4.7 Article

Organ specific responses to first-line lenvatinib plus anti-PD-1 antibodies in patients with unresectable hepatocellular carcinoma: a retrospective analysis

期刊

BIOMARKER RESEARCH
卷 9, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s40364-021-00274-z

关键词

Lenvatinib; Carcinoma; Hepatocellular; Liver neoplasms; Immunotherapy

资金

  1. Leading Investigator Program of the Shanghai municipal government [17XD1401100]
  2. National Key Basic Research Program (973 Program) from the Ministry of Science and Technology of China [2015CB554005]
  3. National Natural Science Foundation of China [81871928, 81672326, 81871929, 82072667]

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The study found that in patients with advanced hepatocellular carcinoma, first-line lenvatinib plus anti-PD-1 antibodies resulted in higher organ-specific response rates for macrovascular tumor thrombi (MVTT), potentially allowing for surgical resection in a proportion of patients.
Background We evaluated organ-specific response rates (OSRRs) to first-line lenvatinib plus anti-PD-1 antibodies in patients with advanced hepatocellular carcinoma (HCC). Methods This retrospective analysis included Chinese patients with unresectable/advanced HCC who received first-line lenvatinib (8 mg/day) plus >= 3 infusions of anti-PD-1 antibodies between October 2018 and May 2020. Tumor and macrovascular tumor thrombi (MVTT) treatment responses were evaluated every 2 months using RECIST v1.1. The overall response rate (ORR)/OSRR was defined as the percentage of patients with a best overall response of complete or partial response (CR or PR). Results In total, 60 patients were included in the analysis; 96.7% had measurable intrahepatic lesions, 55% had MVTT and 26.7% had extrahepatic disease. In all 60 patients, the ORR was 33.3%, median progression-free survival was 7.0 months (95% CI, 1.7-12.3) and median overall survival was not reached. The OSRR for MVTT (54.5%) was higher versus intrahepatic tumors (32.8%), extrahepatic lung metastases (37.5%) and lymph node metastases (33.3%). Among 33 patients with intrahepatic tumors and MVTT, 18 had differential responses in each site, including 13 with a better response in MVTT versus intrahepatic lesions. Among 18 patients whose MVTT achieved a radiographic CR or PR, six underwent surgical resection: 4/6 achieved a pathological CR in MVTT and 2/6 in the intrahepatic tumor. Conclusions First-line lenvatinib plus anti-PD-1 antibodies resulted in better tumor responses in MVTT versus intrahepatic lesions. Complete MVTT necrosis may allow downstaging and subsequent eligibility for surgical resection in a proportion of patients with advanced HCC.

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