铂类化疗失败后转移性非小细胞肺癌患者的临床试验和现实结果。

Yu Yang Soon MBBS , Wesley Furnback BA , Jin Kim MS , Po-Ya Chuang MHA , Gordon Chavez BA , Christina Proescholdt MD , Cloe Ying Chee Koh MS
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引用次数: 0

摘要

引言:进行了一项文献综述,以确定IV期NSCLC患者的临床试验和现实世界研究,这些患者在接受铂类化疗后或之后取得了进展。方法:使用EMBASE和MEDLINE数据库搜索2017年9月28日至2021年9月27日期间发表的英语研究。如果研究(1)是对IV期NSCLC患者的一种或多种治疗方案的临床试验或现实世界分析,这些患者在铂类化疗中或之后取得了进展,(2)包含包括疗效、有效性或安全性在内的终点,以及(3)包括45名或更多患者,则将其纳入综述。结果:总共收录了15篇出版物(9项独特的试验和3项真实世界的研究)。样本量为49至1253名患者。在九项临床试验中的八项试验中,至少有一项治疗组的总有效率≥15%。在临床试验中,中位无进展生存期(PFS)和总生存期分别为1.9至5.2个月和5.4至15.4个月,在现实世界研究中分别为4.4至6.8个月和8.3至18.0个月。在报告中位PFS的研究中,11项临床试验中有8项和两项真实世界研究报告了中位PFS大于或等于3个月。在所有纳入的研究中,因不良事件导致的停药率从1.9%到18%不等。结论:IV期NSCLC患者在接受含铂化疗后,在治疗过程中反应有限,不良事件负担较高。在这种情况下,对额外、有效和可耐受的治疗方案的需求仍然迫切未得到满足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Clinical Trial and Real-World Outcomes of Patients With Metastatic NSCLC in the Post-Platinum–Based Chemotherapy Failure Setting

Introduction

A literature review was undertaken to identify clinical trials and real-world studies of patients with stage IV NSCLC who had progressed on or after treatment with platinum-based chemotherapy.

Methods

The EMBASE and MEDLINE databases were used to search for English-language studies published between September 28, 2017, and September 28, 2021. Studies were included in the review if they (1) were clinical trials or real-world analyses of one or more treatment regimens for patients with stage IV NSCLC who had progressed on or after treatment with platinum-based chemotherapy, (2) contained an end point including efficacy, effectiveness, or safety, and (3) included 45 or more patients.

Results

In total, there were 15 publications (nine unique trials and three real-world studies) included. Sample size ranged from 49 to 1253 patients. At least one treatment arm in eight of the nine clinical trials reported an overall response rate of ≥15%. Median progression-free survival (PFS) and overall survival ranged from 1.9 to 5.2 months and 5.4 to 15.4 months in clinical trials and 4.4 to 6.8 months and 8.3 to 18.0 months in real-world studies, respectively. Within studies reporting median PFS, a median PFS of more than or equal to 3 months was reported in eight of 11 clinical trials and both real-world studies. Discontinuation due to adverse events ranged from 1.9% to 18% across all included studies.

Conclusions

Patients with stage IV NSCLC had limited response and a high burden of adverse events during treatment after progression on platinum-containing chemotherapy. There remains a pressing unmet need for additional, effective, and tolerable treatment options in this setting.

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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
145
审稿时长
19 weeks
期刊最新文献
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