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广泛期小细胞肺癌患者接受化疗时 Trilaciclib 的真实世界结局。

Real-World Outcomes of Trilaciclib Among Patients with Extensive-Stage Small Cell Lung Cancer Receiving Chemotherapy.

机构信息

Blue Ridge Cancer Centers/US Oncology Research, Blacksburg, VA, USA.

Florida Cancer Specialists & Research Institute, Fort Myers, FL, USA.

出版信息

Adv Ther. 2023 Oct;40(10):4189-4215. doi: 10.1007/s12325-023-02601-2. Epub 2023 Jul 25.

Abstract

INTRODUCTION

Trilaciclib was recently approved in the USA for reducing chemotherapy-induced myelosuppression (CIM) among adults with extensive-stage small cell lung cancer (ES-SCLC) when administered prior to chemotherapy. There is limited understanding of real-world outcomes of trilaciclib.

METHODS

A comprehensive literature review was conducted using a keyword search in the MEDLINE, Embase, and conference abstracts. Additional studies were identified through communications with the authors of relevant studies. Published and unpublished real-world studies of trilaciclib- and comparable non-trilaciclib-treated patients with ES-SCLC were included. Evidence on myelosuppressive hematologic adverse events (HAEs), cytopenia-related healthcare utilization, and other reported outcomes (e.g., hospitalizations, dose reduction, and treatment delay) were synthesized. If feasible, outcomes were compared qualitatively between the trilaciclib and historical reference groups, and between first-line trilaciclib initiators and the overall trilaciclib population. Weighted averages were estimated for selected outcomes using sample size as the weight.

RESULTS

The literature search identified five unique studies based on eight records-two included trilaciclib only, two non-trilaciclib only, and one both. In trilaciclib cohorts, the weighted average prevalence of grade ≥ 3 myelosuppressive HAEs in ≥ 1 lineage, ≥ 2 lineages, and all three lineages was 40.5%, 14.5%, and 7.5%, respectively. All rates were numerically lower compared to the historical non-trilaciclib cohorts (58.8%, 28.0%, 13.0% respectively). Cytopenia-related healthcare utilization was also lower in the trilaciclib cohorts. In general, first-line trilaciclib initiators had numerically lower myelosuppressive HAEs and cytopenia-related healthcare utilization than the overall trilaciclib patients.

CONCLUSIONS

The existing evidence suggests that trilaciclib may reduce single and multilineage grade ≥ 3 myelosuppressive HAEs and cytopenia-related healthcare utilization among patients with ES-SCLC in the real world. It is a promising new treatment for CIM prevention in ES-SCLC and may bring greater benefits to first-line trilaciclib initiators. Future studies are recommended to further evaluate the real-world effectiveness of trilaciclib.

摘要

简介

特立昔单抗最近在美国获批用于广泛期小细胞肺癌(ES-SCLC)成人患者,在化疗前使用该药可降低化疗引起的骨髓抑制(CIM)。目前对于特立昔单抗的真实世界结局了解有限。

方法

采用关键词检索在 MEDLINE、Embase 和会议摘要中进行全面的文献检索。通过与相关研究作者的交流确定了其他研究。纳入了特立昔单抗和可比非特立昔单抗治疗的 ES-SCLC 患者的已发表和未发表的真实世界研究。综合评估骨髓抑制性血液学不良事件(HAE)、与细胞减少症相关的医疗保健利用情况以及其他报告的结局(例如住院、剂量减少和治疗延迟)。如果可行,在特立昔单抗组和历史参考组之间以及一线特立昔单抗起始者和总体特立昔单抗人群之间对结局进行定性比较。使用样本量作为权重,对选定结局估计加权平均值。

结果

文献检索确定了基于 8 条记录的 5 项独特研究-2 项仅包括特立昔单抗,2 项仅包括非特立昔单抗,1 项同时包括特立昔单抗和非特立昔单抗。在特立昔单抗队列中,≥1 谱系、≥2 谱系和所有 3 个谱系的重度骨髓抑制性 HAE 的加权平均发生率分别为 40.5%、14.5%和 7.5%。与历史上非特立昔单抗队列相比(分别为 58.8%、28.0%、13.0%),所有这些比率均呈数值性降低。特立昔单抗队列的细胞减少症相关医疗保健利用率也较低。一般而言,一线特立昔单抗起始者的骨髓抑制性 HAE 和细胞减少症相关医疗保健利用率均低于总体特立昔单抗患者。

结论

现有证据表明,特立昔单抗可能会降低真实世界中 ES-SCLC 患者的单谱系和多谱系重度骨髓抑制性 HAE 和与细胞减少症相关的医疗保健利用率。它是预防 ES-SCLC 中 CIM 的一种很有前途的新治疗方法,可能会给一线特立昔单抗起始者带来更大的获益。建议开展未来的研究,进一步评估特立昔单抗的真实世界疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7a/10499684/97a72d35ef9f/12325_2023_2601_Fig1_HTML.jpg

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