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Locoregional therapy and systemic cetuximab to treat colorectal liver metastases

机译:局部区域疗法和全身西妥昔单抗治疗结直肠肝转移

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摘要

AIM: To investigate efficacy and safety of second-line treatment with irinotecan-loaded drug-eluting beads (DEBIRI) and cetuximab (DEBIRITUX) of unresectable colorectal liver metastases.METHODS: Patients with the following characteristics were included in the study: unresectable hepatic metastases from colorectal carcinoma (CRC-LM), progression after first line chemotherapy (any type of chemotherapeutic drug and combination was allowed), second line treatment (mandatory), which included for each patient (unregarding the KRas status) two cycles of DEBIRI (using 100-300 μm beads loaded with irinotecan at a total dose 200 mg) followed by 12 cycles of cetuximab that was administered weekly at a first dose of 400 mg/m2 and then 250 mg/m2; good performance status (0-2) and liver functionality (alanine aminotransferase and gamma-glutamyl transferase not exceeding three times the upper limit of normal, total bilirubin not exceeding 2.5 mg/mL). Data were collected retrospectively and included: tumor response (evaluated monthly for 6 mo then every 3 mo), overall response rate (ORR), KRas status, type and intensity of adverse events (G according to the Common Terminology Criteria for Adverse Events v3.0, CTCAE), overall survival (OS) and progression free survival (PFS).RESULTS: Forty consecutive cases of CRC hepatic metastases were included in the study. Median duration of DEBIRITUX was 4.4 mo (range, 4.0-6.5). Sixteen patients (40%) received the planned 2 cycles of DEBIRI and an average of 10 cetuximab cycles. ORR of the whole sample was 50%, in particular 4 patients were complete responders (10%) and 16 (40%) partial responders. The most observed side effects (G2) were: post-embolization syndrome (30%), diarrhea (25%), skin rushes (38%) and asthenia (35%). The retrospective evaluation of KRas status (24 wild type, 16 mutated) showed that the group of patients with wild type KRas had ORR significantly higher than mutant KRas. Median follow-up was 29 mo (8-48 range); median PFS was 9.8 mo and OS was 20.4 mo. Future randomized trials are required in this setting to establish a role for DEBIRITUX compared with systemic chemotherapy.CONCLUSION: DEBIRITUX seems to be efficacious after first line chemotherapy for the treatment of unresectable CRC-LM.
机译:目的:研究用伊立替康载药洗脱珠(DEBIRI)和西妥昔单抗(DEBIRITUX)治疗无法切除的结直肠肝转移的二线治疗的有效性和安全性。方法:具有以下特征的患者被纳入研究:不可切除的肝转移来自结直肠癌(CRC-LM),一线化疗(允许使用任何类型的化疗药物和联合用药),二线治疗(强制性)后的进展,每例患者(不论KRas状况如何)均包括两个周期的DEBIRI(使用100-300μm的珠粒,总剂量为200 mg的伊立替康,然后连续12个周期的西妥昔单抗,以每周400 mg / m 2 的剂量给药,然后以250 mg / m 2 ;良好的工作状态(0-2)和肝功能(丙氨酸氨基转移酶和γ-谷氨酰转移酶不超过正常上限的三倍,总胆红素不超过2.5 mg / mL)。回顾性收集数据,包括:肿瘤反应(每月评估一次,连续6个月,然后每3个月评估),总体缓解率(ORR),KRas状态,不良事件的类型和强度(根据不良事件通用术语标准v3,G级)。 0,CTCAE),总生存期(OS)和无进展生存期(PFS)。结果:本研究包括连续40例CRC肝转移病例。 DEBIRITUX的中位持续时间为4.4 mo(范围4.0-6.5)。 16名患者(40%)接受了计划的2个DEBIRI周期和平均10个西妥昔单抗周期。整个样本的ORR为50%,特别是4例完全缓解(10%)和16例(40%)部分缓解。观察到最多的副作用(G2)是:栓塞后综合征(30%),腹泻(25%),皮疹(38%)和虚弱(35%)。对KRas状况(24个野生型,16个突变)的回顾性评估表明,野生型KRas患者组的ORR明显高于突变型KRas。随访中位数为29个月(8-48范围); PFS中位数为9.8 mo,OS为20.4 mo。与全身化疗相比,需要在这种情况下进行进一步的随机试验以确定DEBIRITUX的作用。结论:在一线化疗后,DEBIRITUX似乎对于治疗不可切除的CRC-LM是有效的。

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