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Clinical progression is associated with poor prognosis whatever the treatment line in metastatic castration resistant prostate cancer: The CATS international database

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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  • Nicolas Delanoy
  • Anne-Claire Hardy-Bessard
  • Eleni Efstathiou
  • Sylvestre Le Moulec
  • Umberto Basso
  • Alison Birtle
  • Alastair Thomson
  • Michael Krainer
  • Aline Guillot
  • Ugo De Giorgi
  • Ali Hasbini
  • Gedske Daugaard
  • Amit Bahl
  • Simon Chowdhury
  • Orazio Caffo
  • Philippe Beuzeboc
  • Dominique Spaeth
  • Jean-Christophe Eymard
  • Aude Fléchon
  • Jerome Alexandre
  • Carole Helissey
  • Mohamed Butt
  • Frank Priou
  • Eric Lechevallier
  • Jean-Laurent Deville
  • Marine Gross-Goupil
  • Rafael Morales
  • Antoine Thiery-Vuillemin
  • Tatiana Gavrikova
  • Philippe Barthélémy
  • Avishay Sella
  • Karim Fizazi
  • Jean-Marc Ferrero
  • Brigitte Laguerre
  • Constance Thibault
  • Sophie Hans
  • Stéphane Oudard
Vis graf over relationer

AIM OF THE STUDY: Our goal was to evaluate the impact of progression type (prostate-specific antigen [PSA] only, radiological or clinical) at initiation of first-, second- and third life-extending therapy (LET) on treatment outcomes in metastatic castration-resistant prostate cancer (mCRPC) patients, by performing a post-hoc analysis using data from the CATS international registry.

METHODS: The 669 consecutive mCRPC patients of the CATS registry were classified according to their type of progression at initiation of each LET: PSA only (PSA-p), radiological (±PSA) (Radio-p); or clinical (±PSA, ±radiological) progression (Clin-p). Overall survival (OS), the primary endpoint, was calculated from initiation of the first-, second- and third-LET to death for each sequence.

RESULTS: Median OS was shorter in the Clin-p group compared with the PSA-p group (14-month difference in first line; around 7-month difference in second- and third line). Shorter progression-free survival (PFS) was also observed in Clin-p patients, whatever the treatment is. Clinical progression seemed to be associated with a shorter duration of therapy with androgen receptor-targeted therapy (ART) compared with taxanes.

CONCLUSIONS: Clinical progression at initiation of a LET is associated with poor outcomes including shorter PFS and OS as well as clinical and biological features of aggressive disease. Stratifying patients in clinical trials according to disease progression type may prevent selection bias and data heterogeneity. In daily practice, first signs of clinical progression may prompt physicians to consider starting a new LET, independently of PSA levels.

OriginalsprogEngelsk
TidsskriftEuropean journal of cancer (Oxford, England : 1990)
Vol/bind125
Sider (fra-til)153-163
Antal sider11
ISSN0959-8049
DOI
StatusUdgivet - jan. 2020

Bibliografisk note

Copyright © 2019 Elsevier Ltd. All rights reserved.

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