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首页> 外文期刊>Annals of Surgery >Long-term results of adjuvant imatinib mesylate in localized, high-risk, primary gastrointestinal stromal tumor: ACOSOG Z9000 (Alliance) intergroup phase 2 trial
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Long-term results of adjuvant imatinib mesylate in localized, high-risk, primary gastrointestinal stromal tumor: ACOSOG Z9000 (Alliance) intergroup phase 2 trial

机译:甲磺酸伊马替尼辅助治疗局部,高风险,原发性胃肠道间质瘤的长期结果:ACOSOG Z9000(Alliance)组间2期试验

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Objective: To conduct the first adjuvant trial of imatinib mesylate for treatment of gastrointestinal stromal tumor (GIST). Background: GIST is the most common sarcoma. Although surgical resection has been the mainstay of therapy for localized, primary GIST, postoperative tumor recurrence is common. The KIT protooncogene or, less frequently, platelet-derived growth factor receptor alpha is mutated in GIST; the gene products of both are inhibited by imatinib mesylate. Methods: This was a phase II, intergroup trial led by the American College of Surgeons Oncology Group, registered at ClinicalTrials.gov as NCT00025246. From September 2001 to September 2003, we accrued 106 patients who had undergone complete gross tumor removal but were deemed at high risk for recurrence. Patients were prescribed imatinib 400 mg per day for 1 year and followed with serial radiologic evaluation. The primary endpoint was overall survival (OS). Results: After a median follow-up of 7.7 years, the 1-, 3-, and 5-year OS rates were 99%, 97%, and 83%, which compared favorably with a historical 5-year OS rate of 35%. The 1-, 3-, and 5-year recurrence-free survival (RFS) rates were 96%, 60%, and 40%. On univariable analysis, age and mitotic rate were associated with OS. On multivariable analysis, the RFS rate was lower with increasing tumor size, small bowel site, KIT exon 9 mutation, high mitotic rate, and older age. Conclusions: Adjuvant imatinib in patients with primary GIST who are at high risk of recurrence prolongs OS compared with that of historical controls. Optimal duration of adjuvant therapy remains undefined.
机译:目的:进行甲磺酸伊马替尼治疗胃肠道间质瘤(GIST)的首次佐剂试验。背景:GIST是最常见的肉瘤。尽管手术切除一直是局部原发性GIST治疗的主要手段,但术后肿瘤复发很常见。 KIT原癌基因或血小板衍生的生长因子受体α在GIST中发生突变;两者的基因产物均受到甲磺酸伊马替尼的抑制。方法:这是由美国外科医师学会肿瘤小组领导的II期临床试验,在ClinicalTrials.gov上注册为NCT00025246。从2001年9月到2003年9月,我们收集了106例已完全切除肿瘤但被认为具有高复发风险的患者。患者接受每天400 mg伊马替尼的处方治疗1年,然后进行系列放射学评估。主要终点是总体生存期(OS)。结果:中位随访7.7年后,第1年,第3年和第5年OS率分别为99%,97%和83%,与历史5年OS率35%相比是有利的。 1年,3年和5年无复发生存率(RFS)分别为96%,60%和40%。在单变量分析中,年龄和有丝分裂率与OS有关。在多变量分析中,RFS率随肿瘤大小,小肠位点,KIT外显子9突变,有丝分裂率高和年龄增加而降低。结论:与历史对照相比,原发性GIST高复发风险的辅助伊马替尼可延长OS。辅助治疗的最佳持续时间仍然不确定。

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