Guo Ge, Jing Zihan, Dou Wenrui, Wang Guiqin, Dang JunJie, Li Yajie, Wang Ruqiong, Zhang Huan, Sun Jing, Shang Lihua
Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.
Department of Clinical Medicine, Harbin Medical University, Harbin, China.
Front Immunol. 2024 Dec 23;15:1495460. doi: 10.3389/fimmu.2024.1495460. eCollection 2024.
The relationship between immune-related thyroid dysfunction (irTD) and survival rates in cancer patients remains unclear. Furthermore, the impact of variations in immunotherapy line numbers and pathological types among lung cancer patients on this relationship has not been fully elucidated. This study aims to evaluate the potential of irTD as a prognostic marker for immunotherapy in Chinese patients with lung cancer.
A retrospective analysis was conducted on data collected from patients with locally advanced or metastatic lung cancer who received immune checkpoint inhibitor treatment at the Harbin Medical University Cancer Hospital. The study period spanned from December 1, 2016, to November 30, 2023. The primary endpoints were progression-free survival (PFS) and overall survival (OS), while the objective response rate served as the secondary endpoint.
Among the 361 patients in this study, 42.7% developed irTD. Significant differences were observed between the groups with and without irTD regarding inflammatory indices, thyroid-stimulating hormone levels, and thyroid autoantibody positivity (P < 0.05). Patients with irTD demonstrated longer OS (32.5 vs. 22 months, HR: 0.65, 95% CI: 0.49-0.88; P = 0.005). For NSCLC patients, OS was significantly prolonged in those with irTD (40.8 vs. 27.2 months, HR: 0.68, 95% CI: 0.48-0.96; P = 0.028). Similarly, SCLC patients who developed irTD exhibited longer OS (27.9 vs. 13.8 months, HR: 0.51, 95% CI: 0.29-0.90; P = 0.022). Notably, irTD was observed exclusively in patients receiving immunotherapy in the second or later lines, showing a significant association with extended OS (40.8 vs. 19.4 months, HR: 0.56, 95% CI: 0.35-0.88; P = 0.012), while the presence of irTD during first-line immunotherapy did not confer a benefit to patients (32.4 vs 24.5 months, HR: 0.74, 95% CI: 0.50-1.10; P = 0.134). The effects of different irTD types, severities, or clinical symptoms on PFS and OS did not differ significantly (P > 0.05).
irTD demonstrates potential as a predictive marker for long-term survival benefits in Chinese patients with lung cancer. However, our exploratory analysis indicates that this association was exclusively observed in individuals receiving immunotherapy as a second-line or subsequent treatment.
免疫相关甲状腺功能障碍(irTD)与癌症患者生存率之间的关系尚不清楚。此外,肺癌患者免疫治疗线数和病理类型的变化对这种关系的影响尚未完全阐明。本研究旨在评估irTD作为中国肺癌患者免疫治疗预后标志物的潜力。
对哈尔滨医科大学附属肿瘤医院接受免疫检查点抑制剂治疗的局部晚期或转移性肺癌患者收集的数据进行回顾性分析。研究期间为2016年12月1日至2023年11月30日。主要终点为无进展生存期(PFS)和总生存期(OS),客观缓解率作为次要终点。
本研究的361例患者中,42.7%发生了irTD。有和没有irTD的组在炎症指标、促甲状腺激素水平和甲状腺自身抗体阳性方面存在显著差异(P<0.05)。发生irTD的患者表现出更长的OS(32.5个月对22个月,HR:0.65,95%CI:0.49-0.88;P=0.005)。对于非小细胞肺癌(NSCLC)患者,发生irTD的患者OS显著延长(40.8个月对27.2个月,HR:0.68,95%CI:0.48-0.96;P=0.028)。同样,发生irTD的小细胞肺癌(SCLC)患者表现出更长的OS(27.9个月对13.8个月,HR:0.51,95%CI:0.29-0.90;P=0.022)。值得注意的是,irTD仅在接受二线或更晚线免疫治疗的患者中观察到,与延长的OS显著相关(40.8个月对19.4个月,HR:0.56,95%CI:0.35-0.88;P=0.012),而一线免疫治疗期间出现irTD对患者没有益处(32.4个月对24.5个月,HR:0.74,95%CI:0.50-1.10;P=0.134)。不同类型、严重程度或临床症状的irTD对PFS和OS的影响无显著差异(P>0.05)。
irTD显示出作为中国肺癌患者长期生存获益预测标志物的潜力。然而,我们的探索性分析表明,这种关联仅在接受二线或后续免疫治疗的个体中观察到。