A Pilot Study of Anti-CTLA4 Antibody Ipilimumab in Patients with Synovial Sarcoma

Robert G Maki1, Achim A Jungbluth, Sacha Gnjatic

  • 1Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA ; Departments of Medicine, Pediatrics, and Orthopaedics, Mount Sinai School of Medicine, 1 Gustave L. Levy Place, P.O. Box 1208, New York, NY 10029-6574, USA.

Sarcoma
|April 5, 2013
PubMed

Insights

Ipilimumab did not show clinical benefit in advanced synovial sarcoma patients. Despite high cancer-testis antigen expression, no significant immune response or tumor shrinkage was observed.

Area of Science:

  • Immunotherapy
  • Oncology
  • Sarcoma Research

Background:

  • Synovial sarcoma patients with recurrent disease have limited systemic therapy options.
  • Synovial sarcomas often express cancer-testis (CT) antigens like NY-ESO-1.
  • Investigating novel immunotherapies targeting CT antigens is crucial for advanced sarcomas.

Purpose of the Study:

  • To evaluate the clinical activity of ipilimumab, an anti-CTLA4 antibody, in patients with advanced or metastatic synovial sarcoma.
  • To assess if ipilimumab can induce an immune response against CT antigens in synovial sarcoma.
  • To determine if ipilimumab offers a viable treatment option for this patient population.

Main Methods:

  • A Simon two-stage phase II clinical trial design was employed.
  • Patients received ipilimumab 3 mg/kg intravenously every 3 weeks for three cycles.
  • Tumor response was assessed using RECIST 1.0 criteria; immune responses to NY-ESO-1 were monitored via sera and peripheral blood mononuclear cells.

Main Results:

  • Six patients were enrolled, receiving 1-3 cycles of ipilimumab.
  • All patients experienced disease progression, resulting in a 0% RECIST response rate.
  • No clinically significant serologic or delayed type hypersensitivity responses to NY-ESO-1 were detected.

Conclusions:

  • Single-agent ipilimumab demonstrated no clinical benefit or anti-CT antigen immune response in advanced synovial sarcoma.
  • The lack of activity may stem from the inability of synovial sarcoma cell lines to effectively present CT antigens.
  • Further research into antigen presentation mechanisms is warranted to guide future immunotherapy strategies.

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