BRCA Variants Do Not Increase the Risk of Adverse Reactions in Patients With Ovarian Cancer: A Single-Center Real-World Study

Objective To study the correlation between BRCA mutation status and the risk of adverse reactions in patients with ovarian cancer. Method A real-world study was conducted at the largest gynecological oncology center in western China, the West China Second University Hospital of Sichuan University. T...

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Published inFrontiers in oncology Vol. 12; p. 807748
Main Authors Li, Kemin, Zeng, Jing, Zhang, Mengpei, Yin, Rutie, Li, Zhengyu
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 30.06.2022
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Summary:Objective To study the correlation between BRCA mutation status and the risk of adverse reactions in patients with ovarian cancer. Method A real-world study was conducted at the largest gynecological oncology center in western China, the West China Second University Hospital of Sichuan University. The research subjects were patients diagnosed with ovarian cancer who were initially treated in our hospital from January 2016 to January 2020 and had their BRCA gene status evaluated. Multivariate Cox analysis was conducted to investigate the correlation between the BRCA mutation status and adverse reactions in ovarian cancer patients during initial treatment. Results A total of 349 ovarian cancer patients were enrolled, including 79 patients with pathogenic BRCA variants, resulting in a pathogenic mutation rate of 22.6%. Among these 79 patients, 57 had BRCA1 variants and 22 had BRCA2 variants, yielding a pathogenic mutation rate of 16.3% and 6.3%, respectively. Multivariate COX analysis revealed that pathogenic BRCA variants were not related to the risk of adverse reactions, such as myelosuppression and allergies to chemotherapy drugs ( P >0.05), during the initial treatment of ovarian cancer. Conclusion BRCA variants did not increase the risk of adverse reactions, such as myelosuppression and allergies to chemotherapy drugs, in ovarian cancer patients during initial treatment.
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Reviewed by: Athina Christopoulou, General University Hospital of Patras, Greece; Steven Narod, University of Toronto, Canada; Christine Garcia, Kaiser Permanente San Francisco Medical Center, United States
Edited by: Sophia George, University of Miami, United States
These authors have contributed equally to this work
This article was submitted to Gynecological Oncology, a section of the journal Frontiers in Oncology
ISSN:2234-943X
2234-943X
DOI:10.3389/fonc.2022.807748