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Anti-PD-1 monoclonal antibody (specialist)

Dostarlimab

Brand names: Jemperli

Dostarlimab is a monoclonal antibody immune checkpoint inhibitor used in certain advanced cancers, including endometrial cancer with mismatch-repair deficiency.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It binds the programmed death-1 (PD-1) receptor on T cells, blocking its interaction with PD-L1 and PD-L2 and restoring T-cell-mediated antitumour immune responses.

Prescribing in practice

  • It can cause immune-related adverse effects affecting any organ system, including the lungs, bowel, liver and endocrine glands, which may be severe and require corticosteroids and treatment interruption.
  • Mismatch-repair or microsatellite-instability status guides patient selection for the relevant indications.
  • It is given by intravenous infusion under specialist oncology supervision.

Monitoring

Monitor for immune-related adverse reactions, including liver, thyroid, adrenal, lung and bowel involvement, before and during treatment.

Counselling the patient

  • Report new or worsening symptoms such as diarrhoea, cough, breathlessness, rash or unusual tiredness promptly.
  • Carry an alert that you are receiving immunotherapy so other clinicians are aware.

Evidence & guidelines

Dostarlimab is supported by trial evidence in mismatch-repair-deficient tumours and is appraised by NICE within its licensed indications.

Reference: NICE TA779; ESMO; SmPC; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.