*Memorial Sloan-Kettering Cancer Center, New York, NY †Alliance Statistics and Data Center, Mayo Clinic, Rochester, MN ‡Oregon Health Sciences University, Portland, OR §Fox Chase Cancer Center, Philadelphia, PA ¶University of Colorado School of Medicine, Aurora, CO ‖Stanford University School of Medicine, Stanford CA **Mt Sinai School of Medicine, New York, NY ††University of Texas MD Anderson Cancer Center, Houston, TX ‡‡Dana Farber Cancer Institute, Boston, MA; and §§Alliance Statistics and Data Center, Duke University, Durham, NC.
Ann Surg. 2013 Sep;258(3):422-9. doi: 10.1097/SLA.0b013e3182a15eb7.
To conduct the first adjuvant trial of imatinib mesylate for treatment of gastrointestinal stromal tumor (GIST).
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.
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).
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.
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. (NCT00025246).
开展甲磺酸伊马替尼治疗胃肠道间质瘤(GIST)的首个辅助治疗试验。
GIST 是最常见的肉瘤。尽管手术切除一直是局限性原发性 GIST 的主要治疗方法,但术后肿瘤复发很常见。GIST 中 KIT 原癌基因或较少见的血小板衍生生长因子受体 α 发生突变;两者的基因产物均被甲磺酸伊马替尼抑制。
这是由美国外科医师学会肿瘤学组领导的一项 II 期、分组间试验,在美国国立卫生研究院临床试验注册中心注册为 NCT00025246。从 2001 年 9 月到 2003 年 9 月,我们共招募了 106 例已完成肿瘤完全切除但复发风险高的患者。患者每天服用伊马替尼 400mg,持续 1 年,并进行连续影像学评估。主要终点是总生存(OS)。
中位随访 7.7 年后,1、3 和 5 年 OS 率分别为 99%、97%和 83%,与历史上 5 年 OS 率 35%相比具有优势。1、3 和 5 年无复发生存(RFS)率分别为 96%、60%和 40%。单变量分析显示,年龄和有丝分裂率与 OS 相关。多变量分析显示,肿瘤大小、小肠部位、KIT 外显子 9 突变、高有丝分裂率和年龄较大与 RFS 率降低相关。
与历史对照相比,高复发风险的原发性 GIST 患者接受辅助伊马替尼治疗可延长 OS。辅助治疗的最佳持续时间仍未确定。(NCT00025246)。