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Germline BRCA, chemotherapy response scores, and survival in the neoadjuvant treatment of ovarian cancer

DC Field Value Language
dc.contributor.author김상운-
dc.contributor.author김성훈-
dc.contributor.author김영태-
dc.contributor.author김현수-
dc.contributor.author남은지-
dc.contributor.author이용재-
dc.contributor.author이정윤-
dc.date.accessioned2020-12-01T17:58:42Z-
dc.date.available2020-12-01T17:58:42Z-
dc.date.issued2020-03-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/180541-
dc.description.abstractBackground: To analyze the effects of BRCA1/2 mutations on chemotherapy response scores (CRS) and survival in a cohort of patients with advanced-stage ovarian cancer who were treated with neoadjuvant chemotherapy (NAC) followed by interval debulking surgery (IDS). Methods: We retrospectively reviewed the medical records of 169 high-grade serous ovarian cancer patients who underwent a germline BRCA1/2 test and received three cycles of NAC at the Yonsei Cancer Center from 2006 to 2018. Chemotherapy response scores were compared in patients with and without BRCA1/2 mutations. The effects of BRCA1/2 mutations and CRS on survival were evaluated. Results: BRCA1/2 mutations were detected in 47 (28.1%) of the 169 patients. Overall, 16 (34.0%) patients with BRCA1/2 mutations had a CRS 3 to chemotherapy compared to scores of 43 in patients (35.2%) without a mutation. Response scores of 3 in patients with BRCA1/2 mutations were not significantly associated with either improved progression-free survival (PFS) (P = 0.949) or overall survival (OS) (P = 0.168). However, CRS 3 in patients without BRCA mutations was significantly associated with both improved PFS (P = 0.030) and OS (P = 0.039). In patients with CRS1/2, carriers of BRCA1/2 mutations had better PFS (P = 0.0344) and OS (P = 0.043) than wild-type BRCA genotype patients. Conclusion: In ovarian cancer patients treated with NAC, CRS did not predict survival for BRCA 1/2 mutation carriers but did for BRCA wild-type patients.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherBioMed Central-
dc.relation.isPartOfBMC CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHBRCA1 Protein / genetics*-
dc.subject.MESHBRCA2 Protein / genetics*-
dc.subject.MESHCystadenocarcinoma, Serous / genetics-
dc.subject.MESHCystadenocarcinoma, Serous / pathology-
dc.subject.MESHCystadenocarcinoma, Serous / therapy*-
dc.subject.MESHCytoreduction Surgical Procedures-
dc.subject.MESHDrug Therapy / methods*-
dc.subject.MESHFemale-
dc.subject.MESHGerm-Line Mutation*-
dc.subject.MESHGynecologic Surgical Procedures / methods*-
dc.subject.MESHHumans-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoadjuvant Therapy-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHOvarian Neoplasms / genetics-
dc.subject.MESHOvarian Neoplasms / pathology-
dc.subject.MESHOvarian Neoplasms / therapy*-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHSurvival Analysis-
dc.subject.MESHTreatment Outcome-
dc.titleGermline BRCA, chemotherapy response scores, and survival in the neoadjuvant treatment of ovarian cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Obstetrics and Gynecology (산부인과학교실)-
dc.contributor.googleauthorYong Jae Lee-
dc.contributor.googleauthorHyun-Soo Kim-
dc.contributor.googleauthorJohn Hoon Rim-
dc.contributor.googleauthorJung-Yun Lee-
dc.contributor.googleauthorEun Ji Nam-
dc.contributor.googleauthorSang Wun Kim-
dc.contributor.googleauthorSunghoon Kim-
dc.contributor.googleauthorYoung Tae Kim-
dc.identifier.doi10.1186/s12885-020-6688-8-
dc.contributor.localIdA00526-
dc.contributor.localIdA00595-
dc.contributor.localIdA00729-
dc.contributor.localIdA01114-
dc.contributor.localIdA01262-
dc.contributor.localIdA05165-
dc.contributor.localIdA04638-
dc.relation.journalcodeJ00351-
dc.identifier.eissn1471-2407-
dc.identifier.pmid32131779-
dc.subject.keywordChemotherapy response scores-
dc.subject.keywordGermline BRCA-
dc.subject.keywordNeoadjuvant chemotherapy-
dc.subject.keywordOvarian cancer-
dc.contributor.alternativeNameKim, Sang Wun-
dc.contributor.affiliatedAuthor김상운-
dc.contributor.affiliatedAuthor김성훈-
dc.contributor.affiliatedAuthor김영태-
dc.contributor.affiliatedAuthor김현수-
dc.contributor.affiliatedAuthor남은지-
dc.contributor.affiliatedAuthor이용재-
dc.contributor.affiliatedAuthor이정윤-
dc.citation.volume20-
dc.citation.number1-
dc.citation.startPage185-
dc.identifier.bibliographicCitationBMC CANCER, Vol.20(1) : 185, 2020-03-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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