Case Report: A PD-L1-Positive Patient With Pleomorphic Rhabdomyosarcoma Achieving an Impressive Response to Immunotherapy

Front Immunol. 2022 Mar 17:13:815598. doi: 10.3389/fimmu.2022.815598. eCollection 2022.

Abstract

There is currently a lack of effective systemic treatment for patients with advanced pleomorphic rhabdomyosarcoma (PRMS). Although programmed death protein 1 (PD-1) inhibitors have shown efficacy in various solid tumors, their effects on PRMS have not been well established. Here, we present a case of a 12-year-old Chinese male adolescent with metastatic PRMS who benefited from the PD-1 inhibitor nivolumab. The patient initially underwent primary tumor resection but failed to respond to subsequent first-line chemotherapy and second-line pazopanib treatment. Pathological examination showed positive PD-L1 expression and tumor-infiltrating lymphocytes in the tumor tissue, and the patient was administered nivolumab as a posterior-line treatment. After attaining a clinically partial response (PR), surgical resection was performed, which was followed by adjuvant nivolumab. At the time of the submission of this manuscript, the patient achieved recurrence-free survival (RFS) lasting 45 months and counting. This is the first clinical evidence that a patient with refractory PRMS was controlled by anti-PD-1 antibody, with an RFS lasting more than 3 years. This case suggests that PD-L1 expression and T-cell infiltration could be used as potential biomarkers for PRMS immunotherapy.

Keywords: CD8 T cell; PD-L1; immunotherapy; pazopanib; pleomorphic rhabdomyosarcoma.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • B7-H1 Antigen / metabolism
  • Child
  • Humans
  • Immunologic Factors
  • Immunotherapy
  • Male
  • Nivolumab* / therapeutic use
  • Rhabdomyosarcoma* / therapy
  • T-Lymphocytes / metabolism

Substances

  • B7-H1 Antigen
  • Immunologic Factors
  • Nivolumab