Ottawa Hospital Cancer Centre/Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Cross Cancer Institute, Edmonton, Alberta, Canada.
J Thorac Oncol. 2016 Nov;11(11):2018-2021. doi: 10.1016/j.jtho.2016.06.024. Epub 2016 Jul 20.
There is no approved second-line systemic therapy option for malignant pleural mesothelioma (MPM), but targeting angiogenesis is an area of investigation. PF-03446962 is a fully human antibody against activin receptor-like kinase 1, which is commonly expressed in tumor vasculature. We performed a multicenter, open label, single-arm, two-stage phase II study of PF-03446962 in patients with MPM and progressive disease after platinum-based chemotherapy. In total, 17 patients were enrolled, but no partial or complete responses were observed. The trial did not meet the prespecified response criterion for moving to the second stage. There were only three grade 3 (G3) or higher nonhematological toxicities observed (G3 hypertension [n=2] and G3 fatigue [n=1]) and just one episode of G3 lymphopenia. In conclusion, PF-03446962, despite being generally well tolerated, failed to demonstrate efficacy in the treatment of advanced MPM as a single agent. There are no plans for further investigation of this agent in MPM.
对于恶性胸膜间皮瘤(MPM),目前尚无批准的二线系统治疗选择,但靶向血管生成是一个研究领域。PF-03446962 是一种针对激活素受体样激酶 1 的全人抗体,该激酶在肿瘤血管中普遍表达。我们在铂类化疗后疾病进展的 MPM 患者中进行了一项多中心、开放标签、单臂、两阶段 II 期 PF-03446962 研究。共有 17 名患者入组,但未观察到部分或完全缓解。试验未达到进入第二阶段的预设缓解标准。仅观察到 3 例 3 级(G3)或更高等级的非血液学毒性(G3 高血压 [n=2] 和 G3 疲劳 [n=1])和 1 例 G3 淋巴细胞减少症。总之,PF-03446962 尽管总体耐受性良好,但作为单一药物在治疗晚期 MPM 方面未能显示出疗效。目前尚无计划进一步研究该药物在 MPM 中的应用。