Phase II Studies with Refametinib or Refametinib plus Sorafenib in Patients with RAS-Mutated Hepatocellular Carcinoma

Archive ouverte

Lim, Ho Yeong | Merle, Philippe | Weiss, Karl Heinz | Yau, Thomas | Ross, Paul | Mazzaferro, Vincenzo | Blanc, Jean-Frederic | Ma, Yuk Ting | Yen, Chia Jui | Kocsis, Judit | Choo, Su Pin | Sukeepaisarnjaroen, Wattana | Gerolami, Rene | Dufour, Jean-Francois | Gane, Edward J. | Ryoo, Baek-Yeol | Peck-Radosavljevic, Markus | Dao, Thong | Yeo, Winnie | Lamlertthon, Wisut | Thongsawat, Satawat | Teufel, Michael | Roth, Katrin | Reis, Diego | Childs, Barrett H. | Krissel, Heiko | Llovet, Josep M.

Edité par CCSD ; American Association for Cancer Research -

International audience. Purpose: Refametinib, an oral MEK inhibitor, has demonstrated antitumor activity in combination with sorafenib in patients with RAS-mutated hepatocellular carcinoma (HCC). Two phase II studies evaluated the efficacy of refametinib monotherapy and refametinib plus sorafenib in patients with RAS-mutant unresectable or metastatic HCC. Patients and Methods: Eligible patients with RAS mutations of cell-free circulating tumor DNA (ctDNA) determined by beads, emulsion, amplification, and magnetics technology received twice-daily refametinib 50 mg +/- sorafenib 400 mg. Potential biomarkers were assessed in ctDNA via next-generation sequencing (NGS). Results: Of 1,318 patients screened, 59 (4.4%) had a RAS mutation, of whom 16 received refametinib and 16 received refametinib plus sorafenib. With refametinib monotherapy, the objective response rate (ORR) was 0%, the disease control rate (OCR) was 56.3%, overall survival (OS) was 5.8 months, and progression-free survival (PFS) was 1.9 months. With refametinib plus sorafenib, the ORR was 6.3%, the DCR was 43.8%, OS was 12.7 months, and PFS was 1.5 months. In both studies, time to progression was 2.8 months. Treatment-emergent toxicities included fatigue, hypertension, and acneiform rash. Twenty-seven patients had ctDNA samples available for NCS. The most frequently detected mutations were in TERT (63.0%), TP53 (48.1%), and beta-catenin (CTNNBI; 37.0%). Conclusions: Prospective testing for RAS family mutations using ctDNA was a feasible, noninvasive approach for large-scale mutational testing in patients with HCC. A median OS of 12.7 months with refametinib plus sorafenib in this small population of RAS-mutant patients may indicate a synergistic effect between sorafenib and refametinib-this preliminary finding should be further explored. (C) 2018 AACR.

Consulter en ligne

Suggestions

Du même auteur

Outcomes Based on Plasma Biomarkers for the Phase 3 CELESTIAL Trial of Cabozantinib versus Placebo in Advanced Hepatocellular Carcinoma

Archive ouverte | Rimassa, Lorenza | CCSD

International audience. Introduction: Cabozantinib, an inhibitor of MET, AXL, and VEGF receptors, significantly improved overall survival (OS) and progression-free survival (PFS) versus placebo in patients with prev...

Pembrolizumab As Second-Line Therapy in Patients With Advanced Hepatocellular Carcinoma in KEYNOTE-240: A Randomized, Double-Blind, Phase III Trial

Archive ouverte | Finn, Richard | CCSD

International audience. PURPOSE Pembrolizumab demonstrated antitumor activity and safety in the phase II KEYNOTE-224 trial in previously treated patients with advanced hepatocellular carcinoma (HCC). KEYNOTE-240 eva...

Health‐related quality‐of‐life impact of pembrolizumab versus best supportive care in previously systemically treated patients with advanced hepatocellular carcinoma: KEYNOTE‐240

Archive ouverte | Ryoo, Baek‐yeol | CCSD

International audience

Chargement des enrichissements...