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免疫检查点抑制剂引起的甲状腺功能障碍与非小细胞肺癌患者无进展生存期和总生存期的改善相关:一项原始队列研究。

Thyroid dysfunction induced by immune checkpoint inhibitors is associated with a better progression-free survival and overall survival in non-small cell lung cancer: an original cohort study.

机构信息

Department of Endocrinology, University Hospital of Brest, Boulevard Tanguy Prigent, 29609, Brest Cedex, France.

EA GETBO 3878, University Hospital of Brest, Brest Cedex, France.

出版信息

Cancer Immunol Immunother. 2021 Jul;70(7):2023-2033. doi: 10.1007/s00262-020-02802-6. Epub 2021 Jan 9.

Abstract

BACKGROUND

The objective of this study was to investigate the association between the onset of TD and treatment efficacy in NSCLC patients who initiated anti-PD-1 blockade (Nivolumab) and to assess the impact of TD severity and subtype on nivolumab efficacy.

MATERIALS AND METHODS

This study was performed at a referral oncology center between July 20, 2015 and June 30, 2018. Patients with histologically confirmed stage IIIB/IV NSCLC in progression after one or two lines of treatment and who initiated Nivolumab were included. Thyroid function (TSH ± fT4, fT3) was monitored and patients were classified according to TD status [TD(+) versus TD(-)], severity [moderate thyroid dysfunction: TSH level between 0.1 and 0.4 or 4.0 and 10 mIU/L and severe thyroid dysfunction: TSH ≤ 0.1 or ≥ 10mUI/L) and subtype (isolated hypothyroidism, isolated hyperthyroidism and hyperthyroidism then hypothyroidism)]. Clinical endpoints were overall survival (OS) and progression-free survival (PFS).

RESULTS

Among 194 eligible patients, 134 patients (median age, 63 yo; 70.1% male) were included. Forty (29.9%) patients were classified in TD(+) and had a longer OS of 29.8 months (95% CI 18.8-NR) versus 8.1 months (95% CI 5.5-11.5) in TD(-) group (p < 0.001). PFS was also longer (8.7 months (95% CI 5.3-15.1) in TD(+) versus 1.7 months (95% CI 1.6-1.9) in TD(-) group (p < 0.001). In Cox proportional hazards analysis, TD remained an independent predictive factor of OS/PFS. Severity and subtype of TD were not correlated with OS/PFS.

CONCLUSIONS

This study suggested that TD induced by Nivolumab appears to be an independent predictive factor of survival, irrespective of TD severity and subtype.

摘要

背景

本研究旨在探讨 NSCLC 患者起始抗 PD-1 阻断(Nivolumab)后 TD 的发生与治疗疗效之间的关系,并评估 TD 严重程度和亚型对 Nivolumab 疗效的影响。

材料和方法

本研究于 2015 年 7 月 20 日至 2018 年 6 月 30 日在一家肿瘤转诊中心进行。纳入标准为:经组织学证实的 IIIB/IV 期 NSCLC 患者,在一线或二线治疗后进展,且开始接受 Nivolumab 治疗。监测甲状腺功能(TSH ± fT4、fT3),根据 TD 状态[TD(+)与 TD(-)]、严重程度[中度甲状腺功能障碍:TSH 水平在 0.1 至 0.4 或 4.0 至 10 mIU/L 之间和重度甲状腺功能障碍:TSH≤0.1 或≥10mUI/L]和亚型(孤立性甲状腺功能减退、孤立性甲状腺功能亢进和甲状腺功能亢进后甲状腺功能减退)对患者进行分类。临床终点为总生存期(OS)和无进展生存期(PFS)。

结果

在 194 名符合条件的患者中,纳入了 134 名患者(中位年龄 63 岁;70.1%为男性)。40 名(29.9%)患者被归类为 TD(+),其 OS 为 29.8 个月(95%CI 18.8-NR),而 TD(-)组为 8.1 个月(95%CI 5.5-11.5)(p<0.001)。PFS 也更长(TD(+)组为 8.7 个月(95%CI 5.3-15.1),而 TD(-)组为 1.7 个月(95%CI 1.6-1.9)(p<0.001)。在 Cox 比例风险分析中,TD 仍然是 OS/PFS 的独立预测因素。TD 的严重程度和亚型与 OS/PFS 无相关性。

结论

本研究表明,Nivolumab 诱导的 TD 似乎是生存的独立预测因素,与 TD 的严重程度和亚型无关。

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