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口服地塞米松联合多西他赛加雷莫芦单抗治疗经治肺癌的疗效回顾性分析。

A Retrospective Analysis of the Efficacy of Oral Dexamethasone in Combination With Docetaxel Plus Ramucirumab Therapy for Previously Treated Lung Cancer.

机构信息

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

Department of Respiratory Medicine, JA Onomichi General Hospital, Onomichi, Japan.

出版信息

Cancer Control. 2024 Jan-Dec;31:10732748241274615. doi: 10.1177/10732748241274615.

Abstract

INTRODUCTION

Docetaxel plus ramucirumab (DTX + RAM) therapy is a standard treatment for previously treated lung cancer, but many adverse events have been reported. This retrospective study was conducted to examine if the side effects of DTX + RAM therapy can be minimized by the combined use of oral dexamethasone (DEX), and to assess the therapeutic effect of DTX + RAM in patients with recurrent lung cancer.

METHODS

Forty patients with relapsed non-small cell lung cancer who underwent DTX + RAM therapy were divided into two groups based on the concomitant use of oral DEX, and the therapeutic effects and toxicities in the two groups were compared.

RESULTS

The objective response rate (ORR) was significantly better in the DEX group ( = 0.0203). The median progression-free survival (PFS) was 5.20 months vs 2.87 months ( = 0.064) in the DEX and non-DEX groups, respectively. However, the median overall survival (OS) was significantly better in the DEX group (15.17 months vs 7.37 months, = 0.0317). The frequency of fluid retention within six months of the start of treatment was 10.0% vs 42.5% in the DEX and non-DEX groups, respectively, with the fluid retention rate being significantly higher in the non-DEX group ( = 0.039). Concomitant use of oral DEX during DTX + RAM therapy may facilitate the long-term continuation of treatment and contribute to OS prolongation.

摘要

简介

多西他赛联合雷莫芦单抗(DTX+RAM)治疗方案是治疗既往治疗的肺癌的标准治疗方法,但有许多不良反应的报道。本回顾性研究旨在探讨口服地塞米松(DEX)联合使用是否可以减轻 DTX+RAM 治疗的副作用,并评估 DTX+RAM 在复发性肺癌患者中的治疗效果。

方法

40 名接受 DTX+RAM 治疗的复发性非小细胞肺癌患者根据是否同时使用口服 DEX 分为两组,比较两组的治疗效果和毒性。

结果

DEX 组的客观缓解率(ORR)显著更好( = 0.0203)。DEX 组和非 DEX 组的中位无进展生存期(PFS)分别为 5.20 个月和 2.87 个月( = 0.064)。然而,DEX 组的中位总生存期(OS)显著更长(15.17 个月比 7.37 个月, = 0.0317)。治疗开始后 6 个月内发生液体潴留的频率分别为 DEX 组 10.0%和非 DEX 组 42.5%,非 DEX 组的液体潴留率显著更高( = 0.039)。在 DTX+RAM 治疗期间同时使用口服 DEX 可能有助于长期持续治疗,并延长 OS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fab/11316262/7e3c62b07108/10.1177_10732748241274615-fig1.jpg

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