The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study.


Journal

World journal of surgical oncology
ISSN: 1477-7819
Titre abrégé: World J Surg Oncol
Pays: England
ID NLM: 101170544

Informations de publication

Date de publication:
02 Feb 2021
Historique:
received: 25 11 2020
accepted: 28 01 2021
entrez: 3 2 2021
pubmed: 4 2 2021
medline: 15 5 2021
Statut: epublish

Résumé

Disease sites of female genital tract cancers of BRCA1/2-associated hereditary breast and ovarian cancer (HBOC) are less understood than non-hereditary cancers. We aimed to elucidate the disease site distribution of genital cancers in women with the germline BRCA1 and BRCA2 pathogenic variants (BRCA1+ and BRCA2+) of HBOC. For the primary disease site, the proportion of fallopian tube and peritoneal cancer was significantly higher in BRCA2+ (40.5%) compared with BRCA1+ (15.4%) and BRCA- (no pathogenic variant, 12.8%). For the metastatic site, the proportion of peritoneal dissemination was significantly higher in BRCA1+ (71.9%) than BRCA- (55.1%) and not different from BRCA2+ (71.4%). With one of the most extensive patients, this study supported the previous reports showing that the pathogenic variants of BRCA1/2 were involved in the female genitalia's disease sites.

Identifiants

pubmed: 33531027
doi: 10.1186/s12957-021-02151-3
pii: 10.1186/s12957-021-02151-3
pmc: PMC7856749
doi:

Substances chimiques

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

Types de publication

Letter

Langues

eng

Sous-ensembles de citation

IM

Pagination

36

Subventions

Organisme : Takeda Science Foundation
ID : not applicable

Références

J Clin Oncol. 2012 Jul 20;30(21):2654-63
pubmed: 22711857
Jpn J Clin Oncol. 2020 Dec 16;50(12):1380-1385
pubmed: 32676635
J Clin Oncol. 2010 May 20;28(15):2505-11
pubmed: 20406939
Cancer Genet. 2012 Jan-Feb;205(1-2):34-41
pubmed: 22429596
Ann Surg Oncol. 2018 Nov;25(12):3701-3708
pubmed: 30128899
Int J Gynecol Cancer. 2019 Jul;29(6):1043-1049
pubmed: 31263023

Auteurs

Takashi Mitamura (T)

Department of Obstetrics and Gynecology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Kita 14, Nishi 5, Kita-ku, Sapporo, Hokkaido, 060-8648, Japan. takami@huhp.hokudai.ac.jp.
Division of Clinical Genetics, Hokkaido University Hospital, Sapporo, Japan. takami@huhp.hokudai.ac.jp.

Masayuki Sekine (M)

Department of Obstetrics and Gynecology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Masami Arai (M)

Clinical Genetics, Juntendo University, Graduate School of Medicine, Tokyo, Japan.

Yuka Shibata (Y)

Division of Clinical Genetics, Hokkaido University Hospital, Sapporo, Japan.

Momoko Kato (M)

Division of Clinical Genetics, Hokkaido University Hospital, Sapporo, Japan.

Shiro Yokoyama (S)

Division of Breast Surgical Oncology, Department of Surgery, Showa University School of Medicine, Tokyo, Japan.

Hiroko Yamashita (H)

Department of Breast Surgery, Hokkaido University Hospital, Sapporo, Japan.

Hidemichi Watari (H)

Department of Obstetrics and Gynecology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Kita 14, Nishi 5, Kita-ku, Sapporo, Hokkaido, 060-8648, Japan.

Ichiro Yabe (I)

Division of Clinical Genetics, Hokkaido University Hospital, Sapporo, Japan.

Hiroyuki Nomura (H)

Department of Obstetrics and Gynecology, School of Medicine, Fujita Health University, Toyoake, Japan.

Takayuki Enomoto (T)

Department of Obstetrics and Gynecology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Seigo Nakamura (S)

Division of Breast Surgical Oncology, Department of Surgery, Showa University School of Medicine, Tokyo, Japan.

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Classifications MeSH