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dc.contributor.authorTakada, Men
dc.contributor.authorIshiguro, Hen
dc.contributor.authorNagai, Sen
dc.contributor.authorOhtani, Sen
dc.contributor.authorKawabata, Hen
dc.contributor.authorYanagita, Yen
dc.contributor.authorHozumi, Yen
dc.contributor.authorShimizu, Cen
dc.contributor.authorTakao, Sen
dc.contributor.authorSato, Nen
dc.contributor.authorKosaka, Yen
dc.contributor.authorSagara, Yen
dc.contributor.authorIwata, Hen
dc.contributor.authorOhno, Sen
dc.contributor.authorKuroi, Ken
dc.contributor.authorMasuda, Nen
dc.contributor.authorYamashiro, Hen
dc.contributor.authorSugimoto, Men
dc.contributor.authorKondo, Men
dc.contributor.authorNaito, Yen
dc.contributor.authorSasano, Hen
dc.contributor.authorInamoto, Ten
dc.contributor.authorMorita, Sen
dc.contributor.authorToi, Men
dc.contributor.alternative高田, 正泰ja
dc.contributor.alternative戸井, 雅和ja
dc.date.accessioned2015-08-13T01:16:55Z-
dc.date.available2015-08-13T01:16:55Z-
dc.date.issued2014-05-
dc.identifier.issn1573-7217-
dc.identifier.urihttp://hdl.handle.net/2433/199065-
dc.description.abstractWe investigated the disease-free survival (DFS) of HER2-positive primary breast cancer patients treated with neoadjuvant chemotherapy plus trastuzumab, as well as predictive factors for DFS and pathologic response. Data from 829 female patients treated between 2001 and 2010 were collected from 38 institutions in Japan. Predictive factors were evaluated using multivariate analyses. The 3-year DFS rate was 87 % [95 % confidence interval (CI) 85-90]. The pathologic complete response (pCR: ypT0/is + ypN0) rate was 51 %. The pCR rate was higher in the ER/PgR-negative patients than in the ER/PgR-positive patients (64 vs. 36 %, P < 0.001). Patients with pCR showed a higher DFS rate than patients without pCR (93 vs. 82 %, P < 0.001). Multivariate analysis revealed three independent predictors for poorer DFS: advanced nodal stage [hazard ratio (HR) 2.63, 95 % CI 1.36-5.21, P = 0.004 for cN2-3 vs. cN0], histological/nuclear grade 3 (HR 1.81, 95 % CI 1.15-2.91, P = 0.011), and non-pCR (HR 1.98, 95 % CI 1.22-3.24, P = 0.005). In the ER/PgR-negative dataset, non-pCR (HR 2.63, 95 % CI 1.43-4.90, P = 0.002) and clinical tumor stage (HR 2.20, 95 % CI 1.16-4.20, P = 0.017 for cT3-4 vs. cT1-2) were independent predictors for DFS, and in the ER/PgR-positive dataset, histological grade of 3 (HR 3.09, 95 % CI 1.48-6.62, P = 0.003), clinical nodal stage (HR 4.26, 95 % CI 1.53-13.14, P = 0.005 for cN2-3 vs. cN0), and young age (HR 2.40, 95 % CI 1.12-4.94, P = 0.026 for ?40 vs. >40) were negative predictors for DFS. Strict pCR (ypT0 + ypN0) was an independent predictor for DFS in both the ER/PgR-negative and -positive datasets (HR 2.66, 95 % CI 1.31-5.97, P = 0.006 and HR 3.86, 95 % CI 1.13-24.21, P = 0.029, respectively). These results may help assure a more accurate prognosis and personalized treatment for HER2-positive breast cancer patients.en
dc.language.isoeng-
dc.publisherSpringer USen
dc.rightsThe final publication is available at Springer via http://dx.doi.org/10.1007/s10549-014-2907-9en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.rightsThis is not the published version. Please cite only the published version.en
dc.subjectBreast canceren
dc.subjectHER2en
dc.subjectneoadjuvant chemotherapyen
dc.subjectpathologic complete responseen
dc.subjectprognostic factorsen
dc.subjecttrastuzumaben
dc.subject.meshAntibodies, Monoclonal, Humanized/therapeutic useen
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols/therapeutic useen
dc.subject.meshBreast Neoplasms/drug therapyen
dc.subject.meshBreast Neoplasms/mortalityen
dc.subject.meshDisease-Free Survivalen
dc.subject.meshFemaleen
dc.subject.meshHumansen
dc.subject.meshNeoadjuvant Therapyen
dc.subject.meshPrognosisen
dc.subject.meshReceptor, ErbB-2/metabolismen
dc.subject.meshRetrospective Studiesen
dc.titleSurvival of HER2-positive primary breast cancer patients treated by neoadjuvant chemotherapy plus trastuzumab: a multicenter retrospective observational study (JBCRG-C03 study).en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleBreast cancer research and treatmenten
dc.identifier.volume145-
dc.identifier.issue1-
dc.identifier.spage143-
dc.identifier.epage153-
dc.relation.doi10.1007/s10549-014-2907-9-
dc.textversionauthor-
dc.addressDepartment of Breast Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japanen
dc.identifier.pmid24682674-
dcterms.accessRightsopen access-
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