Safety and efficacy of itacitinib, a selective JAK1 inhibitor, in advanced hepatocellular cancer: Phase 1b trial (JAKAL)

Overactivation of the JAK/STAT pathway is one of the drivers for the pathophysiology of hepatocellular carcinoma (HCC). We propose a Phase Ib study to evaluate the safety and efficacy of itacitinib, a selective JAK1 inhibitor, as a second-line treatment for patients with advanced or metastatic HCC.Twenty-five patients will receive 400 mg itacitinib orally daily, 28-day cycle. Safety will be reviewed prior to each cycle. Tumor response assessed every 2 months until disease progression, death or withdrawal. Tumor biopsies and blood samples will be taken for presence of <i>JAK1</i> mutations.Activation of JAK/STAT pathway drives HCC development and is associated with immunotherapy resistance. Itacitinib is hypothesized to be safe and effective in HCC patients that have progressed after first-line therapies.<b>Clinical Trial Registration:</b> EudraCT: 2017-004437-81 NCT04358185 (ClinicalTrials.gov).

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Publication Details

Journal
Future Oncology
Published
2024-09-16
DOI
https://doi.org/10.1080/14796694.2024.2396795
Citations
5
Primary Topic
Cytokine Signaling Pathways and Interactions
Type
article
Field-Weighted Citation Impact
1.41

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article

Safety and efficacy of itacitinib, a selective JAK1 inhibitor, in advanced hepatocellular cancer: Phase 1b trial (JAKAL)

David James Pinato, Charlotte S. Wilhelm-Benartzi, Caroline Ward, María Cristina Quijano Martínez et al.
5 citations
Future Oncology
Cytokine Signaling Pathways and Interactions
1.41
article

Safety and efficacy of itacitinib, a selective JAK1 inhibitor, in advanced hepatocellular cancer: Phase 1b trial (JAKAL)

David James Pinato, Charlotte S. Wilhelm-Benartzi, Caroline Ward, María Cristina Quijano Martínez, Alessandro Troiani, Rohini Sharma
article en
5 citations

Abstract

Overactivation of the JAK/STAT pathway is one of the drivers for the pathophysiology of hepatocellular carcinoma (HCC). We propose a Phase Ib study to evaluate the safety and efficacy of itacitinib, a selective JAK1 inhibitor, as a second-line treatment for patients with advanced or metastatic HCC.Twenty-five patients will receive 400 mg itacitinib orally daily, 28-day cycle. Safety will be reviewed prior to each cycle. Tumor response assessed every 2 months until disease progression, death or withdrawal. Tumor biopsies and blood samples will be taken for presence of <i>JAK1</i> mutations.Activation of JAK/STAT pathway drives HCC development and is associated with immunotherapy resistance. Itacitinib is hypothesized to be safe and effective in HCC patients that have progressed after first-line therapies.<b>Clinical Trial Registration:</b> EudraCT: 2017-004437-81 NCT04358185 (ClinicalTrials.gov).

Future OncologyVol. 20(36)
University Hospital of Wales (GB), Hammersmith Hospital (GB), Imperial College London (GB)
Incyte, National Institute for Health and Care Research, Department of Health and Social Care, Imperial College London, Imperial Experimental Cancer Medicine Centre
Good health and well-being
Openalex Percentile: Top 15%
Cytokine Signaling Pathways and Interactions
1.41
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Safety and efficacy of itacitinib, a selective JAK1 inhibitor, in advanced hepatocellular cancer: Phase 1b trial (JAKAL) — David James Pinato, Charlotte S. Wilhelm-Benartzi, et al. · Future Oncology (2024) | TGRS Research Map | TGRS