Post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desert

In Europe, prostate cancer is the most common cancer among men with 382.000 new cases and 89.000 deaths annually. Historically, androgen deprivation therapy and docetaxel based chemotherapy were the only treatments able to improve survival. Two studies have been published during last few months rega...

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Main Authors: Amelia Altavilla, Roberto Iacovelli, Giuseppe Procopio, Enrico Cortesi
Format: Article
Language:English
Published: SAGE Publishing 2012-06-01
Series:Therapeutic Advances in Urology
Online Access:https://doi.org/10.1177/1756287212440302
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spelling doaj-35d31ff8609344e09768335e3fb088602020-11-25T03:24:03ZengSAGE PublishingTherapeutic Advances in Urology1756-28721756-28802012-06-01410.1177/1756287212440302Post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desertAmelia AltavillaRoberto IacovelliGiuseppe ProcopioEnrico CortesiIn Europe, prostate cancer is the most common cancer among men with 382.000 new cases and 89.000 deaths annually. Historically, androgen deprivation therapy and docetaxel based chemotherapy were the only treatments able to improve survival. Two studies have been published during last few months regarding the management of castration resistant prostate cancer (CRPC) progressed after docetaxel: for the first time second line therapies have been demonstrated to improve prognosis of these patients. The relevance of these trials is the reintroduction of chemotherapy and hormonal therapy in a disease once considered chemotherapy and castration resistant. All these data may change the traditional approach to CRPC but no evidences have came out from recently closed or ongoing clinical trials about the therapeutic algorithm. How to get oriented in this forest? We propose that patient’s conditions, response and toxicities reported with previous treatments and, above all, dynamics and evolution of disease may influence the choice of subsequent therapies in docetaxel progressed CRPC.https://doi.org/10.1177/1756287212440302
collection DOAJ
language English
format Article
sources DOAJ
author Amelia Altavilla
Roberto Iacovelli
Giuseppe Procopio
Enrico Cortesi
spellingShingle Amelia Altavilla
Roberto Iacovelli
Giuseppe Procopio
Enrico Cortesi
Post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desert
Therapeutic Advances in Urology
author_facet Amelia Altavilla
Roberto Iacovelli
Giuseppe Procopio
Enrico Cortesi
author_sort Amelia Altavilla
title Post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desert
title_short Post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desert
title_full Post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desert
title_fullStr Post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desert
title_full_unstemmed Post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desert
title_sort post-docetaxel therapy in castration resistant prostate cancer – the forest is growing in the desert
publisher SAGE Publishing
series Therapeutic Advances in Urology
issn 1756-2872
1756-2880
publishDate 2012-06-01
description In Europe, prostate cancer is the most common cancer among men with 382.000 new cases and 89.000 deaths annually. Historically, androgen deprivation therapy and docetaxel based chemotherapy were the only treatments able to improve survival. Two studies have been published during last few months regarding the management of castration resistant prostate cancer (CRPC) progressed after docetaxel: for the first time second line therapies have been demonstrated to improve prognosis of these patients. The relevance of these trials is the reintroduction of chemotherapy and hormonal therapy in a disease once considered chemotherapy and castration resistant. All these data may change the traditional approach to CRPC but no evidences have came out from recently closed or ongoing clinical trials about the therapeutic algorithm. How to get oriented in this forest? We propose that patient’s conditions, response and toxicities reported with previous treatments and, above all, dynamics and evolution of disease may influence the choice of subsequent therapies in docetaxel progressed CRPC.
url https://doi.org/10.1177/1756287212440302
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