Prophylactic risk-reducing salpingo-oophorectomy in BRCA mutation carriers: what is going on in a region of northern Italy?


Journal

Maturitas
ISSN: 1873-4111
Titre abrégé: Maturitas
Pays: Ireland
ID NLM: 7807333

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 17 04 2020
revised: 07 08 2020
accepted: 24 08 2020
entrez: 14 12 2020
pubmed: 15 12 2020
medline: 17 2 2021
Statut: ppublish

Résumé

BRCA1 mutation carriers are recommended to undergo prophylactic risk-reducing salpingo-oophorectomy (RRSO) between the ages of 35 and 40 or when child bearing is complete, with a possible delay until age 40-45 for BRCA2 mutation carriers. Primary outcome was the rate of unsuspected cancer findings during RRSO in a region of northern Italy (Emilia Romagna) and secondary outcomes were details of RRSO: age at surgical intervention, the venue of the procedures in relation to the surgical/pathological quality and the rate/role of concomitant opportunistic hysterectomies. Multicentre data collection by invitation to report current RRSO practices. A total of 222 RRSOs (54.5 % BRCA1, 34.7 % BRCA2, 1.8 % BRCA1 and BRCA2 combined, 5.8 % BRCA-VUS and 3.2 % BRCA not better specified) were reported from 9 different centres, half in non-university hospitals and the remainder in university hospitals. Breast cancer survivors (56.3 %) underwent the RRSO at a younger age (47.8 vs 50.6 years, p =  0.02). The mean and median ages at surgical intervention (49.0 and 48.0, respectively) were similar for BRCA1 and BRCA2 mutation carriers, as was the temporal trend in age distribution, and proportions treated in university and non-university hospitals. A diagnosis of ovarian invasive cancer was reported in 3.5 % of subjects, all BRCA1 or BRCA-combined subjects, at a median and mean age of 57 years (range 42-68). Abnormal tubal findings, such as serous tubal intraepithelial lesions (STIL) (100 %), secretory cell outgrowth (SCOUT) (100 %) and STIC (71.4 %), were mainly reported by pathologists in university hospitals. Of the 222 procedures, 15 (6.7 %) included hysterectomies: in none of these cases was a primitive uterine endometrioid or serous cancer found. The results from this multicentre regional study should guide future preventive health policies for RRSO in BRCA mutation carriers.

Sections du résumé

BACKGROUND BACKGROUND
BRCA1 mutation carriers are recommended to undergo prophylactic risk-reducing salpingo-oophorectomy (RRSO) between the ages of 35 and 40 or when child bearing is complete, with a possible delay until age 40-45 for BRCA2 mutation carriers.
STUDY QUESTION OBJECTIVE
Primary outcome was the rate of unsuspected cancer findings during RRSO in a region of northern Italy (Emilia Romagna) and secondary outcomes were details of RRSO: age at surgical intervention, the venue of the procedures in relation to the surgical/pathological quality and the rate/role of concomitant opportunistic hysterectomies.
STUDY DESIGN METHODS
Multicentre data collection by invitation to report current RRSO practices.
RESULTS RESULTS
A total of 222 RRSOs (54.5 % BRCA1, 34.7 % BRCA2, 1.8 % BRCA1 and BRCA2 combined, 5.8 % BRCA-VUS and 3.2 % BRCA not better specified) were reported from 9 different centres, half in non-university hospitals and the remainder in university hospitals. Breast cancer survivors (56.3 %) underwent the RRSO at a younger age (47.8 vs 50.6 years, p =  0.02). The mean and median ages at surgical intervention (49.0 and 48.0, respectively) were similar for BRCA1 and BRCA2 mutation carriers, as was the temporal trend in age distribution, and proportions treated in university and non-university hospitals. A diagnosis of ovarian invasive cancer was reported in 3.5 % of subjects, all BRCA1 or BRCA-combined subjects, at a median and mean age of 57 years (range 42-68). Abnormal tubal findings, such as serous tubal intraepithelial lesions (STIL) (100 %), secretory cell outgrowth (SCOUT) (100 %) and STIC (71.4 %), were mainly reported by pathologists in university hospitals. Of the 222 procedures, 15 (6.7 %) included hysterectomies: in none of these cases was a primitive uterine endometrioid or serous cancer found.
CONCLUSIONS CONCLUSIONS
The results from this multicentre regional study should guide future preventive health policies for RRSO in BRCA mutation carriers.

Identifiants

pubmed: 33308637
pii: S0378-5122(20)30361-3
doi: 10.1016/j.maturitas.2020.08.011
pii:
doi:

Substances chimiques

BRCA1 Protein 0
BRCA1 protein, human 0
BRCA2 Protein 0
BRCA2 protein, human 0

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

59-64

Investigateurs

Lorenzo Aguzzoli (L)
Valentina Arcangeli (V)
Roberto Berretta (R)
Laura Cortesi (L)
Roberta De Domenico (R)
Maria De Nuzzo (M)
Stefano Friso (S)
Pantaleo Greco (P)
Federica Rosati (F)
Gennaro Scutiero (G)
Angela Toss (A)

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Giovanni Grandi (G)

Hereditary Breast-Ovarian Cancer Group, University of Modena and Reggio Emilia, Azienda Ospedaliero Universitaria Policlinico, Via del Pozzo 71, 41124, Modena, Italy. Electronic address: giovanni.grandi@unimore.it.

Anna Myriam Perrone (AM)

Gynecologic Oncology Unit, University of Bologna, Policlinico S.Orsola-Malpighi, Via Masserenti 13, 40138, Bologna, Italy.

Antonino Perrone (A)

Gynecology Unit, Ospedale Maggiore, Largo Nigrisoli 2, 40133, Bologna, Italy.

Vincenzo Dario Mandato (VD)

Unit of Obstetrics and Gynecology, Azienda Unità Sanitaria Locale, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Azienda Unità Sanitaria Locale, Viale Risorgimento 80, 42123 Reggio Emilia, Italy.

Giuseppe Comerci (G)

Obstetrics and Gynecology, Hospital "S. Maria delle Croci", Viale Randi 5, 48121, Ravenna, Italy.

Margaret Sammarini (M)

Hereditary Breast-Ovarian Cancer Group, University of Modena and Reggio Emilia, Azienda Ospedaliero Universitaria Policlinico, Via del Pozzo 71, 41124, Modena, Italy.

Carla Merisio (C)

University Hospital of Parma, Viale Gramsci 14, 43126, Parma, Italy.

Andrea Amadori (A)

Gynecology Unit, Hospital of Forlì, Via Forlanini 4, 47121, Forlì, Italy.

Marco Stefanetti (M)

Obstetrics and Gynecology, Infermi Hospital, Viale Settembrini 2, 47923, Rimini, Italy.

Ruby Martinello (R)

Gynecologic Oncology Unit, Arcispedale S. Anna, University Hospital of Ferrara, Via Aldo Moro 8, 44124, Ferrara, Italy.

Fabio Facchinetti (F)

Hereditary Breast-Ovarian Cancer Group, University of Modena and Reggio Emilia, Azienda Ospedaliero Universitaria Policlinico, Via del Pozzo 71, 41124, Modena, Italy.

Pierandrea De Iaco (P)

Gynecologic Oncology Unit, University of Bologna, Policlinico S.Orsola-Malpighi, Via Masserenti 13, 40138, Bologna, Italy.

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Classifications MeSH