Improvement in overall and cancer-specific survival in contemporary, metastatic prostate cancer chemotherapy exposed patients

Prostate. 2021 Dec;81(16):1374-1381. doi: 10.1002/pros.24235. Epub 2021 Sep 15.

Abstract

Introduction: Over the last decade, multiple clinical trials demonstrated improved survival after chemotherapy for metastatic prostate cancer (mPCa). However, real-world data validating this effect within large-scale epidemiological data sets are scarce. We addressed this void.

Materials and methods: Men with de novo mPCa were identified and systemic chemotherapy status was ascertained within the Surveillance, Epidemiology, and End Results database (2004-2016). Patients were divided between historical (2004-2013) versus contemporary (2014-2016). Chemotherapy rates were plotted over time. Kaplan-Meier plots and Cox regression models with additional multivariable adjustments addressed overall and cancer-specific mortality. All tests were repeated in propensity-matched analyses.

Results: Overall, 19,913 patients had de novo mPCa between 2004 and 2016. Of those, 1838 patients received chemotherapy. Of 1838 chemotherapy-exposed patients, 903 were historical, whereas 905 were contemporary. Chemotherapy rates increased from 5% to 25% over time. Median overall survival was not reached in contemporary patients versus was 24 months in historical patients (hazard ratio [HR]: 0.55, p < 0.001). After propensity score matching and additional multivariable adjustment (age, prostate-specific antigen, GGG, cT-stage, cN-stage, cM-stage, and local treatment) a HR of 0.55 (p < 0.001) was recorded. Analyses were repeated for cancer-specific mortality after adjustment for other cause mortality in competing risks regression models and recorded virtually the same findings before and after propensity score matching (HR: 0.55, p < 0.001).

Conclusions: In mPCa patients, chemotherapy rates increased over time. A concomitant increase in survival was also recorded.

Keywords: chemotherapy; contemporary; metastatic prostate cancer; survival.

MeSH terms

  • Adenocarcinoma* / drug therapy
  • Adenocarcinoma* / mortality
  • Adenocarcinoma* / pathology
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Humans
  • Kaplan-Meier Estimate
  • Male
  • Middle Aged
  • Mortality / trends
  • Neoplasm Metastasis / diagnosis*
  • Neoplasm Staging
  • Prognosis
  • Proportional Hazards Models
  • Prostate-Specific Antigen / analysis
  • Prostatic Neoplasms* / drug therapy
  • Prostatic Neoplasms* / mortality
  • Prostatic Neoplasms* / pathology
  • Risk Assessment / methods
  • SEER Program / statistics & numerical data

Substances

  • Prostate-Specific Antigen