Efficacy and Safety of Cabazitaxel Versus Abiraterone or Enzalutamide in Older Patients with Metastatic Castration-resistant Prostate Cancer in the CARD Study.


Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
10 2021
Historique:
received: 11 11 2020
accepted: 28 06 2021
pubmed: 19 7 2021
medline: 11 3 2022
entrez: 18 7 2021
Statut: ppublish

Résumé

In the CARD study (NCT02485691), cabazitaxel significantly improved median radiographic progression-free survival (rPFS) and overall survival (OS) versus abiraterone/enzalutamide in patients with metastatic castration-resistant prostate cancer (mCRPC) who had previously received docetaxel and progressed ≤12 mo on the alternative agent (abiraterone/enzalutamide). To assess cabazitaxel versus abiraterone/enzalutamide in older (≥70 yr) and younger (<70 yr) patients in CARD. Patients with mCRPC were randomized 1:1 to cabazitaxel (25 mg/m Analyses of rPFS (primary endpoint) and safety by age were prespecified; others were post hoc. Treatment groups were compared using stratified log-rank or Cochran-Mantel-Haenszel tests. Of the 255 patients randomized, 135 were aged ≥70 yr (median 76 yr). Cabazitaxel, compared with abiraterone/enzalutamide, significantly improved median rPFS in older (8.2 vs 4.5 mo; hazard ratio [HR] = 0.58; 95% confidence interval [CI] = 0.38-0.89; p = 0.012) and younger (7.4 vs 3.2 mo; HR = 0.47; 95% CI = 0.30-0.74; p < 0.001) patients. The median OS of cabazitaxel versus abiraterone/enzalutamide was 13.9 versus 9.4 mo in older patients (HR = 0.66; 95% CI = 0.41-1.06; p = 0.084), and it was 13.6 versus 11.8 mo in younger patients (HR = 0.66; 95% CI = 0.41-1.08; p = 0.093). Progression-free survival, prostate-specific antigen, and tumor and pain responses favored cabazitaxel, regardless of age. Grade ≥3 treatment-emergent adverse events (TEAEs) occurred in 58% versus 49% of older patients receiving cabazitaxel versus abiraterone/enzalutamide and 48% versus 42% of younger patients. In older patients, cardiac adverse events were more frequent with abiraterone/enzalutamide; asthenia and diarrhea were more frequent with cabazitaxel. Cabazitaxel improved efficacy outcomes versus abiraterone/enzalutamide in patients with mCRPC after prior docetaxel and abiraterone/enzalutamide, regardless of age. TEAEs were more frequent among older patients. The cabazitaxel safety profile was manageable across age groups. Clinical trial data showed that cabazitaxel improved survival versus abiraterone/enzalutamide with manageable side effects in patients with metastatic castration-resistant prostate cancer who had previously received docetaxel and the alternative agent (abiraterone/enzalutamide), irrespective of age.

Sections du résumé

BACKGROUND
In the CARD study (NCT02485691), cabazitaxel significantly improved median radiographic progression-free survival (rPFS) and overall survival (OS) versus abiraterone/enzalutamide in patients with metastatic castration-resistant prostate cancer (mCRPC) who had previously received docetaxel and progressed ≤12 mo on the alternative agent (abiraterone/enzalutamide).
OBJECTIVE
To assess cabazitaxel versus abiraterone/enzalutamide in older (≥70 yr) and younger (<70 yr) patients in CARD.
DESIGN, SETTING, AND PARTICIPANTS
Patients with mCRPC were randomized 1:1 to cabazitaxel (25 mg/m
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS
Analyses of rPFS (primary endpoint) and safety by age were prespecified; others were post hoc. Treatment groups were compared using stratified log-rank or Cochran-Mantel-Haenszel tests.
RESULTS AND LIMITATIONS
Of the 255 patients randomized, 135 were aged ≥70 yr (median 76 yr). Cabazitaxel, compared with abiraterone/enzalutamide, significantly improved median rPFS in older (8.2 vs 4.5 mo; hazard ratio [HR] = 0.58; 95% confidence interval [CI] = 0.38-0.89; p = 0.012) and younger (7.4 vs 3.2 mo; HR = 0.47; 95% CI = 0.30-0.74; p < 0.001) patients. The median OS of cabazitaxel versus abiraterone/enzalutamide was 13.9 versus 9.4 mo in older patients (HR = 0.66; 95% CI = 0.41-1.06; p = 0.084), and it was 13.6 versus 11.8 mo in younger patients (HR = 0.66; 95% CI = 0.41-1.08; p = 0.093). Progression-free survival, prostate-specific antigen, and tumor and pain responses favored cabazitaxel, regardless of age. Grade ≥3 treatment-emergent adverse events (TEAEs) occurred in 58% versus 49% of older patients receiving cabazitaxel versus abiraterone/enzalutamide and 48% versus 42% of younger patients. In older patients, cardiac adverse events were more frequent with abiraterone/enzalutamide; asthenia and diarrhea were more frequent with cabazitaxel.
CONCLUSIONS
Cabazitaxel improved efficacy outcomes versus abiraterone/enzalutamide in patients with mCRPC after prior docetaxel and abiraterone/enzalutamide, regardless of age. TEAEs were more frequent among older patients. The cabazitaxel safety profile was manageable across age groups.
PATIENT SUMMARY
Clinical trial data showed that cabazitaxel improved survival versus abiraterone/enzalutamide with manageable side effects in patients with metastatic castration-resistant prostate cancer who had previously received docetaxel and the alternative agent (abiraterone/enzalutamide), irrespective of age.

Identifiants

pubmed: 34274136
pii: S0302-2838(21)01862-5
doi: 10.1016/j.eururo.2021.06.021
pii:
doi:

Substances chimiques

Androstenes 0
Benzamides 0
Nitriles 0
Taxoids 0
Docetaxel 15H5577CQD
Phenylthiohydantoin 2010-15-3
cabazitaxel 51F690397J
enzalutamide 93T0T9GKNU
Abiraterone Acetate EM5OCB9YJ6
abiraterone G819A456D0
Prednisone VB0R961HZT

Banques de données

ClinicalTrials.gov
['NCT02485691']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

497-506

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Auteurs

Cora N Sternberg (CN)

Englander Institute for Precision Medicine, Weill Cornell Medicine, Meyer Cancer Center, New York, NY, USA. Electronic address: cns9006@med.cornell.edu.

Daniel Castellano (D)

12 de Octubre University Hospital, Madrid, Spain.

Johann de Bono (J)

The Institute of Cancer Research and the Royal Marsden Hospital, London, UK.

Karim Fizazi (K)

Gustave Roussy Institute and University of Paris Saclay, Villejuif, France.

Bertrand Tombal (B)

Institute de Recherche Clinique, Université Catholique de Louvain, Brussels, Belgium.

Christian Wülfing (C)

Department of Urology, Asklepios Tumorzentrum Hamburg, Asklepios Klinik Altona, Hamburg, Germany.

Gero Kramer (G)

Department of Urology, Medical University of Vienna, Vienna, Austria.

Jean-Christophe Eymard (JC)

Jean Godinot Institute, Reims, France.

Aristotelis Bamias (A)

Alexandra Hospital, National and Kapodistrian University of Athens, Athens, Greece.

Joan Carles (J)

Vall d'Hebron Institute of Oncology, Vall d'Hebron University Hospital, Barcelona, Spain.

Roberto Iacovelli (R)

Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy; Fondazione Policlinico Agostino Gemelli IRCCS, Rome, Italy.

Bohuslav Melichar (B)

Palacky University Medical School and Teaching Hospital, Olomouc, Czech Republic.

Ásgerður Sverrisdóttir (Á)

Landspitali University Hospital, Reykjavik, Iceland.

Christine Theodore (C)

Foch Hospital, Suresnes, France.

Susan Feyerabend (S)

Studienpraxis Urologie, Nürtingen, Germany.

Carole Helissey (C)

Hôpital D'Instruction des Armées, Bégin, Saint Mandé, France.

Elizabeth M Poole (EM)

Sanofi, Global Medical Oncology, Cambridge, MA, USA.

Ayse Ozatilgan (A)

Sanofi, Global Medical Oncology, Cambridge, MA, USA.

Christine Geffriaud-Ricouard (C)

Sanofi, Europe Medical Oncology, Paris, France.

Ronald de Wit (R)

Erasmus University Hospital, Rotterdam, The Netherlands.

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Classifications MeSH