Advice

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