國家衛生研究院 NHRI:Item 3990099045/6903

NHRI > National Institute of Cancer Research > Her-Shyong Shiah(1996-2012) > Conference Papers/Meeting Abstract > Item 3990099045/6903

Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/6903

Title:	Early data from a phase I study of nintedanib (BIBF1120) in Asian patients with advanced hepatocellular carcinoma
Authors:	Yen, C;Shen, Y;Shiah, H;Chen, J;Hsu, C;Huang, DC;Hocke, J;Su, W;Cheng, A
Contributors:	National Institute of Cancer Research
Abstract:	Background: Nintedanib is an oral, triple angiokinase inhibitor targeting VEGFRs, PDGFRs and FGFRs. This multicentre, open-label, phase I/randomised phase II study (NCT00987935; phase II ongoing) evaluated the efficacy, safety and pharmacokinetics of nintedanib versus sorafenib in patients ( pts) with advanced hepatocellular carcinoma (HCC) from Asia, where HCC is endemic and has unique clinical features. Phase I data are presented. Methods: Phase I pts had histologically, cytologically or clinically confirmed HCC, ECOG performance status ?2, Child-Pugh (CP) score ?7, and ?1 line of prior systemic therapy. Using a 3 + 3 design, pts were stratified into two groups by liver function and CP score: (I) AST and ALT ?2 x upper limit of normal (ULN), and CP 5–6; (II) AST or ALT >2 x to ?5 x ULN, or CP 7. Nintedanib (given continuously in 28-day courses) was started at 50mg bid (group II) or 100mg bid (group I) and increased in 50mg bid increments up to 200mg bid. Therapy was continued until no clinical benefit or undue toxicity. The phase I primary endpoint was the maximum-tolerated dose (MTD) of nintedanib. Results: Overall, 35 pts have received nintedanib: 11 in group I(100/150/200 mg bid, n = 4/3/4; median [range] duration: 140 [10–337] days) and 24 in group II (50/100/150/200 mg bid, n = 3/7/3/11; median [range] duration: 81 [2–587] days). In group I, no dose-limiting toxicities (DLTs) were seen at any dose during the first course. In group II, one pt experienced a DLT (CTCAE Grade [G] 3 AST increase) at 100 mg bid in Course 1 (dose-escalation phase). The MTD of nintedanib was thus 200 mg bid in both groups. DLTs seen after MTD assessment were G4 gastrointestinal (GI) haemorrhage/anaemia (50 mg bid), G3 ALT increase (150 mg bid), G3 GI haemorrhage (150 mg bid), G3 hypertension (200 mg bid; n = 2) and G4 gastric ulcer (200 mg bid). The most common adverse events, by system organ class, were GI (83%) and general/administration site disorders (51%), and investigations (51%). Hypertension and rash (any grade) occurred in 6 and 8 pts, respectively. Conclusions: Nintedanib has an acceptable safety profile in this Asian HCC population. As in other cancer types and European HCC pts, the MTD of nintedanib was 200 mg bid.
Date:	2012-09
Relation:	Annals of Oncology. 2012 Sep;23(Suppl. 9):246-247.
Link to:	http://dx.doi.org/10.1093/annonc/mds398
JIF/Ranking 2023:	http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0923-7534&DestApp=IC2JCR
Cited Times(WOS):	https://www.webofscience.com/wos/woscc/full-record/WOS:000309409001228
Appears in Collections:	[Her-Shyong Shiah(1996-2012)] Conference Papers/Meeting Abstract

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