Survival Outcomes of Whole-Pelvic Versus Prostate-Only Radiation Therapy for High-Risk Prostate Cancer Patients With Use of the National Cancer Data Base

Purpose/Objectives The addition of whole pelvic (WP) compared with prostate-only (PO) radiation therapy (RT) for clinically node-negative prostate cancer remains controversial. The purpose of our study was to evaluate the survival benefit of adding WPRT versus PO-RT for high-risk, node-negative pros...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2015-12, Vol.93 (5), p.1052-1063
Hauptverfasser: Amini, Arya, MD, Jones, Bernard L., PhD, Yeh, Norman, MD, PhD, Rusthoven, Chad G., MD, Armstrong, Hirotatsu, PhD, Kavanagh, Brian D., MD, MPH
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Sprache:eng
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Zusammenfassung:Purpose/Objectives The addition of whole pelvic (WP) compared with prostate-only (PO) radiation therapy (RT) for clinically node-negative prostate cancer remains controversial. The purpose of our study was to evaluate the survival benefit of adding WPRT versus PO-RT for high-risk, node-negative prostate cancer, using the National Cancer Data Base (NCDB). Methods and Materials Patients with high-risk prostate cancer treated from 2004 to 2006, with available data for RT volume, coded as prostate and pelvis (WPRT) or prostate alone (PO-RT) were included. Multivariate analysis (MVA) and propensity-score matched analysis (PSM) were performed. Recursive partitioning analysis (RPA) based on overall survival (OS) using Gleason score (GS), T stage, and pretreatment prostate-specific antigen (PSA) was also conducted. Results A total of 14,817 patients were included: 7606 (51.3%) received WPRT, and 7211 (48.7%) received PO-RT. The median follow-up time was 81 months (range, 2-122 months). Under MVA, the addition of WPRT for high-risk patients had no OS benefit compared with PO-RT (HR 1.05; P =.100). On subset analysis, patients receiving dose-escalated RT also did not benefit from WPRT (HR 1.01; P =.908). PSM confirmed no survival benefit with the addition of WPRT for high-risk patients (HR 1.05; P =.141). In addition, RPA was unable to demonstrate a survival benefit of WPRT for any subset. Other prognostic factors for inferior OS under MVA included older age (HR 1.25; P
ISSN:0360-3016
1879-355X
DOI:10.1016/j.ijrobp.2015.09.006