AI Article Synopsis

  • The study examines how muscle strength and skeletal muscle mass relate to the survival of patients with unresectable hepatocellular carcinoma (HCC) who are treated with lenvatinib.
  • Researchers found that a significant number of patients had decreased grip strength (33.3%) and skeletal muscle index (34.9%), and those with normal grip strength had better overall survival compared to those with decreased grip strength.
  • The study concludes that apart from liver function, decreased grip strength is a key indicator of poor prognosis in HCC patients undergoing lenvatinib treatment.

Article Abstract

Although sarcopenia is characterized by a loss of muscle strength and skeletal muscle mass, few studies have evaluated the effect of muscle strength on hepatocellular carcinoma (HCC) patients. We evaluated the impact of sarcopenia-related factors (grip strength (GS) and the skeletal muscle index (SMI)) on the survival among lenvatinib-treated unresectable HCC (u-HCC) patients. This single-center cohort study was conducted at a university hospital. The study population included 63 lenvatinib-treated u-HCC patients managed between April 2018 and April 2020. A decreased GS and decreased SMI were found in 21 (33.3%) and 22 (34.9%) patients, respectively. The overall survival (OS) of the normal GS group was significantly higher than that of the decreased GS group, while that of the normal and decreased SMI groups did not differ markedly. There were no significant differences in the progression-free survival between the normal GS and decreased GS groups or the normal SMI and decreased SMI groups. A multivariate Cox proportional hazards model showed that modified albumin-bilirubin-grade (mALBI) 2b (hazard ratio (HR) 4.39) and a decreased GS (HR 3.55) were independently associated with an increased risk of poor prognosis. In addition to the hepatic functional reserve, a decreased GS was a poor prognostic factor in lenvatinib-treated u-HCC patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465794PMC
http://dx.doi.org/10.3390/cancers12082146DOI Listing

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