Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/107009
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dc.contributor.authorCaramelo, Olga L.-
dc.contributor.authorSilva, Cristina M.-
dc.contributor.authorCaramelo, Francisco-
dc.contributor.authorFrutuoso, Cristina-
dc.contributor.authorAlmeida-Santos, Teresa-
dc.date.accessioned2023-05-09T09:13:47Z-
dc.date.available2023-05-09T09:13:47Z-
dc.date.issued2019-
dc.identifier.issn1731-2302pt
dc.identifier.urihttps://hdl.handle.net/10316/107009-
dc.description.abstractBackground: Triple negative breast cancers (TNBC) are associated with an aggressive clinical course, earlier recurrence and short survival. BRCA – mutated tumours represent up to 25% of all TNBC. BRCA status is being studied as a predictive biomarker of response to platinum agents. However, the predictive role of BRCA status is still uncertain in this setting. Since TNBC is a very heterogeneous group of diseases, it is important to identify subsets of TNBC patients that may benefit from platinum-based therapy. This study aims to establish if the presence of a germline BRCA mutation in women with TNBC improves the pathologic complete response (pCR) after neoadjuvant chemotherapy with platinum compounds. Methods: An extensive literature search was performed in MEDLINE, EMBASE and LILACS databases, WHO (WHO International Clinical Trials Registry Platform) and the Cochrane Controlled Trials Register Database, for online trial registries and conference proceedings. The measurement of pCR was assessed by pathology review of breast specimen and lymph nodes. Results: The overall OR was computed using random effects models. Seven studies were included, comprising a total of 808 TNBC patients, among which 159 were BRCA mutated. Among mutated TNBC patients, 93 (93/159; 58.4%) achieved pCR, while 410 wildtype patients (410/808; 50.7%) showed pCR (OR 1.459 CI 95% [0.953–2.34] p = 0.082) although this result did not reach statistical significance. Conclusions: This meta-analysis shows that the addition of platinum to chemotherapy regimens in the neoadjuvant setting increases pCR rate in BRCA – mutated as compared to wild-type TNBC patients. However, this trend did not achieve statistical significance.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectTriple negative breast cancerpt
dc.subjectBRCApt
dc.subjectNeoadjuvant chemotherapypt
dc.subjectCisplatinpt
dc.subjectCarboplatinpt
dc.titleThe effect of neoadjuvant platinum-based chemotherapy in BRCA mutated triple negative breast cancers -systematic review and meta-analysispt
dc.typearticle-
degois.publication.firstPage11pt
degois.publication.issue1pt
degois.publication.titleHereditary Cancer in Clinical Practicept
dc.peerreviewedyespt
dc.identifier.doi10.1186/s13053-019-0111-ypt
degois.publication.volume17pt
dc.date.embargo2019-01-01*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitICBR Coimbra Institute for Clinical and Biomedical Research-
crisitem.author.parentresearchunitFaculty of Medicine-
crisitem.author.orcid0000-0002-0015-8604-
crisitem.author.orcid0000-0001-7423-2996-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
I&D ICBR - Artigos em Revistas Internacionais
FMUC Medicina - Artigos em Revistas Internacionais
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