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Toxicity in combination immune checkpoint inhibitor and radiation therapy: A systematic review and meta-analysis

Journal

RADIOTHERAPY AND ONCOLOGY
Volume 151, Issue -, Pages 141-148

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.radonc.2020.07.035

Keywords

Toxicity; Immune checkpoint inhibitors; Radiotherapy; Stereotactic radiosurgery; Brain metastases; Meta-analysis

Funding

  1. Penn State Cancer Institute
  2. Penn State College of Medicine
  3. National Institutes of Health [LRP 1 L30 CA231572-01]
  4. American Cancer Society - Tri State CEOs Against Cancer Clinician Scientist Development Grant [CSDG-20-013-01-CCE]

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Background and purpose: Immune checkpoint inhibitor with radiation therapy (ICI + RT) is under inves-tigation for improved patient outcome, so we performed a systematic review/meta-analysis of toxicities for ICI + RT compared to immune checkpoint inhibitor (ICI) therapy alone. Materials and methods: A PRISMA-compliant systematic review of studies in MEDLINE (PubMed) and in the National Comprehensive Cancer Network guidelines was conducted, with primary outcome grade 3 + toxicity. Criteria for ICI alone were: phase III/IV trials that compared immunotherapy to placebo, chemotherapy, or alternative immunotherapy; and for ICI + RT: prospective/retrospective studies with an arm treated with ICI + RT. Meta-analysis was performed by random effects models using the DerSimonian and Laird method. The I-2 statistic and Cochran's Q test were used to assess heterogeneity, while funnel plots and Egger's test assessed publication bias. Results: This meta-analysis included 51 studies (n = 15,398), with 35 ICI alone (n =13,956) and 16 ICI + RT studies (n = 1,442). Our models showed comparable grade 3-4 toxicities in ICI + RT (16.3%; 95% CI, 11.1- 22.3%) and ICI alone (22.3%; 95% CI, 18.1-26.9%). Stratification by timing of radiation and irradiated site showed no significant differences, but anti-CTLA-4 therapy and melanoma showed increased toxicity. The grade 5 toxicities were 1.1% and 1.9% for ICI alone and ICI + RT respectively. There was significant heterogeneity, but not publication bias. Conclusions: The random effects model showed comparable grade 3-4 toxicity in using ICI + RT compared to ICI alone in CNS melanoma metastases, NSCLC, and prostate cancer. ICI + RT is safe for future clinical trials in these cancers. (C) 2020 Elsevier B.V. All rights reserved.

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