Blackstein Martin E, Blay Jean-Yves, Corless Christopher, Driman David K, Riddell Robert, Soulières Denis, Swallow Carol J, Verma Shailendra
Medical Oncology Unit, Mount Sinai Hospital, Toronto, Ontario.
Can J Gastroenterol. 2006 Mar;20(3):157-63. doi: 10.1155/2006/434761.
In the multidisciplinary management of gastrointestinal stromal tumours (GISTs), there is a need to coordinate the efforts of pathology, radiology, surgery and oncology. Surgery is the mainstay for resectable nonmetastatic GISTs, but virtually all GISTs are associated with a risk of metastasis. Imatinib 400 mg/day with or without surgery is the recommended first-line treatment for recurrent or metastatic GIST; a higher dose may be considered in patients who progress, develop secondary resistance or present with specific genotypic characteristics. Adjuvant or neoadjuvant imatinib is not advised for resectable nonmetastatic GISTs. Neoadjuvant imatinib may be considered when surgery would result in significant morbidity or loss of organ function. Follow-up computed tomography imaging is recommended every three to six months for at least five years. Patients with metastatic disease should be continued on imatinib due to the high risk of recurrence on discontinuation of therapy. Treatment should be continued until there is progression or intolerable adverse effects. If dose escalation with imatinib fails, a clinical trial with novel agents alone or in combination may be considered. The present recommendations were developed at a surgical subcommittee meeting and a subsequent full Advisory Committee meeting held in Toronto, Ontario, in April 2005, under the sponsorship of Novartis Pharmaceuticals Canada Inc.
在胃肠间质瘤(GIST)的多学科管理中,需要协调病理学、放射学、外科和肿瘤学的工作。手术是可切除的非转移性GIST的主要治疗方法,但几乎所有GIST都有转移风险。伊马替尼400毫克/天,无论是否联合手术,都是复发或转移性GIST的推荐一线治疗方案;对于病情进展、出现继发性耐药或具有特定基因型特征的患者,可考虑更高剂量。不建议对可切除的非转移性GIST使用辅助或新辅助伊马替尼。当手术会导致严重并发症或器官功能丧失时,可考虑新辅助伊马替尼。建议每三到六个月进行一次计算机断层扫描成像随访,至少持续五年。由于停药后复发风险高,转移性疾病患者应继续使用伊马替尼治疗。治疗应持续到病情进展或出现无法耐受的不良反应。如果伊马替尼剂量增加失败,可考虑单独或联合使用新型药物的临床试验。本建议是在2005年4月于安大略省多伦多举行的一次外科小组委员会会议以及随后的一次咨询委员会全体会议上制定的,由加拿大诺华制药公司赞助。