Fertility counseling in women with hereditary cancer syndromes.

Fertility preservation Hereditary cancer syndrome Oocytes cryopreservation Oocytes donation Preimplantation genetic diagnosis

Journal

Critical reviews in oncology/hematology
ISSN: 1879-0461
Titre abrégé: Crit Rev Oncol Hematol
Pays: Netherlands
ID NLM: 8916049

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 30 10 2021
revised: 16 01 2022
accepted: 21 01 2022
pubmed: 30 1 2022
medline: 3 3 2022
entrez: 29 1 2022
Statut: ppublish

Résumé

Hereditary cancer syndromes are a heterogeneous group of genetic conditions that are associated with an increased risk of developing cancer during lifespan. In affected women, parenthood may be accompanied by concerns for the offspring, considering the common autosomal dominant inheritance. Moreover, fertility preservation to prevent the detrimental effects of cancer treatments differs compared to other clinical contexts. The necessity to preserve gametes is indeed predictable and expected to be common. For these reasons, we advocate a personalized and early fertility counseling. Carriers should be aware of the risk of transmission. The possibility to perform elective oocytes cryopreservation, either before (previvors) or after (survivors) cancer diagnosis should be discussed. Finally, they should be informed about the options of preimplantation genetic test (PGT) and oocytes donation. In conclusion, physicians engaged in oncofertility should personalize the counseling for women with hereditary cancer syndromes, being aware of their peculiar needs.

Identifiants

pubmed: 35091060
pii: S1040-8428(22)00028-2
doi: 10.1016/j.critrevonc.2022.103604
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

103604

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Edgardo Somigliana (E)

Infertility Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy; Dept of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy. Electronic address: dadosomigliana@yahoo.it.

Maria Paola Costantini (MP)

Legal Counsultor for Health Human Rights, Law Firm Costantini, Rome, Italy.

Francesca Filippi (F)

Infertility Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Monica Terenziani (M)

Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Alessandra Riccaboni (A)

Infertility Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Valeria Nicotra (V)

Unit of Medical Genetics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Rocco Rago (R)

Physiopathology of Reproduction and Andrology Unit, Sandro Pertini Hospital, Rome, Italy.

Alessio Paffoni (A)

Infertility Unit, Azienda Socio Sanitaria Territoriale Lariana, Cantù, Come, Italy.

Luca Mencaglia (L)

ART Center, Santa Margherita Hospital, Cortona, Italy.

Stefania Magnolfi (S)

ART Center, Santa Margherita Hospital, Cortona, Italy.

Daniela Zuccarello (D)

Unit of Clinical Genetics, Epidemiology and PGT Unit, Dept of Lab Medicine University Hospital of Padova, Padua, Italy.

Laura Rienzi (L)

GeneraLife IVF Centers, Clinica Valle Giulia, Rome, Italy.

Francesca Spinella (F)

Eurofins Genoma Group, Molecular Genetics Laboratories, Rome, Italy.

Antonio Capalbo (A)

Igenomix, Marostica, Italy.

Giulia Scaravelli (G)

ART Italian National Register, National Centre for Diseases Prevention and Health Promotion, National Health Institute, Rome, Italy.

Salvo Testa (S)

Mutagens, Nonprofit Organization, Milan, Italy.

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Classifications MeSH