thalidomide has been researched along with Glial Cell Tumors in 26 studies
Thalidomide: A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects. It has been reintroduced and used for a number of immunological and inflammatory disorders. Thalidomide displays immunosuppressive and anti-angiogenic activity. It inhibits release of TUMOR NECROSIS FACTOR-ALPHA from monocytes, and modulates other cytokine action.
thalidomide : A racemate comprising equimolar amounts of R- and S-thalidomide.
2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione : A dicarboximide that is isoindole-1,3(2H)-dione in which the hydrogen attached to the nitrogen is substituted by a 2,6-dioxopiperidin-3-yl group.
Excerpt | Relevance | Reference |
---|---|---|
"Thalidomide and procarbazine have demonstrated single agent activity against malignant gliomas (MG)." | 9.16 | A phase II trial of thalidomide and procarbazine in adult patients with recurrent or progressive malignant gliomas. ( Case, D; Ellis, TL; Enevold, G; Lesser, GJ; McMullen, KP; McQuellon, RP; Rosdhal, R; Ruiz, J; Shaw, EG; Stieber, VW; Tatter, SB, 2012) |
"A phase II study was conducted to assess the efficacy of administering daily thalidomide concomitantly with radiation and continuing for up to 1 year following radiation in children with brain stem gliomas (BSG) or glioblastoma multiforme (GBM)." | 9.12 | Phase II study of thalidomide and radiation in children with newly diagnosed brain stem gliomas and glioblastoma multiforme. ( Briody, C; Chi, S; Chordas, C; Goumnerova, LC; Kieran, MW; MacDonald, T; Marcus, KJ; Packer, RJ; Poussaint, TY; Scott, RM; Turner, CD; Ullrich, N; Vajapeyam, S; Zimmerman, MA, 2007) |
" Our data demonstrate that thalidomide in combination with BCNU is well tolerated and has antitumor activity in patients with recurrent high-grade gliomas." | 9.10 | Phase II trial of thalidomide and carmustine for patients with recurrent high-grade gliomas. ( Batchelor, T; Borkowf, CB; Figg, WD; Fine, HA; Lakhani, N; Maher, EA; Purow, BW; Viscosi, E; Wen, PY, 2003) |
"Thalidomide is a generally well-tolerated drug that may have antitumor activity in a minority of patients with recurrent high-grade gliomas." | 9.09 | Phase II trial of the antiangiogenic agent thalidomide in patients with recurrent high-grade gliomas. ( Black, PM; Figg, WD; Fine, HA; Jaeckle, K; Kaplan, R; Kyritsis, AP; Levin, VA; Loeffler, JS; Pluda, JM; Wen, PY; Yung, WK, 2000) |
"The efficacy of thalidomide in terms of response in recurrent gliomas is low, with a partial response rate of only 6%." | 9.09 | Thalidomide as an anti-angiogenic agent in relapsed gliomas. ( Brada, M; Dowe, A; Gore, M; Hines, F; Short, SC; Traish, D, 2001) |
"For its numerous abilities including sedation, we have been using thalidomide (TH) as the 'last therapeutic option' in patients with advanced gliomas." | 7.81 | Thalidomide as palliative treatment in patients with advanced secondary glioblastoma. ( Ackerl, M; Dieckmann, KU; Flechl, B; Hainfellner, JA; Hassler, MR; Marosi, C; Prayer, D; Preusser, M; Rössler, K; Sax, C; Woehrer, A, 2015) |
"Human malignant glioma cells U251-MG were cultured and assigned to four groups with different treatments for 3 days: temozolomide group (100 micromol/L), thalidomide group (100 microg/L), temozolomide (100 micromol/L) plus thalidomide group (100 microg/L) and control group." | 7.75 | Mechanism of thalidomide to enhance cytotoxicity of temozolomide in U251-MG glioma cells in vitro. ( Gao, S; Ji, YW; Pan, Q; Yang, XJ; Zhang, WG, 2009) |
"The chemotherapeutic agent temozolomide (TMZ) and the anti-angiogenic agent thalidomide (THD) have both demonstrated anti-tumor activity in patients with recurrent malignant glioma." | 7.73 | Combination treatment with temozolomide and thalidomide inhibits tumor growth and angiogenesis in an orthotopic glioma model. ( Jeon, HJ; Kim, H; Kim, JH; Kim, JS; Kim, JT; Kim, MH; Kim, YJ; Lee, DS; Nam, DH; Park, SY; Shin, T; Son, MJ; Song, HS, 2006) |
"Serial MR imaging was performed in 18 consecutive patients with recurrent malignant gliomas receiving both thalidomide and carboplatin for 12-month periods." | 7.70 | Dynamic contrast-enhanced T2-weighted MR imaging of recurrent malignant gliomas treated with thalidomide and carboplatin. ( Cha, S; Glass, J; Gruber, ML; Johnson, G; Knopp, EA; Litt, A; Lu, S; Zagzag, D, 2000) |
"Malignant gliomas are tumors with a very unfavorable prognosis." | 5.43 | Lenalidomide in an in vitro Dendritic Cell Model for Malignant Gliomas. ( Kramm, CM; Kühnöl, CD; Staege, MS, 2016) |
"Gliomas are highly vascularized tumors, suggesting that the prevention of vessel formation by anti-angiogenic treatment might be effective." | 5.40 | Radiation therapy and concurrent topotecan followed by maintenance triple anti-angiogenic therapy with thalidomide, etoposide, and celecoxib for pediatric diffuse intrinsic pontine glioma. ( Arola, M; Clausen, N; Harila-Saari, A; Holm, S; Kivivuori, SM; Lähteenmäki, P; Lannering, B; Lönnqvist, T; Porkholm, M; Riikonen, P; Saarinen-Pihkala, UM; Schomerus, E; Sehested, A; Thomassen, H; Thorarinsdottir, HK; Valanne, L; Wojcik, D, 2014) |
"Thalidomide treatment also dramatically suppressed the anchorage-independent growth of U-87 MG and other glioma cells by over a thousand fold without affecting its anchorage-dependent growth, which may be accomplished by knocking down endogenous bFGF expression in these cells." | 5.35 | The G-rich promoter and G-rich coding sequence of basic fibroblast growth factor are the targets of thalidomide in glioma. ( Mei, SC; Wu, RT, 2008) |
"Thalidomide is a racemate with known pharmacologic and pharmacokinetic enantioselectivity." | 5.34 | Enantioselectivity of thalidomide serum and tissue concentrations in a rat glioma model and effects of combination treatment with cisplatin and BCNU. ( Boyle, FM; Davey, RA; Gu, XQ; Mather, LE; Murphy, S, 2007) |
"Gliomas are primary brain tumors associated with a poor prognosis partly due to resistance to conventional therapies." | 5.33 | Antiangiogenic agent, thalidomide increases the antitumor effect of single high dose irradiation (gamma knife radiosurgery) in the rat orthotopic glioma model. ( Itasaka, S; Kim, JT; Lee, JI; Nam, DH, 2006) |
"Thalidomide and procarbazine have demonstrated single agent activity against malignant gliomas (MG)." | 5.16 | A phase II trial of thalidomide and procarbazine in adult patients with recurrent or progressive malignant gliomas. ( Case, D; Ellis, TL; Enevold, G; Lesser, GJ; McMullen, KP; McQuellon, RP; Rosdhal, R; Ruiz, J; Shaw, EG; Stieber, VW; Tatter, SB, 2012) |
"A phase II study was conducted to assess the efficacy of administering daily thalidomide concomitantly with radiation and continuing for up to 1 year following radiation in children with brain stem gliomas (BSG) or glioblastoma multiforme (GBM)." | 5.12 | Phase II study of thalidomide and radiation in children with newly diagnosed brain stem gliomas and glioblastoma multiforme. ( Briody, C; Chi, S; Chordas, C; Goumnerova, LC; Kieran, MW; MacDonald, T; Marcus, KJ; Packer, RJ; Poussaint, TY; Scott, RM; Turner, CD; Ullrich, N; Vajapeyam, S; Zimmerman, MA, 2007) |
" Our data demonstrate that thalidomide in combination with BCNU is well tolerated and has antitumor activity in patients with recurrent high-grade gliomas." | 5.10 | Phase II trial of thalidomide and carmustine for patients with recurrent high-grade gliomas. ( Batchelor, T; Borkowf, CB; Figg, WD; Fine, HA; Lakhani, N; Maher, EA; Purow, BW; Viscosi, E; Wen, PY, 2003) |
"Thalidomide is a generally well-tolerated drug that may have antitumor activity in a minority of patients with recurrent high-grade gliomas." | 5.09 | Phase II trial of the antiangiogenic agent thalidomide in patients with recurrent high-grade gliomas. ( Black, PM; Figg, WD; Fine, HA; Jaeckle, K; Kaplan, R; Kyritsis, AP; Levin, VA; Loeffler, JS; Pluda, JM; Wen, PY; Yung, WK, 2000) |
"The efficacy of thalidomide in terms of response in recurrent gliomas is low, with a partial response rate of only 6%." | 5.09 | Thalidomide as an anti-angiogenic agent in relapsed gliomas. ( Brada, M; Dowe, A; Gore, M; Hines, F; Short, SC; Traish, D, 2001) |
"For its numerous abilities including sedation, we have been using thalidomide (TH) as the 'last therapeutic option' in patients with advanced gliomas." | 3.81 | Thalidomide as palliative treatment in patients with advanced secondary glioblastoma. ( Ackerl, M; Dieckmann, KU; Flechl, B; Hainfellner, JA; Hassler, MR; Marosi, C; Prayer, D; Preusser, M; Rössler, K; Sax, C; Woehrer, A, 2015) |
"Human malignant glioma cells U251-MG were cultured and assigned to four groups with different treatments for 3 days: temozolomide group (100 micromol/L), thalidomide group (100 microg/L), temozolomide (100 micromol/L) plus thalidomide group (100 microg/L) and control group." | 3.75 | Mechanism of thalidomide to enhance cytotoxicity of temozolomide in U251-MG glioma cells in vitro. ( Gao, S; Ji, YW; Pan, Q; Yang, XJ; Zhang, WG, 2009) |
"The chemotherapeutic agent temozolomide (TMZ) and the anti-angiogenic agent thalidomide (THD) have both demonstrated anti-tumor activity in patients with recurrent malignant glioma." | 3.73 | Combination treatment with temozolomide and thalidomide inhibits tumor growth and angiogenesis in an orthotopic glioma model. ( Jeon, HJ; Kim, H; Kim, JH; Kim, JS; Kim, JT; Kim, MH; Kim, YJ; Lee, DS; Nam, DH; Park, SY; Shin, T; Son, MJ; Song, HS, 2006) |
"Serial MR imaging was performed in 18 consecutive patients with recurrent malignant gliomas receiving both thalidomide and carboplatin for 12-month periods." | 3.70 | Dynamic contrast-enhanced T2-weighted MR imaging of recurrent malignant gliomas treated with thalidomide and carboplatin. ( Cha, S; Glass, J; Gruber, ML; Johnson, G; Knopp, EA; Litt, A; Lu, S; Zagzag, D, 2000) |
"Malignant gliomas are tumors with a very unfavorable prognosis." | 1.43 | Lenalidomide in an in vitro Dendritic Cell Model for Malignant Gliomas. ( Kramm, CM; Kühnöl, CD; Staege, MS, 2016) |
"Gliomas are highly vascularized tumors, suggesting that the prevention of vessel formation by anti-angiogenic treatment might be effective." | 1.40 | Radiation therapy and concurrent topotecan followed by maintenance triple anti-angiogenic therapy with thalidomide, etoposide, and celecoxib for pediatric diffuse intrinsic pontine glioma. ( Arola, M; Clausen, N; Harila-Saari, A; Holm, S; Kivivuori, SM; Lähteenmäki, P; Lannering, B; Lönnqvist, T; Porkholm, M; Riikonen, P; Saarinen-Pihkala, UM; Schomerus, E; Sehested, A; Thomassen, H; Thorarinsdottir, HK; Valanne, L; Wojcik, D, 2014) |
"Thalidomide treatment also dramatically suppressed the anchorage-independent growth of U-87 MG and other glioma cells by over a thousand fold without affecting its anchorage-dependent growth, which may be accomplished by knocking down endogenous bFGF expression in these cells." | 1.35 | The G-rich promoter and G-rich coding sequence of basic fibroblast growth factor are the targets of thalidomide in glioma. ( Mei, SC; Wu, RT, 2008) |
"Thalidomide is a racemate with known pharmacologic and pharmacokinetic enantioselectivity." | 1.34 | Enantioselectivity of thalidomide serum and tissue concentrations in a rat glioma model and effects of combination treatment with cisplatin and BCNU. ( Boyle, FM; Davey, RA; Gu, XQ; Mather, LE; Murphy, S, 2007) |
"Gliomas are primary brain tumors associated with a poor prognosis partly due to resistance to conventional therapies." | 1.33 | Antiangiogenic agent, thalidomide increases the antitumor effect of single high dose irradiation (gamma knife radiosurgery) in the rat orthotopic glioma model. ( Itasaka, S; Kim, JT; Lee, JI; Nam, DH, 2006) |
"Thalidomide has been previously shown to inhibit angiogenesis induced by basic fibroblast growth factor in vivo, using the rabbit corneal micropocket assay." | 1.30 | Thalidomide and a thalidomide analogue inhibit endothelial cell proliferation in vitro. ( Friedlander, DR; Kaplan, G; Moreira, AL; Shif, B; Zagzag, D, 1999) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (7.69) | 18.2507 |
2000's | 13 (50.00) | 29.6817 |
2010's | 11 (42.31) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Yung, R | 1 |
Seyfoddin, V | 1 |
Guise, C | 1 |
Tijono, S | 1 |
McGregor, A | 1 |
Connor, B | 1 |
Ching, LM | 1 |
Porkholm, M | 1 |
Valanne, L | 2 |
Lönnqvist, T | 2 |
Holm, S | 1 |
Lannering, B | 1 |
Riikonen, P | 2 |
Wojcik, D | 1 |
Sehested, A | 1 |
Clausen, N | 1 |
Harila-Saari, A | 1 |
Schomerus, E | 1 |
Thorarinsdottir, HK | 1 |
Lähteenmäki, P | 1 |
Arola, M | 1 |
Thomassen, H | 1 |
Saarinen-Pihkala, UM | 2 |
Kivivuori, SM | 2 |
Hassler, MR | 1 |
Sax, C | 1 |
Flechl, B | 1 |
Ackerl, M | 1 |
Preusser, M | 1 |
Hainfellner, JA | 1 |
Woehrer, A | 1 |
Dieckmann, KU | 1 |
Rössler, K | 1 |
Prayer, D | 1 |
Marosi, C | 1 |
Milanovic, D | 1 |
Sticht, C | 1 |
Röhrich, M | 1 |
Maier, P | 1 |
Grosu, AL | 1 |
Herskind, C | 1 |
Kuramitsu, S | 1 |
Ohno, M | 1 |
Ohka, F | 1 |
Shiina, S | 1 |
Yamamichi, A | 1 |
Kato, A | 1 |
Tanahashi, K | 1 |
Motomura, K | 1 |
Kondo, G | 1 |
Kurimoto, M | 1 |
Senga, T | 1 |
Wakabayashi, T | 1 |
Natsume, A | 1 |
Kühnöl, CD | 1 |
Staege, MS | 1 |
Kramm, CM | 1 |
Shimizu, T | 1 |
Kurozumi, K | 2 |
Ishida, J | 1 |
Ichikawa, T | 2 |
Date, I | 2 |
Mei, SC | 1 |
Wu, RT | 1 |
Gao, S | 1 |
Yang, XJ | 1 |
Zhang, WG | 1 |
Ji, YW | 1 |
Pan, Q | 1 |
Onishi, M | 1 |
Ruiz, J | 1 |
Case, D | 1 |
Enevold, G | 1 |
Rosdhal, R | 1 |
Tatter, SB | 1 |
Ellis, TL | 1 |
McQuellon, RP | 1 |
McMullen, KP | 1 |
Stieber, VW | 1 |
Shaw, EG | 1 |
Lesser, GJ | 1 |
Giglio, P | 1 |
Dhamne, M | 1 |
Hess, KR | 1 |
Gilbert, MR | 1 |
Groves, MD | 1 |
Levin, VA | 2 |
Kang, SL | 1 |
Ictech, SE | 1 |
Liu, V | 1 |
Colman, H | 1 |
Conrad, CA | 1 |
Loghin, M | 1 |
de Groot, J | 1 |
Yung, WK | 2 |
Puduvalli, VK | 1 |
Fine, HA | 2 |
Wen, PY | 3 |
Maher, EA | 1 |
Viscosi, E | 1 |
Batchelor, T | 1 |
Lakhani, N | 1 |
Figg, WD | 2 |
Purow, BW | 1 |
Borkowf, CB | 1 |
Takano, S | 1 |
Son, MJ | 1 |
Kim, JS | 1 |
Kim, MH | 1 |
Song, HS | 1 |
Kim, JT | 2 |
Kim, H | 1 |
Shin, T | 1 |
Jeon, HJ | 1 |
Lee, DS | 1 |
Park, SY | 1 |
Kim, YJ | 1 |
Kim, JH | 1 |
Nam, DH | 2 |
Lee, JI | 1 |
Itasaka, S | 1 |
Turner, CD | 1 |
Chi, S | 1 |
Marcus, KJ | 1 |
MacDonald, T | 1 |
Packer, RJ | 1 |
Poussaint, TY | 1 |
Vajapeyam, S | 1 |
Ullrich, N | 1 |
Goumnerova, LC | 1 |
Scott, RM | 1 |
Briody, C | 1 |
Chordas, C | 1 |
Zimmerman, MA | 1 |
Kieran, MW | 1 |
Murphy, S | 1 |
Boyle, FM | 1 |
Davey, RA | 1 |
Gu, XQ | 1 |
Mather, LE | 1 |
Kesari, S | 1 |
Schiff, D | 1 |
Doherty, L | 1 |
Gigas, DC | 1 |
Batchelor, TT | 1 |
Muzikansky, A | 1 |
O'Neill, A | 1 |
Drappatz, J | 1 |
Chen-Plotkin, AS | 1 |
Ramakrishna, N | 1 |
Weiss, SE | 1 |
Levy, B | 1 |
Bradshaw, J | 1 |
Kracher, J | 1 |
Laforme, A | 1 |
Black, PM | 2 |
Folkman, J | 1 |
Kieran, M | 1 |
Burton, E | 1 |
Prados, M | 1 |
Moreira, AL | 1 |
Friedlander, DR | 1 |
Shif, B | 1 |
Kaplan, G | 1 |
Zagzag, D | 2 |
Jaeckle, K | 1 |
Kyritsis, AP | 1 |
Loeffler, JS | 1 |
Kaplan, R | 1 |
Pluda, JM | 1 |
Cha, S | 1 |
Knopp, EA | 1 |
Johnson, G | 1 |
Litt, A | 1 |
Glass, J | 1 |
Gruber, ML | 1 |
Lu, S | 1 |
Cohen, MH | 1 |
Short, SC | 1 |
Traish, D | 1 |
Dowe, A | 1 |
Hines, F | 1 |
Gore, M | 1 |
Brada, M | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Phase II Study of Peg-Interferon Alpha-2B (Peg-Intron(TM)) and Thalidomide in Adults With Recurrent High-Grade Gliomas[NCT00047879] | Phase 2 | 7 participants (Actual) | Interventional | 2002-10-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Here are the total number of participants with adverse events. For the detailed list of adverse events see the adverse event module. (NCT00047879)
Timeframe: 4 months
Intervention | Participants (Number) |
---|---|
Glioblastoma Multiforme Stratum | 4 |
Anaplastic Glioma Stratum | 2 |
4 reviews available for thalidomide and Glial Cell Tumors
Article | Year |
---|---|
Adhesion molecules and the extracellular matrix as drug targets for glioma.
Topics: Angiogenesis Inhibitors; Antibodies; Brain Neoplasms; Cell Adhesion Molecules; Disease Progression; | 2016 |
Angiogenesis and invasion in glioma.
Topics: Angiogenesis Inhibitors; Animals; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Bevaciz | 2011 |
[Anti-angiogenesis treatment for brain tumors--present and future].
Topics: Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Bevacizumab; Brain Neoplasms; Clinical Tr | 2005 |
New chemotherapy options for the treatment of malignant gliomas.
Topics: Adult; Antineoplastic Agents; Brain Neoplasms; Camptothecin; Clinical Trials as Topic; Dacarbazine; | 1999 |
7 trials available for thalidomide and Glial Cell Tumors
Article | Year |
---|---|
A phase II trial of thalidomide and procarbazine in adult patients with recurrent or progressive malignant gliomas.
Topics: Adult; Angiogenesis Inhibitors; Antineoplastic Agents; Brain Neoplasms; Female; Follow-Up Studies; G | 2012 |
Phase 2 trial of irinotecan and thalidomide in adults with recurrent anaplastic glioma.
Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasms; Disease-Free Survival; | 2012 |
Phase II trial of thalidomide and carmustine for patients with recurrent high-grade gliomas.
Topics: Adult; Aged; Angiogenesis Inhibitors; Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasm | 2003 |
Phase II study of thalidomide and radiation in children with newly diagnosed brain stem gliomas and glioblastoma multiforme.
Topics: Adolescent; Angiogenesis Inhibitors; Brain Stem Neoplasms; Child; Combined Modality Therapy; Disease | 2007 |
Phase II study of metronomic chemotherapy for recurrent malignant gliomas in adults.
Topics: Adult; Aged; Angiogenesis Inhibitors; Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasm | 2007 |
Phase II trial of the antiangiogenic agent thalidomide in patients with recurrent high-grade gliomas.
Topics: Adult; Aged; Angiogenesis Inhibitors; Biomarkers, Tumor; Chemotherapy, Adjuvant; Combined Modality T | 2000 |
Thalidomide as an anti-angiogenic agent in relapsed gliomas.
Topics: Adult; Angiogenesis Inhibitors; Brain Neoplasms; Disease Progression; Glioma; Humans; Middle Aged; N | 2001 |
15 other studies available for thalidomide and Glial Cell Tumors
Article | Year |
---|---|
Efficacy against subcutaneous or intracranial murine GL261 gliomas in relation to the concentration of the vascular-disrupting agent, 5,6-dimethylxanthenone-4-acetic acid (DMXAA), in the brain and plasma.
Topics: Animals; Antineoplastic Agents; Blood-Brain Barrier; Brain Neoplasms; Cell Line, Tumor; Disease Mode | 2014 |
Radiation therapy and concurrent topotecan followed by maintenance triple anti-angiogenic therapy with thalidomide, etoposide, and celecoxib for pediatric diffuse intrinsic pontine glioma.
Topics: Adolescent; Antineoplastic Combined Chemotherapy Protocols; Brain Stem Neoplasms; Case-Control Studi | 2014 |
Thalidomide as palliative treatment in patients with advanced secondary glioblastoma.
Topics: Adult; Antineoplastic Agents; Female; Glioblastoma; Glioma; Humans; Male; Palliative Care; Retrospec | 2015 |
Inhibition of 13-cis retinoic acid-induced gene expression of reactive-resistance genes by thalidomide in glioblastoma tumours in vivo.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasms; Cell Line, Tumor; Cell Pro | 2015 |
Lenalidomide enhances the function of chimeric antigen receptor T cells against the epidermal growth factor receptor variant III by enhancing immune synapses.
Topics: Animals; Cell Line, Tumor; Combined Modality Therapy; ErbB Receptors; Glioma; Humans; Immunologic Fa | 2015 |
Lenalidomide in an in vitro Dendritic Cell Model for Malignant Gliomas.
Topics: Antineoplastic Agents; Dendritic Cells; Drug Screening Assays, Antitumor; Glioma; Humans; Immunologi | 2016 |
The G-rich promoter and G-rich coding sequence of basic fibroblast growth factor are the targets of thalidomide in glioma.
Topics: Angiogenesis Inhibitors; Brain Neoplasms; Fibroblast Growth Factor 2; Glioma; Guanine; Humans; Promo | 2008 |
Mechanism of thalidomide to enhance cytotoxicity of temozolomide in U251-MG glioma cells in vitro.
Topics: Antineoplastic Agents, Alkylating; Autophagy; Cell Line, Tumor; Cell Proliferation; Dacarbazine; Gli | 2009 |
Antiangiogenic combination therapy after local radiotherapy with topotecan radiosensitizer improved quality of life for children with inoperable brainstem gliomas.
Topics: Adolescent; Angiogenesis Inhibitors; Antineoplastic Combined Chemotherapy Protocols; Brain Stem Neop | 2011 |
Combination treatment with temozolomide and thalidomide inhibits tumor growth and angiogenesis in an orthotopic glioma model.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents, Alkylating; Apoptosis; Brain Neoplasms; Cel | 2006 |
Antiangiogenic agent, thalidomide increases the antitumor effect of single high dose irradiation (gamma knife radiosurgery) in the rat orthotopic glioma model.
Topics: Angiogenesis Inhibitors; Animals; Apoptosis; Brain Neoplasms; Cell Proliferation; Combined Modality | 2006 |
Enantioselectivity of thalidomide serum and tissue concentrations in a rat glioma model and effects of combination treatment with cisplatin and BCNU.
Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Carmustine; Cisplati | 2007 |
Thalidomide and a thalidomide analogue inhibit endothelial cell proliferation in vitro.
Topics: Animals; Cell Division; Cornea; Endothelium, Vascular; Fibroblast Growth Factor 2; Glioma; Humans; N | 1999 |
Dynamic contrast-enhanced T2-weighted MR imaging of recurrent malignant gliomas treated with thalidomide and carboplatin.
Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Brain Neoplasms; Carboplatin; Echo-Plan | 2000 |
Thalidomide in the treatment of high-grade gliomas.
Topics: Angiogenesis Inhibitors; Clinical Trials, Phase II as Topic; Glioma; Humans; Middle Aged; Thalidomid | 2000 |