Hsu Jun-Te, Le Puo-Hsien, Kuo Chang-Fu, Chiou Meng-Jiun, Kuo Chia-Jung, Chen Tsung-Hsing, Lin Chun-Jung, Chen Jen-Shi, Yu Huang-Pin, Yeh Chun-Nan, Jan Yi-Yin, Yeh Ta-Sen
Department of Surgery, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Department of Gastroenterology, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Oncotarget. 2017 Apr 3;8(41):71128-71137. doi: 10.18632/oncotarget.16795. eCollection 2017 Sep 19.
Although treatment with imatinib in advanced gastrointestinal stromal tumor (GIST) patients has led to significant clinical benefits, the disease will eventually progress due to imatinib resistance. Treatment options after failure of first-line imatinib include imatinib dose escalation or shifting to sunitinib. However, there is no large-scale study to compare the efficacy difference between these two treatment strategies or the role of surgery.
This study recruited 521 advanced GIST patients including 246, 125, and 150 placed in groups 1, 2, and 3, respectively. Groups 1 and 2 had significantly longer overall survival (OS) as compared with the group 3 (median 37.5 months versus 16.0 months; < 0.0001). After adjusting for confounding variables, groups 1 and 2 had longer OS than group 3. A favorable survival trend was seen with surgery, although this benefit disappeared after adjusting for confounding factors.
We conducted a nationwide population-based cohort study using data from the Taiwan National Health Insurance Research Database from July 2004 to December 2010. Advanced GIST patients who no longer responded to first-line imatinib were stratified into three groups: imatinib dose escalation (group 1); imatinib dose escalation and a shift to sunitinib (group 2); a direct shift to sunitinib (group 3). The therapeutic success of the three treatment regimens and the effect of surgery were evaluated by overall survival.
For advanced GIST patients who failed first-line imatinib treatment, imatinib dose escalation confers significantly longer OS compared to a direct switch to sunitinib. Surgery does not provide survival benefits.
尽管伊马替尼治疗晚期胃肠道间质瘤(GIST)患者已带来显著的临床益处,但由于伊马替尼耐药,疾病最终仍会进展。一线伊马替尼治疗失败后的治疗选择包括伊马替尼剂量递增或改用舒尼替尼。然而,尚无大规模研究比较这两种治疗策略之间的疗效差异或手术的作用。
本研究招募了521例晚期GIST患者,分别将246例、125例和150例纳入第1组、第2组和第3组。与第3组相比,第1组和第2组的总生存期(OS)显著更长(中位生存期分别为37.5个月和16.0个月;P<0.0001)。在调整混杂变量后,第1组和第2组的OS比第3组长。手术显示出有利的生存趋势,尽管在调整混杂因素后这种益处消失了。
我们利用2004年7月至2010年12月台湾国民健康保险研究数据库的数据进行了一项全国性的基于人群的队列研究。对一线伊马替尼不再有反应的晚期GIST患者被分为三组:伊马替尼剂量递增(第1组);伊马替尼剂量递增并改用舒尼替尼(第2组);直接改用舒尼替尼(第3组)。通过总生存期评估三种治疗方案的治疗成功率和手术效果。
对于一线伊马替尼治疗失败的晚期GIST患者,与直接改用舒尼替尼相比,伊马替尼剂量递增可显著延长总生存期。手术不能提供生存益处。