胸膜间皮瘤患者的实际治疗效果:多地点回顾性队列研究

IF 1.4 4区 医学 Q4 ONCOLOGY Asia-Pacific journal of clinical oncology Pub Date : 2024-06-21 DOI:10.1111/ajco.14098
Kar Ven Cavan Chow, Cassie Turner, Brett Hughes, Zarnie Lwin, Bryan Chan
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引用次数: 0

摘要

目的评估免疫疗法时代胸膜间皮瘤(PM)患者的实际治疗模式和结果。方法这项回顾性审计纳入了2017年1月至2023年7月在澳大利亚昆士兰州三个三级转诊中心确诊的PM患者。记录了患者和治疗特征及结果。数据采用描述性统计和卡普兰-梅耶生存法进行分析:84%为男性,中位年龄为75岁(70-79岁不等),85%的基线东方集团合作组为0-1。亚型包括54%的上皮样癌、17%的双相型癌、12%的肉瘤样癌和17%的不明/未知型癌。57/90的患者(63%)接受了一线治疗,33/90的患者(37%)接受了最佳支持治疗(BSC)。化疗的使用率最高(63%),但自2021年7月ipilimumab/nivolumab获得澳大利亚药品福利计划报销以来,一线免疫疗法的使用率更高。所有患者的12个月总生存期(OS)和无进展生存期分别为53%(95%置信区间[CI]:43-65)和25%(95% CI:15-40)。免疫疗法、化疗和 BSC 的 12 个月 OS 分别为 72%、64% 和 29%。化疗和免疫治疗的生存率无明显差异(危险比 1.28,95% CI:0.65-2.5,P = 0.5)。我们仍然需要更好的治疗方案,尤其是一线治疗方案。参加临床试验对于改善这种使人衰弱的疾病的预后至关重要。
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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Real-world outcomes for patients with pleural mesothelioma: A multisite retrospective cohort study

Aim

To evaluate the real-world treatment patterns and outcomes for patients with pleural mesothelioma (PM) in the era of immunotherapy.

Methods

This retrospective audit included patients with PM diagnosed within three tertiary referral centers in Queensland, Australia from January 2017 to July 2023. Patient and treatment characteristics and outcomes were recorded. Data was analyzed using descriptive statistics and the Kaplan-Meier survival method.

Results

A total of 90 patients were included: 84% were male, the median age was 75 years (range 70–79) and 85% had baseline Eastern Group Cooperative Group of 0–1. Subtypes included 54% epithelioid, 17% biphasic, 12% sarcomatoid, and 17% unspecified/unknown. First-line treatment was received by 57/90 patients (63%) and 33/90 patients (37%) received the best supportive care (BSC). Chemotherapy was most used (63%) overall, but first-line immunotherapy was more commonly used since ipilimumab/nivolumab was reimbursed by the Australian Pharmaceutical Benefits Scheme in July 2021. After first-line treatment, only 40% received second-line treatment and 60% received BSC.

12-month overall survival (OS) and progression-free survival for all patients were 53% (95% confidence interval [CI]: 43–65) and 25% (95% CI 15–40) respectively. 12-month OS was 72%, 64%, and 29% for immunotherapy, chemotherapy, and BSC, respectively. There was no significant difference in survival between chemotherapy and immunotherapy (hazard ratio 1.28, 95% CI: 0.65–2.5, p = 0.5).

Conclusion

In our unselected real-world cohort, both chemotherapy and immunotherapy are active against PM, but the prognosis remains guarded. There remains a need for better treatment options, especially in the first-line setting. Enrolment in clinical trials is crucial to improving outcomes in this debilitating disease.

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来源期刊
CiteScore
3.40
自引率
0.00%
发文量
175
审稿时长
6-12 weeks
期刊介绍: Asia–Pacific Journal of Clinical Oncology is a multidisciplinary journal of oncology that aims to be a forum for facilitating collaboration and exchanging information on what is happening in different countries of the Asia–Pacific region in relation to cancer treatment and care. The Journal is ideally positioned to receive publications that deal with diversity in cancer behavior, management and outcome related to ethnic, cultural, economic and other differences between populations. In addition to original articles, the Journal publishes reviews, editorials, letters to the Editor and short communications. Case reports are generally not considered for publication, only exceptional papers in which Editors find extraordinary oncological value may be considered for review. The Journal encourages clinical studies, particularly prospectively designed clinical trials.
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