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首页> 外文期刊>Journal of Clinical Oncology >Dose Escalation Trial of the Wee1 Inhibitor Adavosertib (AZD1775) in Combination With Gemcitabine and Radiation for Patients With Locally Advanced Pancreatic Cancer
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Dose Escalation Trial of the Wee1 Inhibitor Adavosertib (AZD1775) in Combination With Gemcitabine and Radiation for Patients With Locally Advanced Pancreatic Cancer

机译:WEE1抑制剂Adavosertib(AZD1775)的剂量升级试验与吉西他滨和局部晚期胰腺癌患者的辐射相结合

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PURPOSEAZD1775 (adavosertib) is an inhibitor of the Wee1 kinase. In this study, we built on our preclinical studies to evaluate the safety and efficacy of AZD1775 in combination with gemcitabine and radiation in patients with newly diagnosed locally advanced pancreatic cancer.PATIENTS AND METHODSThirty-four patients with locally advanced pancreatic cancer were enrolled with the intention to receive four 21-day cycles of gemcitabine (1,000 mg/m(2) days 1 and 8) with AZD1775 (once daily on days 1, 2, 8, and 9). Cycles 2 and 3 were administered concurrently with radiation, and cycles 5 to 8 were optional. AZD1775 was dose escalated using a time-to-event continual reassessment method on the basis of the rate of dose-limiting toxicities within the first 15 weeks of therapy. The primary objective was to determine the maximum tolerated dose of AZD1775 given in conjunction with gemcitabine and radiation. Secondary objectives were to estimate overall and progression-free survival and determine pharmacodynamic activity of AZD1775 in surrogate tissues.RESULTSThe recommended phase II dose of AZD1775 was 150 mg/d. Eight patients (24%) experienced a dose-limiting toxicity, most commonly anorexia, nausea, or fatigue. The median overall survival for all patients was 21.7 months (90% CI, 16.7 to 24.8 months), and the median progression-free survival was 9.4 months (90% CI, 8.0 to 9.9 months). Hair follicle biopsy samples demonstrated evidence of Wee1 inhibition with decreased phosphorylation of cyclin-dependent kinase 1 staining by immunohistochemistry after AZD1775 administration at the recommended phase II dose.CONCLUSIONAZD1775 in combination with gemcitabine and radiation therapy was well tolerated at a dose that produced target engagement in a surrogate tissue. The overall survival is substantially higher than prior results combining gemcitabine with radiation therapy and warrants additional investigation.
机译:purposeazd1775(Adavosertib)是WEE1激酶的抑制剂。在这项研究中,我们建立了我们的临床前研究,评估AZD1775与吉西他滨的安全性和有效性与新诊断的局部晚期胰腺癌患者的辐射相结合。患者和方法患有局部晚期胰腺癌的患者患者参与了意图接受吉西他滨的四个21天循环(1,000mg / m(2)天1和8),AZD1775(每日一次每日一次,2,8和9天)。循环2和3与辐射同时施用,并选择循环5至8。 AZD1775在治疗的前15周内的剂量限制毒性率的基础上使用时间持续重新评估方法进行升级。主要目的是确定结合吉西他滨和辐射给予的AZD1775的最大耐受剂量。次要目标是估计总体和无进展生存期,并确定在替代tissues.RESULTSThe AZD1775的药效学活性的推荐的II期剂量AZD1775的为150mg / d。八名患者(24%)经历了一种剂量限制毒性,最常见的厌食,恶心或疲劳。所有患者的中位数全身生存率为21.7个月(90%CI,16.7至24.8个月),中位进展生存率为9.4个月(90%CI,8.0至9.9个月)。毛囊活检样品证明WEE1抑制的证据通过免疫组织化学在推荐的第二阶段II剂量的AZD1775给药后通过免疫组织化学染色的降低磷酸化。结合吉西众红嗪和放射治疗,以产生靶接合的剂量良好耐受耐受替代组织。整体存活率明显高于结合吉西他滨与放射治疗的结果,并认证额外调查。

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