Biochemical progression free and overall survival among Black men with stage IV prostate cancer in South Africa: Results from a prospective cohort study

Author:

Pumpalova Yoanna S.1ORCID,Ramakrishnan Adarsh2,May Michael1,Pentz Audrey3,Minkowitz Shauli4,Doherty Sean4,Singh Elvira5,Chen Wenlong Carl356,Rebbeck Timothy R.78ORCID,Neugut Alfred I.129,Joffe Maureen4

Affiliation:

1. Department of Medicine, Vagelos College of Physicians and Surgeons Columbia University New York City New York USA

2. Department of Epidemiology, Mailman School of Public Health Columbia University New York City New York USA

3. Strengthening Oncology Services Research Unit, Faculty of Health Sciences University of the Witwatersrand Johannesburg South Africa

4. Division of Urology, Department of Surgery, Faculty of Health Sciences University of the Witwatersrand Johannesburg South Africa

5. National Cancer Registry National Health Laboratory Service Johannesburg South Africa

6. Sydney Brenner Institute for Molecular Bioscience Faculty of Health Sciences, University of the Witwatersrand Johannesburg South Africa

7. Dana Farber Cancer Institute Boston Massachusetts USA

8. Harvard T.H. Chan School of Public Health Boston Massachusetts USA

9. Herbert Irving Comprehensive Cancer Center, Vagelos College of Physicians and Surgeons Columbia University New York City New York USA

Abstract

AbstractBackgroundMen of African descent are disproportionately affected by prostate cancer (PCa), and many have metastatic disease at presentation. In South Africa (SA), androgen deprivation therapy (ADT) is the first‐line treatment for stage IV PCa.ObjectiveTo identify predictors of overall survival (OS) in Black South African men with stage IV PCa treated with ADT.Design, Setting, and ParticipantsMen diagnosed with prostate cancer (3/22/2016–10/30/2020) at Chris Hani Baragwanath Academic Hospital in Soweto, Johannesburg, were recruited for the Men of African Descent with Cancer of the Prostate study. We included men with newly diagnosed stage IV PCa treated with ADT who had a prostate‐specific antigen (PSA) level drawn prior to initiation of ADT and had ≥1 PSA drawn ≥12 weeks after ADT start.Outcomes Measures and Statistical AnalysisWe used Kaplan–Meier statistics to estimate OS and Cox regression models to identify predictors of OS.Results and LimitationsOf the 1097 men diagnosed with prostate cancer, we included 153 men with stage IV PCa who received ADT and met PSA requirements. The median age was 68.0 years (interquartile range 64–73 years). Median OS from time of ADT initiation was 3.39 years (95% confidence interval (CI): 3.14%–noncalculable), while biochemical progression‐free survival was 2.36 years (95% CI: 2.03%–3.73%). Biochemical progression (HR 3.52, 95% CI: 1.85%–6.70%), PSA nadir level >4 ng/mL (HR 3.77, 95% CI: 1.86%–7.62%), alkaline phosphatase level at diagnosis >150 IU/dL (HR 3.09, 95% CI: 1.64%–5.83%), and hemoglobin at diagnosis <13.5 g/dL (HR 2.90, 95% CI: 1.28%–6.56%) were associated with worse OS.ConclusionsIn this study, we identified factors associated with poor OS among Black South African men with stage IV PCa treated with ADT. These factors may be useful in identifying patients for upfront treatment escalation, including the use of docetaxel chemotherapy or escalation of therapy at the time of biochemical progression.Patient SummaryIn this study, we found that high alkaline phosphatase level, anemia at diagnosis, and high PSA nadir after initiation of androgen deprivation therapy are associated with worse overall survival among Black South African men treated with androgen deprivation therapy for metastatic prostate cancer.

Funder

Conquer Cancer Foundation

National Institutes of Health

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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