Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.
Department of Medical Oncology, Tom Baker Cancer Centre, Calgary, Alberta, Canada.
Br J Cancer. 2022 Nov;127(8):1473-1478. doi: 10.1038/s41416-022-01903-6. Epub 2022 Jul 22.
Cisplatin 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.
Patients 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.
In 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.
Adding sequential or continuous selumetinib to CisGem failed to improve efficacy and increased toxicity in patients with advanced BTC.
顺铂和吉西他滨(CisGem)是晚期胆道癌(BTC)的标准化疗药物。MEK 抑制剂 selumetinib 与吉西他滨序贯给药时在 BTC 中显示出协同作用。这项随机 2 期试验旨在评估顺铂和吉西他滨联合序贯或连续 selumetinib 的疗效。
晚期 BTC 患者接受 CisGem;A 臂包括每天给予 selumetinib,B 臂:每个周期的第 1-5 天和第 8-19 天给予 selumetinib。C 臂单独接受 CisGem。selumetinib 的剂量为 75mg BID,但由于毒性而修改为 50mg BID。
共有 51 名可评估反应的患者。在第 10 周时,A 臂和 C 臂(-7.8%对-12.8%,P=0.54)或 B 臂和 C 臂(-15%对-12.8%,P=0.78)之间肿瘤大小的平均变化没有显著差异。无进展生存期(6.0、7.0、6.3 个月,P>0.95)或总生存期(11.7、11.7、12.8 个月,P=0.70)在 A、B 和 C 臂之间也没有差异。在含 selumetinib 的臂中,更多的患者发生 3-4 级毒性。在 A 臂中,更多的患者需要减少化疗剂量(P=0.01),在前 10 周期间化疗剂量强度降低。
在晚期 BTC 患者中,添加序贯或连续 selumetinib 到 CisGem 未能提高疗效并增加毒性。