Survival Benefit of Germline BRCA Mutation is Associated with Residual Disease in Ovarian Cancer.
dc.contributor.author | Shi, Tingyan | |
dc.contributor.author | Wang, Pan | |
dc.contributor.author | Tang, Wenbin | |
dc.contributor.author | Jiang, Rong | |
dc.contributor.author | Yin, Sheng | |
dc.contributor.author | Shi, Di | |
dc.contributor.author | Wang, Qing | |
dc.contributor.author | Wei, Qingyi | |
dc.contributor.author | Zang, Rongyu | |
dc.date.accessioned | 2019-05-01T18:18:57Z | |
dc.date.available | 2019-05-01T18:18:57Z | |
dc.date.issued | 2018-01 | |
dc.date.updated | 2019-05-01T18:18:57Z | |
dc.description.abstract | BACKGROUND/AIMS:Prognostic value of germline BRCA1 or BRCA2 (gBRCA1/2) mutations in epithelial ovarian cancer (EOC) remains controversial, especially in the estimation of long-term survival. We previously reported the largest study of gBRCA1/2 mutation prevalence in Chinese EOC patients. The aim of this study is to further illustrate the correlation of residual disease and survival in BRCA-associated EOC in China. METHODS:In the current cohort consisting of 615 cases from the Chinese EOC genome-wide association study, we evaluated the association between gBRCA1/2 mutation and clinical outcomes. RESULTS:Overall, we did not find any significant difference between gBRCA1/2 mutation carriers and non-carriers in both progression-free survival (PFS) and overall survival (OS) (19.3 vs. 18.1 months and 77.2 vs. 73.2 months, P=0.528 and 0.147, HR 0.93 and 0.79, 95%CI 0.74-1.17 and 0.57-1.09, respectively). However, within three years after diagnosis, mutation carriers showed a longer OS than non-carriers (P=0.018, HR 0.53, 95%CI 0.31-0.90). Such a survival advantage decreased along with the extension of follow-up time. Quite interestingly, in the subgroup of patients with gross residual disease, mutation carriers had a longer survival than non-carriers (18.5 vs. 15.1 months and 68.5 vs. 54.3 months, P=0.046 and 0.038, HR 0.74 and 0.65, 95% CI 0.55-1.00 and 0.43-0.98, for PFS and OS respectively). CONCLUSIONS:Our findings provided the evidence that gBRCA1/2 mutation was not associated with survival in Chinese EOC patients, which possibly attributed to more than 37% of the patients without gross residual disease. Survival benefit of gBRCA1/2 mutation was prominent in ovarian cancer patients with gross residual disease. | |
dc.identifier | 000491477 | |
dc.identifier.issn | 1015-8987 | |
dc.identifier.issn | 1421-9778 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | S. Karger AG | |
dc.relation.ispartof | Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology | |
dc.relation.isversionof | 10.1159/000491477 | |
dc.subject | Humans | |
dc.subject | Ovarian Neoplasms | |
dc.subject | Neoplasm, Residual | |
dc.subject | BRCA1 Protein | |
dc.subject | BRCA2 Protein | |
dc.subject | Disease-Free Survival | |
dc.subject | Survival Rate | |
dc.subject | Follow-Up Studies | |
dc.subject | Germ-Line Mutation | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Middle Aged | |
dc.subject | Female | |
dc.title | Survival Benefit of Germline BRCA Mutation is Associated with Residual Disease in Ovarian Cancer. | |
dc.type | Journal article | |
duke.contributor.orcid | Wei, Qingyi|0000-0002-3845-9445 | |
pubs.begin-page | 2088 | |
pubs.end-page | 2096 | |
pubs.issue | 5 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Population Health Sciences | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Medicine, Medical Oncology | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Clinical Science Departments | |
pubs.publication-status | Published | |
pubs.volume | 47 |
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