Neuroendokrine Tumoren: Wirksamkeit der Kombinations-Chemotherapie bestätigt

M. Stahl
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Abstract

Background: Capecitabine and temozolomide combination (CAPTEM) is associated with high response rates in patients with advanced neuroendocrine neoplasms (NENs). We evaluated the real-world activity and safety of CAPTEM from 3 NEN centers. Methods: Clinicopathological characteristics and outcomes of patients treated with CAPTEM for bulky or progressive disease (PD) were retrospectively analyzed. Results: Seventy-nine patients with gastroenteropancreatic (grades 1 - 2 [n = 38], grade 3 [n = 24]) and lung/thymic (n = 17) NENs were included. Median treatment duration was 12.1 months (range 0.6 - 55.6). Overall, partial responses (PRs) occurred in 23 (29.1%), stable (SD) in 24 (30.4%), and PD in 28 (35.4%) patients. Median progression-free survival (PFS) and overall survival (OS) were 10.1 (6 - 14.2) and 102.9 months (43.3-162.5), respectively. On univariate analysis, NENs naive to chemotherapy and low Ki67 were associated with favorable responses (partial response [PR] + SD; p = 0.011 and 0.045), PFS (p < 0.0001 and 0.002) and OS (p = 0.005 and 0.001). Primary site (pancreas and lung/thymus) was also a significant prognostic factor for PFS (p < 0.0001) and OS (p < 0.0001). On multivariate analysis, gastrointestinal and unknown primary NENs (hazard ratio [HR] 0.3, 95% CI 0.1 - 0.8, p = 0.009 and p = 0.018) and prior surgery (HR 2.4, 95% CI 11 - 4.9, p = 0.021) were independent prognostic factors for PFS. Ki-67 was a poor predictor for favorable response in receiver operating characteristic analysis (area under the curve 0.678). Safety analysis of CAPTEM indicated rare events of serious (grades 3 - 4) toxicities (n = 4) and low discontinuation rates (n = 8) even in patients with prolonged administration ( > 12 months). Conclusions: CAPTEM treatment can be an effective and safe treatment even after prolonged administration for patients with NENs of various sites and Ki67 labeling index, associated with significant favorable responses and PFS.
内分泌学:组合治疗的有效性得到确认
背景:卡培他滨联合替莫唑胺(CAPTEM)治疗晚期神经内分泌肿瘤(NENs)的有效率较高。我们评估了来自3个NEN中心的CAPTEM的实际活性和安全性。方法:回顾性分析采用CAPTEM治疗体积大或进展性疾病(PD)患者的临床病理特点及预后。结果:纳入79例胃肠胰(1 ~ 2级[n = 38], 3级[n = 24])和肺/胸腺(n = 17) NENs患者。中位治疗持续时间为12.1个月(范围0.6 - 55.6)。总体而言,23例(29.1%)患者出现部分缓解(pr), 24例(30.4%)患者出现稳定缓解(SD), 28例(35.4%)患者出现PD。中位无进展生存期(PFS)和总生存期(OS)分别为10.1(6 - 14.2)和102.9个月(43.3-162.5)。在单因素分析中,未接受化疗的NENs和低Ki67与良好的反应相关(部分反应[PR] + SD;p = 0.011和0.045),PFS (p < 0.0001和0.002)和OS (p = 0.005和0.001)。原发部位(胰腺和肺/胸腺)也是PFS (p < 0.0001)和OS (p < 0.0001)的重要预后因素。在多因素分析中,胃肠道和未知原发NENs(风险比[HR] 0.3, 95% CI 0.1 - 0.8, p = 0.009和p = 0.018)和既往手术(风险比[HR] 2.4, 95% CI 11 - 4.9, p = 0.021)是PFS的独立预后因素。在受试者工作特征分析中,Ki-67不能作为良好应答的预测因子(曲线下面积0.678)。CAPTEM的安全性分析显示,即使在延长给药时间(> 12个月)的患者中,也很少发生严重(3 - 4级)毒性事件(n = 4)和低停药率(n = 8)。结论:对于不同部位的NENs和Ki67标记指数的患者,CAPTEM治疗可以是一种有效的、安全的治疗方法,即使经过长时间的给药,与显著的有利反应和PFS相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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