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多西他赛联合雷莫芦单抗联合预防性应用聚乙二醇化粒细胞集落刺激因子治疗预处理的非小细胞肺癌:一项 II 期研究。

Administration of docetaxel plus ramucirumab with primary prophylactic pegylated-granulocyte colony-stimulating factor for pretreated non-small cell lung cancer: a phase II study.

机构信息

Innovative Medical Research Center, Gunma University Hospital, Maebashi, Gunma, 371-8511, Japan.

Department of Respiratory Medicine, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.

出版信息

Support Care Cancer. 2020 Oct;28(10):4825-4831. doi: 10.1007/s00520-020-05317-z. Epub 2020 Jan 25.

Abstract

PURPOSE

Although docetaxel plus ramucirumab has shown superior treatment efficacy over docetaxel monotherapy for patients with non-small cell lung cancer (NSCLC), the high rate of febrile neutropenia (FN) presents a clinical problem. This study aimed to validate the primary prophylactic use of pegfilgrastim with docetaxel and ramucirumab treatment in Japanese patients with NSCLC.

METHODS

Patients with NSCLC with progression after at least one round of chemotherapy were enrolled and administered docetaxel (60 mg/m) plus ramucirumab (10 mg/kg) intravenously on day 1, followed by pegylated-granulocyte colony-stimulating factor (3.6 mg) on day 2 of a 21-day treatment cycle. The primary study endpoint was the percentage of patients who developed FN. Secondary endpoints included overall survival, progression-free survival, overall response rate, and safety.

RESULTS

Overall, 20 patients (15 men and 5 women) were enrolled, of whom one developed FN, resulting in an overall FN rate of 5%. The response and disease control rates were 40% and 85%, respectively. The median progression-free survival was 6.6 (95% confidence interval [CI], 0.5-NR) months. The median overall survival was 18.4 (95% CI, 2.2-11.0) months. Six patients aged over 75 years were included in this study, and although most adverse events were durable, ramucirumab-associated adverse events occurred more frequently in these patients.

CONCLUSIONS

We observed a 5% FN rate using primary prophylactic pegylated-granulocyte colony-stimulating factor with docetaxel plus ramucirumab in Japanese patients with NSCLC. While most adverse events were durable, elderly patients should be closely monitored.

摘要

目的

多西他赛联合雷莫芦单抗治疗非小细胞肺癌(NSCLC)患者的疗效优于多西他赛单药治疗,但发热性中性粒细胞减少(FN)的发生率较高,这是一个临床问题。本研究旨在验证培非格司亭联合多西他赛和雷莫芦单抗治疗日本 NSCLC 患者的主要预防作用。

方法

纳入至少接受过一轮化疗后进展的 NSCLC 患者,并给予多西他赛(60mg/m)加雷莫芦单抗(10mg/kg)静脉滴注,第 1 天,随后在 21 天治疗周期的第 2 天给予聚乙二醇化粒细胞集落刺激因子(3.6mg)。主要研究终点为发生 FN 的患者比例。次要终点包括总生存期、无进展生存期、总缓解率和安全性。

结果

共有 20 例患者(15 例男性和 5 例女性)入组,其中 1 例发生 FN,FN 总发生率为 5%。缓解率和疾病控制率分别为 40%和 85%。中位无进展生存期为 6.6 个月(95%置信区间[CI],0.5-NR)。中位总生存期为 18.4 个月(95%CI,2.2-11.0)。本研究纳入了 6 名 75 岁以上的患者,虽然大多数不良事件持续存在,但这些患者更常发生雷莫芦单抗相关的不良事件。

结论

我们观察到在日本 NSCLC 患者中,使用多西他赛联合雷莫芦单抗进行主要预防使用培非格司亭可使 FN 发生率为 5%。虽然大多数不良事件持续存在,但应密切监测老年患者。

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