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

Authors :
Sener U
Webb M
Breen WG
Neth BJ
Laack NN
Routman D
Brown PD
Mahajan A
Frechette K
Dudek AZ
Markovic SN
Block MS
McWilliams RR
Dimou A
Kottschade LA
Montane HN
Kizilbash SH
Campian JL
Source :
Journal of immunotherapy and precision oncology [J Immunother Precis Oncol] 2024 Feb 05; Vol. 7 (1), pp. 1-6. Date of Electronic Publication: 2024 Feb 05 (Print Publication: 2024).
Publication Year :
2024

Abstract

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.<br />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.<br />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.<br />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.<br />Competing Interests: Conflicts of Interest: None.

Details

Language :
English
ISSN :
2590-017X
Volume :
7
Issue :
1
Database :
MEDLINE
Journal :
Journal of immunotherapy and precision oncology
Publication Type :
Academic Journal
Accession number :
38327758
Full Text :
https://doi.org/10.36401/JIPO-23-20