COVID-19疫苗接种与晚期非小细胞肺癌患者抗pd -(L)1免疫治疗疗效增强相关:一项现实世界研究

IF 3.1 2区医学 Q3 IMMUNOLOGY

Infectious Agents and Cancer Pub Date : 2023-09-07 DOI:10.1186/s13027-023-00526-7

Yunfei Qian, Zhuxian Zhu, Yin-Yuan Mo, Ziqiang Zhang

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引用次数: 0

摘要

背景:2019冠状病毒病(COVID-19)疫苗在结束大流行方面发挥了重要作用。然而，COVID-19疫苗对非小细胞肺癌(NSCLC)患者免疫治疗效果的影响尚不清楚。目的:本研究的目的是探讨COVID-19疫苗是否影响免疫检查点抑制剂(ICIs)在NSCLC患者中的疗效。方法:回顾性分析104例接受ici治疗的III-IV期NSCLC患者的生存资料，这些患者接受了COVID-19疫苗接种(n = 25)或未接种疫苗(n = 79)。评估了潜在的危险因素，特别是COVID-19疫苗接种在这些患者的ICIs疗效中的作用。结果:与未接种疫苗组相比，接种疫苗组的ORR(28.0%比11.39%，p = 0.05)和DCR(88.0%比54.43%，p = 0.005)显著提高。在长期生存获益方面，COVID-19疫苗对接受ICIs治疗的NSCLC患者的PFS (HR = 0.16, p = 0.021)和OS (HR = 0.168, p = 0.019)均有深远影响。结论:COVID-19疫苗可增强III-IV期非小细胞肺癌患者的抗pd -1免疫治疗效果，提示COVID-19疫苗可能为非小细胞肺癌患者提供额外的益处。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

COVID-19 vaccination is associated with enhanced efficacy of anti-PD-(L)1 immunotherapy in advanced NSCLC patients: a real-world study.

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COVID-19 vaccination is associated with enhanced efficacy of anti-PD-(L)1 immunotherapy in advanced NSCLC patients: a real-world study.

Background: Coronavirus disease 2019 (COVID-19) vaccine has played a major role in ending the pandemic. However, little is known about the influence of COVID-19 vaccine on the efficacy of immunotherapy in patients with non-small cell lung cancer (NSCLC).

Objectives: The goal of this study is to explore whether COVID-19 vaccine impacts the efficacy of immune checkpoint inhibitors (ICIs) in NSCLC patients.

Methods: We retrospectively analyzed the survival data of ICI-treated 104 patients with stage III-IV NSCLC, who either received COVID-19 vaccination (n = 25) or no vaccination (n = 79). The potential risk factors, in particular roles of COVID-19 vaccination in the efficacy of ICIs in these patients, were evaluated.

Results: Our results showed significantly improved ORR (28.0% vs. 11.39%, p = 0.05) and DCR (88.0% vs. 54.43%, p = 0.005) in the COVID-19 vaccinated group compared with the non-vaccinated group. Regarding the long-term survival benefits, COVID-19 vaccine showed profound influence both on the PFS (HR = 0.16, p = 0.021) and OS (HR = 0.168, p = 0.019) in patients with NSCLC under ICIs treatment. The PFS (p < 0.001) or OS (p < 0.001) was significantly improved in the COVID-19 vaccinated group, compared with the non-vaccinated group. Moreover, CD4 T cell (p = 0.047) level was higher in the COVID-19 vaccinated group than in the non-vaccinated group.

Conclusions: COVID-19 vaccination enhances anti-PD-1 immunotherapy efficacy in patients with stage III-IV NSCLC, suggesting that COVID-19 vaccination may provide additional benefit to NSCLC patients.

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来源期刊

Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY

CiteScore

5.80

自引率

2.70%

发文量

期刊介绍： Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.