Cited 0 times in

Breast Cancer Index and Prediction of Extended Aromatase Inhibitor Therapy Benefit in Hormone Receptor-Positive Breast Cancer from the NRG Oncology/NSABP B-42 Trial

DC Field Value Language
dc.contributor.author백순명-
dc.date.accessioned2025-02-03T08:28:19Z-
dc.date.available2025-02-03T08:28:19Z-
dc.date.issued2024-05-
dc.identifier.issn1078-0432-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/201698-
dc.description.abstractPurpose: BCI (H/I) has been shown to predict extended endocrine therapy (EET) benefit. We examined BCI (H/I) for EET benefit prediction in NSABP B-42, which evaluated extended letrozole therapy (ELT) in patients with hormone receptor-positive breast cancer after 5 years of ET. Experimental design: A stratified Cox model was used to analyze RFI as the primary endpoint, with DR, BCFI, and DFS as secondary endpoints. Because of a nonproportional effect of ELT on DR, time-dependent analyses were performed. Results: The translational cohort included 2,178 patients (45% BCI (H/I)-High, 55% BCI (H/I)-Low). ELT showed an absolute 10-year RFI benefit of 1.6% (P = 0.10), resulting in an underpowered primary analysis (50% power). ELT benefit and BCI (H/I) did not show a significant interaction for RFI (BCI (H/I)-Low: 10 years absolute benefit 1.1% [HR, 0.70; 95% confidence interval (CI), 0.43-1.12; P = 0.13]; BCI (H/I)-High: 2.4% [HR, 0.83; 95% CI, 0.55-1.26; P = 0.38]; Pinteraction = 0.56). Time-dependent DR analysis showed that after 4 years, BCI (H/I)-High patients had significant ELT benefit (HR = 0.29; 95% CI, 0.12-0.69; P < 0.01), whereas BCI (H/I)-Low patients were less likely to benefit (HR, 0.68; 95% CI, 0.33-1.39; P = 0.29; Pinteraction = 0.14). Prediction of ELT benefit by BCI (H/I) was more apparent in the HER2- subset after 4 years (ELT-by-BCI (H/I) Pinteraction = 0.04). Conclusions: BCI (H/I)-High versus BCI (H/I)-Low did not show a statistically significant difference in ELT benefit for the primary endpoint (RFI). However, in time-dependent DR analysis, BCI (H/I)-High patients experienced statistically significant benefit from ELT after 4 years, whereas (H/I)-Low patients did not. Because BCI (H/I) has been validated as a predictive marker of EET benefit in other trials, additional follow-up may enable further characterization of BCI's predictive ability.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherAmerican Association for Cancer Research-
dc.relation.isPartOfCLINICAL CANCER RESEARCH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAromatase Inhibitors* / therapeutic use-
dc.subject.MESHBreast Neoplasms* / drug therapy-
dc.subject.MESHBreast Neoplasms* / metabolism-
dc.subject.MESHBreast Neoplasms* / pathology-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLetrozole* / administration & dosage-
dc.subject.MESHLetrozole* / therapeutic use-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNitriles / therapeutic use-
dc.subject.MESHPrognosis-
dc.subject.MESHReceptors, Estrogen* / metabolism-
dc.subject.MESHReceptors, Progesterone / metabolism-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHTriazoles / administration & dosage-
dc.subject.MESHTriazoles / therapeutic use-
dc.titleBreast Cancer Index and Prediction of Extended Aromatase Inhibitor Therapy Benefit in Hormone Receptor-Positive Breast Cancer from the NRG Oncology/NSABP B-42 Trial-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentBioMedical Science Institute (의생명과학부)-
dc.contributor.googleauthorEleftherios P Mamounas-
dc.contributor.googleauthorHanna Bandos-
dc.contributor.googleauthorPriya Rastogi-
dc.contributor.googleauthorYi Zhang-
dc.contributor.googleauthorKai Treuner-
dc.contributor.googleauthorPeter C Lucas-
dc.contributor.googleauthorCharles E Geyer Jr-
dc.contributor.googleauthorLouis Fehrenbacher-
dc.contributor.googleauthorStephen K Chia-
dc.contributor.googleauthorAdam M Brufsky-
dc.contributor.googleauthorJanice M Walshe-
dc.contributor.googleauthorGamini S Soori-
dc.contributor.googleauthorShaker Dakhil-
dc.contributor.googleauthorSoonmyung Paik-
dc.contributor.googleauthorSandra M Swain-
dc.contributor.googleauthorDennis C Sgroi-
dc.contributor.googleauthorCatherine A Schnabel-
dc.contributor.googleauthorNorman Wolmark-
dc.identifier.doi10.1158/1078-0432.CCR-23-1977-
dc.contributor.localIdA01823-
dc.relation.journalcodeJ00564-
dc.identifier.pmid38376912-
dc.contributor.alternativeNamePaik, Soon Myung-
dc.contributor.affiliatedAuthor백순명-
dc.citation.volume30-
dc.citation.number9-
dc.citation.startPage1984-
dc.citation.endPage1991-
dc.identifier.bibliographicCitationCLINICAL CANCER RESEARCH, Vol.30(9) : 1984-1991, 2024-05-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.