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一项每周紫杉醇 Nab 联合卡铂加胸部放疗治疗非小细胞肺癌的 I 期临床试验。

A Phase I Trial of Weekly Nab-paclitaxel Plus Carboplatin With Thoracic Radiotherapy for Non-small Cell Lung Cancer.

机构信息

Department of Respiratory Medicine and Allergology, Kochi University, Kochi Medical School, Kochi, Japan

Department of Respiratory Medicine and Allergology, Kochi University, Kochi Medical School, Kochi, Japan.

出版信息

In Vivo. 2024 Jan-Feb;38(1):259-263. doi: 10.21873/invivo.13433.

DOI:10.21873/invivo.13433
PMID:38148041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10756434/
Abstract

BACKGROUND/AIM: This study aimed to evaluate the safety and recommended dose of nab-paclitaxel in combination with carboplatin and thoracic radiotherapy for locally advanced non-small cell lung cancer (NSCLC).

PATIENTS AND METHODS

Nab-paclitaxel was administered weekly with escalating doses, combined with carboplatin area under the curve (AUC) 2 and concurrent standard thoracic radiotherapy. Escalating doses of nab-paclitaxel were as follows: level 0, 30 mg/m; level 1, 35 mg/m; level 2, 40 mg/m; level 3, 45 mg/m Results: Twelve patients were enrolled and received the treatment according to the protocol; seven patients (58%) had squamous cell carcinoma and all cases had stage III disease. At level 1, none of the three patients experienced dose limiting toxicity (DLT). At level 2, one of the first three patients experienced a fatal DLT of bronchopulmonary hemorrhage. None of the three more additional patients experienced DLT. At level 3, two of the three patients experienced a DLT of grade 3 febrile neutropenia and grade 4 neutropenia, respectively. Consolidation chemotherapy was provided to 10 of 12 patients. Radiation pneumonitis developed in five of 12 patients (42%). Eight patients (66.7%) showed partial response, and four (33.3%) showed stable disease. For the above reasons, level 2 (40 mg/m) was considered the recommended dose in this study.

CONCLUSION

Concurrent chemoradiotherapy with weekly nab-paclitaxel (40 mg/m) and carboplatin (AUC 2) is a feasible and well-tolerated regimen in patients with previously untreated locally advanced NSCLC. A phase II trial with this regimen is warranted.

摘要

背景/目的:本研究旨在评估纳武利尤单抗联合卡铂和胸部放疗治疗局部晚期非小细胞肺癌(NSCLC)的安全性和推荐剂量。

方法

纳武利尤单抗每周给药,剂量递增,联合卡铂曲线下面积(AUC)2 和同期标准胸部放疗。纳武利尤单抗的递增剂量如下:0 级,30mg/m;1 级,35mg/m;2 级,40mg/m;3 级,45mg/m。

结果

12 例患者按方案接受治疗;7 例(58%)患者患有鳞状细胞癌,所有病例均为 III 期疾病。在 1 级时,3 例患者均未出现剂量限制毒性(DLT)。在 2 级时,前 3 例患者中有 1 例出现致命的 DLT-支气管肺出血。另外 3 例患者均未出现 DLT。在 3 级时,3 例患者中有 2 例发生 3 级发热性中性粒细胞减少症和 4 级中性粒细胞减少症的 DLT。12 例患者中有 10 例接受了巩固化疗。12 例患者中有 5 例发生放射性肺炎(42%)。8 例(66.7%)患者出现部分缓解,4 例(33.3%)患者疾病稳定。基于上述原因,本研究中 40mg/m 被认为是推荐剂量。

结论

每周纳武利尤单抗(40mg/m)联合卡铂(AUC 2)同期放化疗是治疗未经治疗的局部晚期 NSCLC 患者的一种可行且耐受良好的方案。有必要开展该方案的 II 期临床试验。