Literature DB >> 20483588

The interval from the last cycle of docetaxel-based chemotherapy to progression is associated with the efficacy of subsequent docetaxel in patients with prostate cancer.

Yohann Loriot1, Christophe Massard, Marine Gross-Goupil, Mario Di Palma, Bernard Escudier, Alberto Bossi, Anne Chauchereau, Karim Fizazi.   

Abstract

There is currently no standard treatment after first-line docetaxel-based chemotherapy for patients with castration-refractory prostate cancer (CRPC). Some patients are likely to discontinue first-line docetaxel-based chemotherapy because of either completed treatment or the occurrence of manageable side-effects. The aim of this study was to determine whether a rechallenge with docetaxel might be appropriate in patients with CRPC previously treated with docetaxel. Between December 2004 and July 2009, 39 patients diagnosed with metastatic cancer prostate at the Institut Gustave Roussy were administered subsequent docetaxel after front-line docetaxel-based chemotherapy. The medical records of these patients were extracted from the database. The PSA response rate (PSA decline > or =30% and > or =50%), progression-free survival (PFS) and overall survival (OS) of patients receiving docetaxel as a subsequent line of therapy were evaluated using consensus criteria. The effect of pre-treatment variables on efficacy was studied. A PSA decline > or =30% and > or =50% was observed in 64% and 38% of patients, respectively, median PFS was 4.3 months [confidence interval (CI) 95%: 3.6-4.9] and median OS was 15.8 months (CI 95%: 11.7-20.3) in 39 patients who received subsequent docetaxel. The interval between the last cycle of first-line docetaxel and progression [median: 3.0 months; range: 1-30 months] was associated with PFS: median PFS was 3.4 months (CI 95%: 2.6-4.1) and 6.3 months (CI 95%: 3.0-5.6), respectively, in patients with an interval <3.0 months and an interval > or =3.0 months, (p=0.04). Tolerance of re-treatment with docetaxel was acceptable with no toxicity-related death. Re-treatment with subsequent docetaxel in patients with CRPC pretreated with first-line docetaxel is safe and demonstrates some activity. The interval from the last cycle of first-line docetaxel-based chemotherapy to progression is associated with the efficacy of subsequent docetaxel. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20483588     DOI: 10.1016/j.ejca.2010.04.010

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  18 in total

Review 1.  Drug rechallenge and treatment beyond progression--implications for drug resistance.

Authors:  Elizabeth A Kuczynski; Daniel J Sargent; Axel Grothey; Robert S Kerbel
Journal:  Nat Rev Clin Oncol       Date:  2013-09-03       Impact factor: 66.675

Review 2.  Second-line chemotherapy in metastatic docetaxel-resistant prostate cancer: a review.

Authors:  Giuseppe Colloca; Antonella Venturino; Franco Checcaglini
Journal:  Med Oncol       Date:  2011-02-20       Impact factor: 3.064

Review 3.  Perspectives on treatment of metastatic castration-resistant prostate cancer.

Authors:  Axel S Merseburger; Joaquim Bellmunt; Cheryl Jenkins; Chris Parker; John M Fitzpatrick
Journal:  Oncologist       Date:  2013-05-13

4.  [Castration-resistant prostate cancer (CRPC)].

Authors:  W Loidl; F Luger; A Roosen
Journal:  Urologe A       Date:  2014-03       Impact factor: 0.639

Review 5.  Evolving standards in the treatment of docetaxel-refractory castration-resistant prostate cancer.

Authors:  E S Antonarakis; A J Armstrong
Journal:  Prostate Cancer Prostatic Dis       Date:  2011-05-17       Impact factor: 5.554

6.  Is there still a place for docetaxel rechallenge in prostate cancer?

Authors:  Roberto Petrioli; Edoardo Francini; Giandomenico Roviello
Journal:  World J Clin Oncol       Date:  2015-10-10

Review 7.  Overview of the latest treatments for castration-resistant prostate cancer.

Authors:  Mohamed Bishr; Fred Saad
Journal:  Nat Rev Urol       Date:  2013-06-25       Impact factor: 14.432

8.  Docetaxel-rechallenge in castration-resistant prostate cancer: defining clinical factors for successful treatment response and improvement in overall survival.

Authors:  Christian Thomas; Maximilian P Brandt; Stephanie Baldauf; Igor Tsaur; Sebastian Frees; Hendrik Borgmann; Wolfgang Jäger; Georg Bartsch; Meike Schneider; Robert Dotzauer; Andreas Neisius; Axel Haferkamp
Journal:  Int Urol Nephrol       Date:  2018-08-17       Impact factor: 2.370

Review 9.  Evolving landscape and novel treatments in metastatic castrate-resistant prostate cancer.

Authors:  Paul J Toren; Martin E Gleave
Journal:  Asian J Androl       Date:  2013-04-15       Impact factor: 3.285

10.  Increased chemosensitivity via targeting testicular nuclear receptor 4 (TR4)-Oct4-interleukin 1 receptor antagonist (IL1Ra) axis in prostate cancer CD133+ stem/progenitor cells to battle prostate cancer.

Authors:  Dong-Rong Yang; Xian-Fan Ding; Jie Luo; Yu-Xi Shan; Ronghao Wang; Shin-Jen Lin; Gonghui Li; Chiung-Kuei Huang; Jin Zhu; Yuhchyau Chen; Soo Ok Lee; Chawnshang Chang
Journal:  J Biol Chem       Date:  2013-04-22       Impact factor: 5.157

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