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Dasatinib in previously treated metastatic colorectal cancer: a phase II trial of the University of Chicago Phase II Consortium.

机译:达沙替尼在先前已治疗的转移性结直肠癌中:芝加哥大学II期联合体的II期试验。

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Treatment options for metastatic colorectal cancer (CRC) are limited after a fluoropyrimidine, oxaliplatin and irinotecan; novel agents need to be explored in this setting. Dasatinib, an oral inhibitor of Src family kinases, inhibits proliferation in CRC cell lines and has antitumor activity in CRC xenograft models.We conducted a multi-center phase II trial of dasatinib in unresectable, previously-treated metastatic CRC patients. No more than 2 prior chemotherapy regimens were permitted, which must have contained a fluoropyrimidine, oxaliplatin and irinotecan. The primary endpoint was progression-free survival (PFS) at 4 months. The Simon two-stage design required that at least 5 of the first 19 patients be progression-free at 4 months to expand to a second stage.Nineteen patients enrolled at 9 centers. The study was terminated after the first stage due to lack of efficacy. There were no objective responses; 1 patient (5%) had stable disease for 7.3 months. The PFS rate at 4 months was 5.3% (90% CI: 0.3, 22.6). Median PFS was 1.6 months (90% CI: 1.4, 1.8). Median overall survival was 5.1 months (90% CI: 2.4, 6.3). Grade 3/4 toxicities included fatigue in 16% of patients, and anemia, anorexia, nausea/vomiting and dyspnea in 11%.Dasatinib is inactive as a single agent in previously treated metastatic CRC patients.
机译:氟嘧啶,奥沙利铂和伊立替康后,转移性大肠癌的治疗选择受到限制。在这种情况下,需要探索新型代理。达沙替尼是一种Src家族激酶的口服抑制剂,可抑制CRC细胞系增殖并在CRC异种移植模型中具有抗肿瘤活性。我们在无法切除的,先前接受过治疗的转移性CRC患者中进行了达沙替尼的多中心II期临床试验。允许不超过2种先前的化疗方案,这些方案必须包含氟嘧啶,奥沙利铂和伊立替康。主要终点是4个月时无进展生存期(PFS)。西蒙的两阶段设计要求前19名患者中的至少5名在4个月内无进展以扩展至第二阶段.19名患者在9个中心入组。由于缺乏疗效,该研究在第一阶段后终止。没有客观的回应; 1名患者(5%)病情稳定了7.3个月。 4个月时的PFS率为5.3%(90%CI:0.3、22.6)。 PFS中位数为1.6个月(90%CI:1.4、1.8)。中位总生存期为5.1个月(90%CI:2.4、6.3)。 3/4级毒性反应包括16%的患者疲劳,11%的贫血,厌食,恶心/呕吐和呼吸困难。达沙替尼在先前治疗的转移性CRC患者中没有活性。

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