Validation of MiROvaR, a microRNA-based predictor of early relapse in early stage epithelial ovarian cancer as a new strategy to optimise patients' prognostic assessment.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
01 2022
Historique:
received: 02 09 2021
revised: 26 10 2021
accepted: 07 11 2021
pubmed: 19 12 2021
medline: 29 1 2022
entrez: 18 12 2021
Statut: ppublish

Résumé

Early-stage epithelial ovarian cancer (eEOC) patients have a generally favorable prognosis but unpredictable recurrence. Accurate prediction of risk of relapse is still a major concern, essentially to avoid overtreatment. Our robust tissue-based miRNA signature named MiROvaR, predicting early EOC recurrence in mostly advanced-stage EOC patients, is here challenged in an independent cohort to extend its classifying ability in the early-stage EOC setting. We retrospectively selected patients who underwent comprehensive surgical staging at our institution including stages from IA to IIB. miRNA expression profile was analysed in 89 cases and MiROvaR algorithm was applied using the previously validated cut-off for patients' classification. The primary endpoint was progression-free survival (PFS) at 5 years. Complete follow-up time (median = 112 months) was also considered as secondary analysis. MiROvaR was assessable on 87 cases (19 events of disease progression) and classified 68 (78%) low-risk and 19 (22%) high-risk patients. Recurrence rate at primary end-point was 39% for high-risk patients as compared to 9.5% for low-risk ones. Accordingly, their Kaplan-Meier PFS curves were significantly different at both primary and secondary analysis (p = 0.0006 and p = 0.03, respectively). While none of the prominent clinical variables had prognostic relevance, MiROvaR significantly predicted disease recurrence at the 5-year assessment (primary endpoint analysis; HR:5.43, 95%CI:1.82-16.1, p = 0.0024; AUC = 0.78, 95%CI:0.53-0.82) and at complete follow-up time (HR:2.67, 95%CI:1.04-6.8, p = 0.041; AUC:0.68, 95%CI:0.52-0.82). We validated MiROvaR performance in identifying at diagnosis eEOC patients' at higher risk of early relapse thus enabling selection of the most effective therapeutic approach.

Identifiants

pubmed: 34922264
pii: S0959-8049(21)01214-4
doi: 10.1016/j.ejca.2021.11.003
pii:
doi:

Substances chimiques

MicroRNAs 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

55-63

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this article.

Auteurs

Antonino Ditto (A)

Unit of Gynecologic Oncology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Loris De Cecco (L)

Department of Applied Research and Technology Development, Integrated Biology Platform, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Biagio Paolini (B)

Department of Pathology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Paola Alberti (P)

Department of Research, Unit of Molecular Therapies, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Fabio Martinelli (F)

Unit of Gynecologic Oncology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Umberto Leone Roberti Maggiore (U)

Unit of Gynecologic Oncology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Giorgio Bogani (G)

Unit of Gynecologic Oncology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Paolo Chiodini (P)

Medical Statistics Unit, University of Campania "Luigi Vanvitelli", Naples, Italy.

Sandro Pignata (S)

Urogynaecological Medical Oncology Unit, Istituto Nazionale Tumori - IRCCS - "Fondazione G. Pascale", Naples, Italy.

Antonella Tomassetti (A)

Department of Research, Unit of Molecular Therapies, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Francesco Raspagliesi (F)

Unit of Gynecologic Oncology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

Delia Mezzanzanica (D)

Department of Research, Unit of Molecular Therapies, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy. Electronic address: delia.mezzanzanica@istitutotumori.mi.it.

Marina Bagnoli (M)

Department of Research, Unit of Molecular Therapies, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.

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