Adjuvant Whole-Brain Radiation Therapy Compared With Observation After Local Treatment of Melanoma Brain Metastases: A Multicenter, Randomized Phase III Trial

Author:

Hong Angela M.12,Fogarty Gerald B.12,Dolven-Jacobsen Kari3,Burmeister Bryan H.45,Lo Serigne N.16,Haydu Lauren E.7,Vardy Janette L.18,Nowak Anna K.9,Dhillon Haryana M.1,Ahmed Tasnia1,Shivalingam Brindha1210,Long Georgina V.111,Menzies Alexander M.111,Hruby George1211,Drummond Katharine J.1213,Mandel Catherine14,Middleton Mark R.15,Reisse Claudius H.3,Paton Elizabeth J.1,Steel Victoria1,Williams Narelle C.1,Scolyer Richard A.110,Morton Rachael L.1,Thompson John F.110

Affiliation:

1. The University of Sydney, Sydney, NSW, Australia

2. GenesisCare, Mater Hospital, Sydney, NSW, Australia

3. Oslo University Hospital, The Radium Hospital, Oslo, Norway

4. University of Queensland, Brisbane, QLD, Australia

5. GenesisCare, Fraser Coast, QLD, Australia

6. Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia

7. The University of Texas MD Anderson Cancer Center, Houston, TX

8. Concord Cancer Centre, Concord Repatriation General Hospital, Concord, NSW, Australia

9. University of Western Australia, WA, Australia

10. Royal Prince Alfred Hospital, Sydney, NSW, Australia

11. Royal North Shore Hospital, Sydney, NSW, Australia

12. Royal Melbourne Hospital, Parkville, VIC, Australia

13. University of Melbourne, Parkville, VIC, Australia

14. Swinburne University of Technology, Hawthorn, VIC, Australia

15. National Institute for Health Research Oxford Biomedical Research Centre, Oxford, United Kingdom

Abstract

PURPOSE The brain is a common site of metastasis for patients with high-risk melanoma. Although surgery or stereotactic radiosurgery are highly effective local treatments for a small number of metastases, there is a high risk of developing additional brain metastases. The role of adjuvant whole-brain radiotherapy (WBRT) in reducing new metastases is controversial, with a lack of high-level evidence specifically for melanoma. METHODS In this randomized phase III trial, patients who had local treatment of one to three melanoma brain metastases were randomly assigned to WBRT or observation. The primary end point was distant intracranial failure within 12 months, and secondary end points included time to intracranial failure, survival, and time to deterioration in performance status. RESULTS Between April 2009 and September 2017, 215 patients were randomly assigned from 24 centers. Median follow-up was 48.1 months (range, 39.6 to 68 months). Forty-two percent of patients in the WBRT group and 50.5% of those in the observation developed distant intracranial failure within 12 months (odds ratio, 0.71; 95% CI, 0.41 to 1.23; P = .22) and the rates over the entire follow-up period were 52.0% and 57.9%, respectively (odds ratio, 0.79; 95% CI, 0.45 to 1.36; P = .39). Local failure rate was lower after WBRT (20.0% v 33.6%; P = .03). At 12 months, 41.5% of patients in the WBRT group and 51.4% of patients in the observation group had died ( P = .28), with no difference in the rate of neurologic death. Median time to deterioration in performance status was 3.8 months after WBRT and 4.4 months with observation ( P = .32). WBRT was associated with more grade 1 to 2 acute toxicity. CONCLUSION After local treatment of one to three melanoma brain metastases, adjuvant WBRT does not provide clinical benefit in terms of distant intracranial control, survival, or preservation of performance status.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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