Characteristics of patients with longer treatment period of lenvatinib for unresectable hepatocellular carcinoma: A post-hoc analysis of post-marketing surveillance study in Japan

PLoS One. 2024 Mar 8;19(3):e0298420. doi: 10.1371/journal.pone.0298420. eCollection 2024.

Abstract

Patient profiles suitable for long-term lenvatinib treatment for unresectable hepatocellular carcinoma (uHCC) are yet to be fully understood. This post-hoc analysis aimed to identify such patient characteristics and explore the impact of treatment duration and relative dose intensity (RDI) on treatment outcomes. The data were obtained from 703 patients in a multicenter, prospective cohort study in Japan. Lenvatinib-naïve patients with uHCC were enrolled between July 2018 and January 2019 and were followed up for 12 months. Moreover, patients were dichotomized using the median treatment duration into the longer- (≥177 days; n = 352) or shorter-treatment (<177 days; n = 351) groups. The longer-treatment group often had better performance status, lower Child-Pugh score and better modified albumin-bilirubin grade than the shorter treatment group (p<0.05 for all). The objective response rate (47.6% vs. 28.2%; p<0.001) and disease control rate (92.4% vs. 60.2%; p<0.001) were both significantly higher in the longer-treatment groups than in the shorter-treatment groups. The proportion of patients with any adverse drug reactions was generally similar between the two treatment groups. Within the longer-treatment group, the disease control rate was high regardless of dose modification (i.e., RDI <100% vs. ≥100% during the initial 177 days) (91.2% vs. 98.0%). In conclusion, patients with longer treatment tended to have better overall conditions. Lenvatinib dose modifications at the physician's discretion, considering the balance between effectiveness and safety, may contribute to the long-term treatment.

Publication types

  • Multicenter Study

MeSH terms

  • Antineoplastic Agents* / adverse effects
  • Carcinoma, Hepatocellular* / pathology
  • Humans
  • Japan
  • Liver Neoplasms* / pathology
  • Phenylurea Compounds*
  • Product Surveillance, Postmarketing
  • Prospective Studies
  • Quinolines*

Substances

  • lenvatinib
  • Antineoplastic Agents
  • Phenylurea Compounds
  • Quinolines

Grants and funding

This study was funded by Eisai Co., Ltd. The sponsor was involved in the study design, data collection and analysis, decision to publish, and preparation of the manuscript.