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NSABP B-47/NRG Oncology Phase III Randomized Trial Comparing Adjuvant Chemotherapy With or Without Trastuzumab in High-Risk Invasive Breast Cancer Negative for HER2 by FISH and With IHC 1+ or 2+

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dc.contributor.author백순명-
dc.date.accessioned2022-09-06T06:41:53Z-
dc.date.available2022-09-06T06:41:53Z-
dc.date.issued2020-02-
dc.identifier.issn0732-183X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/190270-
dc.description.abstractPURPOSE Adjuvant trastuzumab reduces invasive breast cancer (IBC) recurrence and risk for death in patients with HER2-amplified or overexpressing IBC. A subset of patients in the landmark trastuzumab adjuvant trials who originally tested HER2-positive but were HER2-negative by central HER2 testing appeared to possibly benefit from trastuzumab. The objective for the NSABP B-47 trial was to determine whether the addition of trastuzumab to adjuvant chemotherapy (CRx) would improve invasive disease-free survival (IDFS) in patients with HER2-negative breast cancer. PATIENTS AND METHODS A total of 3,270 women with high-risk primary IBC were randomly assigned to CRx with or without 1 year of trastuzumab. Eligibility criteria included immunohistochemistry (IHC) score 1+ or 2+ with fluorescence in situ hybridization ratio (FISH) < 2.0 or, if ratio was not performed, HER2 gene copy number < 4.0. CRx was either docetaxel plus cyclophosphamide or doxorubicin and cyclophosphamide followed by weekly paclitaxel for 12 weeks. RESULTS At a median follow-up of 46 months, the addition of trastuzumab to CRx did not improve IDFS (5-year IDFS: 89.8% with CRx plus trastuzumab [CRxT] v 89.2% with CRx alone; hazard ratio [HR], 0.98; 95% CI, 0.76 to 1.25; P = .85). These findings did not differ by level of HER2 IHC expression, lymph node involvement, or hormone-receptor status. For distant recurrence-free interval, 5-year estimates were 92.7% with CRxT compared with 93.6% for CRx alone (HR, 1.10; 95% CI, 0.81 to 1.50; P = .55) and for overall survival (OS) were 94.8% with CRxT and 96.3% in CRx alone (HR, 1.33; 95% CI, 0.90 to 1.95; P = .15). There were no unexpected toxicities from the addition of trastuzumab to CRx. CONCLUSION The addition of trastuzumab to CRx did not improve IDFS, distant recurrence-free interval, or OS in women with non-HER2-overexpressing IBC. Trastuzumab does not benefit women without IHC 3+ or FISH ratio-amplified breast cancer. (C) 2019 by American Society of Clinical Oncology-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherAmerican Society of Clinical Oncology-
dc.relation.isPartOfJOURNAL OF CLINICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntineoplastic Agents, Immunological / administration & dosage-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols / therapeutic use*-
dc.subject.MESHBreast Neoplasms / drug therapy*-
dc.subject.MESHBreast Neoplasms / enzymology-
dc.subject.MESHBreast Neoplasms / genetics-
dc.subject.MESHBreast Neoplasms / pathology-
dc.subject.MESHChemotherapy, Adjuvant-
dc.subject.MESHCyclophosphamide / administration & dosage-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHDocetaxel / administration & dosage-
dc.subject.MESHDoxorubicin / administration & dosage-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHImmunohistochemistry-
dc.subject.MESHIn Situ Hybridization, Fluorescence-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNeoplasm Invasiveness-
dc.subject.MESHReceptor, ErbB-2 / biosynthesis*-
dc.subject.MESHReceptor, ErbB-2 / genetics-
dc.subject.MESHRisk Factors-
dc.subject.MESHTrastuzumab / administration & dosage-
dc.titleNSABP B-47/NRG Oncology Phase III Randomized Trial Comparing Adjuvant Chemotherapy With or Without Trastuzumab in High-Risk Invasive Breast Cancer Negative for HER2 by FISH and With IHC 1+ or 2+-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentBioMedical Science Institute (의생명과학부)-
dc.contributor.googleauthorLouis Fehrenbacher-
dc.contributor.googleauthorReena S Cecchini-
dc.contributor.googleauthorCharles E Geyer Jr-
dc.contributor.googleauthorPriya Rastogi-
dc.contributor.googleauthorJoseph P Costantino-
dc.contributor.googleauthorJames N Atkins-
dc.contributor.googleauthorJohn P Crown-
dc.contributor.googleauthorJonathan Polikoff-
dc.contributor.googleauthorJean-Francois Boileau-
dc.contributor.googleauthorLouise Provencher-
dc.contributor.googleauthorChristopher Stokoe-
dc.contributor.googleauthorTimothy D Moore-
dc.contributor.googleauthorAndré Robidoux-
dc.contributor.googleauthorPatrick J Flynn-
dc.contributor.googleauthorVirginia F Borges-
dc.contributor.googleauthorKathy S Albain-
dc.contributor.googleauthorSandra M Swain-
dc.contributor.googleauthorSoonmyung Paik-
dc.contributor.googleauthorEleftherios P Mamounas-
dc.contributor.googleauthorNorman Wolmark-
dc.identifier.doi10.1200/JCO.19.01455-
dc.contributor.localIdA01823-
dc.relation.journalcodeJ01331-
dc.identifier.eissn1527-7755-
dc.identifier.pmid31821109-
dc.contributor.alternativeNamePaik, Soon Myung-
dc.contributor.affiliatedAuthor백순명-
dc.citation.volume38-
dc.citation.number5-
dc.citation.startPage444-
dc.citation.endPage453-
dc.identifier.bibliographicCitationJOURNAL OF CLINICAL ONCOLOGY, Vol.38(5) : 444-453, 2020-02-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers

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