4.7 Article

Adding Short-Term Androgen Deprivation Therapy to Radiation Therapy in Men With Localized Prostate Cancer: Long-Term Update of the NRG/RTOG 9408 Randomized Clinical Trial

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.ijrobp.2021.08.031

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Funding

  1. National Cancer Institute [U10CA180868, U10CA180822, UG1CA189867]

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The study shows that adding short-term androgen deprivation therapy (ADT) to radiation therapy (RT) improves overall survival and reduces disease-specific mortality, biochemical failure, local progression, and distant metastases in men with localized prostate cancer.
Purpose: For men with localized prostate cancer, NRG Oncology/Radiation Therapy Oncology Group (RTOG) 9408 demonstrated that adding short-term androgen deprivation therapy (ADT) to radiation therapy (RT) improved the primary endpoint of overall survival (OS) and improved disease-specific mortality (DSM), biochemical failure (BF), local progression, and freedom from distant metastases (DM). This study was performed to determine whether the short-term ADT continued to improve OS, DSM, BF, and freedom from DM with longer follow-up. Methods and Materials: From 1994 to 2001, NRG/RTOG 9408 randomized 2028 men from 212 North American institutions with T1b-T2b, N0 prostate adenocarcinoma and prostate-specific antigen (PSA) <= 20ng/mL to RT alone or RT plus shortterm ADT. Patients were stratified by PSA, tumor grade, and surgical versus clinical nodal staging. ADT was flutamide with either goserelin or leuprolide for 4 months. Prostate RT (66.6 Gy) was started after 2 months. OS was calculated at the date of death from any cause or at last follow-up. Secondary endpoints were DSM, BF, local progression, and DM. Acute and late toxic effects were assessed using RTOG toxicity scales. Results: Median follow-up in surviving patients was 14.8 years (range, 0.16-21.98). The 10-year and 18-year OS was 56% and 23%, respectively, with RT alone versus 63% and 23% with combined therapy (HR 0.94; 95% confidence interval [CI], 0.85-1.05; P =.94). The hazards were not proportional (P =.003). Estimated restricted mean survival time at 18 years was 11.8 years (95% CI, 11.4-12.1) with combined therapy versus 11.3 years with RT alone (95% CI, 10.9-11.6; P =.05). The 10-year and 18year DSMwas 7% and 14%, respectively, with RT alone versus 3% and 8% with combined therapy (HR 0.56; 95% CI, 0.41-0.75; P <.01). DMand BF favored combined therapy at 18 years. Rates of late grade >= 3 hepatic, gastrointestinal, and genitourinary toxicity were <= 1%, 3%, and 8%, respectively, with combined therapy versus = 1%, 2%, and 5% with RT alone. Conclusions: Further follow-up demonstrates that OS converges at approximately 15 years, by which point the administration of 4 months of ADT had conferred an estimated additional 6 months of life. (C) 2021 Elsevier Inc. All rights reserved.

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