甲状腺免疫相关不良事件对接受检查点抑制剂治疗的非小细胞肺癌(NSCLC)患者临床结局的影响:一项单中心研究

0 MEDICINE, RESEARCH & EXPERIMENTAL
Šejla Cerić, Timur Cerić, Emir Sokolović, Jasmina Dalač, Dragana Miletić, Inga Marijanović, Layan Mattar, Amina Aljić, Selma Agić-Bilalagić, Amera Šadija, Miran Hadžiahmetović, Semir Bešlija
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引用次数: 0

摘要

免疫检查点抑制剂(ICIs)已经改变了非小细胞肺癌(NSCLC)的治疗前景,但与免疫相关不良事件(irAEs)相关,包括甲状腺功能障碍。本研究探讨了在萨拉热窝大学临床中心肿瘤诊所接受ICIs治疗的非小细胞肺癌患者甲状腺功能障碍的发生率和临床影响。在这项回顾性队列研究中,我们收集了50例接受icis治疗的转移性NSCLC患者的数据,这些患者要么联合化疗,要么作为程序性死亡-配体1 (PD-L1)表达≥50%的单药治疗,我们收集了人口统计学、治疗方案、甲状腺功能测试和生存结果的数据。24例(48%)患者发生甲状腺功能障碍,其中12例(24%)发展为甲状腺功能减退,4例(8%)发展为甲状腺功能亢进,8例(16%)经历从甲状腺功能亢进到甲状腺功能减退的过渡。与派姆单抗相比,阿特唑单抗治疗的患者甲状腺功能障碍发生率显著升高(P = 0.04), 87.5%的患者接受阿特唑单抗治疗。甲状腺功能减退的中位发病时间为10个周期(四分位数间距[IQR]: 5),甲状腺功能亢进的中位发病时间为6个周期(IQR: 19)。甲状腺功能障碍患者的无进展生存期(PFS)明显更长,中位PFS未达到,而无甲状腺功能障碍患者的中位PFS为14个月(95% CI: 9.68-18.32) (P = 0.038)。甲状腺功能障碍与患者的年龄或性别之间没有明显的关联。这些发现表明,甲状腺功能障碍是接受ICIs治疗的转移性NSCLC患者常见的irAE,尤其是阿特唑单抗,其发展可能与PFS的改善有关。建议定期监测甲状腺功能,以便在ICI治疗期间及时识别和管理甲状腺异常,潜在地改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of thyroid immune-related adverse events on clinical outcomes in non-small cell lung cancer (NSCLC) patients treated with checkpoint inhibitor therapy: A single center study.

Immune checkpoint inhibitors (ICIs) have transformed the treatment landscape for non-small cell lung carcinoma (NSCLC) but are associated with immune-related adverse events (irAEs), including thyroid dysfunction. This study examines the incidence and clinical impact of thyroid dysfunction in NSCLC patients receiving ICIs at the Clinic of Oncology, Clinical Center University of Sarajevo. In this retrospective cohort study of 50 patients with metastatic NSCLC treated with ICIs-either in combination with chemotherapy or as monotherapy for those with programmed death-ligand 1 (PD-L1) expression ≥ 50%-we collected data on demographics, treatment regimens, thyroid function tests, and survival outcomes. Thyroid dysfunction occurred in 24 patients (48%), with 12 (24%) developing hypothyroidism, 4 (8%) developing hyperthyroidism, and 8 (16%) experiencing a transition from hyperthyroidism to hypothyroidism. The incidence of thyroid dysfunction was significantly higher in patients treated with atezolizumab compared to pembrolizumab (P = 0.04), with 87.5% of affected patients receiving atezolizumab. The median time to onset of thyroid dysfunction was 10 cycles (interquartile range [IQR]: 5) for hypothyroidism and six cycles (IQR: 19) for hyperthyroidism. Progression-free survival (PFS) was significantly longer in patients who developed thyroid dysfunction, with the median PFS not reached, compared to a median PFS of 14 months (95% CI: 9.68-18.32) in patients without thyroid dysfunction (P = 0.038). No significant associations were found between thyroid dysfunction and patient age or gender. These findings suggest that thyroid dysfunction is a common irAE in patients with metastatic NSCLC receiving ICIs, particularly atezolizumab, and its development may be associated with improved PFS. Regular monitoring of thyroid function is recommended to promptly identify and manage thyroid abnormalities during ICI therapy, potentially improving patient outcomes.

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