Cutler Holt S, Ogando Paul, Uhr Joshua H, Gonzalez Dani O, Warner Richard R P, Divino Celia M
Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Am Surg. 2016 Apr;82(4):369-75.
This case series demonstrates the potential of molecular profiling to improve selection of antitumor therapies in the treatment of patients with neuroendocrine and carcinoid tumors. Carcinoid tumors resected at one institution over a 3-year period were sent for molecular profiling to guide choice of treatment. Potentially beneficial therapies were identified based on the measured expression of 20 proteins and oncogenes and a comprehensive review of the chemotherapy response literature. The clinical charts of 41 patients were reviewed retrospectively, and 12 were selected as representatives of the range of effects molecular profiling has on carcinoid treatment. Their presentation, molecular profile results, treatment, and disease progression is reviewed in the following case series. A total of nine patients were treated with drugs identified as potentially beneficial by molecular profile reports. These include capecitabine, 5-fluorouracil, temozolomide, oxaliplatin, and gemcitabine. Based on clinical symptoms, serum markers of disease, and radiographic evidence five of nine patients responded to treatment, two had mixed responses, and two did not respond to treatment. At this early juncture, our critique of molecular profiling for neuroendocrine tumors is favorable, as a significant number of our patients responded to drugs identified by molecular profiling as potentially beneficial.
该病例系列证明了分子谱分析在改善神经内分泌肿瘤和类癌患者抗肿瘤治疗选择方面的潜力。在3年时间里,一家机构切除的类癌被送去进行分子谱分析,以指导治疗选择。根据20种蛋白质和癌基因的测量表达以及对化疗反应文献的全面综述,确定了可能有益的治疗方法。对41例患者的临床病历进行了回顾性分析,选择了12例作为分子谱分析对类癌治疗影响范围的代表。在以下病例系列中回顾了他们的临床表现、分子谱分析结果、治疗情况和疾病进展。共有9例患者接受了分子谱分析报告确定为可能有益的药物治疗。这些药物包括卡培他滨、5-氟尿嘧啶、替莫唑胺、奥沙利铂和吉西他滨。根据临床症状、疾病血清标志物和影像学证据,9例患者中有5例对治疗有反应,2例有混合反应,2例对治疗无反应。在这个早期阶段,我们对神经内分泌肿瘤分子谱分析的评价是积极的,因为我们的大量患者对分子谱分析确定为可能有益的药物有反应。