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OncoMatch/Clinical Trials/NCT06180733

Neo-adjuvant Pembrolizumab as an Alternative Treatment for MMRd Uterine Cancer

Is NCT06180733 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Pembrolizumab for endometrial cancer.

Phase 2RecruitingUniversity Medical Center GroningenNCT06180733Data as of May 2026

Treatment: PembrolizumabThe goal of this clinical trial is to establish the fraction of patients that achieve a major pathological response (MPR) after 9 cycles of pembrolizumab, with the ultimate aim of informing a follow-up randomized trial. Participants will receive 9 cycles of pembrolizumab before their standard of care hysterectomy.

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Extracted eligibility criteria

Cancer type

Endometrial Cancer

Biomarker criteria

Required: MMR deficient

G3/CC MMRd uterine cancer

Disease stage

Grade: G3

histologically confirmed primary diagnosis of G3/CC MMRd uterine cancer

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: anti-PD-1/PD-L1/PD-L2 or co-inhibitory T-cell receptor therapy

Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti PD L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, CTLA-4, OX-40, CD137).

Cannot have received: systemic anti-cancer therapy

Exception: within 4 weeks prior to allocation

Has received prior systemic anti-cancer therapy including investigational agents within 4 weeks [could consider shorter interval for kinase inhibitors or other short half-life drugs] prior to allocation.

Cannot have received: radiotherapy

Exception: within 2 weeks of start of study treatment or radiation-related toxicities requiring corticosteroids. Note: Two weeks or fewer of palliative radiotherapy for non-CNS disease with a 1-week washout is permitted.

Has received prior radiotherapy within 2 weeks of start of study treatment or radiation-related toxicities requiring corticosteroids.

Cannot have received: investigational agent/device

Exception: within 4 weeks prior to study intervention administration

Has received an investigational agent or has used an investigational device within 4 weeks prior to study intervention administration.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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