Long-Term Analysis of NRG Oncology RTOG 0415: A Randomized Phase III Noninferiority Study Comparing Two Fractionation Schedules in Patients With Low-Risk Prostate Cancer

Author:

Lee W. Robert1ORCID,Dignam James J.23,Amin Mahul B.4,Bruner Deborah W.5ORCID,Low Daniel6,Swanson Gregory P.7ORCID,Shah Amit B.8,D'Souza David9,Michalski Jeff M.10ORCID,Dayes Ian S.11ORCID,Seaward Samantha A.12ORCID,Hall William A.13ORCID,Nguyen Paul L.14,Pisansky Thomas M.15,Faria Sergio L.16,Chen Yuhchyau17,Rodgers Joseph P.3,Sandler Howard M.4ORCID

Affiliation:

1. Duke University Medical Center, Durham, NC

2. Department of Public Health Sciences, University of Chicago, Chicago, IL

3. NRG Oncology Statistics and Data Management Center, Philadelphia, PA

4. Cedars-Sinai Medical Center, Los Angeles, CA

5. Emory University, Atlanta, GA

6. University of California, Los Angeles, Los Angeles, CA

7. Baylor Scott & White Healthcare Temple Clinic, Temple, TX

8. York Cancer Center, York, PA

9. London Regional Cancer Program, London, ON, Canada

10. Washington University School of Medicine, St Louis, MO

11. McMaster University, Hamilton, ON, Canada

12. Kaiser Permanente Northern California, Santa Clara, CA

13. Medical College of Wisconsin, Milwaukee, WI

14. Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, MA

15. Mayo Clinic, Rochester, MN

16. McGill University Health Center, Montreal, QC, Canada

17. University of Rochester Medical Center, Wilmot Cancer Institute, Rochester, NY

Abstract

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported. NRG Oncology RTOG 0415 is a randomized phase III noninferiority (NI) clinical trial comparing conventional fractionation (73.8 Gy in 41 fractions) radiotherapy (C-RT) with hypofractionation (H-RT; 70 Gy in 28) in patients with low-risk prostate cancer. The study included 1,092 protocol-eligible patients initially reported in 2016 with a median follow-up of 5.8 years. Updated results with median follow-up of 12.8 years are now presented. The estimated 12-year disease-free survival (DFS) is 56.1% (95% CI, 51.5 to 60.5) for C-RT and 61.8% (95% CI, 57.2 to 66.0) for H-RT. The DFS hazard ratio (H-RT/C-RT) is 0.85 (95% CI, 0.71 to 1.03), confirming NI ( P < .001). Twelve-year cumulative incidence of biochemical failure (BF) was 17.0% (95% CI, 13.8 to 20.5) for C-RT and 9.9% (95% CI, 7.5 to 12.6) for H-RT. The HR (H-RT/C-RT) comparing biochemical recurrence between the two arms was 0.55 (95% CI, 0.39 to 0.78). Late grade ≥3 GI adverse event (AE) incidence is 3.2% (C-RT) versus 4.4% (H-RT), with relative risk (RR) for H-RT versus C-RT 1.39 (95% CI, 0.75 to 2.55). Late grade ≥3 genitourinary (GU) AE incidence is 3.4% (C-RT) versus 4.2% (H-RT), RR 1.26 (95% CI, 0.69 to 2.30). Long-term DFS is noninferior with H-RT compared with C-RT. BF is less with H-RT. No significant differences in late grade ≥3 GI/GU AEs were observed between assignments (ClinicalTrials.gov identifier: NCT00331773 ).

Publisher

American Society of Clinical Oncology (ASCO)

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