...
首页> 外文期刊>Journal of Clinical Oncology >Initial and late resistance to imatinib in advanced gastrointestinal stromal tumors are predicted by different prognostic factors: a European organisation for research and treatment of cancer-italian sarcoma group-australasian gastrointestinal trials
【24h】

Initial and late resistance to imatinib in advanced gastrointestinal stromal tumors are predicted by different prognostic factors: a European organisation for research and treatment of cancer-italian sarcoma group-australasian gastrointestinal trials

机译:通过不同的预后因素可以预测晚期胃肠道间质瘤对伊马替尼的初始和晚期耐药性:欧洲一家研究和治疗癌症的机构-意大利肉瘤组-澳大利亚胃肠道试验

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

PURPOSE The aim of this study was to identify factors predicting initial and late resistance of GI stromal tumor (GIST) patients to imatinib and to document the dose-response relationship in the prognostic subgroups. This study is based on the European Organisation for Research and Treatment of Cancer-Italian Sarcoma Group-Australasian Gastrointestinal Trials Group randomized trial comparing two doses of imatinib in advanced disease. PATIENTS AND METHODS Initial resistance was defined as progression within 3 months of randomization, and late resistance was defined as progression beyond 3 months. Investigated cofactors include imatinib dose, age, sex, performance status, original disease site, site and size of lesions at trial entry, and baseline hematologic and biologic parameters. Results Initial resistance was recorded for 116 (12%) of 934 assessable patients and was independently predicted by the presence of lung and absence of liver metastases, low hemoglobin level, and high granulocyte count. Among 818 patients who were alive and progression free at 3 months, 347 subsequent progressions were recorded, and late resistance was independently predicted by high baseline granulocyte count, primary tumor outside of the stomach, large tumor size, and low initial imatinib dose. The impact of initial dose on late resistance was mainly significant in patients with a high baseline granulocyte count (> 5.10(9)/L) and in patients with tumors of GI origin outside of the stomach and small intestine. CONCLUSION Our study identifies patients for whom initial and/or long-term treatment needs to be improved and patients who require a high initial dose. Correlation of these results with immunohistochemistry and molecular parameters may further help to understand the biologic mechanisms of resistance.
机译:目的本研究的目的是确定预测胃肠道间质瘤(GIST)患者对伊马替尼的初始和晚期耐药性的因素,并记录预后亚组中的剂量反应关系。这项研究是基于欧洲癌症研究和治疗组织-意大利肉瘤组-澳大利亚胃肠道试验组进行的随机试验,比较了伊马替尼在晚期疾病中的两种剂量。患者和方法最初的耐药性定义为随机分配后3个月内的进展,晚期耐药性定义为超过3个月的进展。研究的辅助因子包括伊马替尼的剂量,年龄,性别,行为状态,原始疾病部位,试验进入时病变的部位和大小以及基线血液学和生物学参数。结果934例可评估患者中有116例(12%)记录了初始耐药,并通过肺的存在和肝转移的缺乏,低血红蛋白水平和高粒细胞计数独立预测。在818例存活且3个月内无进展的患者中,记录了347个随后的进展,并且通过高基线粒细胞计数,胃外原发肿瘤,大肿瘤尺寸和低伊马替尼初始剂量独立预测了晚期耐药。初始剂量对晚期耐药的影响主要在基线粒细胞计数高(> 5.10(9)/ L)的患者以及胃肠道起源于胃和小肠之外的肿瘤患者中显着。结论我们的研究确定了需要改善初始和/或长期治疗的患者以及需要高初始剂量的患者。这些结果与免疫组织化学和分子参数的相关性可能进一步有助于了解耐药性的生物学机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号