Genome-wide Copy-number Alterations in Circulating Tumor DNA as a Novel Biomarker for Patients with High-grade Serous Ovarian Cancer.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
01 05 2021
Historique:
received: 01 09 2020
revised: 27 10 2020
accepted: 11 12 2020
pubmed: 17 12 2020
medline: 17 3 2022
entrez: 16 12 2020
Statut: ppublish

Résumé

High-grade serous epithelial ovarian cancer (HGS-EOC) is defined by high levels of somatic copy-number alterations (SCNA) with marked spatial and temporal tumor heterogeneity. Biomarkers serving to monitor drug response and detect disease recurrence are lacking, a fact which reflects an unmet clinical need. A total of 185 plasma samples and 109 matched tumor biopsies were collected from 46 patients with HGS-EOC, and analyzed by shallow whole-genome sequencing (sWGS). The percentage of tumor fraction (TF) in the plasma was used to study the biological features of the disease at the time of diagnosis (T0) and correlated with patients' survival. Longitudinal analysis of TF was correlated with CA-125 levels and radiological images to monitor disease recurrence. Gain in the clonal regions, Our results support the notion that sWGS is an inexpensive and useful tool for the genomic analysis of ctDNA in patients with HGS-EOC to monitor disease evolution and to anticipate relapse better than serum CA-125, the routinely used clinical biomarker.

Identifiants

pubmed: 33323403
pii: 1078-0432.CCR-20-3345
doi: 10.1158/1078-0432.CCR-20-3345
doi:

Substances chimiques

Biomarkers, Tumor 0
Circulating Tumor DNA 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2549-2559

Commentaires et corrections

Type : CommentIn

Informations de copyright

©2020 American Association for Cancer Research.

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Auteurs

Lara Paracchini (L)

Department of Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

Luca Beltrame (L)

Department of Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

Tommaso Grassi (T)

Department of Obstetrics and Gynaecology, Università degli Studi Milano-Bicocca, San Gerardo Hospital, Monza, Italy.

Alessia Inglesi (A)

Department of Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

Robert Fruscio (R)

Department of Obstetrics and Gynaecology, Università degli Studi Milano-Bicocca, San Gerardo Hospital, Monza, Italy.

Fabio Landoni (F)

Department of Obstetrics and Gynaecology, Università degli Studi Milano-Bicocca, San Gerardo Hospital, Monza, Italy.

Davide Ippolito (D)

Department of Obstetrics and Gynaecology, Università degli Studi Milano-Bicocca, San Gerardo Hospital, Monza, Italy.

Martina Delle Marchette (M)

Department of Obstetrics and Gynaecology, Università degli Studi Milano-Bicocca, San Gerardo Hospital, Monza, Italy.

Mariachiara Paderno (M)

Department of Obstetrics and Gynaecology, Università degli Studi Milano-Bicocca, San Gerardo Hospital, Monza, Italy.

Marco Adorni (M)

Department of Obstetrics and Gynaecology, Università degli Studi Milano-Bicocca, San Gerardo Hospital, Monza, Italy.

Marta Jaconi (M)

Department of Pathology, Università degli Studi Milano-Bicocca, San Gerardo Hospital, Monza, Italy.

Chiara Romualdi (C)

Department of Biology, University of Padova, Padova, Italy.

Maurizio D'Incalci (M)

Department of Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy. maurizio.dincalci@marionegri.it.

Giulia Siravegna (G)

Cancer Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.

Sergio Marchini (S)

Department of Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.

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