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Circulating Tumor Cell Detection by Liquid Biopsy during Early-Stage Endometrial Cancer Surgery: A Pilot Study

Affiliation
Department of Gynecological and Breast Surgery, Montpellier University Hospital, 34000 Montpellier, France
Francini, Sarah;
ORCID
0000-0001-8126-7927
Affiliation
Department of Gynecological and Breast Surgery, Montpellier University Hospital, 34000 Montpellier, France
Duraes, Martha;
Affiliation
Department of Gynecological and Breast Surgery, Montpellier University Hospital, 34000 Montpellier, France
Rathat, Gauthier;
ORCID
0000-0002-1323-301X
Affiliation
Clinical Research and Epidemiology Unit, Montpellier University Hospital, 34000 Montpellier, France
Macioce, Valérie;
Affiliation
Clinical Research and Epidemiology Unit, Montpellier University Hospital, 34000 Montpellier, France
Mollevi, Caroline;
Affiliation
Clinical Research and Epidemiology Unit, Montpellier University Hospital, 34000 Montpellier, France
Pages, Laurence;
Affiliation
Department of Gynecological and Breast Surgery, Nimes University Hospital, 30000 Nimes, France
Ferrer, Catherine;
ORCID
0000-0002-6124-7029
Affiliation
Laboratory of Rare Human Circulating Cells, University Medical Center of Montpellier, 34000 Montpellier, France
Cayrefourcq, Laure;
ORCID
0000-0002-6401-2903
Affiliation
Laboratory of Rare Human Circulating Cells, University Medical Center of Montpellier, 34000 Montpellier, France
Alix-Panabières, Catherine

The recurrence of non-metastatic endometrial carcinoma (EC) (6 to 21%) might be due to disseminated tumor cells. This feasibility study investigated whether circulating tumor cells (CTCs) were detectable in blood samples from the peripheral and ovarian veins of 10 patients undergoing laparoscopic resection of stage I-II EC between July 2019 and September 2021. CTCs were detected using the CellSearch ® system (i) preoperatively (T0) in peripheral blood, (ii) after ovary suspensory ligament pediculation in ovarian vein blood (T1), and (iii) before colpotomy in peripheral blood (T2). CTCs were detected only in ovarian vein samples in 8/10 patients. The CTC median number did not differ with patient age (37 (min-max: 0–91) in <70-year-old vs. 11 (0–65) in ≥70 year-old women, p = 0.59), tumor grade (15 (0–72) for grade 1 vs. 15 (0–91) for grade 2, p = 0.97), FIGO stage (72 (27–91) vs. 2 (0–65) vs. 3 (0–6]) for stage IA, B, and II, respectively; p = 0.08), and tumor size (40 (2–72) for size < 30 mm vs. 4 (0–91) for size ≥ 30 mm, p = 0.39). Estrogen receptor-positive CTCs and CTC clusters were identified. The prognostic and therapeutic values of CTCs released during EC surgery need to be determined.

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