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Myosteatosis on computed tomography as a predictor of therapeutic response to CDK4/6 inhibitors plus aromatase inhibitors in patients with advanced breast cancer

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dc.contributor.authorKim, Min Hwan-
dc.contributor.authorKim, Hyunwook-
dc.contributor.authorBaek, Seungjin-
dc.contributor.authorHan, Sookyeong-
dc.contributor.authorKim, Gun Min-
dc.contributor.authorSohn, Joohyuk-
dc.contributor.authorRhee, Yumie-
dc.contributor.authorHong, Namki-
dc.contributor.author김현욱-
dc.date.accessioned2026-05-15T02:48:07Z-
dc.date.available2026-05-15T02:48:07Z-
dc.date.created2026-05-04-
dc.date.issued2024-05-
dc.identifier.issn0732-183X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/212348-
dc.description.abstractBackground: Recent evidence indicates that a dysregulated host metabolism influences treatment outcomes in patients with breast cancer. We investigated the association of computed tomography (CT)-derived body composition indices as imaging biomarkers of host metabolic status with therapeutic responses in patients with hormone receptor-positive, HER2-negative advanced breast cancer (ABC) on endocrine plus CDK4/6 inhibitor (CDK4/6i) treatment. Methods: The study involved a prospective cohort of patients with ABC at the Yonsei Cancer Center who received CDK4/6i and aromatase inhibitors as first-line therapy. Body composition parameters were estimated from the pretreatment non-enhanced CT images of the third lumbar spine. Myosteatosis was defined as skeletal muscle radiodensity (SMD) of low tertile (#28.7 Hounsfield Units). The primary outcome was progression-free survival (PFS). Results: Among the 247 participants (mean age, 54.8 years; body mass index [BMI], 23.7 kg/m2), 45.7% had events during a median follow-up of 36.4 months. Low SMD was an independent predictor of worse PFS after adjusting for age and visceral metastases (adjusted hazard ratio [HR]=1.20 per standard deviation decrement, p=0.041), whereas BMI, muscle area, and fat area did not. Participants with myosteatosis had a higher risk of progression than those without (PFS, 27.2 vs. 51.1 months; p=0.009; adjusted HR 1.84, p=0.003). Strong associations between myosteatosis and poor PFS were observed in groups with pre-menopause status (HR, 3.04 vs. 1.19 in post-menopause; p for interaction,0.05) and without visceral metastases (HR, 2.95 vs. 1.19 in with visceral metastases; p for interaction,0.05). Conclusions: CT-derived myosteatosis predicts poor treatment outcomes in patients with ABC undergoing first-line treatment with aromatase inhibitors and CDK4/6i. Research Sponsor: Severance Hospital; Korea Health Industry Development Institute; Ministry of Science and ICT; RS-2023-00231864. © (2024), (Lippincott Williams and Wilkins). All rights reserved.-
dc.languageEnglish-
dc.publisherAmerican Society of Clinical Oncology-
dc.relation.isPartOfJournal of Clinical Oncology-
dc.relation.isPartOfJOURNAL OF CLINICAL ONCOLOGY-
dc.titleMyosteatosis on computed tomography as a predictor of therapeutic response to CDK4/6 inhibitors plus aromatase inhibitors in patients with advanced breast cancer-
dc.typeArticle-
dc.contributor.googleauthorKim, Min Hwan-
dc.contributor.googleauthorKim, Hyunwook-
dc.contributor.googleauthorBaek, Seungjin-
dc.contributor.googleauthorHan, Sookyeong-
dc.contributor.googleauthorKim, Gun Min-
dc.contributor.googleauthorSohn, Joohyuk-
dc.contributor.googleauthorRhee, Yumie-
dc.contributor.googleauthorHong, Namki-
dc.identifier.doi10.1200/JCO.2024.42.16_suppl.1030-
dc.relation.journalcodeJ01331-
dc.identifier.eissn1527-7755-
dc.identifier.urlhttps://ascopubs.org/doi/pdf/10.1200/JCO.2024.42.16_suppl.1030-
dc.contributor.affiliatedAuthorKim, Min Hwan-
dc.contributor.affiliatedAuthorKim, Hyunwook-
dc.contributor.affiliatedAuthorBaek, Seungjin-
dc.contributor.affiliatedAuthorKim, Gun Min-
dc.contributor.affiliatedAuthorSohn, Joohyuk-
dc.contributor.affiliatedAuthorRhee, Yumie-
dc.contributor.affiliatedAuthorHong, Namki-
dc.identifier.scopusid2-s2.0-105023389256-
dc.citation.volume42-
dc.citation.number16 Sup-
dc.identifier.bibliographicCitationJournal of Clinical Oncology, Vol.42(16 Sup), 2024-05-
dc.identifier.rimsid92730-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.articleno1030-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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