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(Liver Cancer) Efficacy of Nivolumab in Cancer Patients with Impaired Liver Function

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(Liver Cancer) Efficacy of Nivolumab in Cancer Patients with Impaired Liver Function

(Liver Cancer) Efficacy of Nivolumab in Cancer Patients with Impaired Liver Function

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Anti-PD-1 Antibody Nivolumab in Liver Cancer

  • February 27, 2019
  • Reading time: 1 minute

Efficacy of the anti-PD-1 antibody nivolumab in patients with advanced hepatocellular carcinoma and impaired liver function

At the ASCO GI 2019 Gastrointestinal Cancers Symposium held in San Francisco, January 17–19, 2019, Dr. Masatoshi Kudo of the Gastroenterology Division, Kinki University Hospital, presented CheckMate 040 Phase 2 clinical trial results for the anti-PD-1 antibody nivolumab in 49 patients with hepatocellular carcinoma and impaired liver function.

The trial administered nivolumab 240 mg every two weeks to patients with hepatocellular carcinoma, continuing until disease progression or intolerable adverse reactions. Primary endpoints included ORR (objective response rate) and DOR (duration of response).

Key results:

  • ORR (objective response rate): 10.2%
  • DCR (disease control rate): 55.1%
  • TTR (time to response): Mean 2.7 months
  • DOR (duration of response): Mean 9.9 months

Overall survival (OS):

  • Sorafenib-naive patients: OS 9.8 months
  • Sorafenib-pretreated patients: OS 7.3 months

Safety: Adverse event rate was 51% (25/49 patients), but the treatment discontinuation rate due to adverse events was only 4.1% (2/49 patients).

Based on these results, continuous nivolumab treatment demonstrated efficacy in patients with advanced hepatocellular carcinoma and impaired liver function, with a low rate of treatment discontinuation due to side effects.

Source: Checkmate-040: Nivolumab (NIVO) in patients (pts) with advanced hepatocellular carcinoma (aHCC) and Child-Pugh B (CPB) status. (ASCO GI 2019, Abstract No. 327)

Tags: #LiverCancer

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