Therapeutic Response

MSI-H status confers therapeutic sensitivity to Carboplatin in combination with Dostarlimab and Paclitaxel in patients with Endometrial Carcinoma.

Statements

Source and description
Jemperli (dostarlimab) [package insert]. FDA. The U.S. Food and Drug Administration granted approval to dostarlimab in combination with carboplatin and paclitaxel, followed by dostarlimab as a single agent, for the treatment of adult patients with primary advanced or recurrent endometrial cancer that is mismatch repair deficient (dMMR), as determined by an FDA-approved test, or microstallite instability-high (MSI-H).
Jemperli (dostarlimab) [product information]. EMA. The European Medicines Agency (EMA) has authorized dostarlimab in combination with carboplatin and paclitaxel for the treatment of adult patients with mismatch repair deficient (dMMR) / microsatellite instability-high (MSI-H) primary advanced or recurrent endometrial cancer (EC) who are candidates for systemic therapy.