Yao Xu, Qiuhong Zhang, Jie Gao, Shiyuan Yao, Chan Tian, Tuo He, Ming Zhang, Hu Shan, Jie Shi, Bo Yuan, Lei Wang, Xia Yang
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High-sensitivity troponin I (hs-TnI), α-hydroxybutyrate dehydrogenase (HBDH), creatine kinase (CK), creatine kinase MB (CK-MB), and coagulation indices exhibited significant changes (p < .05), while the cardiac ultrasound result remained unchanged. In subgroup analysis, the severe group demonstrated lower overall survival (OS) (43 months vs. 56 months) (p = .008) and progression-free survival (PFS) (15 months vs. 20 months, p < .001) compared to the non-severe group. Meanwhile, the severe PAD/AoD ratio progression served as independent predictors of prognosis in lung cancer patients receiving ICI treatment, but immune-related pneumonia(CIP) did not significantly influence the PAD/AoD ratio progression (p > .999). Therefore, in lung cancer patients receiving ICIs, pulmonary vascular involvement can occur within the initial 3 months and needs to be monitored with chest CT and echocardiography.</p>","PeriodicalId":180,"journal":{"name":"International Journal of Cancer","volume":" ","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of immune checkpoint inhibitors on the pulmonary circulation in lung cancer patients.\",\"authors\":\"Yao Xu, Qiuhong Zhang, Jie Gao, Shiyuan Yao, Chan Tian, Tuo He, Ming Zhang, Hu Shan, Jie Shi, Bo Yuan, Lei Wang, Xia Yang\",\"doi\":\"10.1002/ijc.70110\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Immune checkpoint inhibitors (ICIs) are effective anti-tumor agents, but new immune-related side effects (irAEs) are emerging. 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引用次数: 0
摘要
免疫检查点抑制剂(ICIs)是一种有效的抗肿瘤药物,但新的免疫相关副作用(irAEs)正在出现。本回顾性队列研究调查了461例接受ICIs治疗2年以上的肺癌患者,通过胸部计算机断层扫描(CT)分析治疗后基线、治疗后3个月、6个月、1年和2年肺动脉直径(PAD)、主动脉直径(AoD)和肺动脉/主动脉直径(PAD/AoD)比的变化。PAD由25.19 mm增加到26.33 mm (p .999)。因此,在接受ICIs的肺癌患者中,肺血管受累可在最初3个月内发生,需要通过胸部CT和超声心动图进行监测。
Effects of immune checkpoint inhibitors on the pulmonary circulation in lung cancer patients.
Immune checkpoint inhibitors (ICIs) are effective anti-tumor agents, but new immune-related side effects (irAEs) are emerging. This retrospective cohort study investigated 461 lung cancer patients treated with ICIs over 2 years, analyzing changes in pulmonary artery diameter (PAD), aortic diameter (AoD), and the pulmonary artery/aortic diameter (PAD/AoD) ratio through chest computed tomography (CT) at baseline, 3 months, 6 months, 1 year, and 2 years post-treatment. The PAD increased from 25.19 to 26.33 mm (p < .001) and the PAD/AoD ratio increased from 0.70 to 0.73 (p < .001) during ICI treatment over a 2-year follow-up period, as early as within the first 3 months. High-sensitivity troponin I (hs-TnI), α-hydroxybutyrate dehydrogenase (HBDH), creatine kinase (CK), creatine kinase MB (CK-MB), and coagulation indices exhibited significant changes (p < .05), while the cardiac ultrasound result remained unchanged. In subgroup analysis, the severe group demonstrated lower overall survival (OS) (43 months vs. 56 months) (p = .008) and progression-free survival (PFS) (15 months vs. 20 months, p < .001) compared to the non-severe group. Meanwhile, the severe PAD/AoD ratio progression served as independent predictors of prognosis in lung cancer patients receiving ICI treatment, but immune-related pneumonia(CIP) did not significantly influence the PAD/AoD ratio progression (p > .999). Therefore, in lung cancer patients receiving ICIs, pulmonary vascular involvement can occur within the initial 3 months and needs to be monitored with chest CT and echocardiography.
期刊介绍:
The International Journal of Cancer (IJC) is the official journal of the Union for International Cancer Control—UICC; it appears twice a month. IJC invites submission of manuscripts under a broad scope of topics relevant to experimental and clinical cancer research and publishes original Research Articles and Short Reports under the following categories:
-Cancer Epidemiology-
Cancer Genetics and Epigenetics-
Infectious Causes of Cancer-
Innovative Tools and Methods-
Molecular Cancer Biology-
Tumor Immunology and Microenvironment-
Tumor Markers and Signatures-
Cancer Therapy and Prevention