OncoMatch/Clinical Trials/NCT05635344
A Feasibility Window Study of Pembrolizumab Prior to Second Evacuation for Post-molar Gestational Trophoblastic Neoplasia
Is NCT05635344 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Pembrolizumab for gestational trophoblastic disease.
Treatment: Pembrolizumab — Gestational Trophoblastic Diseases (GTD) are a variety of rare, pregnancy related cell multiplication disorders of cells of the placenta which can range from pre-cancerous growths to more serious lesions that can spread to nearby tissues that can cause serious health issues. Most patients that develop GTD are diagnosed at the precancerous stage early in pregnancy and undergo surgical removal of the disease from the uterus. Around 15% of patients are not cured by surgical removal alone and need to undergo further treatment with chemotherapy or further surgery; of which roughly one-third of patients are cured with a second round of surgery alone. Anti-cancer treatment with chemotherapy carries many short- and long-term side effects that can negatively affect a person's quality of living. Finding less harmful anticancer therapies that can be paired with surgery is therefore of great benefit to patients with recurrent GTD. An alternative is to pair surgery with another class of anticancer treatments, known as immunotherapies. Immunotherapy aims to encourage the bodies natural defences to fight the cancer cells. Pembrolizumab, an immunotherapeutic agent which works by preventing cancer cells from hiding from the immune system; has been proven to be an extremely safe form of anticancer therapy and is an attractive alternative to more toxic chemotherapeutic agents. The RESOLVE study aims to determine how feasible it is to deliver pre-surgical pembrolizumab to patients and determine if this is a desirable alternative; potentially leading to a larger more definitive study. 20 patients will be recruited onto the study and will be evenly split into two arms: * 10 patients to receive second evacuation alone * 10 patients to receive single dose of Pembrolizumab followed by surgery All patients that take part in the study will be recruited from Charing Cross Hospital and will be followed up for a year after the date of their surgery.
Check if I qualifyExtracted eligibility criteria
Cancer type
Tumor Agnostic
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received: primary surgical evacuation
histologically confirmed CHM after primary surgical evacuation with no intervening treatment
Lab requirements
Blood counts
absolute neutrophil count ≥ 1.5 x 10^9 /l; platelet count ≥ 100 x 10^9 /l; haemoglobin ≥ 9.0 g/dl (may have been blood transfused)
Kidney function
creatinine clearance ≥ 30 ml/min (cockcroft-gault formula)
Liver function
serum bilirubin ≤ 1.5 x uln; ast/alt ≤ 2.5 x uln
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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