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Anti-EGFR Therapy in Metastatic Small Bowel Adenocarcinoma: Myth or Reality?

机译:抗EGFR治疗转移性小肠腺癌:神话或现实?

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Background: Due to the relative rarity of small bowel adenocarcinoma (SBA), prospective trials, helping to guide therapeutic decisions, are lacking and the optimal therapy for advanced SBA is unknown. The role of targeted agents, such as anti–epidermal growth factor receptor (EGFR) and anti–vascular endothelial growth factor (VEGF), is unknown. Patients and Methods: This is a retrospective multicenter observational study that included patients with metastatic SBA treated with anti-EGFR antibodies (cetuximab or panitumumab)?±?chemotherapy in the first (I) or second (II) line. Results: Thirteen patients with metastatic SBA, recruited from 5 Italian referral institutions, were included in the present retrospective analysis. All patients received anti-EGFR inhibitors as a single agent or in association with chemotherapy. More common G2 treatment–related side effects were skin reaction (8 patients, 53.8%), hypomagnesemia (6 patients, 46.2%), and diarrhea (8 patients, 61.5%). Grade 3 diarrhea was observed in only 1 patient. Conjunctivitis was not reported in any patients. Grade 4 toxicity was not reported. In the overall population, median progression-free survival was 5.526?months (95% confidence interval [CI]: 3.684-12.467). Median overall survival was 15.86?months (95% CI: 14.43-24.30). Complete response was observed in 15% of patients, partial response in 39% of patients, stable disease in 23% of patients, and progression disease in 15% of patients. Conclusions: In this retrospective analysis, anti-EGFR inhibitors showed to be a suitable addendum to chemotherapy in the I and II line, with an excellent tolerance and safety profile both in I and II line.
机译:背景:由于小肠腺癌(SBA)的相对罕见,缺乏预期试验,有助于指导治疗决策,缺乏和先进的SBA的最佳治疗未知。靶向剂的作用,例如抗表皮生长因子受体(EGFR)和抗血管内皮生长因子(VEGF)是未知的。患者和方法:这是一种回顾性多中心观察研究,包括用抗EGFR抗体(西妥昔单抗或Panitumumab)α±±化疗在第一(I)或第二(II)线中处理的转移SBA患者。结果:来自5例意大利推荐机构的13例转移SBA患者,包括在本发明回顾性分析中。所有患者均接受抗EGFR抑制剂作为单一剂或与化疗结合。更常见的G2治疗相关的副作用是皮肤反应(8名患者,53.8%),血清血症(6例,46.2%)和腹泻(8例,61.5%)。仅在1例患者中观察到3级腹泻。任何患者都没有报道结膜炎。没有报告4级毒性。在整体人口中,中位进展生存率为5.526?月份(95%置信区间[CI]:3.684-12.467)。中位数总生存率为15.86?月份(95%CI:14.43-24.30)。在15%的患者中观察到完全反应,39%的患者的部分反应,23%的患者稳定的疾病,以及15%的患者的进展疾病。结论:在这种回顾性分析中,抗EGFR抑制剂表现为I和II线中化疗的合适附录,I和II线II和II线均具有优异的耐受性和安全性。

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