Clinical activity of pembrolizumab in refractory MDM2-amplified advanced intimal sarcomas

Author:

Ribeiro Mauricio Fernando1ORCID,Demicco Elizabeth G.2,Razak Albiruni Ryan Abdul34

Affiliation:

1. Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada

2. Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada

3. Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, Suit 6-445.13, 600 University Avenue, Toronto, ON M5G 1X5, Canada

4. Division of Medical Oncology, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada

Abstract

Intimal sarcoma (InS) is an ultra-rare and aggressive subtype of soft tissue sarcoma (STS). It usually arises in large mediastinal arteries and the heart. In the advanced setting, sequential cytotoxic chemotherapy is often used, mainly based on retrospective studies and case series but with modest benefit. The use of immune checkpoint inhibitors is a promising strategy for some STS, but identifying biomarkers of response remains challenging due to disease rarity and heterogeneity. A reactive and pro-inflammatory tumor microenvironment (TME) is believed to be associated with better outcomes for patients receiving anti-PD-1-based regimens, generating the rationale to explore this strategy in malignancies with this characteristic, such as InS. We report three cases of advanced InS patients experiencing partial response to pembrolizumab-based therapy despite low tumor mutational burden and absence of mismatch-repair deficiency. We hypothesize that TME-related characteristics such as PD-L1 expression and the presence of tertiary lymphoid structures might explain this phenomenon.

Publisher

SAGE Publications

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