Influence of Comorbidity on the Risk of Mortality in Men With Unfavorable-Risk Prostate Cancer Undergoing High-Dose Radiation Therapy Alone
Creators
- 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.2016.03.004Additional 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
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48097328
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BRACHYTHERAPY; DIABETES MELLITUS; HEART FAILURE; MEN; MORTALITY; MYOCARDIAL INFARCTION; NEOPLASMS; PROSTATE; REGRESSION ANALYSIS
- Descriptors DEC
- ANIMALS; BODY; CARDIOVASCULAR DISEASES; DISEASES; ENDOCRINE DISEASES; GLANDS; MALE GENITALS; MALES; MAMMALS; MAN; MATHEMATICS; MEDICINE; METABOLIC DISEASES; NUCLEAR MEDICINE; ORGANS; PRIMATES; RADIOLOGY; RADIOTHERAPY; STATISTICS; SYMPTOMS; THERAPY; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.