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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+
DC Field | Value | Language |
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dc.contributor.author | 백순명 | - |
dc.date.accessioned | 2022-09-06T06:41:53Z | - |
dc.date.available | 2022-09-06T06:41:53Z | - |
dc.date.issued | 2020-02 | - |
dc.identifier.issn | 0732-183X | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/190270 | - |
dc.description.abstract | PURPOSE 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.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | American Society of Clinical Oncology | - |
dc.relation.isPartOf | JOURNAL OF CLINICAL ONCOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Antineoplastic Agents, Immunological / administration & dosage | - |
dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols / therapeutic use* | - |
dc.subject.MESH | Breast Neoplasms / drug therapy* | - |
dc.subject.MESH | Breast Neoplasms / enzymology | - |
dc.subject.MESH | Breast Neoplasms / genetics | - |
dc.subject.MESH | Breast Neoplasms / pathology | - |
dc.subject.MESH | Chemotherapy, Adjuvant | - |
dc.subject.MESH | Cyclophosphamide / administration & dosage | - |
dc.subject.MESH | Disease-Free Survival | - |
dc.subject.MESH | Docetaxel / administration & dosage | - |
dc.subject.MESH | Doxorubicin / administration & dosage | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Immunohistochemistry | - |
dc.subject.MESH | In Situ Hybridization, Fluorescence | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoplasm Invasiveness | - |
dc.subject.MESH | Receptor, ErbB-2 / biosynthesis* | - |
dc.subject.MESH | Receptor, ErbB-2 / genetics | - |
dc.subject.MESH | Risk Factors | - |
dc.subject.MESH | Trastuzumab / administration & dosage | - |
dc.title | 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+ | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | BioMedical Science Institute (의생명과학부) | - |
dc.contributor.googleauthor | Louis Fehrenbacher | - |
dc.contributor.googleauthor | Reena S Cecchini | - |
dc.contributor.googleauthor | Charles E Geyer Jr | - |
dc.contributor.googleauthor | Priya Rastogi | - |
dc.contributor.googleauthor | Joseph P Costantino | - |
dc.contributor.googleauthor | James N Atkins | - |
dc.contributor.googleauthor | John P Crown | - |
dc.contributor.googleauthor | Jonathan Polikoff | - |
dc.contributor.googleauthor | Jean-Francois Boileau | - |
dc.contributor.googleauthor | Louise Provencher | - |
dc.contributor.googleauthor | Christopher Stokoe | - |
dc.contributor.googleauthor | Timothy D Moore | - |
dc.contributor.googleauthor | André Robidoux | - |
dc.contributor.googleauthor | Patrick J Flynn | - |
dc.contributor.googleauthor | Virginia F Borges | - |
dc.contributor.googleauthor | Kathy S Albain | - |
dc.contributor.googleauthor | Sandra M Swain | - |
dc.contributor.googleauthor | Soonmyung Paik | - |
dc.contributor.googleauthor | Eleftherios P Mamounas | - |
dc.contributor.googleauthor | Norman Wolmark | - |
dc.identifier.doi | 10.1200/JCO.19.01455 | - |
dc.contributor.localId | A01823 | - |
dc.relation.journalcode | J01331 | - |
dc.identifier.eissn | 1527-7755 | - |
dc.identifier.pmid | 31821109 | - |
dc.contributor.alternativeName | Paik, Soon Myung | - |
dc.contributor.affiliatedAuthor | 백순명 | - |
dc.citation.volume | 38 | - |
dc.citation.number | 5 | - |
dc.citation.startPage | 444 | - |
dc.citation.endPage | 453 | - |
dc.identifier.bibliographicCitation | JOURNAL OF CLINICAL ONCOLOGY, Vol.38(5) : 444-453, 2020-02 | - |
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