Cited 27 times in
Palbociclib plus endocrine therapy significantly enhances overall survival of HR+/HER2- metastatic breast cancer patients compared to endocrine therapy alone in the second-line setting: A large institutional study
DC Field | Value | Language |
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dc.contributor.author | 하민진 | - |
dc.date.accessioned | 2022-08-23T00:09:27Z | - |
dc.date.available | 2022-08-23T00:09:27Z | - |
dc.date.issued | 2022-06 | - |
dc.identifier.issn | 0020-7136 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/189284 | - |
dc.description.abstract | Cyclin-dependent-kinase-4/6 inhibitor (CDK4/6i) plus endocrine therapy (ET) is standard of care for patients with advanced hormone receptor (HR)-positive, HER2-negative breast cancer (BC). The Breast Medical Oncology database at MD Anderson Cancer Center (MDACC) was analyzed to assess effectiveness of the CDK4/6i palbociclib plus ET compared to ET alone. From a total of 5402 advanced HR+ HER2- BC patients referred to MDACC between 1997 and 2020, we identified eligible patients who received palbociclib in combination with first-line (n = 778) and second-line (n = 410) ET. We further identified "control" patients who received ET alone in the first-line (n = 2452) and second-line (n = 1183) settings. Propensity score matching analysis was conducted to balance baseline demographic and clinical characteristics between palbociclib and control cohorts to assess the effect of palbociclib treatment on progression-free survival (PFS) and overall survival (OS). For propensity-matched-cohort in the first-line setting (n = 708), palbociclib group had significantly longer median PFS (17.4 vs 11.1 months; P < .0001) compared to controls. Median OS (44.3 vs 40.2 months) did not show a statistically significant benefit in the first line setting. However, in the second-line setting, with 380 propensity-matched-cohort, the palbociclib group had significantly longer PFS (10 vs 5 months, P < .0001) as well as OS (33 vs 24 months; P < .022), compared to controls. We conclude that in this single center analysis of a large cohort of metastatic HR+ HER2- BC patients, palbociclib in combination with ET was associated with improved PFS in both first-line and second-line settings and OS in the second-line setting compared to ET alone cohort. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Wiley-Liss | - |
dc.relation.isPartOf | INTERNATIONAL JOURNAL OF CANCER | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Antineoplastic Combined Chemotherapy Protocols / therapeutic use | - |
dc.subject.MESH | Breast Neoplasms* / drug therapy | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Piperazines | - |
dc.subject.MESH | Protein Kinase Inhibitors / therapeutic use | - |
dc.subject.MESH | Pyridines | - |
dc.subject.MESH | Receptor, ErbB-2 | - |
dc.subject.MESH | Receptors, Estrogen | - |
dc.title | Palbociclib plus endocrine therapy significantly enhances overall survival of HR+/HER2- metastatic breast cancer patients compared to endocrine therapy alone in the second-line setting: A large institutional study | - |
dc.type | Article | - |
dc.contributor.college | Graduate School of Public Health (보건대학원) | - |
dc.contributor.department | Graduate School of Public Health (보건대학원) | - |
dc.contributor.googleauthor | Min Jin Ha | - |
dc.contributor.googleauthor | Akshara Singareeka Raghavendra | - |
dc.contributor.googleauthor | Nicole M Kettner | - |
dc.contributor.googleauthor | Wei Qiao | - |
dc.contributor.googleauthor | Senthil Damodaran | - |
dc.contributor.googleauthor | Rachel M Layman | - |
dc.contributor.googleauthor | Kelly K Hunt | - |
dc.contributor.googleauthor | Yu Shen | - |
dc.contributor.googleauthor | Debu Tripathy | - |
dc.contributor.googleauthor | Khandan Keyomarsi | - |
dc.identifier.doi | 10.1002/ijc.33959 | - |
dc.contributor.localId | A06302 | - |
dc.relation.journalcode | J01092 | - |
dc.identifier.eissn | 1097-0215 | - |
dc.identifier.pmid | 35133007 | - |
dc.identifier.url | https://onlinelibrary.wiley.com/doi/10.1002/ijc.33959 | - |
dc.subject.keyword | CDK4/6 inhibitors | - |
dc.subject.keyword | Propensity matching | - |
dc.subject.keyword | aromatase inhibitors | - |
dc.subject.keyword | endocrine therapy | - |
dc.subject.keyword | fulvestrant | - |
dc.subject.keyword | hormone receptor | - |
dc.subject.keyword | metastatic breast cancer | - |
dc.subject.keyword | overall survival | - |
dc.subject.keyword | progression-free survival | - |
dc.contributor.alternativeName | Ha, Min Jin | - |
dc.contributor.affiliatedAuthor | 하민진 | - |
dc.citation.volume | 150 | - |
dc.citation.number | 12 | - |
dc.citation.startPage | 2025 | - |
dc.citation.endPage | 2037 | - |
dc.identifier.bibliographicCitation | INTERNATIONAL JOURNAL OF CANCER, Vol.150(12) : 2025-2037, 2022-06 | - |
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