suramin has been researched along with Cancer of Prostate in 155 studies
Suramin: A polyanionic compound with an unknown mechanism of action. It is used parenterally in the treatment of African trypanosomiasis and it has been used clinically with diethylcarbamazine to kill the adult Onchocerca. (From AMA Drug Evaluations Annual, 1992, p1643) It has also been shown to have potent antineoplastic properties.
suramin : A member of the class of phenylureas that is urea in which each of the amino groups has been substituted by a 3-({2-methyl-5-[(4,6,8-trisulfo-1-naphthyl)carbamoyl]phenyl}carbamoyl)phenyl group. An activator of both the rabbit skeletal muscle RyR1 and sheep cardiac RyR2 isoform ryanodine receptor channels, it has been used for the treatment of human African trypanosomiasis for over 100 years.
Excerpt | Relevance | Reference |
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"The goal of the current study was to determine the prostate-specific antigen (PSA) and objective response rates and the pharmacokinetics associated with a monthly x 3 one-hour infusion of suramin in 58 patients with hormone-refractory prostate carcinoma." | 9.11 | A Phase II trial of suramin monthly x 3 for hormone-refractory prostate carcinoma. ( Arrieta, R; Cohn, H; Garcia, J; Giannone, L; Karrison, T; Kugler, J; Ratain, MJ; Stadler, WM; Troeger, T; Vogelzang, NJ; Vokes, EE, 2004) |
"Using a fixed higher-dose schedule, the efficacy and toxicity of suramin plus hydrocortisone were assessed in patients with metastatic hormone-refractory prostate carcinoma (HRPC)." | 9.09 | Fixed higher dose schedule of suramin plus hydrocortisone in patients with hormone refractory prostate carcinoma a multicenter Phase II study. ( Beltrán, C; Berián, JM; Brugarolas, A; Calvo, E; Cortés, J; de Irala, J; Martínez-Monge, R; Rebollo, J; Rodríguez, J; Sureda, M, 2001) |
" Absolute hypophosphatemia developed in two patients with more prolonged suramin treatment due to Fanconi's syndrome." | 9.07 | Suramin-induced weakness from hypophosphatemia and mitochondrial myopathy. Association of suramin with mitochondrial toxicity in humans. ( Miles, JM; Rago, RP; Spriggs, DR; Sufit, RL; Wilding, G, 1994) |
"This paper presents a retrospective review of 6 cases of severe neutropenia attributed to suramin, the response to granulocyte-colony stimulating factor (G-CSF) and the possible mechanism." | 7.69 | Suramin-induced neutropenia. ( Dawson, NA; Figg, WD; Headlee, DJ; Lush, RM; Steinberg, SM; Tompkins, AC, 1996) |
"The antiparasitic drug, suramin, has antiproliferative effects in human carcinoma cells." | 7.68 | Disruption of cellular energy balance by suramin in intact human prostatic carcinoma cells, a likely antiproliferative mechanism. ( Cheng, AL; Mitchen, J; Oberley, T; Rago, R; Wilding, G, 1991) |
"Suramin is a polyanionic agent which has been found to be an effective antineoplastic agent against various human tumors including adrenal, renal and prostatic cancer, and osteosarcoma." | 5.29 | Suramin suppresses hypercalcemia and osteoclastic bone resorption in nude mice bearing a human squamous cancer. ( Boyce, BF; Dunstan, C; Mundy, GR; Rhine, C; Williams, P; Yoneda, T, 1995) |
"The goal of the current study was to determine the prostate-specific antigen (PSA) and objective response rates and the pharmacokinetics associated with a monthly x 3 one-hour infusion of suramin in 58 patients with hormone-refractory prostate carcinoma." | 5.11 | A Phase II trial of suramin monthly x 3 for hormone-refractory prostate carcinoma. ( Arrieta, R; Cohn, H; Garcia, J; Giannone, L; Karrison, T; Kugler, J; Ratain, MJ; Stadler, WM; Troeger, T; Vogelzang, NJ; Vokes, EE, 2004) |
"Patients with histologically confirmed advanced hormone-refractory adenocarcinoma of the prostate were randomized to receive suramin at a low dose (n = 129; median age, 69 years), an intermediate dose (n = 129; median age, 71 years), or a high dose (n = 127; median age, 70 years) as part of the Intergroup 0159/Cancer and Leukemia Group B 9480 trial." | 5.11 | Quality of life impact of three different doses of suramin in patients with metastatic hormone-refractory prostate carcinoma: results of Intergroup O159/Cancer and Leukemia Group B 9480. ( Ahles, TA; Herndon, JE; Holland, JC; Kornblith, AB; Marshall, ME; Palchak, D; Petrylak, D; Ratain, MJ; Small, EJ; Stadler, W; Vogelzang, NJ; Wilding, G, 2004) |
"Overall mean reductions in combined pain and opioid analgesic intake were greater for suramin plus HC (rank sum P =." | 5.09 | Suramin therapy for patients with symptomatic hormone-refractory prostate cancer: results of a randomized phase III trial comparing suramin plus hydrocortisone to placebo plus hydrocortisone. ( Chen, L; Eisenberger, M; Lenehan, PF; Marshall, ME; Meyer, M; Meyers, FJ; Natale, RB; Reyno, LM; Slichenmyer, WJ; Small, EJ, 2000) |
"Using a fixed higher-dose schedule, the efficacy and toxicity of suramin plus hydrocortisone were assessed in patients with metastatic hormone-refractory prostate carcinoma (HRPC)." | 5.09 | Fixed higher dose schedule of suramin plus hydrocortisone in patients with hormone refractory prostate carcinoma a multicenter Phase II study. ( Beltrán, C; Berián, JM; Brugarolas, A; Calvo, E; Cortés, J; de Irala, J; Martínez-Monge, R; Rebollo, J; Rodríguez, J; Sureda, M, 2001) |
" Absolute hypophosphatemia developed in two patients with more prolonged suramin treatment due to Fanconi's syndrome." | 5.07 | Suramin-induced weakness from hypophosphatemia and mitochondrial myopathy. Association of suramin with mitochondrial toxicity in humans. ( Miles, JM; Rago, RP; Spriggs, DR; Sufit, RL; Wilding, G, 1994) |
"Suramin has shown promising activity against prostate and breast cancer but is severely neurotoxic." | 5.07 | Suramin for breast and prostate cancer: a pilot study of intermittent short infusions without adaptive control. ( George, N; Howell, A; Margison, J; Ranson, M; Thomson, Y; van der Water, L; Woll, PJ, 1994) |
" As a result, mitoxantrone plus prednisone has been demonstrated to be a useful palliative therapy that provides improvements in pain and quality of life for approximately 40% of those treated." | 4.81 | Treatment of hormone refractory prostate cancer. ( Knox, JJ; Moore, MJ, 2001) |
"This paper presents a retrospective review of 6 cases of severe neutropenia attributed to suramin, the response to granulocyte-colony stimulating factor (G-CSF) and the possible mechanism." | 3.69 | Suramin-induced neutropenia. ( Dawson, NA; Figg, WD; Headlee, DJ; Lush, RM; Steinberg, SM; Tompkins, AC, 1996) |
"The antiparasitic drug, suramin, has antiproliferative effects in human carcinoma cells." | 3.68 | Disruption of cellular energy balance by suramin in intact human prostatic carcinoma cells, a likely antiproliferative mechanism. ( Cheng, AL; Mitchen, J; Oberley, T; Rago, R; Wilding, G, 1991) |
" There was a dose-response relationship between dose and toxicity." | 2.70 | Randomized study of three different doses of suramin administered with a fixed dosing schedule in patients with advanced prostate cancer: results of intergroup 0159, cancer and leukemia group B 9480. ( Halabi, S; Hars, V; Marshall, E; Palchak, D; Petrylak, D; Rago, R; Ratain, MJ; Rosner, G; Small, EJ; Stadler, W; Vogelzang, NJ; Wilding, G, 2002) |
"Suramin was administered on a 78-day fixed dosing schedule (one cycle), and suramin treatment cycles were repeated every 6 months for a total of four cycles." | 2.69 | Androgen deprivation and four courses of fixed-schedule suramin treatment in patients with newly diagnosed metastatic prostate cancer: A Southwest Oncology Group Study. ( Crawford, ED; Eisenberger, MA; Fisher, EI; Hussain, M; O'Connor, J; Petrylak, DP; Small, EJ; Wood, DP, 2000) |
"Suramin was given i." | 2.69 | Phase I study of suramin combined with doxorubicin in the treatment of androgen-independent prostate cancer. ( Amato, RJ; Banks, ME; Bugazia, NA; Logothetis, CJ; Madden, T; Millikan, RE; Newman, RA; Pagliaro, LC; Tu, SM, 1998) |
"Suramin has limited, but significant, efficacy even in chemotherapy- and hormone-refractory prostate cancer, without serious toxicity." | 2.69 | Suramin treatment in hormone- and chemotherapy-refractory prostate cancer. ( Allolio, B; Garcia-Schürmann, JM; Haupt, G; Pastor, J; Schulze, H; Senge, T, 1999) |
"Suramin was administered initially as a 6-day continuous infusion for 10 consecutive weeks and then for 6 days every 28 days for a maximum of 6 months." | 2.69 | Suramin in combination with weekly epirubicin for patients with advanced hormone-refractory prostate carcinoma. ( Allegrini, G; Antonuzzo, A; Conte, P; Danesi, R; Del Tacca, M; Falcone, A; Masi, G; Monica, L; Pfanner, E; Ricci, S, 1999) |
"Management of prostate cancer progression after failure of initial hormonal therapy is controversial." | 2.69 | Phase II study of suramin plus aminoglutethimide in two cohorts of patients with androgen-independent prostate cancer: simultaneous antiandrogen withdrawal and prior antiandrogen withdrawal. ( Bergan, R; Brawley, OW; Cooper, MR; Dawson, N; Figg, WD; Headlee, D; Linehan, WM; Patronas, N; Reed, E; Sartor, O; Sausville, E; Senderowicz, A; Steinberg, SM; Sutherland, M, 1998) |
"Significant neurologic toxicity can result from therapy with suramin, even when dosing is designed to avoid exposure to plasma concentrations greater than 350 micrograms/mL." | 2.68 | Pharmacologic variables associated with the development of neurologic toxicity in patients treated with suramin. ( Bitton, RJ; Bowden, C; Cooper, MR; Dalakas, MC; Figg, WD; Headlee, D; Myers, CE; Reed, E; Venzon, DJ, 1995) |
"Ten patients with hormone-refractory prostate cancer received a fixed dosing scheme of suramin infusion in combination with weekly epidoxorubicin at 25 mg/m2." | 2.68 | Suramin/epidoxorubicin association in hormone-refractory prostate cancer: preliminary results of a pilot phase II study. ( Boccardo, F; Canobbio, L; Esposito, M; Granetto, C; Miglietta, L; Vannozzi, MO, 1997) |
"Patients with stage D2 and poor-prognosis stage D1 prostate cancer were given suramin on a pharmacokinetically derived dosing schedule to maintain suramin concentrations between 175 and 300 micrograms/mL." | 2.68 | Phase II trial of suramin, leuprolide, and flutamide in previously untreated metastatic prostate cancer. ( Bergan, RC; Cooper, MR; Dawson, NA; Figg, WD; Myers, CE; Reed, E; Sartor, O; Sausville, EA; Senderowicz, AM; Steinberg, SM; Tompkins, A; Weinberger, B, 1997) |
"Suramin is an investigational drug that has shown therapeutic activity in hormone-refractory metastatic prostate cancer in Phase I/II trials." | 2.68 | A prospective study of suramin-induced peripheral neuropathy. ( Chaudhry, V; Cornblath, DR; Eisenberger, MA; Griffin, JW; Sheikh, K; Sinibaldi, VJ, 1996) |
"We used population pharmacokinetic-parameter estimates and designed a fixed dosing schedule to maintain plasma suramin concentrations between 100 and 300 micrograms/mL and then evaluated its performance." | 2.68 | Development and validation of a pharmacokinetically based fixed dosing scheme for suramin. ( Egorin, MJ; Eisenberger, MA; Reyno, LM; Sinibaldi, VJ; Sridhara, R; Zuhowski, EG, 1995) |
" We conclude that: (1) serial electrophysiologic monitoring is helpful for early detection of suramin-induced neuropathy; and (2) fixed dosing schedule of suramin without adaptive control does not lead to an increased incidence of demyelinating neuropathy when compared to adaptively controlled dosing schedules." | 2.68 | Evaluation of neuropathy in patients on suramin treatment. ( Arora, R; Dhand, UK; Janisch, L; Kobayashi, K; Martin, B; Petersen, MV; Ratain, MJ; Soliven, B; Vogelzang, NJ; Vokes, EE, 1997) |
" There appeared to be a cumulative dose-response relationship to the development of glucocorticoid insufficiency, with no instances being observed at doses < 4." | 2.68 | Mineralocorticoid insufficiency due to suramin therapy. ( Janisch, L; Kobayashi, K; Ratain, MJ; Vogelzang, NJ; Vokes, EE; Weiss, RE, 1996) |
"Suramin is a newer agent employed in the management of prostate cancer." | 2.68 | Suramin as adjuvant therapy with radical prostatectomy. ( Chou, P; Guinan, P; Ray, V; Rubenstein, M; Saffrin, R; Shaw, M, 1996) |
"Using this dosing schedule, suramin has limited activity against hormone-refractory metastatic prostate cancer." | 2.68 | Suramin in hormone-refractory metastatic prostate cancer: a drug with limited efficacy. ( Belldegrun, A; deKernion, J; Graves, MC; Landaw, EM; McBride, JH; Mendoza, EF; Mondino, B; Rosen, PJ; Turcillo, P, 1996) |
"Suramin was given as intermittent infusions at fixed doses on days 1-5 and thereafter dosing was guided by adaptive control with feedback to maintain plasma suramin concentrations between 300-175 micrograms/ml." | 2.68 | Antitumor activity of suramin in hormone-refractory prostate cancer controlling for hydrocortisone treatment and flutamide withdrawal as potentially confounding variables. ( Bergan, RC; Cooper, MR; Dawson, NA; Figg, WD; Headlee, DJ; Myers, CE; Sartor, O; Sausville, EA; Steinberg, SM; Thibault, A, 1995) |
"Suramin has limited efficacy in patients with androgen-independent prostate cancer who have had disease progression after hydrocortisone." | 2.68 | Prospective evaluation of hydrocortisone and suramin in patients with androgen-independent prostate cancer. ( Curley, T; Dnistrian, A; Kelly, WK; Leibretz, C; Scher, HI; Schwartz, M, 1995) |
"Suramin is a synthetic polysulfonated naphthylurea which has been used for the treatment of African trypanosomiasis and onchocerciasis, but since the mid-1980s has received attention as a possible antiretroviral and antineoplastic agent." | 2.68 | A phase I/II study of continuous infusion suramin in patients with hormone-refractory prostate cancer: toxicity and response. ( Bitton, RJ; Bowden, CJ; Cooper, MR; Dawson, NA; Figg, WD; Headlee, D; Myers, CE; Reed, E; Sartor, O; Weinberger, MS, 1996) |
"This phase I study was designed with the following objectives: (1) to describe the overall and dose-limiting toxicity (DLT) of suramin administered by intermittent short intravenous infusions until DLT or disease progression; (2) to determine the ability of an adaptive control with feedback (ACF) dosing strategy to maintain suramin plasma concentrations within a preselected range; (3) to develop a population model of suramin pharmacokinetics; and (4) to identify preliminary evidence of antitumor activity." | 2.68 | Phase I and clinical evaluation of a pharmacologically guided regimen of suramin in patients with hormone-refractory prostate cancer. ( Eisenberger, MA; Hemady, RK; Jacobs, SC; Jodrell, DI; Lowitt, MH; Reyno, LM; Sinibaldi, VJ; Sridhara, R; Tkaczuk, KH; Zuhowski, EG, 1995) |
"Suramin is a promising agent for the treatment of hormone-refractory metastatic prostate cancer." | 2.68 | Phase I study of suramin given by intermittent infusion without adaptive control in patients with advanced cancer. ( Janish, L; Kobayashi, K; Ratain, MJ; Soliven, B; Vogelzang, NJ; Vokes, EE, 1995) |
"Three cohorts of patients with advanced prostate cancer that progressed despite castrate levels of testosterone received oral hydrocortisone plus suramin administered in the following manners: (1) a loading dose of suramin followed by a continuous infusion using an adaptive control program (cohort A); (2) an intermittent schedule using a simplified adaptive control schedule (cohort B); and (3) an empiric dosing regimen (cohort C)." | 2.68 | Suramin and hydrocortisone: determining drug efficacy in androgen-independent prostate cancer. ( Cohen, L; Curley, T; Dnistrian, A; Kelly, WK; Leibertz, C; Mazumdar, M; Pfister, D; Scher, HI; Schwartz, M; Vlamis, V, 1995) |
"This study aimed to (1) develop a population pharmacokinetic model for suramin; (2) use Bayesian methods to assess suramin pharmacokinetics in individual patients; (3) use individual patients' pharmacokinetic parameter estimates to individualize suramin dose and schedule and maintain plasma suramin concentrations within predetermined target ranges; and (4) assess the feasibility of outpatient administration of suramin by intermittent, short infusions." | 2.67 | Suramin: development of a population pharmacokinetic model and its use with intermittent short infusions to control plasma drug concentration in patients with prostate cancer. ( Egorin, MJ; Eisenberger, MA; Jodrell, DI; Novak, MJ; Reyno, LM; Sinibaldi, VJ; Sridhara, R; Tkaczuk, KH; Zuhowski, EG, 1994) |
"Suramin is known to inhibit the growth of malignant prostate carcinoma cells in vitro." | 2.67 | Suramin: a novel growth factor antagonist with activity in hormone-refractory metastatic prostate cancer. ( Choyke, P; Cooper, M; Dawson, N; LaRocca, R; Myers, C; Stein, C; Steinberg, S; Uhrich, MM; Walther, MM; Weiss, G, 1992) |
"Mitomycin C 12 mg/m2 was given every 5 weeks starting on day 14." | 2.67 | Suramin in combination with mitomycin C in hormone-resistant prostate cancer. A phase II clinical study. ( de Wet, M; Falkson, G; Lotz, BP; Potgieter, HC; Raats, JI; Rapoport, BL, 1993) |
"Hormone refractory prostate cancer remains a challenge." | 2.43 | Clinical trials in metastatic prostate cancer--has there been real progress in the past decade? ( Bhandari, MS; Hussain, M; Petrylak, DP, 2005) |
"Suramin has significantly enhanced the evolution of our knowledge in several areas of prostate cancer biology and treatment." | 2.41 | Suramin's development: what did we learn? ( Dahut, W; Figg, WD; Kaur, M; Reed, E; Sartor, O, 2002) |
"Death from prostate cancer is associated with objective and biochemical progression following hormonal manipulations often described as hormone refractory prostate cancer (HRPCA)." | 2.41 | Current status of cytotoxic chemotherapy in hormone refractory prostate cancer. ( Heidenreich, A; Hofmann, R; von Knobloch, R, 2001) |
"In the United States, prostate cancer is the most commonly diagnosed cancer and the second leading cause of cancer death in men." | 2.40 | Chemotherapy in advanced prostate cancer. ( Beedassy, A; Cardi, G, 1999) |
"Metastatic prostate cancer is a leading cause of cancer-related death in men." | 2.40 | Treatment options in androgen-independent prostate cancer. ( Lara, PN; Meyers, FJ, 1999) |
"Historically, hormone-refractory prostate cancer has not been routinely treated with chemotherapy, based on perceptions that single agents were not all that active, this patient population was too fragile to receive such therapy, responses were virtually impossible to verify given the rarity of bidimensionally measurable disease, and, if seen, responses were not clinically meaningful." | 2.40 | Androgen-independent prostate cancer: not so chemorefractory after all. ( Roth, BJ, 1999) |
"The term "hormone-refractory" prostate cancer has evolved to include patients with a spectrum of diseases." | 2.39 | Hormone-refractory (D3) prostate cancer: refining the concept. ( Kelly, WK; Scher, HI; Steineck, G, 1995) |
"Suramin has been reintroduced in trials of chemohormonal intervention." | 2.39 | [Recent multicenter study protocols in the USA for patients with metastatic prostatic carcinoma]. ( Crawford, ED; DeAntoni, E, 1995) |
"the majority." | 2.39 | Apoptosis: therapeutic significance in the treatment of androgen-dependent and androgen-independent prostate cancer. ( Kyprianou, N, 1994) |
"By 1994, the number of cases of prostate cancer diagnosed will increase by 50% over a 2-year period." | 2.39 | Prostate cancer: how can a common disease be so controversial? ( Kelly, WK; Scher, HI, 1994) |
"The treatment against hormone relapsing prostate cancer was examined clinically, experimentally and by a review of the literature." | 2.39 | [Treatment of advanced prostate cancer]. ( Akino, H; Aoki, Y; Fujita, T; Iwaoka, K; Miwa, Y; Okada, K; Saikawa, S; Suzuki, Y, 1994) |
"In recent years immunotherapy of prostate cancer has developed into an innovative field of investigation." | 2.38 | [Immunotherapy of prostate cancer]. ( Schulze, H; Sommerfeld, HJ, 1993) |
"Previous in vitro studies on prostate cancer cells suggest a role for PAR-2 in prostate cancer metastasis." | 1.33 | The membrane-anchored serine protease, TMPRSS2, activates PAR-2 in prostate cancer cells. ( Greer, B; Hawthorne, S; Hooper, J; Quigley, J; Walker, B; Wilson, S; Zijlstra, A, 2005) |
"A higher dosage of suramin (200 mumol/L) had a cytotoxic effect on PC-3M cells, while lower dosages from 10 to 100 mumol/L produced a predominant inhibiting effect." | 1.32 | [Influence of suramin on the proliferation of prostatic carcinoma cells PC-3M]. ( Feng, W; Lu, GC; Xiao, YJ; Xing, YF; Zeng, FQ; Zhang, QJ, 2003) |
"Suramin has been shown to have an effect on bone resorption in in vitro models." | 1.31 | Suramin administration is associated with a decrease in serum calcium levels. ( Figg, WD; Linehan, WM; Myers, CE; Rehak, NN; Venzon, D; Walther, MM, 2000) |
"Exposure of 1E8 and 2B4 prostate cancer cells to ATP resulted in p38 activation in a concentration- and time-dependent manner." | 1.31 | [Activation of p38 and c-Jun NH2-terminal kinase mitogen-activated protein kinases in human prostate carcinoma cell lines with different metastatic potentials]. ( Fang, W; He, C; Heng, W; Li, H; Wu, B; You, J; Zheng, J, 2001) |
"Hormone-refractory prostate cancer (HRPC) patients often have nonmeasurable disease." | 1.30 | Evaluation of biomarkers of survival response in hormone-refractory prostate cancer patients treated with suramin. ( Egorin, MJ; Eisenberger, MA; Reyno, LM; Sinibaldi, VJ; Sridhara, R, 1998) |
"Micrometastases were identified in bone and liver 1 day after inoculation and grew to form established metastatic foci in all embryos." | 1.30 | A chick embryo model for metastatic human prostate cancer. ( Endo, Y; Imao, T; Kobayashi, T; Koshida, K; Namiki, M; Sasaki, T; Uchibayashi, T, 1998) |
"Suramin is a novel cytostatic/cytotoxic agent that is currently undergoing clinical trials in the treatment of hormone- and chemo-refractory tumors." | 1.30 | Apoptosis and clonogenic cell death in PC3 human prostate cancer cells after treatment with gamma radiation and suramin. ( Bump, EA; Coleman, CN; Palayoor, ST; Teicher, BA, 1997) |
"Suramin has demonstrated modest activity against prostate cancer and is being investigated in clinical trials." | 1.30 | Acute renal failure in a patient receiving treatment with suramin. ( Harbour, D; Liebmann, J; Smith, A, 1997) |
"Human prostate cancer cells (PC-3) were exposed to single doses of ionizing irradiation, and the immediate protein phosphorylation events were temporally correlated with induction of apoptosis." | 1.30 | Transient tyrosine phosphorylation of p34cdc2 is an early event in radiation-induced apoptosis of prostate cancer cells. ( Bains, A; Kyprianou, N; Rhee, JG, 1997) |
"No significant difference in time to disease progression or survival was observed between African Americans (n = 4) and the other 39 patients." | 1.30 | Similar clinical outcomes in African-American and non-African-American males treated with suramin for metastatic prostate cancer. ( Bergan, RC; Dawson, NA; Figg, WD; Headlee, D; Reed, E; Steinberg, SM; Tompkins, A; Walls, RG, 1997) |
"Metastatic prostate cancer is a growing health problem and is the second leading cause of cancer death in men." | 1.30 | Management of progressive metastatic prostate cancer. ( Dawson, NA; Waselenko, JK, 1997) |
"Suramin is an experimental antineoplastic agent which is currently being tested in clinical trials for its utility in treating breast and prostate cancer." | 1.30 | Role of ceramide in suramin-induced cancer cell death. ( Gill, JS; Windebank, AJ, 1997) |
"Suramin is an anthelmintic drug that recently has been shown to have clinical efficacy in the treatment of patients with some advanced malignancies, including prostate carcinoma." | 1.29 | Effect of suramin on the mitogenic response of the human prostate carcinoma cell line PC-3. ( Ewing, MW; Gnarra, JR; Linehan, WM; Liu, SC; Meyers, CE; Walther, MM, 1993) |
"Suramin treatment prior to irradiation inhibited this radiation-induced cell death." | 1.29 | Combined antitumor effect of suramin plus irradiation in human prostate cancer cells: the role of apoptosis. ( Eddy, HA; Jacobs, SC; Kyprianou, N; Sklar, GN, 1993) |
"Suramin has long been used in the treatment of onchocerciasis and trypanosomiasis." | 1.29 | [Cutaneous drug reaction caused by suramin in 4 patients with metastatic prostate cancer]. ( Dieckmann, KP; Gollnick, H; Handke, A; Tebbe, B; Wichterich, K, 1994) |
"His suramin therapy was discontinued, but his serum creatinine level continued to rise to 10." | 1.29 | Acute renal toxicity associated with suramin in the treatment of prostate cancer. ( Bergan, RC; Cooper, MR; Figg, WD; Headlee, D; Humphrey, J; Reed, E; Sartor, O; Thibault, A, 1994) |
"Suramin is an effective antitumor agent in hormone-refractory prostate cancer, but its mechanism(s) of action is not well understood." | 1.29 | Inhibition of fibroblast hyaluronic acid production by suramin. ( August, EM; Cysyk, RL; Duncan, KL; Malinowski, NM, 1993) |
"Suramin has shown antitumour activity in vitro and in vivo." | 1.29 | The synergistic and antagonistic effects of cytotoxic and biological agents on the in vitro antitumour effects of suramin. ( Lopez Lopez, R; Peters, GJ; Pinedo, HM; van Rijswijk, RE; Wagstaff, J, 1994) |
"Dunning-G rat prostate cancer cells transfected with a bcl-2 expression vector demonstrated resistance to apoptosis induced by adriamycin and, to a lesser extent, suramin." | 1.29 | Combination adriamycin and suramin induces apoptosis in bcl-2 expressing prostate carcinoma cells. ( Campbell, ML; Fernandez, A; Marin, MC; McConnell, K; McDonnell, TJ; Tu, SM; von Eschenbach, AC, 1995) |
"Suramin is a polyanionic agent which has been found to be an effective antineoplastic agent against various human tumors including adrenal, renal and prostatic cancer, and osteosarcoma." | 1.29 | Suramin suppresses hypercalcemia and osteoclastic bone resorption in nude mice bearing a human squamous cancer. ( Boyce, BF; Dunstan, C; Mundy, GR; Rhine, C; Williams, P; Yoneda, T, 1995) |
"Upon testing this hypothesis in prostate cancer cell lines, we found that the most conspicuous effect of suramin was to increase the tyrosine phosphorylation of several distinct proteins." | 1.28 | Suramin rapidly alters cellular tyrosine phosphorylation in prostate cancer cell lines. ( Borner, MM; McLellan, CA; Myers, CE; Sartor, O, 1992) |
"have previously reported that prostate cancer cell motility was essential for tumor cell metastasis." | 1.28 | The effects of basic fibroblast growth factor and suramin on cell motility and growth of rat prostate cancer cells. ( Coffey, DS; Isaacs, WB; Pienta, KJ; Vindivich, D, 1991) |
"Suramin is a trypanocidal drug that has generated recent interest as an antineoplastic agent because of its ability to inhibit the binding of growth factors to their cell surface receptors." | 1.28 | Inhibition of prostatic tumor cell proliferation by suramin: alterations in TGF alpha-mediated autocrine growth regulation and cell cycle distribution. ( Kim, JH; Kozlowski, JM; Lee, C; Sherwood, ER; Sutkowski, DM, 1991) |
" The same dosing regimen found to be ineffective in blocking the restoration of the involuted prostate of castrated rats resulted in a significant reduction in the growth rate of AT-2 tumors." | 1.28 | Differential effects of growth factor antagonists on neoplastic and normal prostatic cells. ( Isaacs, JT; Isaacs, WB; Morton, RA, 1990) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (0.65) | 18.7374 |
1990's | 124 (80.00) | 18.2507 |
2000's | 28 (18.06) | 29.6817 |
2010's | 1 (0.65) | 24.3611 |
2020's | 1 (0.65) | 2.80 |
Authors | Studies |
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Wang, Y | 1 |
Ma, S | 1 |
Ruzzo, WL | 1 |
Atkinson, TM | 1 |
Halabi, S | 4 |
Bennett, AV | 1 |
Rogak, L | 1 |
Sit, L | 1 |
Li, Y | 1 |
Kaplan, E | 1 |
Basch, E | 1 |
Sauer, H | 2 |
Stanelle, R | 1 |
Hescheler, J | 2 |
Wartenberg, M | 2 |
Small, EJ | 7 |
Ratain, MJ | 6 |
Rosner, G | 1 |
Stadler, W | 2 |
Palchak, D | 2 |
Marshall, E | 1 |
Rago, R | 4 |
Hars, V | 1 |
Wilding, G | 7 |
Petrylak, D | 2 |
Vogelzang, NJ | 8 |
Autorino, R | 1 |
Di Lorenzo, G | 1 |
Damiano, R | 1 |
De Placido, S | 1 |
D'Armiento, M | 1 |
Xing, YF | 1 |
Lu, GC | 1 |
Xiao, YJ | 1 |
Zeng, FQ | 1 |
Zhang, QJ | 1 |
Feng, W | 1 |
Karrison, T | 1 |
Stadler, WM | 1 |
Garcia, J | 1 |
Cohn, H | 1 |
Kugler, J | 1 |
Troeger, T | 1 |
Giannone, L | 1 |
Arrieta, R | 1 |
Vokes, EE | 4 |
Cao, LY | 1 |
Huang, H | 1 |
Ni, JH | 1 |
Ahles, TA | 1 |
Herndon, JE | 1 |
Kornblith, AB | 1 |
Marshall, ME | 2 |
Holland, JC | 1 |
Wilson, S | 1 |
Greer, B | 1 |
Hooper, J | 1 |
Zijlstra, A | 1 |
Walker, B | 1 |
Quigley, J | 1 |
Hawthorne, S | 1 |
Zhao, L | 1 |
Wientjes, MG | 5 |
Au, JL | 5 |
Bhandari, MS | 1 |
Petrylak, DP | 4 |
Hussain, M | 2 |
DeAntoni, E | 1 |
Crawford, ED | 2 |
Tatoud, R | 1 |
Desgrandchamps, F | 1 |
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Peehl, DM | 2 |
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Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A PHASE III STUDY OF THREE DIFFERENT DOSES OF SURAMIN (NSC #34936) ADMINISTERED WITH A FIXED DOSING SCHEDULE IN PATIENTS WITH ADVANCED PROSTATE CANCER[NCT00002723] | Phase 3 | 390 participants (Actual) | Interventional | 1996-01-31 | Completed | ||
Phase II Trial of Phenylbutyrate Given as a Continuous Infusion in Pediatric Patients With Progressive or Recurrent CNS Malignancy[NCT00006450] | Phase 2 | 120 participants | Interventional | 2000-11-30 | Completed | ||
Phase I and Pharmacokinetic Trial of Phenylbutyrate Given as a Continuous Infusion in Pediatric Patients With Refractory Malignancy[NCT00001565] | Phase 1 | 35 participants | Interventional | 1996-12-31 | Completed | ||
A Phase II Study of AZD2171 in Metastatic Androgen Independent Prostate Cancer[NCT00436956] | Phase 2 | 59 participants (Actual) | Interventional | 2006-10-16 | Completed | ||
A Phase II Study of Oral Calcitriol in Combination With Ketoconazole in Castration Resistant Prostate Cancer, Progressing Despite Primary ADT and Abiraterone[NCT03261336] | Phase 2 | 1 participants (Actual) | Interventional | 2017-01-06 | Terminated (stopped due to can not meet enrollment) | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Time from treatment start date until date of death or date last known alive. (NCT00436956)
Timeframe: 44 months
Intervention | Months (Median) |
---|---|
20 mg AZD2171 Daily | 11.7 |
20 mg AZD2171 + 10mg Prednisone Daily | 9.9 |
Time interval from start of treatment to documented evidence of disease progression. (NCT00436956)
Timeframe: up to 14.9 months based on a Kaplan-Meier analysis.
Intervention | Months (Median) |
---|---|
20 mg AZD2171 Daily | 3.6 |
20 mg AZD2171 + 10mg Prednisone Daily | 3.7 |
Here is the number of participants with adverse events. For a detailed list of adverse events, see the adverse event module. (NCT00436956)
Timeframe: Date treatment consent signed to date off study, approximately 61.5 months
Intervention | Participants (Count of Participants) |
---|---|
All Participants- AZD2171 & Prednisone | 59 |
PFS is the proportion of subjects who progress or die by 6 months after the start of the combined therapy. PFS is determined by prostatic specific antigen (PSA) consensus criteria and the Response Evaluation Criteria in Solid Tumors (RECIST). PSA consensus criteria is defined as PSA decline of >/= 50% or PSA progression. RECIST is defined as the following: Complete response (CR) is disappearance of all target lesions; partial response (PR) is at least a 30% decline in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD; and stable disease is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease ((PD) at least a 20% increase in the sum of the LD of target lesions, or the appearance of one or more lesions), taking as reference the smallest sum LD since the treatment started. Data is estimated and the probability of PFS as a function of time was determined using the Kaplan-Meier method. (NCT00436956)
Timeframe: 6 months
Intervention | percent probability (Number) |
---|---|
All Participants - AZD2171 & Prednisone | 43.9 |
Here is the number of Grade 2 (moderate) toxicities. (NCT00436956)
Timeframe: 61.5 months
Intervention | toxicities (Number) | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hypertension | Fatigue | Anorexia | Weight loss | Hypothyroidism | Dehydration | Prolonged QTc | Nausea | Diarrhea | Hypoalbuminemia | Proteinuria | Elevated alkaline phosphatase | Aspartate transaminase | Vomiting | Hyperbilirubinemia | Muscle weakness | |
20 mg AZD2171 + 10mg Prednisone Daily | 8 | 4 | 6 | 4 | 6 | 2 | 2 | 3 | 0 | 3 | 3 | 2 | 3 | 2 | 1 | 1 |
20 mg AZD2171 Daily | 17 | 15 | 12 | 11 | 7 | 8 | 8 | 7 | 8 | 5 | 5 | 4 | 3 | 4 | 4 | 2 |
Here is the number of Grade 3 (severe) toxicities. (NCT00436956)
Timeframe: 61.5 months
Intervention | toxicities (Number) | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Hypertension | Fatigue | Anorexia | Weight loss | Hypothyroidism | Dehydration | Prolonged QTc | Nausea | Diarrhea | Hypoalbuminemia | Proteinuria | Elevated alkaline phosphatase | Aspartate transaminase | Vomiting | Hyperbilirubinemia | Muscle weakness | |
20 mg AZD2171 + 10mg Prednisone Daily | 0 | 2 | 1 | 0 | 0 | 3 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
20 mg AZD2171 Daily | 0 | 4 | 1 | 2 | 0 | 3 | 1 | 1 | 0 | 0 | 0 | 5 | 2 | 1 | 1 | 3 |
Response was evaluated by the RECIST. Complete response (CR) is disappearance of all target lesions. Partial response (PR) is at least a 30% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD. Progressive disease (PD)is at least a 20% increase in the sum of the LD of target lesions, taking as reference the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions. Stable disease (SD) is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum LD since the treatment started. (NCT00436956)
Timeframe: Every 2 cycles (approximately 56 days)
Intervention | Participants (Count of Participants) | |||
---|---|---|---|---|
Complete Response | Confirmed Partial Response | Unconfirmed Partial Response | Not Evaluable | |
All Participants - AZD2171 & Prednisone | 0 | 6 | 1 | 1 |
Descriptive analysis of observed toxicity and patient reports of tolerating experimental treatment (NCT03261336)
Timeframe: 2 years
Intervention | Participants (Count of Participants) |
---|---|
Calcitriol, Ketoconazole, Hydrocortisone | 1 |
33 reviews available for suramin and Cancer of Prostate
Article | Year |
---|---|
Role of chemotherapy in hormone-refractory prostate cancer. Old issues, recent advances and new perspectives.
Topics: Aged; Anthracyclines; Antineoplastic Agents; Antineoplastic Agents, Hormonal; Biopsy, Needle; Bridge | 2003 |
[Progress in researches on drugs for prostate cancer].
Topics: Androgen Antagonists; Antineoplastic Agents; Goserelin; Humans; Male; Prostatic Neoplasms; Sulfonami | 2003 |
Clinical trials in metastatic prostate cancer--has there been real progress in the past decade?
Topics: Angiogenesis Inhibitors; Antineoplastic Agents; Antineoplastic Agents, Phytogenic; Clinical Trials a | 2005 |
[Recent multicenter study protocols in the USA for patients with metastatic prostatic carcinoma].
Topics: Antineoplastic Agents, Hormonal; Combined Modality Therapy; Flutamide; Humans; Leuprolide; Male; Mul | 1995 |
[Peptide growth factors in the prostate].
Topics: Adenocarcinoma; Epidermal Growth Factor; Fibroblast Growth Factors; Humans; Interleukin-6; Male; Ner | 1993 |
New agents in the therapy of hormone-refractory patients with prostate cancer.
Topics: Antineoplastic Combined Chemotherapy Protocols; Bone Neoplasms; Humans; Male; Mitoxantrone; Prostate | 1995 |
Hormone-refractory (D3) prostate cancer: refining the concept.
Topics: Aminoglutethimide; Clinical Trials as Topic; Cortisone; Dexamethasone; Drug Therapy, Combination; Hu | 1995 |
New treatment strategies for hormone refractory prostate cancer.
Topics: Estramustine; Etoposide; Humans; Male; Prostatic Neoplasms; Suramin; Vinblastine | 1995 |
Apoptosis: therapeutic significance in the treatment of androgen-dependent and androgen-independent prostate cancer.
Topics: Androgens; Animals; Antineoplastic Agents; Apoptosis; Combined Modality Therapy; Humans; Male; Prost | 1994 |
[Treatment of advanced prostate cancer].
Topics: Animals; Antineoplastic Agents; Combined Modality Therapy; Diphosphonates; Humans; Male; Mice; Mice, | 1994 |
Suramin.
Topics: Drug Administration Schedule; Drug Monitoring; Humans; Male; Neoplasms; Prostatic Neoplasms; Suramin | 1994 |
Prostate cancer: how can a common disease be so controversial?
Topics: Cell Differentiation; Humans; Male; Neoplasm Staging; Oncogenes; Prostatectomy; Prostatic Neoplasms; | 1994 |
[Immunotherapy of prostate cancer].
Topics: Antibodies, Monoclonal; Coumarins; Humans; Immunotherapy; Immunotherapy, Active; Immunotherapy, Adop | 1993 |
The treatment of hormone refractory prostate cancer.
Topics: Androgen Antagonists; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Estramu | 1996 |
Other chemotherapy regimens including mitoxantrone and suramin.
Topics: Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Clinical Trials as Topic; Cyc | 1997 |
Novel therapies for advanced prostate cancer.
Topics: Animals; Antineoplastic Agents; Bombesin; Diet; Enzyme Inhibitors; Epoprostenol; Genetic Therapy; Hu | 1997 |
Therapy for hormone-resistant prostate cancer: no longer a myth.
Topics: Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protocols; Drug Resistance, Ne | 1996 |
Treatment options in androgen-independent prostate cancer.
Topics: Adenocarcinoma; Androgen Antagonists; Androgens; Antibodies, Monoclonal; Antineoplastic Agents; Anti | 1999 |
Serologic tumor markers, clinical biology, and therapy of prostatic carcinoma.
Topics: Androgen Antagonists; Antineoplastic Agents; Cyclohexanes; Humans; Male; O-(Chloroacetylcarbamoyl)fu | 1999 |
Chemotherapy for hormone refractory prostate cancer.
Topics: Anthracyclines; Antineoplastic Combined Chemotherapy Protocols; Camptothecin; Cyclophosphamide; Estr | 1999 |
Differentiating agents and nontoxic therapies.
Topics: Antineoplastic Agents; Cell Transformation, Neoplastic; Fatty Acids; Humans; Male; Phenylacetates; P | 1999 |
Chemotherapy in advanced prostate cancer.
Topics: Antineoplastic Agents; Antineoplastic Agents, Alkylating; Antineoplastic Agents, Hormonal; Clinical | 1999 |
Androgen-independent prostate cancer: not so chemorefractory after all.
Topics: Antineoplastic Combined Chemotherapy Protocols; Estramustine; Humans; Male; Mitoxantrone; Prostatic | 1999 |
Current status of cytotoxic chemotherapy in hormone refractory prostate cancer.
Topics: Anthracyclines; Antineoplastic Agents; Estramustine; Humans; Male; Prognosis; Prostatic Neoplasms; R | 2001 |
Treatment of hormone refractory prostate cancer.
Topics: Adenocarcinoma; Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protocols; Est | 2001 |
Controversies in chemotherapy of prostate cancer.
Topics: Adenocarcinoma; Adrenal Cortex Hormones; Androgen Antagonists; Antigens, Neoplasm; Antineoplastic Ag | 2002 |
Suramin's development: what did we learn?
Topics: Antineoplastic Agents; Clinical Trials as Topic; Half-Life; Humans; Male; Metabolic Clearance Rate; | 2002 |
Hormone refractory prostatic cancer: the role of radiolabelled diphosphonates and growth factor inhibitors.
Topics: Animals; Bone Neoplasms; Dogs; Drug Screening Assays, Antitumor; Etidronic Acid; Growth Substances; | 1992 |
Suramin as an archetypical compound in the development of growth factor antagonists for inhibition of genitourinary tumors.
Topics: Growth Inhibitors; Humans; Male; Prostatic Neoplasms; Suramin; Tumor Cells, Cultured; Urogenital Neo | 1992 |
Therapeutic alternatives for hormone-refractory prostatic cancer.
Topics: Antigens, Neoplasm; Biomarkers, Tumor; Bone Neoplasms; Combined Modality Therapy; Humans; Immunother | 1992 |
Cell motility as a chemotherapeutic target.
Topics: Animals; Antibodies; Antineoplastic Agents, Phytogenic; Cell Division; Cell Movement; Cytoskeleton; | 1991 |
[New substances in therapy of advanced prostate cancer].
Topics: Androgen Antagonists; Humans; Imidazoles; Immunologic Factors; Male; Neoplasm Staging; Palliative Ca | 1991 |
Use of suramin in treatment of prostatic carcinoma refractory to conventional hormonal manipulation.
Topics: Adrenal Cortex; Animals; Enzymes; Growth Substances; Humans; Male; Prostatic Neoplasms; Suramin; Tum | 1991 |
39 trials available for suramin and Cancer of Prostate
Article | Year |
---|---|
Measurement of affective and activity pain interference using the Brief Pain Inventory (BPI): Cancer and Leukemia Group B 70903.
Topics: Adenocarcinoma; Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Factor Analysis, Statistical; | 2012 |
Randomized study of three different doses of suramin administered with a fixed dosing schedule in patients with advanced prostate cancer: results of intergroup 0159, cancer and leukemia group B 9480.
Topics: Aged; Antineoplastic Agents; Disease-Free Survival; Dose-Response Relationship, Drug; Humans; Male; | 2002 |
A Phase II trial of suramin monthly x 3 for hormone-refractory prostate carcinoma.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Antineoplastic Agents, Hormonal; Carcinoma; D | 2004 |
Quality of life impact of three different doses of suramin in patients with metastatic hormone-refractory prostate carcinoma: results of Intergroup O159/Cancer and Leukemia Group B 9480.
Topics: Adenocarcinoma; Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Antineoplastic Agents, Hormon | 2004 |
Prospective evaluation of hydrocortisone and suramin in patients with androgen-independent prostate cancer.
Topics: Aged; Drug Administration Schedule; Drug Therapy, Combination; Humans; Hydrocortisone; Infusions, In | 1995 |
UK studies on suramin therapy in hormone resistant prostate cancer.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Drug Resistance; Flutamide; Humans; Male; Midd | 1995 |
Phase I and clinical evaluation of a pharmacologically guided regimen of suramin in patients with hormone-refractory prostate cancer.
Topics: Adaptation, Physiological; Aged; Anorexia; Bayes Theorem; Cohort Studies; Drug Monitoring; Drug Resi | 1995 |
Development and validation of a pharmacokinetically based fixed dosing scheme for suramin.
Topics: Adult; Aged; Aged, 80 and over; Disease-Free Survival; Drug Administration Schedule; Drug Monitoring | 1995 |
Phase I study of suramin given by intermittent infusion without adaptive control in patients with advanced cancer.
Topics: Adaptation, Physiological; Adult; Aged; Cohort Studies; Drug Administration Schedule; Drug Monitorin | 1995 |
Suramin and hydrocortisone: determining drug efficacy in androgen-independent prostate cancer.
Topics: Adaptation, Physiological; Aged; Aged, 80 and over; Anemia; Cohort Studies; Drug Administration Sche | 1995 |
Pharmacologic variables associated with the development of neurologic toxicity in patients treated with suramin.
Topics: Adult; Aged; Aged, 80 and over; Humans; Logistic Models; Male; Melanoma; Middle Aged; Motor Neuron D | 1995 |
Antigrowth factor strategies.
Topics: Apoptosis; Cell Division; Extracellular Matrix; Growth Inhibitors; Growth Substances; Humans; Male; | 1993 |
Suramin for breast and prostate cancer: a pilot study of intermittent short infusions without adaptive control.
Topics: Adult; Aged; Ambulatory Care; Breast Neoplasms; Drug Administration Schedule; Feasibility Studies; F | 1994 |
Suramin-induced weakness from hypophosphatemia and mitochondrial myopathy. Association of suramin with mitochondrial toxicity in humans.
Topics: Electron Transport Complex IV; Fanconi Syndrome; Humans; Hypophosphatemia; Male; Mitochondria, Muscl | 1994 |
Suramin: development of a population pharmacokinetic model and its use with intermittent short infusions to control plasma drug concentration in patients with prostate cancer.
Topics: Adult; Aged; Antineoplastic Agents; Bayes Theorem; Drug Administration Schedule; Feasibility Studies | 1994 |
Suramin in combination with mitomycin C in hormone-resistant prostate cancer. A phase II clinical study.
Topics: Antineoplastic Combined Chemotherapy Protocols; Drug Resistance; Humans; Male; Mitomycin; Prostatic | 1993 |
Suramin, an active drug for prostate cancer: interim observations in a phase I trial.
Topics: Aged; Antineoplastic Agents; Drug Administration Schedule; Humans; Infusions, Intravenous; Male; Mid | 1993 |
Severe thrombocytopenia in patients treated with suramin: evidence for an immune mechanism in one.
Topics: Antineoplastic Agents; Humans; Immunoglobulin G; Male; Middle Aged; Neoplasm Metastasis; Platelet Ag | 1996 |
Suramin as adjuvant therapy with radical prostatectomy.
Topics: Animals; Antineoplastic Agents; Antineoplastic Agents, Alkylating; Chemotherapy, Adjuvant; Cyclophos | 1996 |
Suramin in hormone-refractory metastatic prostate cancer: a drug with limited efficacy.
Topics: Adenocarcinoma; Aged; Aged, 80 and over; Ambulatory Care; Half-Life; Humans; Male; Middle Aged; Neop | 1996 |
Antitumor activity of suramin in hormone-refractory prostate cancer controlling for hydrocortisone treatment and flutamide withdrawal as potentially confounding variables.
Topics: Aged; Antineoplastic Agents; Flutamide; Humans; Hydrocortisone; Male; Middle Aged; Prospective Studi | 1995 |
Mineralocorticoid insufficiency due to suramin therapy.
Topics: Addison Disease; Adrenal Cortex Diseases; Adrenocorticotropic Hormone; Aged; Aldosterone; Antineopla | 1996 |
A phase I/II study of continuous infusion suramin in patients with hormone-refractory prostate cancer: toxicity and response.
Topics: Aged; Aged, 80 and over; Antineoplastic Agents; Antineoplastic Agents, Hormonal; Dose-Response Relat | 1996 |
Evaluation of neuropathy in patients on suramin treatment.
Topics: Adult; Aged; Aged, 80 and over; Demyelinating Diseases; Female; Humans; Male; Middle Aged; Motor Neu | 1997 |
A prospective study of suramin-induced peripheral neuropathy.
Topics: Aged; Antineoplastic Agents; Axons; Clinical Trials as Topic; Humans; Male; Middle Aged; Neural Cond | 1996 |
Phase II trial of suramin, leuprolide, and flutamide in previously untreated metastatic prostate cancer.
Topics: Adult; Aged; Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protocols; Diseas | 1997 |
Suramin/epidoxorubicin association in hormone-refractory prostate cancer: preliminary results of a pilot phase II study.
Topics: Adenocarcinoma; Antineoplastic Combined Chemotherapy Protocols; Epirubicin; Humans; Male; Pilot Proj | 1997 |
Phase II study of suramin plus aminoglutethimide in two cohorts of patients with androgen-independent prostate cancer: simultaneous antiandrogen withdrawal and prior antiandrogen withdrawal.
Topics: Adult; Aged; Aged, 80 and over; Aminoglutethimide; Androgen Antagonists; Antineoplastic Combined Che | 1998 |
Phase I study of suramin combined with doxorubicin in the treatment of androgen-independent prostate cancer.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Digestive System; Do | 1998 |
Suramin treatment in hormone- and chemotherapy-refractory prostate cancer.
Topics: Aged; Analgesia; Antineoplastic Agents; Humans; Male; Middle Aged; Pain; Prostatic Neoplasms; Surami | 1999 |
Suramin in combination with weekly epirubicin for patients with advanced hormone-refractory prostate carcinoma.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Area Under Curve; Bayes The | 1999 |
Androgen deprivation and four courses of fixed-schedule suramin treatment in patients with newly diagnosed metastatic prostate cancer: A Southwest Oncology Group Study.
Topics: Adult; Aged; Androgens; Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protoc | 2000 |
Suramin therapy for patients with symptomatic hormone-refractory prostate cancer: results of a randomized phase III trial comparing suramin plus hydrocortisone to placebo plus hydrocortisone.
Topics: Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Dise | 2000 |
Serum prostate-specific antigen decline as a marker of clinical outcome in hormone-refractory prostate cancer patients: association with progression-free survival, pain end points, and survival.
Topics: Adenocarcinoma; Adult; Aged; Anti-Inflammatory Agents; Antineoplastic Agents; Biomarkers, Tumor; Dis | 2001 |
Phase 1 drug interaction study of suramin and warfarin in patients with prostate cancer.
Topics: Anti-Inflammatory Agents; Anticoagulants; Antineoplastic Agents; Blood Coagulation; Drug Interaction | 2001 |
Prognostic significance of reverse transcriptase polymerase chain reaction for prostate-specific antigen in men with hormone-refractory prostate cancer.
Topics: Adenocarcinoma; Aged; Antineoplastic Agents; Biomarkers, Tumor; Drug Resistance, Neoplasm; Humans; M | 2001 |
Fixed higher dose schedule of suramin plus hydrocortisone in patients with hormone refractory prostate carcinoma a multicenter Phase II study.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Carcinoma; Disease Progress | 2001 |
Hormone refractory prostatic cancer: the role of radiolabelled diphosphonates and growth factor inhibitors.
Topics: Animals; Bone Neoplasms; Dogs; Drug Screening Assays, Antitumor; Etidronic Acid; Growth Substances; | 1992 |
Suramin: a novel growth factor antagonist with activity in hormone-refractory metastatic prostate cancer.
Topics: Aged; Aged, 80 and over; Antigens, Neoplasm; Biomarkers, Tumor; Bone Neoplasms; Growth Inhibitors; H | 1992 |
84 other studies available for suramin and Cancer of Prostate
Article | Year |
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Spatial modeling of prostate cancer metabolic gene expression reveals extensive heterogeneity and selective vulnerabilities.
Topics: Arachidonic Acid; Cysteine; Databases, Factual; Humans; Male; Metabolic Networks and Pathways; Organ | 2020 |
The DC electrical-field-induced Ca(2+) response and growth stimulation of multicellular tumor spheroids are mediated by ATP release and purinergic receptor stimulation.
Topics: Adenosine Triphosphate; Animals; Antineoplastic Agents; Apyrase; Calcium; Calcium Signaling; Cell Di | 2002 |
[Influence of suramin on the proliferation of prostatic carcinoma cells PC-3M].
Topics: Animals; Antineoplastic Agents; Apoptosis; Cattle; Cell Cycle; Cell Line, Tumor; Cell Proliferation; | 2003 |
The membrane-anchored serine protease, TMPRSS2, activates PAR-2 in prostate cancer cells.
Topics: Boron Compounds; Calcium; Catalysis; Cell Line, Tumor; Humans; Male; Prostatic Neoplasms; Receptor, | 2005 |
Evaluation of combination chemotherapy: integration of nonlinear regression, curve shift, isobologram, and combination index analyses.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Doxorubicin; Drug Interactions; Inhibitory | 2004 |
Keratin expression: a measure of phenotypic modulation of human prostatic epithelial cells by growth inhibitory factors.
Topics: Cell Division; Cells, Cultured; Epithelial Cells; Epithelium; Glucose; Growth Substances; Humans; In | 1994 |
Combination adriamycin and suramin induces apoptosis in bcl-2 expressing prostate carcinoma cells.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Doxorubicin; Drug Resistance; Dr | 1995 |
American studies on suramin therapy in hormone resistant prostate cancer.
Topics: Drug Resistance; Flutamide; Humans; Male; Prostatic Neoplasms; Suramin | 1995 |
Suramin and prostate cancer: where do we go from here?
Topics: Drug Monitoring; Humans; Male; Prostatic Neoplasms; Suramin; Survival Rate | 1995 |
Reversal by transferrin of growth-inhibitory effect of suramin on hormone-refractory human prostate cancer cells.
Topics: Androgens; Apoproteins; Humans; Male; Prostatic Neoplasms; Receptors, Transferrin; RNA, Messenger; S | 1995 |
Effects of suramin on the proliferation of primary epithelial cell cultures derived from normal, benign hyperplastic and cancerous human prostates.
Topics: Cell Adhesion; Cell Division; Cell Survival; Cells, Cultured; Dose-Response Relationship, Drug; Epit | 1993 |
Workshop on suramin with emphasis on prostate cancer: re-evaluation of response criteria.
Topics: Bone Neoplasms; Humans; Male; Prognosis; Prostate-Specific Antigen; Prostatic Neoplasms; Suramin | 1993 |
Clinical trials referral resource. Prostate cancer II.
Topics: Clinical Trials, Phase III as Topic; Drug Administration Schedule; Humans; Male; Prostatic Neoplasms | 1995 |
Suramin suppresses hypercalcemia and osteoclastic bone resorption in nude mice bearing a human squamous cancer.
Topics: Adenocarcinoma; Animals; Bone and Bones; Bone Resorption; Calcium; Carcinoma, Squamous Cell; Cell Di | 1995 |
Re: Reversal by transferrin of growth-inhibitory effect of suramin on hormone-refractory human prostate cancer cells.
Topics: Cell Division; Humans; In Vitro Techniques; Male; Prostatic Neoplasms; Suramin; Transferrin; Tumor C | 1995 |
Erythema multiforme induced by suramin.
Topics: Aged; Drug Eruptions; Erythema Multiforme; Humans; Injections, Intravenous; Male; Prostatic Neoplasm | 1995 |
The synergistic and antagonistic effects of cytotoxic and biological agents on the in vitro antitumour effects of suramin.
Topics: Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Breast Neoplasms; Cell Divisi | 1994 |
In vitro sequence-dependent synergistic effect of suramin and camptothecin.
Topics: Camptothecin; Cell Cycle; Cell Division; DNA Topoisomerases, Type I; Dose-Response Relationship, Dru | 1994 |
Effects of suramin on expression of proliferation associated nuclear antigens in DU-145 prostate carcinoma cells.
Topics: Antigens, Neoplasm; Cell Cycle; Cell Division; Cell Line; Cyclins; DNA, Neoplasm; Dose-Response Rela | 1994 |
Adaptive control with feedback of suramin using intermittent infusions.
Topics: Drug Administration Schedule; Humans; Infusions, Intravenous; Male; Prostatic Neoplasms; Suramin | 1994 |
Inhibition of fibroblast hyaluronic acid production by suramin.
Topics: 3T3 Cells; Animals; Cell Division; Culture Media; DNA; Dose-Response Relationship, Drug; Fibroblasts | 1993 |
Acute renal toxicity associated with suramin in the treatment of prostate cancer.
Topics: Acute Kidney Injury; Antineoplastic Combined Chemotherapy Protocols; Carcinoma; Combined Modality Th | 1994 |
The effects of coumarin and suramin on the growth of malignant renal and prostatic cell lines.
Topics: Carcinoma, Renal Cell; Cell Division; Coumarins; Humans; Kidney Neoplasms; Male; Prostatic Neoplasms | 1994 |
[Cutaneous drug reaction caused by suramin in 4 patients with metastatic prostate cancer].
Topics: Aged; Biopsy; Drug Eruptions; Drug Therapy, Combination; Humans; Infusions, Intravenous; Male; Middl | 1994 |
Suramin decreases circulating levels of insulin-like growth factor-I.
Topics: Analysis of Variance; Humans; Insulin-Like Growth Factor I; Male; Prospective Studies; Prostatic Neo | 1994 |
[Potentiation of cytotoxicity of electromagnetic shock waves by suramin, "in vitro" study].
Topics: Adenocarcinoma; Cell Division; Combined Modality Therapy; Dose-Response Relationship, Radiation; Hum | 1994 |
[The enhancement of the chemotherapeutic effects on human prostate cancer cell--the combination with the growth factor interaction inhibitor (suramin)].
Topics: Animals; Antineoplastic Agents; Cell Division; Cisplatin; Drug Interactions; Drug Synergism; Humans; | 1993 |
Suramin inhibits DNA damage in human prostate cancer cells treated with topoisomerase inhibitors in vitro.
Topics: Amsacrine; Camptothecin; Cell Survival; Chemical Precipitation; DNA Damage; Dose-Response Relationsh | 1993 |
Combined antitumor effect of suramin plus irradiation in human prostate cancer cells: the role of apoptosis.
Topics: Apoptosis; Clusterin; Combined Modality Therapy; DNA, Neoplasm; Dose-Response Relationship, Drug; Do | 1993 |
Effect of suramin on the mitogenic response of the human prostate carcinoma cell line PC-3.
Topics: Blotting, Northern; Cell Cycle; Cell Division; Culture Media, Serum-Free; Dose-Response Relationship | 1993 |
Suramin: here to stay!?
Topics: Antineoplastic Agents; Drug Administration Schedule; Humans; Male; Prostatic Neoplasms; Suramin | 1993 |
Selective growth arrest and phenotypic reversion of prostate cancer cells in vitro by nontoxic pharmacological concentrations of phenylacetate.
Topics: Animals; Cell Division; Cell Survival; DNA Replication; Female; Glutamine; HLA-A3 Antigen; Humans; M | 1993 |
Selective growth arrest and phenotypic reversion of prostate cancer cells in vitro by nontoxic pharmacological concentrations of phenylacetate.
Topics: Animals; Cell Division; Cell Survival; DNA Replication; Female; Glutamine; HLA-A3 Antigen; Humans; M | 1993 |
Selective growth arrest and phenotypic reversion of prostate cancer cells in vitro by nontoxic pharmacological concentrations of phenylacetate.
Topics: Animals; Cell Division; Cell Survival; DNA Replication; Female; Glutamine; HLA-A3 Antigen; Humans; M | 1993 |
Selective growth arrest and phenotypic reversion of prostate cancer cells in vitro by nontoxic pharmacological concentrations of phenylacetate.
Topics: Animals; Cell Division; Cell Survival; DNA Replication; Female; Glutamine; HLA-A3 Antigen; Humans; M | 1993 |
Evaluation of prostate-specific antigen as a surrogate marker for response of hormone-refractory prostate cancer to suramin therapy.
Topics: Adult; Aged; Analysis of Variance; Antineoplastic Agents; Antineoplastic Agents, Hormonal; Biomarker | 1995 |
Ocular symptoms and signs associated with suramin sodium treatment for metastatic cancer of the prostate.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Corneal Diseases; Eye Diseases; Humans; Infus | 1996 |
How much can we rely on the level of prostate-specific antigen as an end point for evaluation of clinical trials? A word of caution!
Topics: Antineoplastic Agents; Biomarkers, Tumor; Clinical Trials as Topic; Humans; Male; Predictive Value o | 1996 |
Suramin-induced decrease in prostate-specific antigen expression with no effect on tumor growth in the LNCaP model of human prostate cancer.
Topics: Analysis of Variance; Androgens; Animals; Antineoplastic Agents; Blotting, Northern; Castration; Gen | 1996 |
New molecules and treatment modulation in advanced prostatic cancer.
Topics: Androgen Antagonists; Anilides; Antineoplastic Agents; Antineoplastic Agents, Hormonal; Flutamide; H | 1996 |
Suramin-induced neutropenia.
Topics: Adult; Aged; Antineoplastic Agents; Bayes Theorem; Fibroblast Growth Factor 2; Granulocyte Colony-St | 1996 |
Induction of apoptosis in malignant and camptothecin-resistant human cells.
Topics: Androgens; Antineoplastic Agents; Apoptosis; bcl-2-Associated X Protein; Camptothecin; Cell Cycle; C | 1996 |
Apoptosis and clonogenic cell death in PC3 human prostate cancer cells after treatment with gamma radiation and suramin.
Topics: Antineoplastic Agents; Apoptosis; Cell Cycle; Cell Survival; Combined Modality Therapy; DNA Fragment | 1997 |
Acute renal failure in a patient receiving treatment with suramin.
Topics: Acute Kidney Injury; Adenocarcinoma; Androgen Antagonists; Anti-Inflammatory Agents; Antineoplastic | 1997 |
Transient tyrosine phosphorylation of p34cdc2 is an early event in radiation-induced apoptosis of prostate cancer cells.
Topics: Apoptosis; CDC2 Protein Kinase; Cell Survival; DNA Fragmentation; DNA, Neoplasm; Dose-Response Relat | 1997 |
Similar clinical outcomes in African-American and non-African-American males treated with suramin for metastatic prostate cancer.
Topics: Aged; Aged, 80 and over; Antineoplastic Agents; Black People; Disease Progression; Humans; Male; Mid | 1997 |
Management of progressive metastatic prostate cancer.
Topics: Androgen Antagonists; Androgens; Diphosphonates; Disease Progression; Hormones; Humans; Male; Prosta | 1997 |
Suramin keratosis: a unique skin eruption in a patient receiving suramin for metastatic prostate cancer.
Topics: Adenocarcinoma; Aged; Antineoplastic Agents; Drug Eruptions; Humans; Keratosis; Male; Prostatic Neop | 1997 |
Role of ceramide in suramin-induced cancer cell death.
Topics: Animals; Antineoplastic Agents; Apoptosis; Breast Neoplasms; Cell Survival; Ceramides; DNA Fragmenta | 1997 |
Evaluation of biomarkers of survival response in hormone-refractory prostate cancer patients treated with suramin.
Topics: Acid Phosphatase; Adult; Aged; Aged, 80 and over; Analysis of Variance; Antineoplastic Agents; Bioma | 1998 |
A chick embryo model for metastatic human prostate cancer.
Topics: Animals; Antineoplastic Agents; Bone and Bones; Cell Division; Cell Transplantation; Chick Embryo; C | 1998 |
The role of a new liquid-solid scintillator, a mixture of DPO, POPOP and Epon 812, for enhancement of autoradiograms with tritium agents.
Topics: Animals; Antineoplastic Agents; Autoradiography; Epoxy Resins; Humans; Indicators and Reagents; Male | 1998 |
The embryoid body as a novel in vitro assay system for antiangiogenic agents.
Topics: Animals; Capillaries; Cell Culture Techniques; Cell Differentiation; Cells, Cultured; Doxorubicin; E | 1998 |
Cell surface binding and cellular internalization properties of suramin, a novel antineoplastic agent.
Topics: Antineoplastic Agents; Binding, Competitive; Cell Membrane; Exocytosis; HL-60 Cells; Humans; Kinetic | 1995 |
Antiproliferative and cytotoxic effects of geldanamycin, cytochalasin E, suramin and thiacetazone in human prostate xenograft tumor histocultures.
Topics: Animals; Antineoplastic Agents; Benzoquinones; Cell Division; Culture Techniques; Cytochalasins; Hum | 1998 |
Efficacy of suramin against human prostate carcinoma DU145 xenografts in nude mice.
Topics: Animals; Antineoplastic Agents; Dose-Response Relationship, Drug; Humans; Male; Mice; Mice, Inbred B | 1999 |
Enhanced activity of estramustine, vinblastine, etoposide, and suramin in prostate carcinoma.
Topics: Antineoplastic Combined Chemotherapy Protocols; Cell Division; Dose-Response Relationship, Drug; Dru | 1999 |
Suramin potently inhibits the enzymatic activity of PSM.
Topics: Antigens, Surface; Antineoplastic Agents; Carboxypeptidases; Chromatography, Ion Exchange; Dipeptide | 2000 |
Fibroblast growth factors: an epigenetic mechanism of broad spectrum resistance to anticancer drugs.
Topics: Adenocarcinoma; Animals; Antineoplastic Agents; Cell Division; Culture Media, Conditioned; Doxorubic | 2000 |
Suramin administration is associated with a decrease in serum calcium levels.
Topics: Anti-Inflammatory Agents; Antineoplastic Agents; Antineoplastic Agents, Hormonal; Antineoplastic Com | 2000 |
Vascular endothelial growth factor and basic fibroblast growth factor urine levels as predictors of outcome in hormone-refractory prostate cancer patients: a cancer and leukemia group B study.
Topics: Aged; Antineoplastic Agents; Antineoplastic Agents, Hormonal; Biomarkers, Tumor; Clinical Trials, Ph | 2001 |
Nontoxic doses of suramin enhance activity of paclitaxel against lung metastases.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Culture Media, Conditioned; Dose-Response R | 2001 |
Nontoxic doses of suramin enhance activity of doxorubicin in prostate tumors.
Topics: Algorithms; Animals; Antibiotics, Antineoplastic; Antineoplastic Agents; Culture Media, Conditioned; | 2001 |
Suramin-induced neuropathy in an animal model.
Topics: Animals; Antineoplastic Agents; Axons; Cell Size; Disease Models, Animal; Dose-Response Relationship | 2001 |
[Activation of p38 and c-Jun NH2-terminal kinase mitogen-activated protein kinases in human prostate carcinoma cell lines with different metastatic potentials].
Topics: Adenosine Triphosphate; Cell Line, Tumor; Humans; Imidazoles; JNK Mitogen-Activated Protein Kinases; | 2001 |
Suramin for prostate carcinoma.
Topics: Humans; Hydrocortisone; Male; Prostate-Specific Antigen; Prostatic Neoplasms; Suramin | 1992 |
Suramin rapidly alters cellular tyrosine phosphorylation in prostate cancer cell lines.
Topics: 3T3 Cells; Animals; Dose-Response Relationship, Drug; Humans; Male; Mice; Molecular Weight; Neoplasm | 1992 |
Prognostic factors for survival of patients with bidimensionally measurable metastatic hormone-refractory prostatic cancer treated with single-agent chemotherapy.
Topics: Aged; Analysis of Variance; Antineoplastic Agents; Humans; Male; Middle Aged; Neoplasms, Hormone-Dep | 1992 |
Disruption of mitochondrial function by suramin measured by rhodamine 123 retention and oxygen consumption in intact DU145 prostate carcinoma cells.
Topics: Adenosine Triphosphate; Fluorescent Dyes; Humans; Male; Mitochondria; Oxygen Consumption; Prostatic | 1992 |
Suramin-induced skin reactions.
Topics: Carcinoma; Drug Eruptions; Drug Evaluation; Humans; Infusions, Intravenous; Male; Prostatic Neoplasm | 1992 |
Suramin inhibits gonadotropin action in rat testis: implications for treatment of advanced prostate cancer.
Topics: Animals; Cells, Cultured; Dose-Response Relationship, Drug; Follicle Stimulating Hormone; Luteinizin | 1992 |
Suramin and prostate cancer: the role of hydrocortisone.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Humans; Hydrocortisone; Mal | 1992 |
Cytostatic effects of suramin on prostate cancer cells cultured from primary tumors.
Topics: Cell Division; Growth Substances; Humans; Immunoblotting; In Vitro Techniques; Male; Prostate; Prost | 1991 |
Use of adaptive control with feedback to individualize suramin dosing.
Topics: Adenocarcinoma; Aged; Algorithms; Humans; Male; Middle Aged; Prostatic Neoplasms; Suramin; Time Fact | 1992 |
Suramin, an active nonhormonal cytotoxic drug for treatment of prostate cancer: compelling reasons for testing in patients with hormone-refractory breast cancer.
Topics: Antineoplastic Agents; Breast Neoplasms; Cell Division; Clinical Trials as Topic; Female; Humans; Ma | 1992 |
Disruption of cellular energy balance by suramin in intact human prostatic carcinoma cells, a likely antiproliferative mechanism.
Topics: Biological Transport; Calcium; Carcinoma; Cell Division; Energy Metabolism; Epidermal Growth Factor; | 1991 |
Effect of suramin on human prostate cancer cells in vitro.
Topics: Adenocarcinoma; Androstenedione; Antineoplastic Agents; Cell Line; Dehydroepiandrosterone; Dehydroep | 1991 |
The effect of suramin, tumor necrosis factor and interferon gamma on human prostate carcinoma.
Topics: Antineoplastic Agents; Cell Line; Drug Screening Assays, Antitumor; Humans; In Vitro Techniques; Int | 1991 |
Determination of suramin in clinical samples using HPLC.
Topics: Antineoplastic Agents; Chemical Precipitation; Chromatography, High Pressure Liquid; Humans; Male; P | 1991 |
Growth factors in human prostate cancer cells: implications for an improved treatment of prostate cancer.
Topics: Cell Division; Culture Media, Serum-Free; Dihydrotestosterone; Epidermal Growth Factor; ErbB Recepto | 1991 |
The effects of basic fibroblast growth factor and suramin on cell motility and growth of rat prostate cancer cells.
Topics: Animals; Cell Movement; Cell Survival; Dose-Response Relationship, Drug; Drug Interactions; Drug Scr | 1991 |
Inhibition of prostatic tumor cell proliferation by suramin: alterations in TGF alpha-mediated autocrine growth regulation and cell cycle distribution.
Topics: Antineoplastic Agents; Cell Cycle; Cell Division; Cell Line; Depression, Chemical; Dose-Response Rel | 1991 |
Suramin for prostatic cancer: a phase I/II study in advanced extensively pretreated disease.
Topics: Drug Administration Schedule; Drug Evaluation; Humans; Infusions, Intravenous; Male; Prostatic Neopl | 1990 |
Antiproliferative effects of suramin on androgen responsive tumour cells.
Topics: Androgen Antagonists; Animals; Cell Cycle; Cell Division; Cricetinae; Drug Screening Assays, Antitum | 1990 |
Differential effects of growth factor antagonists on neoplastic and normal prostatic cells.
Topics: Animals; Growth Inhibitors; Male; Neoplasm Transplantation; Prostate; Prostatic Neoplasms; Protamine | 1990 |
Synergistic activity of suramin with tumor necrosis factor alpha and doxorubicin on human prostate cancer cell lines.
Topics: Antineoplastic Combined Chemotherapy Protocols; Cell Division; Dose-Response Relationship, Drug; Dox | 1990 |
Heparin analogues: a new family of anticancer drugs.
Topics: Antineoplastic Agents; Humans; Kidney Neoplasms; Male; Prostatic Neoplasms; Suramin | 1989 |