following a full submission assessed under the end of life and orphan equivalent medicine process:
dostarlimab (Jemperli®) is not recommended for use within NHSScotland.
Indication under review: in combination with platinum-containing chemotherapy for the treatment of adult patients with primary advanced or recurrent endometrial cancer and who are candidates for systemic therapy.
In a phase III study, dostarlimab compared with placebo, numerically improved progression-free survival in adults with primary advanced or first recurrence of endometrial cancer who had proficient mismatch repair (pMMR)/microsatellite stable (MSS) disease.
The submitting company’s justification of the treatment’s cost in relation to its health benefits was not sufficient and in addition the company did not present a sufficiently robust economic analysis to gain acceptance by SMC.
This advice takes account of the views from a Patient and Clinician Engagement (PACE) meeting.
SMC has previously accepted dostarlimab for use in combination with platinum-containing chemotherapy for the treatment of adult patients with mismatch repair deficient (dMMR)/microsatellite instability-high (MSI-H) primary advanced or recurrent endometrial cancer and who are candidates for systemic therapy (SMC2635). This advice remains valid.
The submitting company has indicated their intention to make a resubmission.
Medicine details
- Medicine name:
- dostarlimab (Jemperli)
- SMC ID:
- SMC2828
- Indication:
In combination with platinum-containing chemotherapy for the treatment of adult patients with primary advanced or recurrent endometrial cancer (EC) and who are candidates for systemic therapy.
- Pharmaceutical company
- GlaxoSmithKline UK Ltd
- BNF chapter
- Malignant disease and immunosuppression
- Submission type
- Full
- Status
- Not recommended
- Date advice published
- 13 April 2026