TEAM Study: Upfront Docetaxel Treatment in Patients With Metastatic Hormone-Sensitive Prostate Cancer: A Real-World, Multicenter, Retrospective Analysis.

Docetaxel Metastatic hormone-sensitive prostate cancer Prognostic factors Triplet therapy

Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
07 Sep 2023
Historique:
received: 08 07 2023
revised: 18 08 2023
accepted: 28 08 2023
medline: 6 10 2023
pubmed: 6 10 2023
entrez: 5 10 2023
Statut: aheadofprint

Résumé

Treatment of metastatic hormone-sensitive prostate cancer (mHSPC) dramatically changed. PEACE-1 and ARASENS trials established triplet therapy efficacy. Identifying prognostic factors supporting treatment choice is pivotal. TEAM is an observational, retrospective study to evaluate prognostic role of variables in mHSPC patients receiving upfront docetaxel in 11 Italian centers. Outcome measures were progression-free survival (PFS) and overall-survival (OS). From September 2014 to December 2020, 147 patients were included. Median PFS and OS were 11.6 and 37.4 months. At univariate analysis, PFS-related variables were Gleason Score (GS) (P = .001), opioid use (P = .004), bone metastases number (P < .001), baseline PSA (P = .006), Hb (P < .001), ALP (P < .001) and LDH (P = .002), time between ADT and docetaxel start (P = .018), 3-month PSA (P < .001) and ALP (P < .001), and number of docetaxel cycles (P < .001). OS-related variables were PSA at diagnosis (P = .024), primary tumor treatment (P = .022), baseline pain (P = .015), opioid use (P < .001), bone metastases number (P < . 001), baseline Hb (P < .001), ALP (P < .001) and LDH (P = .001), NLR ratio (P = .039), 3-month PSA (P < .001) and ALP (P < .001) and docetaxel cycles number (P < .001). At multivariate analysis, independent prognostic variables were GS, opioid use, baseline LDH and time between ADT and docetaxel initiation for PFS, and baseline Hb and LDH for OS. Patients receiving upfront docetaxel with high GS, high disease burden, pain or opioid use, baseline unfavorable laboratory values had worse outcomes. Patients had greater docetaxel benefit when initiated early after ADT start. These parameters could be taken into account when selecting candidates for triplet therapy.

Sections du résumé

BACKGROUND BACKGROUND
Treatment of metastatic hormone-sensitive prostate cancer (mHSPC) dramatically changed. PEACE-1 and ARASENS trials established triplet therapy efficacy. Identifying prognostic factors supporting treatment choice is pivotal.
METHODS METHODS
TEAM is an observational, retrospective study to evaluate prognostic role of variables in mHSPC patients receiving upfront docetaxel in 11 Italian centers. Outcome measures were progression-free survival (PFS) and overall-survival (OS).
RESULTS RESULTS
From September 2014 to December 2020, 147 patients were included. Median PFS and OS were 11.6 and 37.4 months. At univariate analysis, PFS-related variables were Gleason Score (GS) (P = .001), opioid use (P = .004), bone metastases number (P < .001), baseline PSA (P = .006), Hb (P < .001), ALP (P < .001) and LDH (P = .002), time between ADT and docetaxel start (P = .018), 3-month PSA (P < .001) and ALP (P < .001), and number of docetaxel cycles (P < .001). OS-related variables were PSA at diagnosis (P = .024), primary tumor treatment (P = .022), baseline pain (P = .015), opioid use (P < .001), bone metastases number (P < . 001), baseline Hb (P < .001), ALP (P < .001) and LDH (P = .001), NLR ratio (P = .039), 3-month PSA (P < .001) and ALP (P < .001) and docetaxel cycles number (P < .001). At multivariate analysis, independent prognostic variables were GS, opioid use, baseline LDH and time between ADT and docetaxel initiation for PFS, and baseline Hb and LDH for OS.
CONCLUSION CONCLUSIONS
Patients receiving upfront docetaxel with high GS, high disease burden, pain or opioid use, baseline unfavorable laboratory values had worse outcomes. Patients had greater docetaxel benefit when initiated early after ADT start. These parameters could be taken into account when selecting candidates for triplet therapy.

Identifiants

pubmed: 37798164
pii: S1558-7673(23)00200-8
doi: 10.1016/j.clgc.2023.08.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure All authors have no conflict of interest to declare.

Auteurs

Chiara Pisano (C)

Department of Medical Oncology, S Croce e Carle Hospital, Cuneo, Italy.

Fabio Turco (F)

Department of Oncology, San Luigi Gonzaga University Hospital, University of Turin, Orbassano, Italy.

Elena Arnaudo (E)

Department of Oncology, San Luigi Gonzaga University Hospital, University of Turin, Orbassano, Italy.

Elena Fea (E)

Department of Medical Oncology, S Croce e Carle Hospital, Cuneo, Italy.

Paola Vanella (P)

Department of Medical Oncology, S Croce e Carle Hospital, Cuneo, Italy.

Fiorella Ruatta (F)

Department of Medical Oncology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.

Roberto Filippi (R)

Department of Oncology, San Luigi Gonzaga University Hospital, University of Turin, Orbassano, Italy; Division of Medical Oncology 1, Department of Oncology, Città della Salute e della Scienza Hospital, Turin, Italy.

Federica Brusa (F)

Department of Medical Oncology, Cardinal Massaia Hospital, Asti, Italy.

Veronica Prati (V)

Department of Medical Oncology, Michele e Pietro Ferrero Hospital, Verduno-Azienda Sanitaria Locale CN2, Alba-Bra, Cuneo, Italy.

Federica Vana (F)

Department of Oncology, San Giovanni Bosco Hospital, Turin, Italy.

Alessia Mennitto (A)

Medical Oncology-Department of Translational Medicine (DIMET), Università del Piemonte Orientale (UPO), Maggiore della Carità University Hospital, Novara, Italy.

Carlo Cattrini (C)

Medical Oncology-Department of Translational Medicine (DIMET), Università del Piemonte Orientale (UPO), Maggiore della Carità University Hospital, Novara, Italy.

Francesca Vignani (F)

Department of Oncology, Ordine Mauriziano Hospital, University of Turin, Turin, Italy.

Rossana Dionisio (R)

Department of Oncology, Ordine Mauriziano Hospital, University of Turin, Turin, Italy.

Massimiliano Icardi (M)

Division of Medical Oncology 2, Department of Oncology, Città della Salute e della Scienza Hospital, Turin, Italy.

Pamela Guglielmini (P)

Oncology Unit, S. Spirito Hospital, Casale Monferrato, Alessandria, Italy.

Roberta Buosi (R)

Oncology Unit, S. Spirito Hospital, Casale Monferrato, Alessandria, Italy.

Ilaria Stevani (I)

Oncology Unit, S. Spirito Hospital, Casale Monferrato, Alessandria, Italy.

Roberto Vormola (R)

Department of Oncology, Ivrea Community Hospital, Ivrea, Italy.

Gianmauro Numico (G)

Department of Medical Oncology, S Croce e Carle Hospital, Cuneo, Italy.

Ilaria Depetris (I)

Division of Medical Oncology 1, Department of Oncology, Città della Salute e della Scienza Hospital, Turin, Italy.

Alessandro Comandone (A)

Department of Oncology, San Giovanni Bosco Hospital, Turin, Italy.

Alessandra Gennari (A)

Medical Oncology-Department of Translational Medicine (DIMET), Università del Piemonte Orientale (UPO), Maggiore della Carità University Hospital, Novara, Italy.

Mario Airoldi (M)

Division of Medical Oncology 2, Department of Oncology, Città della Salute e della Scienza Hospital, Turin, Italy.

Maura Rossi (M)

Oncology Unit, S. Spirito Hospital, Casale Monferrato, Alessandria, Italy.

Giorgio Vellani (G)

Department of Oncology, Ivrea Community Hospital, Ivrea, Italy.

Cinzia Ortega (C)

Department of Medical Oncology, Michele e Pietro Ferrero Hospital, Verduno-Azienda Sanitaria Locale CN2, Alba-Bra, Cuneo, Italy.

Marcello Tucci (M)

Department of Medical Oncology, Cardinal Massaia Hospital, Asti, Italy. Electronic address: marcello.tucci@gmail.com.

Massimo Di Maio (MD)

Department of Oncology, Ordine Mauriziano Hospital, University of Turin, Turin, Italy.

Consuelo Buttigliero (C)

Department of Oncology, San Luigi Gonzaga University Hospital, University of Turin, Orbassano, Italy.

Classifications MeSH