An Exceptional Response to Dostarlimab in Mismatch Repair Deficient, Microsatellite Instability-High and Platinum

Michele Bartoletti1, Giorgio Giorda2, Alessandra Viel3

  • 1Unit of Medical Oncology and Cancer Prevention, Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO), 33081 Aviano, Italy.

Insights

Immunotherapy with dostarlimab offers a rapid, effective treatment for advanced endometrial cancer in patients with mismatch repair deficiency, even after platinum-based therapies fail.

Area of Science:

  • Oncology
  • Immunotherapy
  • Gynecologic Oncology

Background:

  • Advanced endometrial cancer often lacks effective treatment options after progression on platinum-based chemotherapy.
  • Immunotherapy, specifically anti-PD-1/PD-L1 antibodies, is emerging as a promising treatment modality.
  • Microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) tumors are particularly responsive to PD-1 blockade.

Observation:

  • This case report details a patient with advanced, platinum-refractory endometrial cancer.
  • The patient's tumor was characterized by high disease burden and mismatch repair deficiency (dMMR).

Findings:

  • The patient received dostarlimab, an anti-PD-1 monoclonal antibody.
  • An exceptional and rapid treatment response was observed with dostarlimab therapy.

Implications:

  • Dostarlimab demonstrates significant potential as a therapeutic option for a subset of advanced endometrial cancer patients.
  • This finding supports the role of immunotherapy in mismatch repair deficient gynecologic malignancies.
  • Further research into PD-1 blockade in endometrial cancer is warranted.