Sarcoma in patients with Lynch syndrome and response to immunotherapy

Abstract

AbstractBackgroundLynch syndrome (LS) is an autosomal dominant genetic predisposition to multiple malignancies and is characterized by deficient DNA mismatch repair. Increased incidence of sarcomas is not formally ascribed to LS; however, increasing evidence suggests a preponderance of these malignancies in affected families. Sarcomas typically possess a low tumor mutational burden and incite a poor immune infiltrate, thereby rendering them poorly responsive to immunotherapy.MethodsWe searched the University of California, Los Angeles (UCLA) sarcoma program database for patients with a diagnosis of sarcoma and LS from 2016 to 2023. Three such patients were identified and all three were treated with PD1 blockade.ResultsWe present three cases of LS‐associated sarcomas (two soft tissue sarcoma and one osteosarcoma) with increased tumor mutational burdens. These patients were each treated with an anti‐PD1 antibody and experienced a response far superior to that reported for non‐LS‐associated sarcomas.ConclusionsIncreased mutational burden and immune infiltrate are observed for sarcomas associated with LS. Although unselected patients with sarcoma have demonstrated poor response rates to immunotherapy, our findings suggest that patients with Lynch‐associated sarcomas are more likely to respond to treatment with anti‐PD1. These patients should be given consideration for immunotherapy.