International phase II randomized placebo-controlled study investigating the combination of YIV-906 plus sorafenib (SORA) in HBV (+) patients (Pts) with advanced hepatocellular carcinoma.
Year: 2025
Type: conference-abstract
Abstract: e16244 Background: YIV-906 (formerly PHY906/KD018), inspired by an 1800-year traditional botanical medicine formulation, is being developed under the FDA’s botanical drug guidance (IND’s 138525 and 62627) for treating gastrointestinal ailments associated with chemotherapeutics or chemoradiation. Multi-targeted tyrosine kinase inhibitors, SORA and Lenvatinib, are first-line systemictreatment options for advanced HCC pts, are limited by high rates of grade ≥ 3 treatment-related adverse events. Preclinical data suggests YIV-906 increases tumor microenvironment inflammation by M1 macrophage activation/proliferation resulting in HCC tumor rejection in vivo and reduces SORA-associated toxicity, suggesting improved safety and potential clinical benefit for pts. Methods: An international, multicenter, double-blind, placebo-controlled, randomized phase 2 study was conducted examining YIV-906's impact on SORA in advanced HCC pts (NCT04000737), stratified by metastatic status and ECOG Performance Status. The primary endpoint was progression-free survival (PFS). Secondary endpoints were TTP, ORR, and DCR by RECIST1.1; OS, QoL, and safety by CTCAE version 5.0. Per Protocol Set (PPS) analysis exclude patients with misrandomizations and major protocol violations impacting data integrity and quality. Translational correlatives include pharmacokinetics and exploratory soluble biomarkers analysis. Results: From 18 Feb 2020 to 03 Jun 2023, 107 pts were screened across 20 study sites in 4 regions (US and Asia). 62 chronic HBV(+) HCC systemic treatment naïve pts with Child-Pugh A liver function were randomized to a 2:1 ratio, (41 pts YIV-906 arm, 20 pts placebo arm). The Investigator-assessed mPFS per RECIST 1.1 was slightly longer in the YIV-906 arm than the placebo arm in ITT group (N = 62). PPS Subgroup analyses indicated: significant improvement in PFS in pts completing at least 2 treatment cycles (N = 49); YIV-906 arm mPFS is 5.6 months (95% CI: 3.6, 7.2) vs. placebo arm 2.3 months (95% CI: 1.9, 3.9) respectively; a 69% reduction in risk of disease progression or death (HR = 0.31 [95% CI: 0.13, 0.72]; p = 0.004). The YIV-906 arm mOS was 14.3 months (95% CI: 8.2, 18.8) vs placebo arm 8.0 months (95% CI: 4.6, 32.1), HR of 0.97 (95% CI: 0.51, 1.84; p = 0.92). In the secondary endpoint ORR, improvement was also observed by the investigator. YIV-906 arm pts tolerated SORA longer, with manageable toxicity profile. No new safety signals in YIV-906 + SORA treated pts were identified compared with sorafenib monotherapy. Conclusions: In this limited cohort of patients with confirmed HBV (+) HCC diagnosis, our findings suggest that YIV-906 is effective for increasing SORA’s therapeutic index and clinical activity, and supports further studies of YIV-906. Clinical trial information: NCT04000737 .
Source: Journal of Clinical Oncology
Authors: Ghassan K. Abou-Alfa, Yun Yen, James J. Harding, Jacqueline Whang-Peng, Yuankai Shi, Man Fung Yuen, Xiuhui Li, Shanzhi Gu, Chenghai Liu, Long-Bin Jeng, Chia Jui Yen, Calvin Q Pan, San-Chi Chen, Jason Chia-Hsun Hsieh, M Wasif Saif, Shwu-Huey Liu, Fangyong Li, Wing Lam, Edward Chu, Yung-Chi Tommy Cheng
Institutions: Memorial Sloan Kettering Cancer Center, Trinity College Dublin, Cornell University, Taipei Medical University, Weill Cornell Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Cancer Hospital of Chinese Academy of Medical Sciences, Queen Mary Hospital, University of Hong Kong, Capital Medical University, Beijing YouAn Hospital, Central South University, Hunan Cancer Hospital, Shanghai University of Traditional Chinese Medicine, Shuguang Hospital, China Medical University, China Medical University Hospital, National Cheng Kung University Hospital, Taipei Veterans General Hospital, Linkou Chang Gung Memorial Hospital, Wayne State University, The Barbara Ann Karmanos Cancer Institute, Yale University, Albert Einstein College of Medicine, Montefiore Einstein Comprehensive Cancer Center
Language: English
Subfield: Hepatology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
OpenAlex ID: W4410814242