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广泛期小细胞肺癌透析患者改良 IMpower133 方案的耐受性和疗效:两例报告。

Tolerability and efficacy of IMpower133 regimen modified for dialysis patients with extensive-stage small cell lung cancer: Two case reports.

机构信息

Department of Respiratory Medicine, Hiroshima University Hospital, Hiroshima, Japan.

出版信息

Thorac Cancer. 2021 Nov;12(21):2956-2960. doi: 10.1111/1759-7714.14166. Epub 2021 Sep 29.

DOI:10.1111/1759-7714.14166
PMID:34587368
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8563152/
Abstract

The IMpower133 regimen, composed of atezolizumab/etoposide (VP-16)/carboplatin (CBDCA), is the standard first-line treatment for extensive-stage small cell lung cancer (ES-SCLC). However, the safety and efficacy of triplet therapy in patients receiving dialysis have not been sufficiently evaluated. Here, we report two cases of dialysis patients with ES-SCLC who received the modified IMpower133 regimen. Patient 1 was a 69-year-old man, and patient 2 was a 73-year-old man who received dialysis because of end-stage renal failure caused by diabetic nephropathy. Both patients received a modified IMpower133 regimen in the following order: atezolizumab (1200 mg/body) on day 1, VP-16 (50 mg/m ) on days 1 and 3, and CBDCA (300 mg/m ) on day 1. Four hours of dialysis was performed 1 hour after completing the administration of CBDCA on Day 1 and 2 hours after completing the administration of VP-16 on Day 3. Both patients achieved a partial response and received atezolizumab maintenance therapy after four cycles of triplet therapy without uncontrollable adverse events. By modifying the dosage, the order of drugs, and the timing of dialysis, the IMpower133 regimen may be tolerable and effective for patients receiving dialysis.

摘要

IMpower133 方案由阿替利珠单抗/依托泊苷(VP-16)/卡铂(CBDCA)组成,是广泛期小细胞肺癌(ES-SCLC)的标准一线治疗方案。然而,接受透析的患者中三联疗法的安全性和疗效尚未得到充分评估。在此,我们报告了 2 例接受改良 IMpower133 方案治疗的透析患者。患者 1 为 69 岁男性,患者 2 为 73 岁男性,因糖尿病肾病导致终末期肾衰竭而接受透析。两名患者均按照以下顺序接受改良 IMpower133 方案治疗:第 1 天给予阿替利珠单抗(1200mg/体),第 1 天和第 3 天给予 VP-16(50mg/m ),第 1 天给予 CBDCA(300mg/m )。第 1 天 CBDCA 给药完成后 1 小时进行 4 小时透析,第 3 天 VP-16 给药完成后 2 小时进行 4 小时透析。两名患者均获得部分缓解,在接受四周期三联治疗后未出现不可控的不良事件,继续接受阿替利珠单抗维持治疗。通过调整剂量、药物顺序和透析时机,IMpower133 方案可能对接受透析的患者是耐受且有效的。

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