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Proton Craniospinal Irradiation with Immunotherapy in Two Patients with Leptomeningeal Disease from Melanoma.
Sener, Ugur; Webb, Mason; Breen, William G; Neth, Bryan J; Laack, Nadia N; Routman, David; Brown, Paul D; Mahajan, Anita; Frechette, Kelsey; Dudek, Arkadiusz Z; Markovic, Svetomir N; Block, Matthew S; McWilliams, Robert R; Dimou, Anastasios; Kottschade, Lisa A; Montane, Heather N; Kizilbash, Sani H; Campian, Jian L.
Afiliação
  • Sener U; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Webb M; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Breen WG; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Neth BJ; Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
  • Laack NN; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Routman D; Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
  • Brown PD; Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
  • Mahajan A; Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
  • Frechette K; Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
  • Dudek AZ; Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.
  • Markovic SN; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Block MS; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • McWilliams RR; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Dimou A; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Kottschade LA; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Montane HN; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Kizilbash SH; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
  • Campian JL; Department of Oncology, Mayo Clinic, Rochester, MN, USA.
J Immunother Precis Oncol ; 7(1): 1-6, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38327758
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.

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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Immunother Precis Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Immunother Precis Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos