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Article: Germline mutation in BRCA1 or MRCA2 and ten-year survival for women diagnosed with epithelial ovarian cancer
Title | Germline mutation in BRCA1 or MRCA2 and ten-year survival for women diagnosed with epithelial ovarian cancer |
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Authors | |
Issue Date | 2015 |
Publisher | American Association for Cancer Research. The Journal's web site is located at http://clincancerres.aacrjournals.org/ |
Citation | Clinical Cancer Research, 2015, v. 21 n. 3, p. 652-657 How to Cite? |
Abstract | Purpose:To analyse the effect of germline mutations in BRCA1 and BRCA2 on mortality in ovarian cancer patients up to ten years after diagnosis. Experimental Design:We used unpublished survival time data for 2,242 patients from two case-control studies and extended survival-time data for 4,314 patients from previously reported studies. All participants had been screened for deleterious germline mutations in BRCA1 and BRCA2. Survival time was analysed for the combined data using Cox proportional hazard models with BRCA1 and BRCA2 as time-varying covariates. Competing risks were analysed using Fine and Gray model. Results: The combined 10-year overall survival was 30% (95% CI, 28%-31%) for non-carriers, 25% (95% CI, 22%-28%) for BRCA1 carriers, and 35% (95% CI, 30%-41%) for BRCA2 carriers. The hazard ratio for BRCA1 was 0.53 at time zero and increased over time becoming greater than one at 4.8 years. For BRCA2, the hazard ratio was 0.42 at time zero and increased over time (predicted to become greater than one at 10.5 years). The results were similar when restricted to 3,202 patients with high-grade serous tumors, and to ovarian cancer specific mortality. Conclusions: BRCA1/2 mutations are associated with better short-term survival, but this advantage decreases over time and, in BRCA1 carriers is eventually reversed. This may have important implications for therapy of both primary and relapsed disease and for analysis of long-term survival in clinical trials of new agents, particularly those that are effective in BRCA1/2 mutation carriers. |
Persistent Identifier | http://hdl.handle.net/10722/206832 |
ISSN | 2023 Impact Factor: 10.0 2023 SCImago Journal Rankings: 4.623 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Candido Dos Reis, FJ | en_US |
dc.contributor.author | Song, H | en_US |
dc.contributor.author | Goode, EL | en_US |
dc.contributor.author | Cunningham, JM | en_US |
dc.contributor.author | Dicks, E | en_US |
dc.contributor.author | Mitchell, G | en_US |
dc.contributor.author | Michie, C | en_US |
dc.contributor.author | Cass, I | en_US |
dc.contributor.author | Andrulis, IL | en_US |
dc.contributor.author | Lazaro, C | en_US |
dc.contributor.author | Montagna, M | en_US |
dc.contributor.author | Kwong, A | en_US |
dc.contributor.author | Neuhausen, SL | en_US |
dc.contributor.author | Mai, PL | en_US |
dc.contributor.author | Toland, AE | en_US |
dc.contributor.author | Brenton, JD | en_US |
dc.contributor.author | Antoniou, AC | en_US |
dc.contributor.author | Bowtell, DD | en_US |
dc.date.accessioned | 2014-12-02T10:06:04Z | - |
dc.date.available | 2014-12-02T10:06:04Z | - |
dc.date.issued | 2015 | en_US |
dc.identifier.citation | Clinical Cancer Research, 2015, v. 21 n. 3, p. 652-657 | en_US |
dc.identifier.issn | 1078-0432 | - |
dc.identifier.uri | http://hdl.handle.net/10722/206832 | - |
dc.description.abstract | Purpose:To analyse the effect of germline mutations in BRCA1 and BRCA2 on mortality in ovarian cancer patients up to ten years after diagnosis. Experimental Design:We used unpublished survival time data for 2,242 patients from two case-control studies and extended survival-time data for 4,314 patients from previously reported studies. All participants had been screened for deleterious germline mutations in BRCA1 and BRCA2. Survival time was analysed for the combined data using Cox proportional hazard models with BRCA1 and BRCA2 as time-varying covariates. Competing risks were analysed using Fine and Gray model. Results: The combined 10-year overall survival was 30% (95% CI, 28%-31%) for non-carriers, 25% (95% CI, 22%-28%) for BRCA1 carriers, and 35% (95% CI, 30%-41%) for BRCA2 carriers. The hazard ratio for BRCA1 was 0.53 at time zero and increased over time becoming greater than one at 4.8 years. For BRCA2, the hazard ratio was 0.42 at time zero and increased over time (predicted to become greater than one at 10.5 years). The results were similar when restricted to 3,202 patients with high-grade serous tumors, and to ovarian cancer specific mortality. Conclusions: BRCA1/2 mutations are associated with better short-term survival, but this advantage decreases over time and, in BRCA1 carriers is eventually reversed. This may have important implications for therapy of both primary and relapsed disease and for analysis of long-term survival in clinical trials of new agents, particularly those that are effective in BRCA1/2 mutation carriers. | en_US |
dc.language | eng | en_US |
dc.publisher | American Association for Cancer Research. The Journal's web site is located at http://clincancerres.aacrjournals.org/ | en_US |
dc.relation.ispartof | Clinical Cancer Research | en_US |
dc.title | Germline mutation in BRCA1 or MRCA2 and ten-year survival for women diagnosed with epithelial ovarian cancer | en_US |
dc.type | Article | en_US |
dc.identifier.email | Kwong, A: avakwong@hkucc.hku.hk | en_US |
dc.identifier.authority | Kwong, A=rp01734 | en_US |
dc.identifier.doi | 10.1158/1078-0432.CCR-14-2497 | en_US |
dc.identifier.pmcid | PMC4338615 | - |
dc.identifier.scopus | eid_2-s2.0-84961291899 | - |
dc.identifier.hkuros | 241543 | en_US |
dc.identifier.eissn | 1557-3265 | - |
dc.identifier.isi | WOS:000348908500020 | - |
dc.identifier.issnl | 1078-0432 | - |