Published July 15, 2016 | Version v1
Journal article

Influence of Comorbidity on the Risk of Mortality in Men With Unfavorable-Risk Prostate Cancer Undergoing High-Dose Radiation Therapy Alone

  • 1. Harvard Radiation Oncology Program, Brigham and Women's Hospital, Boston, Massachusetts (United States)
  • 2. Department of Statistics, University of Connecticut, Storrs, Connecticut (United States)
  • 3. Prostate Cancer Foundation of Chicago, Westmont, Illinois (United States)
  • 4. Department of Radiation Oncology, Brigham and Women's Hospital–Dana-Farber Cancer Institute, Boston, Massachusetts (United States)

Description

Purpose: To explore whether a subgroup of men with unfavorable-risk prostate cancer (PC) exists in whom high-dose radiation therapy (RT) alone is sufficient to avoid excess PC death due to competing risk from cardiometabolic comorbidity. Methods and Materials: This was a cohort study of 7399 men in whom comorbidity (including congestive heart failure, diabetes mellitus, or myocardial infarction) was assessed and recorded with T1-3NxM0 PC treated with brachytherapy with or without neoadjuvant RT, October 1997 to May 2013 at a single providing institution. Cox and competing risks regression analyses were used to assess whether men with unfavorable–intermediate/high-risk versus favorable–intermediate/low-risk PC were at increased risk of PC-specific, all-cause, or other-cause mortality (PCSM, ACM, OCM), adjusting for number of comorbidities, age at and year of brachytherapy, RT use, and an RT treatment propensity score. Results: After a median follow-up of 7.7 years, 935 men died: 80 of PC and 855 of other causes. Among men with no comorbidity, PCSM risk (adjusted hazard ratio [AHR] 2.74 [95% confidence interval (CI) 1.49-5.06], P=.001) and ACM risk (AHR 1.30 [95% CI 1.07-1.58], P=.007) were significantly increased in men with unfavorable–intermediate/high-risk PC versus favorable–intermediate/low-risk PC, with no difference in OCM (P=.07). Although PCSM risk was increased in men with 1 comorbidity (AHR 2.87 [95% CI 1.11-7.40], P=.029), ACM risk was not (AHR 1.03 [95% CI 0.78-1.36], P=.84). Neither PCSM risk (AHR 4.39 [95% CI 0.37-51.98], P=.24) or ACM risk (AHR 1.43 [95% CI 0.83-2.45], P=.20) was increased in men with 2 comorbidities. Conclusions: To minimize death from PC, high-dose RT alone may be sufficient treatment in men with 2 or more cardiometabolic comorbidities and unfavorable–intermediate- and high-risk PC.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2016.03.004

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2016.03.004;
PII
S0360-3016(16)00295-9;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
95
Journal Issue
4
Journal Page Range
p. 1158-1167
ISSN
0360-3016
CODEN
IOBPD3

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.