Journal of Immunotherapy and Precision Oncology (Feb 2024)

Proton Craniospinal Irradiation with Immunotherapy in Two Patients with Leptomeningeal Disease from Melanoma

  • Ugur Sener,
  • Mason Webb,
  • William G. Breen,
  • Bryan J. Neth,
  • Nadia N. Laack,
  • David Routman,
  • Paul D. Brown,
  • Anita Mahajan,
  • Kelsey Frechette,
  • Arkadiusz Z. Dudek,
  • Svetomir N. Markovic,
  • Matthew S. Block,
  • Robert R. McWilliams,
  • Anastasios Dimou,
  • Lisa A. Kottschade,
  • Heather N. Montane,
  • Sani H. Kizilbash,
  • Jian L. Campian

DOI
https://doi.org/10.36401/JIPO-23-20
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 6

Abstract

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Introduction Proton craniospinal irradiation (pCSI) is a treatment option for leptomeningeal disease (LMD), which permits whole neuroaxis treatment while minimizing toxicity. Despite this, patients inevitably experience progression. Adding systemic therapy to pCSI may improve outcomes. Methods In this single-institution retrospective case series, we present the feasibility of treatment with pCSI (30Gy, 10 fractions) and an immune checkpoint inhibitor (ICI) in two sequential patients with LMD from melanoma. Results The first patient developed LMD related to BRAF V600E-mutant melanoma after prior ICI and BRAF-targeted therapy. After pCSI with concurrent nivolumab, the addition of relatlimab, and BRAF-targeted therapy, he remained alive 7 months after LMD diagnosis despite central nervous system progression. The second patient developed LMD related to BRAF-wildtype melanoma after up-front ICI. He received pCSI with concurrent ipilimumab and nivolumab, then nivolumab maintenance. Though therapy was held for ICI hepatitis, the patient remained progression-free 5 months after LMD diagnosis. Conclusion Adding an ICI to pCSI is feasible for patients with LMD and demonstrates a tolerable toxicity profile. While prospective evaluation is ultimately warranted, pCSI with ICI may confer survival benefits, even after prior ICI.

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