Itacitinib in advanced hepatocellular cancer following first line therapy.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
19 patients were enrolled.
I · Intervention 중재 / 시술
400 mg of itacitinib QID every 28 days
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Itacitinib either as second- or third-line therapy showed promising activity. We identified a transcriptomic signature predictive of response.
Hepatocellular carcinoma (HCC) develops on background chronic liver disease where uncontrolled inflammation drives hepatocarcinogenesis.
- p-value p = 0.016
- 95% CI 2.6 - 4.5
- 추적기간 3.5 months
APA
Troiani A, Hung L, et al. (2026). Itacitinib in advanced hepatocellular cancer following first line therapy.. NPJ precision oncology, 10(1), 67. https://doi.org/10.1038/s41698-026-01273-9
MLA
Troiani A, et al.. "Itacitinib in advanced hepatocellular cancer following first line therapy.." NPJ precision oncology, vol. 10, no. 1, 2026, pp. 67.
PMID
41673081 ↗
Abstract 한글 요약
Hepatocellular carcinoma (HCC) develops on background chronic liver disease where uncontrolled inflammation drives hepatocarcinogenesis. First-line therapies have limited response. There are no agents that specifically target the underlying liver inflammation. We investigated the safety and efficacy of itacitinib, a highly selective JAK1 inhibitor, as a potential second- or third-line therapy. Biomarkers of response were investigated. Participants with advanced stage HCC, Child Pugh ≤B7 who had progressed through at least one previous line of therapy received 400 mg of itacitinib QID every 28 days. Treatment-related adverse events (trAEs) were assessed weekly during cycle 1 then every 28 days (CTC-AE version 4.03). Response was assessed 8-weekly using RECIST 1.1. Progression-free (PFS) and overall survival (OS) were reported as secondary endpoints. Tumour samples were analysed for targeted transcriptomics. Sequential serum samples were assessed for metabonomic determinants of toxicity and response. 19 patients were enrolled. The most common trAEs were thrombocytopenia (31%), fatigue (26%) and palmar-plantar erythrodysesthesia syndrome (26%); four episodes of dose-limiting thrombocytopaenia were observed. Over a median follow-up of 3.5 months, the best overall response was stable disease (47%). Median PFS and OS were 3.5 (95% CI: 2.6 - 4.5 months) and 7.4 months (95% CI: 4.3-10.5 months), respectively. Subgroup analysis illustrated a significantly increased risk of progression for patients that had received combination immunotherapy prior to itacitinib (HR 4.7, 95%CI 1.3-16.6, p = 0.016). Untargeted tumour and serum transcriptomics identified a signature predictive of response. Itacitinib either as second- or third-line therapy showed promising activity. We identified a transcriptomic signature predictive of response.