Division of Hematology/Oncology, Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611-6189, USA.
Chemotherapy. 2012;58(1):30-3. doi: 10.1159/000333386. Epub 2012 Feb 11.
Gastrointestinal stromal tumors (GIST) arise from precursor cells in the myenteric plexus and comprise the most common mesenchymal tumors of the gastrointestinal tract. Surgical resection is the mainstay of therapy for localized disease. Recurrent, unresectable, and metastatic tumors are associated with a poor prognosis given their resistance to conventional chemotherapy and radiation. Advances in the understanding of molecular pathophysiology of GIST and the use of targeted small-molecule therapies have resulted in dramatic increases in survival. Preliminary data have demonstrated benefits in using imatinib in a neoadjuvant setting; however, there are no studies to date analyzing the use of neoadjuvant sunitinib in primary advanced GIST. Here we present the case of a patient with locally advanced primary GIST who developed severe toxicity on imatinib therapy and was successfully treated with sunitinib in the neoadjuvant setting to achieve complete surgical resection.
胃肠道间质瘤(GIST)起源于肌间神经丛的前体细胞,是胃肠道最常见的间叶性肿瘤。手术切除是局限性疾病的主要治疗方法。对于复发性、不可切除和转移性肿瘤,由于其对常规化疗和放疗的耐药性,预后较差。对 GIST 分子病理生理学的认识不断提高,以及靶向小分子治疗药物的应用,使得患者的生存率显著提高。初步数据表明,在新辅助治疗中使用伊马替尼具有益处;然而,目前尚无研究分析新辅助舒尼替尼在原发性晚期 GIST 中的应用。本文报告了一例局部晚期原发性 GIST 患者,该患者在接受伊马替尼治疗时发生严重毒性反应,随后成功地在新辅助治疗中使用舒尼替尼进行治疗,从而实现了完全手术切除。