Literature DB >> 14713785

Alternative antiandrogens to treat prostate cancer relapse after initial hormone therapy.

Satoko Kojima1, Hiroyoshi Suzuki, Koichiro Akakura, Masaki Shimbo, Tomohiko Ichikawa, Haruo Ito.   

Abstract

PURPOSE: We studied the efficiency of second or third line hormonal therapy for prostate cancer relapse after hormone therapy.
MATERIALS AND METHODS: The study included 70 patients with advanced prostate cancer treated with hormonal therapy, androgen deprivation monotherapy or maximum androgen blockade including surgical or medical castration combined with steroidal antiandrogen, 100 mg chlormadinone acetate daily or nonsteroidal antiandrogens, 375 mg flutamide (FLT) daily or 80 mg bicalutamide (BCL) daily. When the disease relapsed, we discontinued the antiandrogen and evaluated the patient for the antiandrogen withdrawal syndrome (AWS). Thereafter we administrated an alternative antiandrogen and evaluated its effect.
RESULTS: The incidence of the AWS after first, second and third line hormonal therapy was 35.8%, 8.0% and 0%, respectively. The efficiency of subsequent hormonal therapy was not related to the occurrence of the AWS. Nonsteroidal antiandrogens as alternative therapies for disease relapse from primary therapy were effective in second line (FLT 38.1%, BCL 44.4%) or in third line (FLT 30.0%, BCL 28.6%) hormonal therapy. Of 5 (80%) patients who responded to second line therapy 4 (80%) had effective third line therapy, while only 1 of 12 (8.3%) second line nonresponders had effective third line therapy (p = 0.003). The survival of second line responders was significantly better than that of nonresponders (5-year survival rate 92.3% vs 23.9%, p <0.001), indicating a potential predictive value for second line responsiveness. No significant clinical factor identified second line responsiveness.
CONCLUSIONS: Subsequent nonsteroidal antiandrogen therapies were effective against prostate cancer relapse after hormonal therapy. The response to third line therapy was more effective and survival was improved from the time of first line therapy relapse among second line responders than that in nonresponders. Our data support the notion that second line responders are androgen independent but still hormonally sensitive.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14713785     DOI: 10.1097/01.ju.0000106190.32540.6c

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  21 in total

Review 1.  [Local recurrence of prostate cancer: hormone therapy].

Authors:  J E Altwein; T Ebert
Journal:  Urologe A       Date:  2006-10       Impact factor: 0.639

Review 2.  Switching and withdrawing hormonal agents for castration-resistant prostate cancer.

Authors:  David Lorente; Joaquin Mateo; Zafeiris Zafeiriou; Alan D Smith; Shahneen Sandhu; Roberta Ferraldeschi; Johann S de Bono
Journal:  Nat Rev Urol       Date:  2015-01       Impact factor: 14.432

3.  Cranial nerve deficit caused by skull metastasis of prostate cancer: three Japanese castration-resistant prostate cancer cases.

Authors:  Kouji Izumi; Atsushi Mizokami; Kazutaka Narimoto; Kazuhiro Sugimoto; Eitetsu Koh; Tomoyasu Kumano; Mikio Namiki
Journal:  Int J Clin Oncol       Date:  2010-06-05       Impact factor: 3.402

4.  Ligand fishing using new chitosan based functionalized Androgen Receptor magnetic particles.

Authors:  Michał Piotr Marszałł; Wiktor Dariusz Sroka; Adam Sikora; Dorota Chełminiak; Marta Ziegler-Borowska; Tomasz Siódmiak; Ruin Moaddel
Journal:  J Pharm Biomed Anal       Date:  2016-05-04       Impact factor: 3.935

5.  Efficacy of tegafur-uracil (UFT) administration in castration-resistant prostate cancer patients with a history of both alternative antiandrogen therapy and estramustine phosphate sodium hydrate therapy.

Authors:  Nozomi Hayakawa; Kazuhiro Matsumoto; Atsuko Sato; Hirofumi Sakamoto; Taisuke Ezaki; Takahiro Maeda; Akiharu Ninomiya; So Nakamura
Journal:  Int Urol Nephrol       Date:  2013-12-20       Impact factor: 2.370

6.  Tumor infiltrating T lymphocytes expressing FoxP3, CCR7 or PD-1 predict the outcome of prostate cancer patients subjected to salvage radiotherapy after biochemical relapse.

Authors:  Valerio Nardone; Cirino Botta; Michele Caraglia; Elodia Claudia Martino; Maria Raffaella Ambrosio; Tommaso Carfagno; Paolo Tini; Leonardo Semeraro; Gabriella Misso; Anna Grimaldi; Mariarosaria Boccellino; Gaetano Facchini; Massimiliano Berretta; Gianluca Vischi; Bruno Jim Rocca; Aurora Barone; Pierfrancesco Tassone; Pierosandro Tagliaferri; Maria Teresa Del Vecchio; Luigi Pirtoli; Pierpaolo Correale
Journal:  Cancer Biol Ther       Date:  2016-11       Impact factor: 4.742

Review 7.  The androgen receptor in hormone-refractory prostate cancer.

Authors:  Hai-Lei Mao; Zhi-Qi Zhu; Charlie Degui Chen
Journal:  Asian J Androl       Date:  2008-12-01       Impact factor: 3.285

8.  Inhibition of prostate cancer cell growth by second-site androgen receptor antagonists.

Authors:  James D Joseph; Bryan M Wittmann; Mary A Dwyer; Huaxia Cui; Delita A Dye; Donald P McDonnell; John D Norris
Journal:  Proc Natl Acad Sci U S A       Date:  2009-07-02       Impact factor: 11.205

9.  Clinical outcomes of anti-androgen withdrawal and subsequent alternative anti-androgen therapy for advanced prostate cancer following failure of initial maximum androgen blockade.

Authors:  Hiroyuki Momozono; Hideaki Miyake; Hiromoto Tei; Ken-Ichi Harada; Masato Fujisawa
Journal:  Mol Clin Oncol       Date:  2016-03-10

10.  Outcomes and predictive factors of prostate cancer patients with extremely high prostate-specific antigen level.

Authors:  Kouji Izumi; Wen-Jye Lin; Hiroshi Miyamoto; Chiung-Kuei Huang; Aerken Maolake; Yasuhide Kitagawa; Yoshifumi Kadono; Hiroyuki Konaka; Atsushi Mizokami; Mikio Namiki
Journal:  J Cancer Res Clin Oncol       Date:  2014-04-19       Impact factor: 4.553

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.