Department of Endocrinology, University Hospital of Brest, Boulevard Tanguy Prigent, 29609, Brest Cedex, France.
EA GETBO 3878, University Hospital of Brest, Brest Cedex, France.
Cancer Immunol Immunother. 2021 Jul;70(7):2023-2033. doi: 10.1007/s00262-020-02802-6. Epub 2021 Jan 9.
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.
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).
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.
This study suggested that TD induced by Nivolumab appears to be an independent predictive factor of survival, irrespective of TD severity and subtype.
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。
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)。
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。
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。