Classifying high-risk versus very high-risk prostate cancer: is it relevant to outcomes of conformal radiotherapy and androgen deprivation?
Creators
- 1. Departments of Radiation Oncology, Chaim Sheba Medical Center, Tel Aviv University Sackler School of Medicine, Tel Hashomer, 52621 Ramat Gan (Israel)
- 2. Medical Oncology, Chaim Sheba Medical Center, Tel Aviv University Sackler School of Medicine, Tel-Hashomer, 52621 (Israel)
- 3. Nuclear Medicine, Chaim Sheba Medical Center, Tel Aviv University Sackler School of Medicine, Tel-Hashomer, 52621 (Israel)
Description
To evaluate outcomes in prostate cancer patients classified as high-risk (HR) or very high-risk (VHR) who were treated with conformal radiation therapy (CRT) and androgen deprivation therapy (ADT). Between 11/2001 and 3/2012, 203 patients with HR disease received CRT to the prostate (78–82 Gy) and pelvic lymph nodes (46–50 Gy) with ADT (6 m-2 years). Median follow-up was 50 months (12 m-142 m). Biochemical failure was defined according to Phoenix definition. Imaging studies were used to identify local, regional or metastatic failure. Four different VHR/HR groupings were formed using the 2014 and revised 2015 NCCN guidelines. Differences were examined using Kaplan Meier (KM) estimates with log rank test and uni- and multivariate Cox regression analysis (MVA). Failure occurred in 30/203 patients (15%). Median time to failure was 30 m (4 m-76 m). KM estimate of 4 year biochemical disease free survival (b-DFS) for the entire cohort was 87% (95%CI: 82–92%). Four year KM survival estimates for b-DFS, PCSS and OS were comparable for each NCCN subgroup. On univariate analysis, the NCCN subgroups were not predictive of b-DFS at 4 years, however, DMFS was worse for both VHR subgroups (p = .03and .01) respectively. Cox univariate analysis was also significant for: PSA ≥40 ng/ml p = 0.001; clinical stages T2c p = .004, T3b p = .02 and > 4 cores with Gleason score 8–10 p < .03. On MVA, only PSA ≥ 40 ng/ml was predictive for b-DFS or MFS at 4 years (HR: 3.75 and 3.25, p < 0.005). Patients with HR and VHR disease treated with CRT and ADT had good outcomes. Stratification into HR and VHR sub-groups provided no predictive value. Only PSA ≥40 ng/ml predicted poor outcomes on MVA. Distant failure was dominant and local recurrence rare, suggesting that improved systemic treatment rather than intensification of local therapy is needed. Patients with high-risk prostate cancer are most often treated with conformal dose escalated radiation therapy with androgen deprivation. Stratification into high versus very high-risk subgroups using 2014 or revised 2015 National Comprehensive Cancer Network (NCCN) criteria did not impact treatment outcomes. Only Prostate Serum Antigen (PSA) ≥40 ng/ml was predictive of poor prognosis. Distant failure was dominant and local recurrence uncommon which challenges the notion that intensification of local therapy will further improve outcomes in patients with high-risk disease.
Availability note (English)
Available from http://dx.doi.org/10.1186/s13014-016-0743-2; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216523Additional details
Identifiers
Publishing Information
- Journal Title
- Radiation Oncology (Online)
- Journal Volume
- 12
- Journal Page Range
- vp.
- ISSN
- 1748-717X
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49082317
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ANDROGENS; GY RANGE 10-100; LYMPH NODES; MULTIVARIATE ANALYSIS; NEOPLASMS; PATIENTS; PROSTATE; RADIATION DOSES; RADIATION HAZARDS; RADIOTHERAPY
- Descriptors DEC
- ABSORBED DOSE RANGE; ANDROSTANES; BODY; DISEASES; DOSES; GLANDS; GY RANGE; HAZARDS; HEALTH HAZARDS; HORMONES; LYMPHATIC SYSTEM; MALE GENITALS; MATHEMATICS; MEDICINE; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; ORGANS; RADIATION DOSE RANGES; RADIOLOGY; STATISTICS; STEROID HORMONES; STEROIDS; THERAPY
Optional Information
- Copyright
- Copyright (c) The Author(s). 2017
- Notes
- PMCID: PMC5216523; PMID: 28061904; PUBLISHER-ID: 743; OAI: oai:pubmedcentral.nih.gov:5216523