Related Experiment Video
Updated: May 12, 2026

A Mouse Model of Incompletely Resected Soft Tissue Sarcoma for Testing (Neo)adjuvant Therapies
Published on: July 28, 2020
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.
Abstract:
Background. Patients with recurrent synovial sarcomas have few options for systemic therapy. Since they express large amounts of endogenous CT (cancer testis) antigens such as NY-ESO-1, we investigated the clinical activity of single agent anti-CTLA4 antibody ipilimumab in patients with advanced or metastatic synovial sarcoma. Methods. A Simon two-stage phase II design was used to determine if there was sufficient activity to pursue further. The primary endpoint was tumor response rate by RECIST 1.0. Patients were treated with ipilimumab 3 mg/kg intravenously every 3 weeks for three cycles and then restaged. Retreatment was possible for patients receiving an extra three-week break from therapy. Sera and peripheral blood mononuclear cells were collected before and during therapy to assess NY-ESO-1-specific immunity. Results. Six patients were enrolled and received 1-3 cycles of ipilimumab. All patients showed clinical or radiological evidence of disease progression after no more than three cycles of therapy, for a RECIST response rate of 0%. The study was stopped for slow accrual, lack of activity, and lack of immune response. There was no evidence of clinically significant either serologic or delayed type hypersensitivity responses to NY-ESO-1 before or after therapy. Conclusion. Despite high expression of CT antigens by synovial sarcomas of patients treated in this study, there was neither clinical benefit nor evidence of anti-CT antigen serological responses. Assessment of the ability of synovial sarcoma cell lines to present cancer-germ cell antigens may be useful in determining the reason for the observed lack of immunological or clinical activity.
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.
Related Concept Videos
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF
Tumor Immunotherapy
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents

