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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 |
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dc.contributor.author | 백순명 | - |
dc.date.accessioned | 2025-02-03T08:28:19Z | - |
dc.date.available | 2025-02-03T08:28:19Z | - |
dc.date.issued | 2024-05 | - |
dc.identifier.issn | 1078-0432 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/201698 | - |
dc.description.abstract | Purpose: 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.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | American Association for Cancer Research | - |
dc.relation.isPartOf | CLINICAL CANCER RESEARCH | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aromatase Inhibitors* / therapeutic use | - |
dc.subject.MESH | Breast Neoplasms* / drug therapy | - |
dc.subject.MESH | Breast Neoplasms* / metabolism | - |
dc.subject.MESH | Breast Neoplasms* / pathology | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Letrozole* / administration & dosage | - |
dc.subject.MESH | Letrozole* / therapeutic use | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Nitriles / therapeutic use | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Receptors, Estrogen* / metabolism | - |
dc.subject.MESH | Receptors, Progesterone / metabolism | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Triazoles / administration & dosage | - |
dc.subject.MESH | Triazoles / therapeutic use | - |
dc.title | 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.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | BioMedical Science Institute (의생명과학부) | - |
dc.contributor.googleauthor | Eleftherios P Mamounas | - |
dc.contributor.googleauthor | Hanna Bandos | - |
dc.contributor.googleauthor | Priya Rastogi | - |
dc.contributor.googleauthor | Yi Zhang | - |
dc.contributor.googleauthor | Kai Treuner | - |
dc.contributor.googleauthor | Peter C Lucas | - |
dc.contributor.googleauthor | Charles E Geyer Jr | - |
dc.contributor.googleauthor | Louis Fehrenbacher | - |
dc.contributor.googleauthor | Stephen K Chia | - |
dc.contributor.googleauthor | Adam M Brufsky | - |
dc.contributor.googleauthor | Janice M Walshe | - |
dc.contributor.googleauthor | Gamini S Soori | - |
dc.contributor.googleauthor | Shaker Dakhil | - |
dc.contributor.googleauthor | Soonmyung Paik | - |
dc.contributor.googleauthor | Sandra M Swain | - |
dc.contributor.googleauthor | Dennis C Sgroi | - |
dc.contributor.googleauthor | Catherine A Schnabel | - |
dc.contributor.googleauthor | Norman Wolmark | - |
dc.identifier.doi | 10.1158/1078-0432.CCR-23-1977 | - |
dc.contributor.localId | A01823 | - |
dc.relation.journalcode | J00564 | - |
dc.identifier.pmid | 38376912 | - |
dc.contributor.alternativeName | Paik, Soon Myung | - |
dc.contributor.affiliatedAuthor | 백순명 | - |
dc.citation.volume | 30 | - |
dc.citation.number | 9 | - |
dc.citation.startPage | 1984 | - |
dc.citation.endPage | 1991 | - |
dc.identifier.bibliographicCitation | CLINICAL CANCER RESEARCH, Vol.30(9) : 1984-1991, 2024-05 | - |
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