塞鲁美替尼
吉西他滨
医学
化疗
MEK抑制剂
毒性
顺铂
内科学
泌尿科
肿瘤科
胃肠病学
外科
癌症
药理学
MAPK/ERK通路
激酶
结直肠癌
生物
细胞生物学
克拉斯
作者
Mark K. Doherty,Vincent C. Tam,Mairéad G McNamara,Raymond Jang,David Hedley,Eric Chen,Neesha Dhani,Patricia Tang,Hao-Wen Sim,Natasha B. Leighl,Stephanie DeLuca,Lisa Wang,Theresa Pedutem,Jennifer J. Knox
标识
DOI:10.1038/s41416-022-01903-6
摘要
IntroductionCisplatin and gemcitabine (CisGem) are standard chemotherapy for advanced biliary tract cancer (BTC). The MEK inhibitor selumetinib showed synergy with gemcitabine when administered sequentially in BTC. This randomised Phase 2 trial aimed to assess the efficacy of sequential or continuous selumetinib with CisGem.MethodsPatients with advanced BTC received CisGem; arm A included selumetinib every day, arm B: selumetinib, days 1–5, 8–19 each cycle. Arm C received CisGem alone. Selumetinib was dosed at 75 mg BID but amended to 50 mg BID due to toxicity.ResultsIn all, 51 participants were evaluable for response. No significant difference was seen in mean change in tumour size at 10 weeks between arms A and C (−7.8% vs −12.8%, P = 0.54) or arms B and C (−15% vs −12.8%, P = 0.78). There was no difference in median progression-free survival (6.0, 7.0, 6.3 months, P > 0.95) or overall survival (11.7, 11.7, 12.8 months, P = 0.70) for arms A, B and C, respectively. More participants experienced grade 3–4 toxicities in selumetinib-containing arms. More participants in arm A required chemotherapy dose reductions (P = 0.01) with lower chemotherapy dose intensity during the first 10 weeks.ConclusionAdding sequential or continuous selumetinib to CisGem failed to improve efficacy and increased toxicity in patients with advanced BTC.
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