PD-1, PD-L1, NY-ESO-1, and MAGE-A4 expression in cutaneous angiosarcoma: A case report

Kazuhiko Hashimoto1, Shunji Nishimura, Yu Shinyashiki

  • 1Department of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama City, Osaka, Japan.

Medicine
|July 15, 2022
PubMed
Abstract

Insights

This case study highlights a successful treatment for cutaneous angiosarcoma (cAS) using immunotherapy combined with surgery. The patient showed no recurrence after one year, suggesting potential therapeutic targets in specific biomarkers.

Area of Science:

  • Oncology
  • Immunotherapy
  • Surgical Oncology

Background:

  • Cutaneous angiosarcoma (cAS) presents complex genomic alterations, with controversial immunotherapy efficacy and poor prognosis.
  • This report details a cAS case associated with programmed cell death 1 (PD-1), programmed cell death ligand-1 (PD-L1), New York esophageal squamous cell carcinoma-1 (NY-ESO-1), and melanoma-associated antigen 4 (MAGE-A4).

Observation:

  • A 69-year-old male presented with left thumb pain and a soft tissue mass.
  • Initial MRI revealed a soft tissue tumor; a marginal excisional biopsy was performed.
  • Pathology confirmed angiosarcoma characterized by high-flow serpentine vessels.

Findings:

  • Surgical excision with wide margins was performed.
  • Histopathology revealed positivity for programmed cell death 1 (PD-1), programmed cell death ligand-1 (PD-L1), New York esophageal squamous cell carcinoma-1 (NY-ESO-1), and melanoma-associated antigen 4 (MAGE-A4).
  • One year post-treatment, the patient experienced no recurrence, metastasis, or complications.

Implications:

  • The identified biomarkers (PD-1, PD-L1, NY-ESO-1, MAGE-A4) may represent viable therapeutic targets for cAS.
  • Combining immunotherapy with surgical intervention could offer an effective treatment strategy for cutaneous angiosarcoma.
  • This case suggests a promising approach for managing cAS, potentially improving patient outcomes.

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