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Study dataset

Mismatch Repair Deficient Endometrial Cancer

Genomic and clinical data contrasting mutational and epigenetic MMRd at MSK.

Memorial Sloan Kettering Cancer Center · Listed May 4, 2026

  • Genomic
  • Clinical
  • Endometrial

Overview

The findings suggest that distinguishing between these subtypes can improve treatment strategies, such as using PD-1 inhibitors for mutational types and exploring organ preservation for early-stage cases.

Research from Memorial Sloan Kettering (MSK) between 2022 and 2023 reveals that mismatch repair deficient (MMRd) endometrial cancer is heterogeneous, with prognosis and immunotherapy response driven by whether the deficiency is caused by genetic mutations (better prognosis) or epigenetic silencing (worse prognosis). The findings suggest that distinguishing between these subtypes can improve treatment strategies, such as using PD-1 inhibitors for mutational types and exploring organ preservation for early-stage cases.

Publications

Contributors

Investigators
  • Alexia Iasonos ORCID
  • Arnaud Da Cruz Paula, Memorial Sloan-Kettering Cancer Center ORCID
  • Beryl Manning-Geist ORCID
  • Britta Weigelt ORCID
  • Carol Aghajanian ORCID
  • Claire F. Friedman, Memorial Sloan Kettering Cancer Center ORCID
  • Diana L. Mandelker, Memorial Sloan Kettering Cancer Center ORCID
  • Dmitriy Zamarin, MD, PhD, Icahn School of Medicine at Mount Sinai ORCID
  • Kelly A. Devereaux ORCID
  • Lea A. Moukarzel, Memorial Sloan Kettering Cancer Center ORCID
  • Lora H. Ellenson ORCID
  • Maria M. Rubinstein ORCID
  • Nadeem R Abu-Rustum ORCID
  • Ozge Ceyhan-Birsoy, Memorial Sloan Kettering Cancer Center ORCID
  • Pier Selenica ORCID
  • Sushmita Gordhandas, Memorial Sloan Kettering Cancer Center ORCID
  • Timothy J. Hoang ORCID
  • Weining Ma, Memorial Sloan Kettering Cancer Center ORCID
  • Ying L. Liu ORCID
  • Zsofia K. Stadler, Memorial Sloan Kettering Cancer Center ORCID
Institutions
Memorial Sloan Kettering Cancer Center, Weill Cornell Medicine