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Weekly administration of docetaxel for symptomatic metastatic hormone‐refractory prostate carcinoma

BACKGROUND The current Phase II study investigated the clinical benefit, impact on quality of life (QOL), and tolerability of weekly docetaxel in symptomatic patients with metastatic hormone‐refractory prostate carcinoma (HRPC). METHODS Patients received weekly docetaxel 35 mg/m2 intravenously for 6...

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Published in:Cancer 2003-10, Vol.98 (8), p.1627-1634
Main Authors: Gravis, Gwenaelle, Bladou, Franck, Salem, Naji, Macquart‐Moulin, Geneviève, Serment, Gérard, Camerlo, Jacques, Genre, Dominique, Bardou, Valérie‐Jeanne, Maraninchi, Dominique, Viens, Patrice
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container_end_page 1634
container_issue 8
container_start_page 1627
container_title Cancer
container_volume 98
creator Gravis, Gwenaelle
Bladou, Franck
Salem, Naji
Macquart‐Moulin, Geneviève
Serment, Gérard
Camerlo, Jacques
Genre, Dominique
Bardou, Valérie‐Jeanne
Maraninchi, Dominique
Viens, Patrice
description BACKGROUND The current Phase II study investigated the clinical benefit, impact on quality of life (QOL), and tolerability of weekly docetaxel in symptomatic patients with metastatic hormone‐refractory prostate carcinoma (HRPC). METHODS Patients received weekly docetaxel 35 mg/m2 intravenously for 6 consecutive weeks followed by a 2‐week rest repeatedly for a maximum of 24 weeks of treatment. Clinical benefit evaluations, based on Karnofsky performance status (KPS) and pain, were assessed weekly during therapy. A clinical benefit response was defined as a sustained (≥ 4‐week) improvement in at least one of these parameters without worsening in the other. Patient‐assessed QOL (using the European Organization for Research and Treatment of Cancer QLQ‐C30), changes in prostate‐specific antigen (PSA) levels, tumoral response, and toxicity also were evaluated. RESULTS Thirty men (median age, 67 years), 15 of whom had received previous chemotherapy, were treated. Overall, 46% of patients achieved a positive pain response and 48% achieved a 50%‐or‐greater reduction in PSA. KPS was high at baseline (80%), and no significant changes in this parameter were observed. Compared with baseline, all scores improved after the first cycle of therapy, particularly emotional (P = 0.015), pain (P = 0.001), constipation (P = 0.001), and global QOL (P = 0.011) scores. After the second cycle, dyspnea scores decreased (P = 0.010). At the last QOL assessment, there also was deterioration in terms of fatigue (P = 0.013), dyspnea (P = 0.010), and physical functioning (P = 0.017). Toxicity was mild and included neutropenia (Grade 3–4, n = 2). CONCLUSIONS Of these elderly symptomatic patients with HRPC, half had received previous chemotherapy. Weekly docetaxel was found to be associated with improvements in clinical benefit response and in QOL and was well tolerated. Cancer 2003. © 2003 American Cancer Society. DOI 10.1002/cncr.11687 A Phase II study involving weekly docetaxel in symptomatic men with metastatic hormone‐refractory prostate carcinoma was associated with improvements in clinical benefit response, quality of life, and drug tolerance.
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METHODS Patients received weekly docetaxel 35 mg/m2 intravenously for 6 consecutive weeks followed by a 2‐week rest repeatedly for a maximum of 24 weeks of treatment. Clinical benefit evaluations, based on Karnofsky performance status (KPS) and pain, were assessed weekly during therapy. A clinical benefit response was defined as a sustained (≥ 4‐week) improvement in at least one of these parameters without worsening in the other. Patient‐assessed QOL (using the European Organization for Research and Treatment of Cancer QLQ‐C30), changes in prostate‐specific antigen (PSA) levels, tumoral response, and toxicity also were evaluated. RESULTS Thirty men (median age, 67 years), 15 of whom had received previous chemotherapy, were treated. Overall, 46% of patients achieved a positive pain response and 48% achieved a 50%‐or‐greater reduction in PSA. KPS was high at baseline (80%), and no significant changes in this parameter were observed. Compared with baseline, all scores improved after the first cycle of therapy, particularly emotional (P = 0.015), pain (P = 0.001), constipation (P = 0.001), and global QOL (P = 0.011) scores. After the second cycle, dyspnea scores decreased (P = 0.010). At the last QOL assessment, there also was deterioration in terms of fatigue (P = 0.013), dyspnea (P = 0.010), and physical functioning (P = 0.017). Toxicity was mild and included neutropenia (Grade 3–4, n = 2). CONCLUSIONS Of these elderly symptomatic patients with HRPC, half had received previous chemotherapy. Weekly docetaxel was found to be associated with improvements in clinical benefit response and in QOL and was well tolerated. Cancer 2003. © 2003 American Cancer Society. DOI 10.1002/cncr.11687 A Phase II study involving weekly docetaxel in symptomatic men with metastatic hormone‐refractory prostate carcinoma was associated with improvements in clinical benefit response, quality of life, and drug tolerance.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.11687</identifier><identifier>PMID: 14534878</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Aged, 80 and over ; Antineoplastic Agents, Phytogenic - administration &amp; dosage ; docetaxel ; hormone‐refractory prostate carcinoma ; Humans ; Male ; Middle Aged ; Neoplasm Metastasis ; Paclitaxel - administration &amp; dosage ; Paclitaxel - adverse effects ; Paclitaxel - analogs &amp; derivatives ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - drug therapy ; Prostatic Neoplasms - mortality ; Prostatic Neoplasms - psychology ; Quality of Life ; taxanes ; Taxoids ; weekly</subject><ispartof>Cancer, 2003-10, Vol.98 (8), p.1627-1634</ispartof><rights>Copyright © 2003 American Cancer Society</rights><rights>Copyright 2003 American Cancer Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2397-3817a2ca53403c73a1903e82dc75b12c94dee304c6123bce21dcb5af1c96ddc93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14534878$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gravis, Gwenaelle</creatorcontrib><creatorcontrib>Bladou, Franck</creatorcontrib><creatorcontrib>Salem, Naji</creatorcontrib><creatorcontrib>Macquart‐Moulin, Geneviève</creatorcontrib><creatorcontrib>Serment, Gérard</creatorcontrib><creatorcontrib>Camerlo, Jacques</creatorcontrib><creatorcontrib>Genre, Dominique</creatorcontrib><creatorcontrib>Bardou, Valérie‐Jeanne</creatorcontrib><creatorcontrib>Maraninchi, Dominique</creatorcontrib><creatorcontrib>Viens, Patrice</creatorcontrib><title>Weekly administration of docetaxel for symptomatic metastatic hormone‐refractory prostate carcinoma</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND The current Phase II study investigated the clinical benefit, impact on quality of life (QOL), and tolerability of weekly docetaxel in symptomatic patients with metastatic hormone‐refractory prostate carcinoma (HRPC). 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Compared with baseline, all scores improved after the first cycle of therapy, particularly emotional (P = 0.015), pain (P = 0.001), constipation (P = 0.001), and global QOL (P = 0.011) scores. After the second cycle, dyspnea scores decreased (P = 0.010). At the last QOL assessment, there also was deterioration in terms of fatigue (P = 0.013), dyspnea (P = 0.010), and physical functioning (P = 0.017). Toxicity was mild and included neutropenia (Grade 3–4, n = 2). CONCLUSIONS Of these elderly symptomatic patients with HRPC, half had received previous chemotherapy. Weekly docetaxel was found to be associated with improvements in clinical benefit response and in QOL and was well tolerated. Cancer 2003. © 2003 American Cancer Society. DOI 10.1002/cncr.11687 A Phase II study involving weekly docetaxel in symptomatic men with metastatic hormone‐refractory prostate carcinoma was associated with improvements in clinical benefit response, quality of life, and drug tolerance.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antineoplastic Agents, Phytogenic - administration &amp; dosage</subject><subject>docetaxel</subject><subject>hormone‐refractory prostate carcinoma</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Metastasis</subject><subject>Paclitaxel - administration &amp; dosage</subject><subject>Paclitaxel - adverse effects</subject><subject>Paclitaxel - analogs &amp; derivatives</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - drug therapy</subject><subject>Prostatic Neoplasms - mortality</subject><subject>Prostatic Neoplasms - psychology</subject><subject>Quality of Life</subject><subject>taxanes</subject><subject>Taxoids</subject><subject>weekly</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpFUMtKxEAQHERx19WLHyDzA1nnkWSSowRfsCiIorcw6elgNJMJk4jm5if4jX6Js7uKp67uqm6qi5BjzpacMXEKHfgl52mmdsics1xFjMdil8wZY1mUxPJpRg6G4SW0SiRyn8x4nMg4U9mc4CPiaztRbWzTNcPo9di4jrqaGgc46g9sae08HSbbj84GFqgN82HcwGfnrevw-_PLY-01jM5PtPduTSMF7aHpwtYh2at1O-DRb12Qh4vz--IqWt1eXhdnqwiEDLZlxpUWoIM5JkFJzXMmMRMGVFJxAXlsECWLIeVCVoCCG6gSXXPIU2Mglwtysr3bv1UWTdn7xmo_lX__BgHfCt6bFqd_npXrJMt1kuUmybK4Ke42SP4Ahn1qmg</recordid><startdate>20031015</startdate><enddate>20031015</enddate><creator>Gravis, Gwenaelle</creator><creator>Bladou, Franck</creator><creator>Salem, Naji</creator><creator>Macquart‐Moulin, Geneviève</creator><creator>Serment, Gérard</creator><creator>Camerlo, Jacques</creator><creator>Genre, Dominique</creator><creator>Bardou, Valérie‐Jeanne</creator><creator>Maraninchi, Dominique</creator><creator>Viens, Patrice</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20031015</creationdate><title>Weekly administration of docetaxel for symptomatic metastatic hormone‐refractory prostate carcinoma</title><author>Gravis, Gwenaelle ; Bladou, Franck ; Salem, Naji ; Macquart‐Moulin, Geneviève ; Serment, Gérard ; Camerlo, Jacques ; Genre, Dominique ; Bardou, Valérie‐Jeanne ; Maraninchi, Dominique ; Viens, Patrice</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2397-3817a2ca53403c73a1903e82dc75b12c94dee304c6123bce21dcb5af1c96ddc93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antineoplastic Agents, Phytogenic - administration &amp; dosage</topic><topic>docetaxel</topic><topic>hormone‐refractory prostate carcinoma</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Metastasis</topic><topic>Paclitaxel - administration &amp; dosage</topic><topic>Paclitaxel - adverse effects</topic><topic>Paclitaxel - analogs &amp; derivatives</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms - drug therapy</topic><topic>Prostatic Neoplasms - mortality</topic><topic>Prostatic Neoplasms - psychology</topic><topic>Quality of Life</topic><topic>taxanes</topic><topic>Taxoids</topic><topic>weekly</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gravis, Gwenaelle</creatorcontrib><creatorcontrib>Bladou, Franck</creatorcontrib><creatorcontrib>Salem, Naji</creatorcontrib><creatorcontrib>Macquart‐Moulin, Geneviève</creatorcontrib><creatorcontrib>Serment, Gérard</creatorcontrib><creatorcontrib>Camerlo, Jacques</creatorcontrib><creatorcontrib>Genre, Dominique</creatorcontrib><creatorcontrib>Bardou, Valérie‐Jeanne</creatorcontrib><creatorcontrib>Maraninchi, Dominique</creatorcontrib><creatorcontrib>Viens, Patrice</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gravis, Gwenaelle</au><au>Bladou, Franck</au><au>Salem, Naji</au><au>Macquart‐Moulin, Geneviève</au><au>Serment, Gérard</au><au>Camerlo, Jacques</au><au>Genre, Dominique</au><au>Bardou, Valérie‐Jeanne</au><au>Maraninchi, Dominique</au><au>Viens, Patrice</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Weekly administration of docetaxel for symptomatic metastatic hormone‐refractory prostate carcinoma</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2003-10-15</date><risdate>2003</risdate><volume>98</volume><issue>8</issue><spage>1627</spage><epage>1634</epage><pages>1627-1634</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>BACKGROUND The current Phase II study investigated the clinical benefit, impact on quality of life (QOL), and tolerability of weekly docetaxel in symptomatic patients with metastatic hormone‐refractory prostate carcinoma (HRPC). METHODS Patients received weekly docetaxel 35 mg/m2 intravenously for 6 consecutive weeks followed by a 2‐week rest repeatedly for a maximum of 24 weeks of treatment. Clinical benefit evaluations, based on Karnofsky performance status (KPS) and pain, were assessed weekly during therapy. A clinical benefit response was defined as a sustained (≥ 4‐week) improvement in at least one of these parameters without worsening in the other. Patient‐assessed QOL (using the European Organization for Research and Treatment of Cancer QLQ‐C30), changes in prostate‐specific antigen (PSA) levels, tumoral response, and toxicity also were evaluated. RESULTS Thirty men (median age, 67 years), 15 of whom had received previous chemotherapy, were treated. Overall, 46% of patients achieved a positive pain response and 48% achieved a 50%‐or‐greater reduction in PSA. KPS was high at baseline (80%), and no significant changes in this parameter were observed. Compared with baseline, all scores improved after the first cycle of therapy, particularly emotional (P = 0.015), pain (P = 0.001), constipation (P = 0.001), and global QOL (P = 0.011) scores. After the second cycle, dyspnea scores decreased (P = 0.010). At the last QOL assessment, there also was deterioration in terms of fatigue (P = 0.013), dyspnea (P = 0.010), and physical functioning (P = 0.017). Toxicity was mild and included neutropenia (Grade 3–4, n = 2). CONCLUSIONS Of these elderly symptomatic patients with HRPC, half had received previous chemotherapy. Weekly docetaxel was found to be associated with improvements in clinical benefit response and in QOL and was well tolerated. Cancer 2003. © 2003 American Cancer Society. 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source Wiley-Blackwell Read & Publish Collection; EZB Electronic Journals Library
subjects Aged
Aged, 80 and over
Antineoplastic Agents, Phytogenic - administration & dosage
docetaxel
hormone‐refractory prostate carcinoma
Humans
Male
Middle Aged
Neoplasm Metastasis
Paclitaxel - administration & dosage
Paclitaxel - adverse effects
Paclitaxel - analogs & derivatives
Prostate-Specific Antigen - blood
Prostatic Neoplasms - drug therapy
Prostatic Neoplasms - mortality
Prostatic Neoplasms - psychology
Quality of Life
taxanes
Taxoids
weekly
title Weekly administration of docetaxel for symptomatic metastatic hormone‐refractory prostate carcinoma
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