Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancer

J Immunother Cancer. 2023 Jan;11(1):e005847. doi: 10.1136/jitc-2022-005847.

Abstract

Adoptive transfer of autologous tumor-specific lymphocytes represents a viable treatment method for patients with advanced malignancies. Here, we report a patient's case with metastatic hormone-refractory New York esophageal squamous cell carcinoma 1 (NY-ESO-1) expressing prostate cancer treated with in vitro expanded tumor-infiltrating lymphocytes (TILs) in conjunction with IL-2 and immune-checkpoint blockade. Complete and durable tumor remission was observed after three TIL infusions consisting of 1.4×109, 2.0×109, and 8.0×109 T cells, respectively, lasting now for more than 3.5 years. Immunological correlates to the clinical development were the decrease of tumor-driven NY-ESO-1 serum antibody and the drop of prostate-specific antigen to <0.01 µg/L. TILs were reactive against cancer-testis antigen NY-ESO-1, individual tumor mutational proteins (eg, PRPF8, TRPS1), and the androgen receptor splice variant 12.

Keywords: Cell Engineering; Immunotherapy, Adoptive; Lymphocytes, Tumor-Infiltrating.

Publication types

  • Case Reports

MeSH terms

  • Antibodies
  • Esophageal Neoplasms* / metabolism
  • Esophageal Squamous Cell Carcinoma*
  • Humans
  • Lymphocytes, Tumor-Infiltrating
  • Male
  • Prostatic Neoplasms* / metabolism
  • Prostatic Neoplasms* / therapy
  • Repressor Proteins / metabolism
  • T-Lymphocytes

Substances

  • Antibodies
  • TRPS1 protein, human
  • Repressor Proteins