Retrospective analysis of safety and efficacy of anti-PD-1 therapy and radiation therapy in advanced melanoma: A bi-institutional study

医学 内科学 回顾性队列研究 放射治疗 黑色素瘤 比例危险模型 队列 胃肠病学 外科 肿瘤科 癌症研究
作者
Yvonne M. Mowery,Kirtesh R. Patel,Mudit Chowdhary,Christel Rushing,Kingshuk Roy Choudhury,Jared R. Lowe,Adam C. Olson,Amy J. Wisdom,Joseph K. Salama,Brent A. Hanks,Mohammad K. Khan,April K.S. Salama
出处
期刊:Radiotherapy and Oncology [Elsevier]
卷期号:138: 114-120 被引量:12
标识
DOI:10.1016/j.radonc.2019.06.013
摘要

Background and purpose Antibodies against programmed cell death protein 1 (PD-1) are standard treatments for advanced melanoma. Palliative radiation therapy (RT) is commonly administered for this disease. Safety and optimal timing for this combination for melanoma has not been established. Materials and methods In this retrospective cohort study, records for melanoma patients who received anti-PD-1 therapy at Duke University or Emory University (1/1/2013–12/30/2015) were reviewed. Patients were categorized by receipt of RT and RT timing relative to anti-PD-1. Results 151 patients received anti-PD-1 therapy. Median follow-up was 12.9 months. Patients receiving RT (n = 85) had worse baseline prognostic factors than patients without RT (n = 66). One-year overall survival (OS) was lower for RT patients than patients without RT (66%, 95% CI: 55–77% vs 83%, 95% CI: 73–92%). One-year OS was 61% for patients receiving RT before anti-PD-1 (95% CI: 46−76%), 78% for RT during anti-PD-1 (95% CI: 60–95%), and 58% for RT after anti-PD-1 (95% CI: 26–89%). On Cox regression, OS for patients without RT did not differ significantly from patients receiving RT during anti-PD-1 (HR 1.07, 95% CI: 0.41–2.84) or RT before anti-PD-1 (HR 0.56, 95% CI: 0.21–1.45). RT and anti-PD-1 therapy administered within 6 weeks of each other was well tolerated. Conclusion RT can be safely administered with anti-PD-1 therapy. Despite worse baseline prognostic characteristics for patients receiving RT, OS was similar for patients receiving concurrent RT with anti-PD-1 therapy compared to patients receiving anti-PD-1 therapy alone.

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