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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.
Abstract:
Until recently, effective therapies for advanced endometrial cancer progressing to a platinum-based combination were lacking. In this setting, immunotherapy with anti PD-1/PDL-1 monoclonal antibodies is rising as a new paradigm in particular for patients with microsatellites instability/mismatch repair deficiency. In this case report, we describe an exceptional and rapid response to dostarlimab in a platinum refractory endometrial cancer patient with high disease burden harboring a mismatch repair deficiency.
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.
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