Page last updated: 2024-10-27

flutamide and Androgen-Independent Prostatic Cancer

flutamide has been researched along with Androgen-Independent Prostatic Cancer in 24 studies

Flutamide: An antiandrogen with about the same potency as cyproterone in rodent and canine species.

Research Excerpts

ExcerptRelevanceReference
"Men with nonmetastatic prostate cancer were treated with 9 months of leuprolide and flutamide followed by a variable off-treatment interval; AD was resumed when prostate specific antigen (PSA) reached a prespecified value (1 ng/mL, radical prostatectomy; 4 ng/mL, intact prostate)."2.80Relationships between times to testosterone and prostate-specific antigen rises during the first off-treatment interval of intermittent androgen deprivation are prognostic for castration resistance in men with nonmetastatic prostate cancer. ( Gambol, TE; Gulati, R; Hall, SP; Higano, CS; Hunter-Merrill, R; Kuo, KF; Yu, EY, 2015)
"In contrast, in androgen-independent prostate cancer cell lines, TROP2high cells did not exhibit a differential treatment response but were characterized by their high self-renewal ability."1.43High expression of TROP2 characterizes different cell subpopulations in androgen-sensitive and androgen-independent prostate cancer cells. ( Butler, L; Hollande, F; Mølck, C; Paquet-Fifield, S; Sloan, E; Ventura, S; Xie, J, 2016)

Research

Studies (24)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's16 (66.67)24.3611
2020's8 (33.33)2.80

Authors

AuthorsStudies
Endo, S1
Oguri, H1
Segawa, J1
Kawai, M1
Hu, D1
Xia, S2
Okada, T1
Irie, K1
Fujii, S2
Gouda, H1
Iguchi, K1
Matsukawa, T1
Fujimoto, N1
Nakayama, T1
Toyooka, N1
Matsunaga, T1
Ikari, A1
Uemura, H1
Kobayashi, K2
Yokomizo, A1
Hinotsu, S1
Horie, S1
Kakehi, Y1
Nonomura, N1
Ogawa, O2
Oya, M1
Suzuki, K1
Saito, A1
Asakawa, K1
Uno, S1
Naito, S1
Wang, H3
Wei, X3
Zhang, D3
Li, W3
Hu, Y3
Madan, RA1
Bilusic, M1
Stein, MN1
Donahue, RN1
Arlen, PM1
Karzai, F1
Plimack, E1
Wong, YN1
Geynisman, DM1
Zibelman, M1
Mayer, T1
Strauss, J1
Chen, G1
Rauckhorst, M1
McMahon, S1
Couvillon, A1
Steinberg, S1
Figg, WD1
Dahut, WL1
Schlom, J1
Gulley, JL1
Fukuoka, K1
Teishima, J1
Nagamatsu, H1
Inoue, S1
Hayashi, T1
Mita, K1
Shigeta, M1
Kajiwara, M1
Kadonishi, Y1
Tacho, T1
Matsubara, A1
Iguchi, T3
Tamada, S3
Kato, M3
Yasuda, S3
Machida, Y1
Ohmachi, T1
Ishii, K1
Iwata, H1
Yamamoto, S1
Kanamaru, T1
Morimoto, K1
Hase, T1
Tashiro, K1
Harimoto, K1
Deguchi, T1
Adachi, T1
Iwamoto, K1
Takegaki, Y1
Nakatani, T3
Kobayashi, T1
Terada, N1
Kimura, T1
Matsubara, N1
Murakami, K1
Mori, K1
Fujimoto, Y1
Akamatsu, S1
Inoue, T2
Muramatsu, T1
Funahashi, Y1
Yamamoto, A1
Sassa, N1
Matsukawa, Y1
Gotoh, M1
Koga, H1
Negishi, M1
Kinoshita, M1
Mori, S1
Ishigami-Yuasa, M1
Kawachi, E1
Kagechika, H1
Tanatani, A1
Smith, TAD1
Phyu, SM1
Alzyoud, KS1
Tseng, CC1
Nakai, Y1
Tanaka, N2
Miyake, M1
Anai, S1
Fujimoto, K1
Pimenta, RC1
Viana, NI1
Amaral, GQ1
Park, R1
Morais, DR1
Pontes, J1
Guimaraes, VR1
Camargo, JA1
Leite, KR1
Nahas, WC1
Srougi, M1
Reis, ST1
Otoshi, T1
Hamada, K1
Yamasaki, T2
Yamaguchi, N1
Morizane, S1
Yumioka, T1
Iwamoto, H1
Hikita, K1
Sejima, T1
Honda, M1
Takenaka, A1
Shen, P1
Sun, J1
Xu, G1
Zhang, L1
Yang, Z1
Wang, Y1
Liu, Y1
Shi, G1
Matsumoto, K1
Hagiwara, M1
Hayakawa, N1
Ito, Y1
Maeda, T1
Ninomiya, A1
Nagata, H1
Nakamura, S1
Höfner, T1
Vallet, S1
Hadaschik, BA1
Pahernik, S1
Duensing, S1
Hohenfellner, M1
Jäger, D1
Grüllich, C1
Kuo, KF1
Hunter-Merrill, R1
Gulati, R1
Hall, SP1
Gambol, TE1
Higano, CS1
Yu, EY1
Hoang, DT1
Gu, L1
Liao, Z1
Shen, F1
Talati, PG1
Koptyra, M1
Tan, SH1
Ellsworth, E1
Gupta, S1
Montie, H1
Dagvadorj, A1
Savolainen, S1
Leiby, B1
Mirtti, T1
Merry, DE1
Nevalainen, MT1
Murray, NP1
Reyes, E1
Fuentealba, C1
Jacob, O1
Orellana, N1
Lallous, N1
Volik, SV1
Awrey, S1
Leblanc, E1
Tse, R1
Murillo, J1
Singh, K1
Azad, AA1
Wyatt, AW1
LeBihan, S1
Chi, KN1
Gleave, ME1
Rennie, PS1
Collins, CC1
Cherkasov, A1
Xie, J1
Mølck, C1
Paquet-Fifield, S1
Butler, L1
Sloan, E1
Ventura, S1
Hollande, F1

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Multicenter, Prospective, Randomised and Comparative Study of AA Therapy and Early Administrating Enzalutamide in Participants With CRPC Previously Treated With CAB Therapy Using Bicalutamide.[NCT02346578]Phase 2104 participants (Actual)Interventional2014-12-31Completed
A Prospective Study of Intermittent Androgen Suppression (IAS) in Men With Localized Prostate Cancer Who Have Biochemical Relapse After Radiation Therapy or Radical Prostatectomy[NCT00223665]Phase 2102 participants (Actual)Interventional1997-01-08Completed
A Randomized Phase II Trial Comparing Biomarker Directed Therapy Versus Clinician's Choice of Enzalutamide or Docetaxel in Patients With Advanced Prostate Cancer Post Abiraterone[NCT04015622]Phase 2100 participants (Anticipated)Interventional2020-10-07Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Development of Osteopenia (Bone Loss) During IAS

Dual-energy x-ray absorptiometry (DEXA) scans were performed prior to first cycle of ADT, after completion of the first cycle of ADT, and prior to the start of the second cycle of ADT. Bone Mineral Density (BMD) was a assessed in g/cm^2 as a indicator of bone health for each patient at each time point. This measure was defined as the percentage of participants with normal BMD scores at baseline who developed Osteopenia after the first cycle of ADT. (NCT00223665)
Timeframe: From screening prior to first dose of ADT through the start of the second cycle of ADT.

Interventionpercent of participants (Number)
Intermittent Androgen Suppression (IAS)13.2

Effect of IAS on Overall Survival.

Assessment of overall survival measured as median time from completion of first full cycle of IAS until date of death from any cause. (NCT00223665)
Timeframe: From date of first treatment until the date of death or study withdrawal, whichever came first, assessed up to 16 years.

Interventionyears (Median)
Intermittent Androgen Suppression (IAS)6.6

Time to Androgen Independence of Serum Prostate-Specific Antigen (PSA)

Monthly Prostate-Specific Antigen (PSA) testing to assess the point at which each patient's disease stops responding to Androgen Deprivation Therapy (ADT). Androgen Independence (AI), also know as Castrate Resistance (CR), was defined as 2 serial rises in PSA while on ADT with Testosterone levels <50 ng/dL. (NCT00223665)
Timeframe: From date of first treatment until the date of development of CR, metastatic progression, or study withdrawal, whichever came first, assessed up to 16 years.

Interventionyears (Median)
Intermittent Androgen Suppression (IAS)4.0

Change in Standardized Bone Mineral Density (BMD) of the Left Hip During IAS

Dual-energy x-ray absorptiometry (DEXA) scans were performed prior to first cycle of ADT, after completion of the first cycle of ADT, and prior to the start of the second cycle of ADT. Bone Mineral Density (BMD) was a assessed in g/cm^2 as a indicator of bone health. Percent change was assess for each patient at each time point. (NCT00223665)
Timeframe: From screening prior to first dose of ADT through the start of the second cycle of ADT.

InterventionPercent change of BMD (Number)
Post Cycle 1 versus BaselinePre Cycle 2 versus Post Cycle 1
Intermittent Androgen Suppression (IAS)-1.2-0.2

Change in Standardized Bone Mineral Density (BMD) of the Spine During IAS

Dual-energy x-ray absorptiometry (DEXA) scans were performed prior to first cycle of ADT, after completion of the first cycle of ADT, and prior to the start of the second cycle of ADT. Bone Mineral Density (BMD) was a assessed in g/cm^2 as a indicator of bone health for each patient at each time point. (NCT00223665)
Timeframe: From screening prior to first dose of ADT through the start of the second cycle of ADT.

InterventionPercent change in BMD (Number)
Post Cycle 1 versus BaselinePre Cycle 2 versus Post Cycle 1
Intermittent Androgen Suppression (IAS)-3.41.4

Estradiol Levels During First Cycle of IAS

Estradiol was measured at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

Interventionpg/ml (Mean)
BaselineMeasurement at Month 3Measurement at Month 9Measurement at Month 12
Intermittent Androgen Suppression (IAS)33.6023.1222.7624.35

Score on Executive Function Testing (Stroop Task) During First Cycle of IAS

Executive Function was assessed at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT. This assessment was based on the Stroop Color Word Interference Task. Subjects are asked to read 100 color words (red, green, blue), followed by identification of color blocks followed by reading the color of the ink and ignoring the word (e.g., the word 'blue' printed in green letters). Assessment was based on the amount of time needed to time to complete the assessment. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

Interventionminutes to complete the assessment (Mean)
BaselineScore at Month 3Score at Month 9Score at Month 12
Intermittent Androgen Suppression (IAS)51.0055.5247.5848.82

Score on Spatial Ability Test (Block Design) During First Cycle of IAS

Spatial Ability was assessed at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT. This assessment was based on the Wechsler Adult Intelligence Scale-Revised, Block Design sub-test and measures participants' ability to analyze and construct abstract figures from their component parts. The test allows a time limit of 3 minutes per design, for a total of nine designs. Score is based on total number of designs completed (max 9, min 0). (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

InterventionNumber of correctly completed designs (Mean)
BaselineScore at Month 3Score at Month 9Score at Month 12
Combined Androgen Blockade8.657.208.828.47

Score on Spatial Ability Test (Mental Rotation) During First Cycle of IAS

Spatial Ability (Mental Rotation) was assessed at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT. This assessment was based on the Vandenberg & Kuse (1978) Mental Rotation Test. Subjects are presented with line drawings of complex, three dimensional cubes on a computer screen. The subject must compare the two drawings and decide if they match. Score is based on number of correctly identified figures. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

InterventionNumber of correctly identified figures (Mean)
BaselineScore at Month 3Score at Month 9Score at Month 12
Intermittent Androgen Suppression (IAS)16.1213.0016.5215.53

Score on Spatial Memory Testing During First Cycle of IAS

Spatial Memory was assessed at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT using the Puget Sound Route Learning Test. This test measured the ability to navigate a short route within a room. Three trials were administered followed by three trials of a new route using pictures placed on the floor as landmarks. A delayed recall is administered after twenty minutes. Performance was assessed based on number of correctly recalled sequences after a delay. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

Interventionnumber of correctly recalled sequences (Mean)
BaselineScore at Month 3Score at Month 9Score at Month 12
Intermittent Androgen Suppression (IAS)19.5022.0023.7624.12

Score on Verbal Ability/Fluency Testing During First Cycle of IAS

Verbal Ability/Fluency was assessed at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT. Participants were asked to verbally generate as many words beginning with a particular letter (e.g. P) within a 60 second period. Two trials were administered with two different letters. The total number of words generated was recorded for each letter and summed and analyzed. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

InterventionNumber of words generated (Mean)
BaselineScore at Month 3Score at Month 9Score at Month 12
Intermittent Androgen Suppression (IAS)24.6526.1526.2925.70

Score on Verbal Memory Testing (Proactive Interference) During First Cycle of IAS

Verbal Memory was assessed at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT via the Proactive Interference (PI) task. The PI task involves participants listening to a list of 10 words from the same semantic category (e.g., articles of clothing), and then recalling as many of these words as possible.The procedure is repeated for a total of 4 trials. Assessment is based on the total number of words recalled. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

InterventionNumber of correctly recalled words (Mean)
BaselineScore at Month 3Score at Month 9Score at Month 12
Intermittent Androgen Suppression (IAS)21.3122.9022.7022.70

Score on Verbal Memory Testing (Story Recall) During First Cycle of IAS

Verbal Memory was assessed at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT via Story Recall. This task is based on the well known Wechsler Memory Scale -Revised Logical Memory task. Participants listened to two brief narratives (stories) and were asked to recall as much as possible immediately after hearing each story and following a 20-minute delay. Assessment was based on number of correctly recalled pieces of information after a delay. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

Interventionnumber of correctly recalled data points (Mean)
BaselineScore at Month 3Score at Month 9Score at Month 12
Intermittent Androgen Suppression (IAS)35.0637.8639.3841.16

Score on Visual Working Memory Test During First Cycle of IAS

Visual Working Memory was assessed at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT. This task is based on the Subject Ordered Pointing Task (SOPT). The participant is shown a grid array of 10, 12 or 16 abstract designs and they must choose a new design with each refresh of the screen. Assessment is based on total number of errors. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

Interventiontotal number of errors (Mean)
BaselineScore at Month 3Score at Month 9Score at Month 12
Intermittent Androgen Suppression (IAS)13.2215.6612.3514.00

Testosterone Levels During IAS

Testosterone was measured at baseline, and at Month 3, Month 9, and Month 12 after the start of the first cycle of ADT. (NCT00223665)
Timeframe: Baseline, Month 3, Month 9, and Month 12

Interventionng/ml (Mean)
BaselineMeasurement at Month 3Measurement at Month 9Measurement at Month 12
Intermittent Androgen Suppression (IAS)4060.280.202.45

Reviews

1 review available for flutamide and Androgen-Independent Prostatic Cancer

ArticleYear
Third-line hormonal therapy to treat prostate cancer relapse after initial and second-line hormonal therapy: report of 52 cases and literature review.
    Asian Pacific journal of cancer prevention : APJCP, 2014, Volume: 15, Issue:8

    Topics: Aged; Aged, 80 and over; Androgen Antagonists; Anilides; Antineoplastic Agents, Hormonal; Antineopla

2014

Trials

4 trials available for flutamide and Androgen-Independent Prostatic Cancer

ArticleYear
Flutamide With or Without PROSTVAC in Non-metastatic Castration Resistant (M0) Prostate Cancer.
    The oncologist, 2023, 07-05, Volume: 28, Issue:7

    Topics: Androgen Antagonists; Castration; Flutamide; Humans; Male; Prostate-Specific Antigen; Prostatic Neop

2023
Enzalutamide versus flutamide for castration-resistant prostate cancer after combined androgen blockade therapy with bicalutamide: the OCUU-CRPC study.
    International journal of clinical oncology, 2020, Volume: 25, Issue:3

    Topics: Aged; Aged, 80 and over; Androgen Antagonists; Anilides; Antineoplastic Combined Chemotherapy Protoc

2020
Enzalutamide versus flutamide for castration-resistant prostate cancer after combined androgen blockade therapy with bicalutamide: study protocol for a multicenter randomized phase II trial (the OCUU-CRPC study).
    BMC cancer, 2019, Apr-11, Volume: 19, Issue:1

    Topics: Antineoplastic Combined Chemotherapy Protocols; Benzamides; Clinical Protocols; Flutamide; Humans; M

2019
Relationships between times to testosterone and prostate-specific antigen rises during the first off-treatment interval of intermittent androgen deprivation are prognostic for castration resistance in men with nonmetastatic prostate cancer.
    Clinical genitourinary cancer, 2015, Volume: 13, Issue:1

    Topics: Aged; Aged, 80 and over; Flutamide; Humans; Leuprolide; Male; Middle Aged; Prospective Studies; Pros

2015

Other Studies

19 other studies available for flutamide and Androgen-Independent Prostatic Cancer

ArticleYear
Development of Novel AKR1C3 Inhibitors as New Potential Treatment for Castration-Resistant Prostate Cancer.
    Journal of medicinal chemistry, 2020, 09-24, Volume: 63, Issue:18

    Topics: Aldo-Keto Reductase Family 1 Member C3; Animals; Antineoplastic Agents; Apoptosis; Cell Proliferatio

2020
Health-related quality of life with enzalutamide versus flutamide in castration-resistant prostate cancer from the AFTERCAB study.
    International journal of clinical oncology, 2022, Volume: 27, Issue:10

    Topics: Androgen Antagonists; Androgens; Benzamides; Disease-Free Survival; Flutamide; Humans; Male; Nitrile

2022
Lncap-AI prostate cancer cell line establishment by Flutamide and androgen-free environment to promote cell adherent.
    BMC molecular and cell biology, 2022, Nov-28, Volume: 23, Issue:1

    Topics: Androgen Antagonists; Androgens; Cell Line; Flutamide; Humans; Male; Prostate-Specific Antigen; Pros

2022
Lncap-AI prostate cancer cell line establishment by Flutamide and androgen-free environment to promote cell adherent.
    BMC molecular and cell biology, 2022, Nov-28, Volume: 23, Issue:1

    Topics: Androgen Antagonists; Androgens; Cell Line; Flutamide; Humans; Male; Prostate-Specific Antigen; Pros

2022
Lncap-AI prostate cancer cell line establishment by Flutamide and androgen-free environment to promote cell adherent.
    BMC molecular and cell biology, 2022, Nov-28, Volume: 23, Issue:1

    Topics: Androgen Antagonists; Androgens; Cell Line; Flutamide; Humans; Male; Prostate-Specific Antigen; Pros

2022
Lncap-AI prostate cancer cell line establishment by Flutamide and androgen-free environment to promote cell adherent.
    BMC molecular and cell biology, 2022, Nov-28, Volume: 23, Issue:1

    Topics: Androgen Antagonists; Androgens; Cell Line; Flutamide; Humans; Male; Prostate-Specific Antigen; Pros

2022
Predictors of poor response to first-generation anti-androgens as criteria for alternate treatments for patients with non-metastatic castration-resistant prostate cancer.
    International urology and nephrology, 2020, Volume: 52, Issue:1

    Topics: Adenocarcinoma; Aged; Aged, 80 and over; Androgen Antagonists; Anilides; Chlormadinone Acetate; Flut

2020
Sequential Use of Androgen Receptor Axis-targeted Agents in Chemotherapy-naive Castration-resistant Prostate Cancer: A Multicenter Retrospective Analysis With 3-Year Follow-up.
    Clinical genitourinary cancer, 2020, Volume: 18, Issue:1

    Topics: Abiraterone Acetate; Aged; Aged, 80 and over; Androgen Receptor Antagonists; Anilides; Antineoplasti

2020
A case of advanced prostate cancer controlled for the long term by flutamide after bicalutamide failure.
    Nagoya journal of medical science, 2019, Volume: 81, Issue:4

    Topics: Aged; Anilides; Disease Progression; Flutamide; Humans; Male; Nitriles; Prostatic Neoplasms; Prostat

2019
Development of Androgen-Antagonistic Coumarinamides with a Unique Aromatic Folded Pharmacophore.
    International journal of molecular sciences, 2020, Aug-04, Volume: 21, Issue:15

    Topics: Androgen Receptor Antagonists; Androgens; Cell Line, Tumor; Cell Proliferation; Coumarins; Flutamide

2020
Response Detection of Castrate-Resistant Prostate Cancer to Clinically Utilised and Novel Treatments by Monitoring Phospholipid Metabolism.
    BioMed research international, 2017, Volume: 2017

    Topics: Cell Line, Tumor; Cell Proliferation; Choline; Flutamide; Humans; Male; Paclitaxel; Phospholipids; P

2017
Response to flutamide, as second-line therapy after bicalutamide, predicts efficacy of abiraterone, not that of enzalutamide.
    BMC research notes, 2018, May-29, Volume: 11, Issue:1

    Topics: Aged; Aged, 80 and over; Androstenes; Anilides; Antineoplastic Agents; Benzamides; Disease-Free Surv

2018
MicroRNA-23b and microRNA-27b plus flutamide treatment enhances apoptosis rate and decreases CCNG1 expression in a castration-resistant prostate cancer cell line.
    Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2018, Volume: 40, Issue:11

    Topics: Apoptosis; Cell Line, Tumor; Cyclin G1; Flutamide; G1 Phase; Gene Expression Regulation, Neoplastic;

2018
Enzalutamide versus flutamide for castration-resistant prostate cancer after combined androgen blockade therapy with bicalutamide: a retrospective study.
    International journal of clinical oncology, 2019, Volume: 24, Issue:7

    Topics: Aged; Aged, 80 and over; Androgen Antagonists; Antineoplastic Agents; Benzamides; Disease Progressio

2019
Flutamide as an Alternative Anti-androgen Agent and Predictor of the Efficacy of Novel Androgen Receptor-targeted Agents.
    Anticancer research, 2019, Volume: 39, Issue:7

    Topics: Abiraterone Acetate; Aged; Aged, 80 and over; Androgen Antagonists; Antineoplastic Combined Chemothe

2019
Enzalutamide shows strong activity in prostate cancer.
    Cancer discovery, 2014, Volume: 4, Issue:4

    Topics: Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Clinica

2014
KLF9, a transcription factor induced in flutamide-caused cell apoptosis, inhibits AKT activation and suppresses tumor growth of prostate cancer cells.
    The Prostate, 2014, Volume: 74, Issue:9

    Topics: Animals; Apoptosis; Blotting, Western; Cell Growth Processes; Cell Line, Tumor; Cell Survival; Flow

2014
Docetaxel followed by abiraterone in metastatic castration-resistant prostate cancer: efficacy and predictive parameters in a large single center cohort.
    World journal of urology, 2015, Volume: 33, Issue:6

    Topics: Aged; Androgen Antagonists; Androstenes; Anilides; Antineoplastic Agents, Hormonal; Antineoplastic C

2015
Inhibition of Stat5a/b Enhances Proteasomal Degradation of Androgen Receptor Liganded by Antiandrogens in Prostate Cancer.
    Molecular cancer therapeutics, 2015, Volume: 14, Issue:3

    Topics: Androgen Antagonists; Androgens; Anilides; Benzamides; Cell Line, Tumor; Cell Survival; Flutamide; G

2015
Possible Role of HER-2 in the Progression of Prostate Cancer from Primary Tumor to Androgen Independence.
    Asian Pacific journal of cancer prevention : APJCP, 2015, Volume: 16, Issue:15

    Topics: Age Factors; Aged; Androgen Antagonists; Antineoplastic Agents, Hormonal; Blood Vessels; Disease Pro

2015
Functional analysis of androgen receptor mutations that confer anti-androgen resistance identified in circulating cell-free DNA from prostate cancer patients.
    Genome biology, 2016, Jan-26, Volume: 17

    Topics: Androgen Receptor Antagonists; Anilides; Benzamides; DNA; Drug Resistance, Neoplasm; Flutamide; High

2016
High expression of TROP2 characterizes different cell subpopulations in androgen-sensitive and androgen-independent prostate cancer cells.
    Oncotarget, 2016, Jul-12, Volume: 7, Issue:28

    Topics: Androgen Antagonists; Animals; Antigens, Neoplasm; Antineoplastic Agents; Antineoplastic Combined Ch

2016