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首页> 外文期刊>Tumori. >Fluorouracil, leucovorin and irinotecan combined with intra-arterial hepatic infusion of drugeluting beads preloaded with irinotecan in unresectable colorectal liver metastases: Side effects and results of a concomitant treatment schedule. Clinical investigation
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Fluorouracil, leucovorin and irinotecan combined with intra-arterial hepatic infusion of drugeluting beads preloaded with irinotecan in unresectable colorectal liver metastases: Side effects and results of a concomitant treatment schedule. Clinical investigation

机译:氟尿嘧啶,亚叶酸钙蛋白和伊立替康联合动脉内输注预先装载有伊立替康的药物洗脱珠在不可切除的结直肠肝转移中的副作用和伴随的治疗方案。临床调查

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摘要

Aim. Safety evaluation of concomitant systemic chemotherapy and liver chemoembolization in patients with colorectal cancer. Patients and methods. Seven patients with metastases confined to the liver were included and stratified into two groups, depending of dosage of systemic chemotherapy. The first group received systemic chemotherapy (FOLFIRI) with 20% dose reduction, and the second group received the full dose of the same chemotherapy. In both groups, chemoembolization of liver metastases with drug-eluting bead irinotecan (DEBIRI) was performed following the application of systemic chemotherapy. The toxicity profiles of the two groups were compared.Results. Of the 7 patients included, 4 received the reduced systemic chemotherapy dose and 3 received the full chemotherapy dose. DEBIRI was performed in all 7 patients. The main toxicities observed in the reduced chemotherapy dose group were leukopenia (25%), anorexia (75%), diarrhea (25%), vomiting (25%), right upper abdominal quadrant pain (100%) and elevated serum amylase level (25%). Main toxicities observed in the full chemotherapy dose group were anorexia (66.6%), vomiting (33.3%), right upper abdominal quadrant pain (100%), and elevated serum amylase level (66.6%). There were no significant differences between the two groups (P =0.78541).Conclusions. Patients with isolated liver metastases from a colorectal primary can safely be treated with DEBIRI chemoembolization and a full dose of systemic chemotherapy (FOLFIRI).
机译:目标。大肠癌患者同时进行全身化疗和肝化学栓塞的安全性评估。患者和方法。根据全身化疗剂量,将7例转移灶局限于肝脏的患者分为两组。第一组接受减量20%的全身化疗(FOLFIRI),第二组接受相同剂量的全剂量化疗。在两组中,在应用全身化学疗法后,均用药物洗脱微珠伊立替康(DEBIRI)进行了肝转移的化学栓塞。比较了两组的毒性特征。结果。纳入的7例患者中,有4例接受了降低的全身化疗剂量,有3例接受了全化疗剂量。所有7例患者均进行了DEBIRI检查。在减少化疗剂量组中观察到的主要毒性是白细胞减少症(25%),厌食症(75%),腹泻(25%),呕吐(25%),右上腹象限疼痛(100%)和血清淀粉酶水平升高( 25%)。在完全化疗剂量组中观察到的主要毒性为厌食(66.6%),呕吐(33.3%),右上腹象限疼痛(100%)和血清淀粉酶水平升高(66.6%)。两组之间无显着差异(P = 0.78541)。结直肠原发性肝转移患者可以安全地接受DEBIRI化学栓塞和全剂量全身化疗(FOLFIRI)治疗。

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