Department of Clinical & Experimental Medicine, Geriatrics Unit, University of Pisa, Italy.
Department of Oncology, Unit of Oncology 1, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.
Eur J Cancer. 2020 Jul;133:66-73. doi: 10.1016/j.ejca.2020.04.023. Epub 2020 May 20.
Free triiodothyronine (FT3)/free thyroxine (FT4) ratio is an index estimating the peripheral activity of thyroid hormones. In a previous experience, we identified a prognostic role for FT3/FT4 ratio in chemorefractory patients treated with regorafenib. Therefore, we planned this post hoc analysis of the phase III CORRECT trial of regorafenib versus placebo.
Seven hundred fifty-eight out of 760 randomised patients (503 in the regorafenib and 255 in the placebo arm) were evaluable for the present analyses, based on availability of FT3 and FT4 baseline values. Co-primary objectives were to explore the predictive role of FT3/FT4 ratio in patients treated with regorafenib compared with placebo and to validate the prognostic value of FT3/FT4 ratio in the CORRECT trial.
For patients randomised to regorafenib, median overall survival (OS) was 4.0, 7.5 and 9.8 months in low, intermediate and high FT3/FT4 ratio subgroups, respectively. Hazard ratio (HR) for OS was 0.40 (p < 0.0001) when comparing intermediate versus low and 0.32 (p < 0.0001) when comparing high versus low FT3/FT4 ratio. In the placebo arm, median OS was 3.3, 5.6 and 7.7 months, in the three subgroups. HR for OS was 0.47 (p < 0.0001) when comparing intermediate versus low and 0.33 (p < 0.0001) when comparing high versus low. FT3/FT4 ratio retained its association with OS in the multivariate model in both arms.
While rejecting the predictive effect of baseline FT3/FT4 ratio, present data strengthen the prognostic role of the ratio, pave the way for direct clinical application, underline the need for a better biological understanding and suggest possible therapeutic implications for thyroid hormones.
游离三碘甲状腺原氨酸(FT3)/游离甲状腺素(FT4)比值是评估甲状腺激素外周活性的指标。在之前的研究中,我们发现 FT3/FT4 比值在接受regorafenib 治疗的化疗耐药患者中具有预后作用。因此,我们计划对regorafenib 与安慰剂的 III 期 CORRECT 试验进行事后分析。
根据 FT3 和 FT4 基线值的可用性,对 760 名随机患者中的 758 名(regorafenib 组 503 名,安慰剂组 255 名)进行了本分析。主要目的是探索 FT3/FT4 比值在接受 regorafenib 治疗的患者中的预测作用,以及在 CORRECT 试验中验证 FT3/FT4 比值的预后价值。
对于随机接受 regorafenib 治疗的患者,FT3/FT4 比值低、中、高亚组的中位总生存期(OS)分别为 4.0、7.5 和 9.8 个月。OS 的风险比(HR)为 0.40(p<0.0001),比较中间与低;0.32(p<0.0001),比较高与低。在安慰剂组中,OS 的中位值分别为 3.3、5.6 和 7.7 个月,三个亚组之间。OS 的 HR 为 0.47(p<0.0001),比较中间与低;0.33(p<0.0001),比较高与低。在两个治疗组的多变量模型中,FT3/FT4 比值均与 OS 相关。
虽然拒绝了 FT3/FT4 比值的预测作用,但目前的数据加强了该比值的预后作用,为直接临床应用铺平了道路,强调了对甲状腺激素的生物学理解的必要性,并提示了可能的治疗意义。