Doyon C, Sidéris L, Leblanc G, Leclerc Y E, Boudreau D, Dubé P
Department of Surgery, Maisonneuve-Rosemont Hospital, University of Montreal, Montreal, QC, Canada H1T 2M4.
Int J Surg Oncol. 2012;2012:761576. doi: 10.1155/2012/761576. Epub 2012 Dec 17.
Purpose. Proven efficacy of imatinib mesylate in gastrointestinal stromal tumour (GIST) has led to its use in advanced disease and, more recently, in adjuvant and neoadjuvant settings. The purpose of this study was to evaluate the optimal neoadjuvant imatinib duration to reduce the morbidity of surgery and increase the possibility of resection completeness in advanced tumours. Patients and Method. Patients with advanced GIST were enrolled into a registered open-label multicenter trial and received imatinib daily for a maximum of 12 months, followed by en bloc resection. Data were prospectively collected regarding tumour assessment, response rate, surgical characteristics, recurrence, and survival. Results. Fourteen patients with advanced GIST were enrolled. According to RECIST criteria, 6 patients had partial response and 8 had stable disease. The overall tumour size reduction was 25% (0-62.5%), and there was no tumour progression. Eleven patients underwent tumour resection, and all had R0 resection. After a median followup of 48 months, 4-year OS and DFS were 100% and 64%, respectively. Conclusion. This prospective trial showed that one year of neoadjuvant imatinib in advanced GIST is safe and associated with high rate of complete microscopic resection. It is not associated with increased resistance, progression, or complication rates.
目的。甲磺酸伊马替尼在胃肠道间质瘤(GIST)中的疗效已得到证实,这使其可用于晚期疾病,最近还用于辅助和新辅助治疗。本研究的目的是评估新辅助伊马替尼的最佳用药时长,以降低手术 morbidity 并提高晚期肿瘤完整切除的可能性。患者与方法。晚期 GIST 患者被纳入一项注册的开放标签多中心试验,每日接受伊马替尼治疗,最长 12 个月,随后进行整块切除。前瞻性收集有关肿瘤评估、缓解率、手术特征、复发和生存的数据。结果。14 例晚期 GIST 患者入组。根据 RECIST 标准,6 例患者部分缓解,8 例病情稳定。肿瘤总体缩小 25%(0 - 62.5%),无肿瘤进展。11 例患者接受了肿瘤切除,均实现 R0 切除。中位随访 48 个月后,4 年总生存率(OS)和无病生存率(DFS)分别为 100%和 64%。结论。这项前瞻性试验表明,晚期 GIST 患者新辅助使用一年伊马替尼是安全的,且与高比例的显微镜下完全切除相关。它与耐药性增加、疾病进展或并发症发生率升高无关。