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10/22/2024 8:28:50 AM | Browse: 253 | Download: 984
Publication Name World Journal of Clinical Oncology
Manuscript ID 98996
Country Lebanon
Received
2024-07-10 20:44
Peer-Review Started
2024-07-10 20:44
First Decision by Editorial Office Director
2024-08-11 17:17
Return for Revision
2024-08-11 17:17
Revised
2024-08-23 12:44
Publication Fee Transferred
Second Decision by Editor
2024-10-11 02:34
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2024-10-11 09:30
Articles in Press
2024-10-11 09:30
Edit the Manuscript by Language Editor
Typeset the Manuscript
2024-10-16 08:07
Publish the Manuscript Online
2024-10-22 08:28
ISSN 2218-4333 (online)
Open Access This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Copyright © The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Oncology
Manuscript Type Retrospective Study
Article Title Germline pathogenic variants among high hereditary risk patients with breast and ovarian cancer and unaffected subjects in Lebanese Arab women
Manuscript Source Unsolicited Manuscript
All Author List Hiba A Moukadem, Mohammad A Fakhreddine, Nada Assaf, Nadine Safi, Ahmad Al Masry, Monita Al Darazi, Rami Mahfouz and Nagi S El Saghir
ORCID
Author(s) ORCID Number
Nada Assaf http://orcid.org/0000-0002-3352-2660
Monita Al Darazi http://orcid.org/0000-0002-6274-0464
Nagi S El Saghir http://orcid.org/0000-0001-9612-4224
Funding Agency and Grant Number
Corresponding Author Nagi S El Saghir, MD, Professor, Division of Hematology/Oncology, Department of Internal Medicine, American University of Beirut Medical Center, Cairo Street, PO Box 11-0236, Riad El Solh, Beirut 1107 2020, Lebanon. ns23@aub.edu.lb
Key Words Breast cancer; Ovarian cancer; Breast cancer susceptibility gene 1/2; Germline pathogenic variant; High hereditary risk
Core Tip This is the first study on referred patients with breast and/or ovarian cancer and subjects at high hereditary risk for germline pathogenic variant testing among ethnic Lebanese Arab women. The prevalence of pathogenic variants was 8.63% in patients with breast cancer and 15.1% in patients with ovarian cancer. Among the relatives of patients with breast cancer susceptibility gene (BRCA) 1/2 pathogenic variants, 31% tested positive for the same variant, while 5.3% of subjects who tested positive due to a family history of breast cancer had a BRCA pathogenic variant. The results of this study support the hypothesis that the c.131G > T nucleotide change is a founder pathogenic variant in this population.
Publish Date 2024-10-22 08:28
Citation

Moukadem HA, Fakhreddine MA, Assaf N, Safi N, Al Masry A, Al Darazi M, Mahfouz R, El Saghir NS. Germline pathogenic variants among high hereditary risk patients with breast and ovarian cancer and unaffected subjects in Lebanese Arab women. World J Clin Oncol 2024; 15(12): 1481-1490

URL https://www.wjgnet.com/2218-4333/full/v15/i12/1481.htm
DOI https://dx.doi.org/10.5306/wjco.v15.i12.1481
Full Article (PDF) WJCO-15-1481-with-cover.pdf