ctDNA for Prognostication and Monitoring in Patients with Metastatic Endometrial Carcinoma Treated with Olaparib: Validation in the GINECO-UTOLA Trial

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Authors: Guillaume Beinse, V. Taly, A. Leary, Aurelia Baures, I. Ray-Coquard, Benoît You, Manuel Jorge Rodrigues, Laurence Gladieff, Sophie Abadie‐Lacourtoisie, Leïla Bengrine-Lefevre, Pierre-Emmanuel Brachet, Coriolan Lebreton
+18 more Guillaume Meynard, P. Fournel, Jean‐Sébastien Frenel, F. Selle, Rémy Largillier, Cyril Foa, Corina Cornila, Emilie Kaczmarek, Anne-Claire Hardy-Bessard, V. D'Hondt, Isabelle Cojean Zelek, Sophie Roche, Delphine Duliege, Marie Ange Mouret-Reynier, Patrick Bouchaert, Pierre Laurent-Puig, Florence Joly, Jérôme Alexandre
Cited by: 1
References: 44

Abstract

PURPOSE: ctDNA may offer a noninvasive means to evaluate tumor response and anticipate disease dynamics before radiologic changes in advanced endometrial carcinoma. EXPERIMENTAL DESIGN: This ancillary analysis included patients from the multicenter, randomized, phase II GINECO-UTerin OLAparib (UTOLA) trial (NCT03745950) evaluating olaparib/placebo as maintenance after first-line platinum-based chemotherapy. Plasma samples were collected at screening after chemotherapy (baseline), 3 months (M3), and progression. ctDNA detection was assessed by a validated methylation-based Droplet Digital PCR (MethddPCR) assay targeting DNA positions universally methylated in endometrial carcinoma. RESULTS: Among 130 evaluable patients, ctDNA was detected in 25 of 129 (19%, 1 technical fail) at baseline, 15 of 80 (19%) at M3, and 33 of 52 (63%) at progression. Baseline ctDNA positivity was independently associated with poorer progression-free survival (PFS) [median 1.81 vs. 7.39 months; adjusted HR = 5.33 (3.17-8.97)] and overall survival (OS) [10.3 vs. 24.7 months; adjusted HR = 3.98 (2.28-6.91); adjusted for age, stage IV at diagnosis, p53abn subgroup, and residual measurable lesions after chemotherapy]. Patients with baseline ctDNA had median OS of 9.36 months under olaparib versus 19.6 months under placebo (log-rank P = 0.05). Patients with increasing ctDNA at M3 had median PFS of 1.67 months, versus 9.64 months without, and median OS of 18.8 versus 25.8 months. ctDNA rising was predictive of poor postprogression OS under olaparib but not under placebo (interaction test, P < 0.001). CONCLUSIONS: MethddPCR-ctDNA is an independent prognostic biomarker for OS in advanced/metastatic endometrial carcinoma. MethddPCR-ctDNA may identify patients unlikely to benefit from PARP inhibition, guide therapeutic decisions, and should be further evaluated as a new stratification parameter in future endometrial carcinoma trials.

Fields of Study & Subjects

Cancer Genomics and Diagnostics Endometrial and Cervical Cancer Treatments Cancer Cells and Metastasis

Publication details

Journal / source
Clinical Cancer Research
Publisher
American Association for Cancer Research (AACR)
Volume
32
Issue
7
Pages
1302–1312
Publication date
15 January 2026
Language
EN