Schindler C G, Armbrust T, Gunawan B, Langer C, Füzesi L, Ramadori G
Department of Gastroenterology and Endocrinology, Georg August University, Göttingen, Germany.
Z Gastroenterol. 2005 Mar;43(3):267-73. doi: 10.1055/s-2004-813756.
The tyrosine kinase inhibitor imatinib has been introduced into the treatment of gastrointestinal stromal tumors (GIST). Here we report our results of prolonged treatment in comparison to a similar group of GIST patients who had died before imatinib became available.
Fourteen patients with recurrent or metastatic GIST were treated with imatinib. Clinical data and tumor samples of ten patients from the pre-imatinib era were available for comparison. Comparative genomic hybridisation (CGH) was performed on tumors to identify changes that may predict response to treatment.
Fourteen patients were treated, mean treatment time 22.3 months (1 non-response, 2 progression after initial response, 2 stable diseases, 8 partial responses, 1 complete response). Adverse side effects were mild in general. Survival was higher in the treated group (41.1 months vs. 34.8 months in the historical group). Eleven treated patients are alive. CGH analysis showed comparable numbers of chromosomal aberations in both groups.
Prolonged treatment with imatinib is safe and effective in patients with recurrent or metastatic GIST.
酪氨酸激酶抑制剂伊马替尼已被用于治疗胃肠道间质瘤(GIST)。在此,我们报告与一组在伊马替尼可用之前就已死亡的类似GIST患者相比,长期治疗的结果。
14例复发性或转移性GIST患者接受伊马替尼治疗。可获得10例伊马替尼治疗前时代患者的临床数据和肿瘤样本用于比较。对肿瘤进行比较基因组杂交(CGH)以识别可能预测治疗反应的变化。
14例患者接受治疗,平均治疗时间22.3个月(1例无反应,2例初始反应后进展,2例病情稳定,8例部分缓解,1例完全缓解)。总体不良反应较轻。治疗组的生存率更高(41.1个月对历史组的34.8个月)。11例接受治疗的患者存活。CGH分析显示两组染色体畸变数量相当。
伊马替尼长期治疗对复发性或转移性GIST患者安全有效。