Overall Survival of Black and White Men With Metastatic Castration-Resistant Prostate Cancer Treated With Docetaxel.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
10 02 2019
Historique:
pubmed: 24 12 2018
medline: 18 12 2019
entrez: 22 12 2018
Statut: ppublish

Résumé

Several studies have reported that among patients with localized prostate cancer, black men have a shorter overall survival (OS) time than white men, but few data exist for men with advanced prostate cancer. The primary goal of this analysis was to compare the OS in black and white men with metastatic castration-resistant prostate cancer (mCRPC) who were treated in phase III clinical trials with docetaxel plus prednisone (DP) or a DP-containing regimen. Individual participant data from 8,820 men with mCRPC randomly assigned in nine phase III trials to DP or a DP-containing regimen were combined. Race was based on self-report. The primary end point was OS. The Cox proportional hazards regression model was used to assess the prognostic importance of race (black v white) adjusted for established risk factors common across the trials (age, prostate-specific antigen, performance status, alkaline phosphatase, hemoglobin, and sites of metastases). Of 8,820 men, 7,528 (85%) were white, 500 (6%) were black, 424 (5%) were Asian, and 368 (4%) were of unknown race. Black men were younger and had worse performance status, higher testosterone and prostate-specific antigen, and lower hemoglobin than white men. Despite these differences, the median OS was 21.0 months (95% CI, 19.4 to 22.5 months) versus 21.2 months (95% CI, 20.8 to 21.7 months) in black and white men, respectively. The pooled multivariable hazard ratio of 0.81 (95% CI, 0.72 to 0.91) demonstrates that overall, black men have a statistically significant decreased risk of death compared with white men ( P < .001). When adjusted for known prognostic factors, we observed a statistically significant increased OS in black versus white men with mCRPC who were enrolled in these clinical trials. The mechanism for these differences is not known.

Identifiants

pubmed: 30576268
doi: 10.1200/JCO.18.01279
pmc: PMC6804881
doi:

Substances chimiques

Docetaxel 15H5577CQD
Mitoxantrone BZ114NVM5P
Prednisone VB0R961HZT

Types de publication

Journal Article Meta-Analysis Research Support, U.S. Gov't, Non-P.H.S. Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

403-410

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189974
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014089
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180888
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180819
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180830
Pays : United States

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Auteurs

Susan Halabi (S)

1 Duke University Medical Center, Durham, NC.

Sandipan Dutta (S)

1 Duke University Medical Center, Durham, NC.

Catherine M Tangen (CM)

2 Fred Hutchinson Cancer Research Center, Seattle, WA.

Mark Rosenthal (M)

3 The Royal Melbourne Hospital, Parkville, VIC, Australia.

Daniel P Petrylak (DP)

4 Yale University School of Medicine, New Haven, CT.

Ian M Thompson (IM)

5 UT Health Science Center, San Antonio, TX.

Kim N Chi (KN)

6 BC Cancer Agency Vancouver Centre, Vancouver, BC.

John C Araujo (JC)

7 The University of Texas MD Anderson Cancer Center, Houston, TX.

Christopher Logothetis (C)

7 The University of Texas MD Anderson Cancer Center, Houston, TX.

David I Quinn (DI)

8 University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA.

Karim Fizazi (K)

9 Gustave Roussy, Villejuif, France.

Michael J Morris (MJ)

10 Memorial Sloan Kettering Cancer Center, New York, NY.

Mario A Eisenberger (MA)

11 The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University, Baltimore, MD.

Daniel J George (DJ)

1 Duke University Medical Center, Durham, NC.

Johann S De Bono (JS)

12 The Institute of Cancer Research and The Royal Marsden National Health Service Foundation Trust, Sutton, United Kingdom.

Celestia S Higano (CS)

2 Fred Hutchinson Cancer Research Center, Seattle, WA.

Ian F Tannock (IF)

13 Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

Eric J Small (EJ)

14 University of California San Francisco, San Francisco, CA.

William Kevin Kelly (WK)

15 Sidney Kimmel Cancer Center at Thomas Jefferson University, Philadelphia, PA.

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Classifications MeSH