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Updated: Feb 7, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
Response to Immune Checkpoint Inhibition in Two Patients with Alveolar Soft-Part Sarcoma
Jeremy Lewin1, Scott Davidson2,3, Nathaniel D Anderson3
1Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, Canada.
Abstract:
Alveolar soft-part sarcoma (ASPS) is a morphologically distinctive mesenchymal tumor characterized by a canonical ASPL-TFE3 fusion product. In the metastatic setting, standard cytotoxic chemotherapies are typically ineffective. Studies have suggested modest clinical response to multitargeted receptor tyrosine kinase inhibitors. Here, we report sustained partial responses in two patients with immune checkpoint inhibition treated with either durvalumab (anti-PD-L1) alone or in combination with tremelimumab (anti-CTLA-4), which appeared unrelated to tumor immune infiltrates or mutational burden. Genomic analysis of these patients, and other cases of ASPS, demonstrated molecular mismatch-repair deficiency signatures. These findings suggest that immune checkpoint blockade may be a useful therapeutic strategy for ASPS. Cancer Immunol Res; 6(9); 1001-7. ©2018 AACR.
Insights
Immune checkpoint inhibitors show promise for treating metastatic alveolar soft-part sarcoma (ASPS), a rare cancer. This study found durable responses in patients treated with PD-L1 or CTLA-4 blockade, suggesting a new therapeutic avenue.
Area of Science:
- Oncology
- Immunology
- Genetics
Background:
- Alveolar soft-part sarcoma (ASPS) is a rare mesenchymal tumor with a characteristic ASPL-TFE3 fusion.
- Metastatic ASPS is challenging to treat, with limited efficacy of conventional chemotherapy and modest responses to tyrosine kinase inhibitors.
- The role of immunotherapy in ASPS remains largely unexplored.
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