Poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancer

BACKGROUND AND OBJECTIVES: Since previous studies have indicated there are improvements in overall survival, the aim of this phase II clinical study was to evaluate docetaxel every three weeks plus prednisone as first-line chemotherapy for treatment of hormone-refractory metastatic prostate cancer (...

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Main Authors: Abd El Halim Mohamed Abu-Hamar, Saleh Mansour, Mohamed El Shebiney, Naser Mohamed Abd El Bary, Emad Sadaka, Alaa Maria
Format: Article
Language:English
Published: Elsevier 2010-07-01
Series:Hematology/Oncology and Stem Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S1658387610500220
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spelling doaj-51d2cf50b5c442269402772c0697c5862020-11-24T21:41:31ZengElsevierHematology/Oncology and Stem Cell Therapy1658-38762010-07-0133121127Poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancerAbd El Halim Mohamed Abu-Hamar0Saleh Mansour1Mohamed El Shebiney2Naser Mohamed Abd El Bary3Emad Sadaka4Alaa Maria5Abd El Halim Mohamed Abu Hamar MD · Clinical Oncology Department, Faculty of Medicine, Tanta University Hospital, Al Gaish St., Tanta, Gharbia 11312, Egypt; Tanta University Hospital, Tanta, Gharbia, EgyptTanta University Hospital, Tanta, Gharbia, EgyptTanta University Hospital, Tanta, Gharbia, EgyptTanta University Hospital, Tanta, Gharbia, EgyptTanta University Hospital, Tanta, Gharbia, EgyptTanta University Hospital, Tanta, Gharbia, EgyptBACKGROUND AND OBJECTIVES: Since previous studies have indicated there are improvements in overall survival, the aim of this phase II clinical study was to evaluate docetaxel every three weeks plus prednisone as first-line chemotherapy for treatment of hormone-refractory metastatic prostate cancer (HRMPC). METHODS: Thirty-five metastatic HRPC patients were treated with docetaxel 70 /m2 every 3 weeks plus oral prednisolone 5  twice daily at the clinical oncology departments of Tanta, Mansoura and Menofia University Hospitals during the period from June 2006 to December 2008. The primary endpoint was assessment of the overall tumor response rate. Secondary endpoints were assessment of PSA response rate, overall survival rate, and the time to disease progression. RESULTS: The median number of cycles administered was 6 cycles. Partial response was observed in 15 patients (42.9%) with evaluable measurable disease. Median survival from protocol entry was 15 months. Median time-to-disease progression was 10 months. Prostate-specific antigen (PSA) declined ≥50% in 9 patients (25.7%). The most common grade 3/4 toxicity associated with studied protocol was neutropenia (85.7%). CONCLUSIONS: When given with prednisone, treatment with docetaxel every three weeks does not improve survival, so the benefit of docetaxel-based therapy is not clear this high risk and poor prognostic group of patients.http://www.sciencedirect.com/science/article/pii/S1658387610500220
collection DOAJ
language English
format Article
sources DOAJ
author Abd El Halim Mohamed Abu-Hamar
Saleh Mansour
Mohamed El Shebiney
Naser Mohamed Abd El Bary
Emad Sadaka
Alaa Maria
spellingShingle Abd El Halim Mohamed Abu-Hamar
Saleh Mansour
Mohamed El Shebiney
Naser Mohamed Abd El Bary
Emad Sadaka
Alaa Maria
Poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancer
Hematology/Oncology and Stem Cell Therapy
author_facet Abd El Halim Mohamed Abu-Hamar
Saleh Mansour
Mohamed El Shebiney
Naser Mohamed Abd El Bary
Emad Sadaka
Alaa Maria
author_sort Abd El Halim Mohamed Abu-Hamar
title Poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancer
title_short Poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancer
title_full Poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancer
title_fullStr Poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancer
title_full_unstemmed Poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancer
title_sort poor survival outcome of docetaxel every three weeks plus prednisone for treatment of patients with hormone-refractory metastatic prostate cancer
publisher Elsevier
series Hematology/Oncology and Stem Cell Therapy
issn 1658-3876
publishDate 2010-07-01
description BACKGROUND AND OBJECTIVES: Since previous studies have indicated there are improvements in overall survival, the aim of this phase II clinical study was to evaluate docetaxel every three weeks plus prednisone as first-line chemotherapy for treatment of hormone-refractory metastatic prostate cancer (HRMPC). METHODS: Thirty-five metastatic HRPC patients were treated with docetaxel 70 /m2 every 3 weeks plus oral prednisolone 5  twice daily at the clinical oncology departments of Tanta, Mansoura and Menofia University Hospitals during the period from June 2006 to December 2008. The primary endpoint was assessment of the overall tumor response rate. Secondary endpoints were assessment of PSA response rate, overall survival rate, and the time to disease progression. RESULTS: The median number of cycles administered was 6 cycles. Partial response was observed in 15 patients (42.9%) with evaluable measurable disease. Median survival from protocol entry was 15 months. Median time-to-disease progression was 10 months. Prostate-specific antigen (PSA) declined ≥50% in 9 patients (25.7%). The most common grade 3/4 toxicity associated with studied protocol was neutropenia (85.7%). CONCLUSIONS: When given with prednisone, treatment with docetaxel every three weeks does not improve survival, so the benefit of docetaxel-based therapy is not clear this high risk and poor prognostic group of patients.
url http://www.sciencedirect.com/science/article/pii/S1658387610500220
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