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首页> 外文期刊>Targeted oncology >Regorafenib-Induced Hypothyroidism as a Predictive Marker for Improved Survival in Metastatic or Unresectable Colorectal Cancer Refractory to Standard Therapies: A Prospective Single-Center Study
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Regorafenib-Induced Hypothyroidism as a Predictive Marker for Improved Survival in Metastatic or Unresectable Colorectal Cancer Refractory to Standard Therapies: A Prospective Single-Center Study

机译:Regorafenib诱导的甲状腺功能减退症作为预测标志物,用于改善转移或不可切入的结肠直肠癌难治度对标准疗法的难治性:一个预期单中心研究

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摘要

Background Tyrosine kinase inhibitor-induced hypothyroidism is associated with favorable survival in patients with various cancers. Objective We aimed to investigate the incidence of regorafenib-induced hypothyroidism and assess its prognostic value in patients with metastatic or unresectable colorectal cancer (CRC) receiving regorafenib. Patients and Methods This study included 68 patients treated at Asan Medical Center (Seoul, Republic of Korea) between 2014 and 2016 with metastatic or unresectable CRC refractory to standard therapies. Regorafenib (160 mg/day on days 1-21 followed by a 7-day break) was administered. Results The median patient age was 58 (range 26-72) years; 61.8% of patients were male. Among the 68 patients, 50 (73.5%) showed hypothyroidism; 39 (57.4%) had subclinical and 11 (16.2%) had symptomatic hypothyroidism. Overall, the objective response rate (ORR) and disease control rate (DCR) were 7.4% and 70.6%, respectively; both were significantly higher in patients with symptomatic or subclinical hypothyroidism than in euthyroid patients (ORR 27.3% vs. 5.1% vs. 0.0%, P = 0.001; DCR 100% vs. 76.9% vs. 38.9%, P = 0.001). Median progression-free survival (PFS) and overall survival (OS) were longer in patients with symptomatic hypothyroidism than in those with subclinical hypothyroidism (median PFS 9.1 vs. 3.8 months, P = 0.018; median OS: 19.2 vs. 9.4 months, P = 0.012) or with euthyroid status (median PFS 9.1 vs. 1.8 months, P < 0.001; median OS 19.2 vs. 4.7 months, P = 0.001). Symptomatic hypothyroidism was a significant protective factor for PFS (hazard ratio (HR) = 0.37, P = 0.006) and OS (HR = 0.35, P = 0.007); no other adverse events were associated with survival. Conclusions Regorafenib-induced hypothyroidism frequently occurs in patients with metastatic CRC receiving regorafenib and is associated with improved survival. Thyroid function status should be actively monitored in CRC patients receiving regorafenib.
机译:背景技术酪氨酸激酶抑制剂诱导的甲状腺功能亢进症与各种癌症患者有利的存活相关。目的我们旨在探讨令人噬菌体诱导的甲状腺功能亢进的发病率,并评估其在转移或不可切除的结直肠癌(CRC)患者中的预后价值接受Regorafenib。患者和方法本研究包括2014年和2016年在2014年和2016年间Asan Medical Center(首尔)治疗的68名患者,其转移或不可切除的CRC难以解决标准疗法。施用Regorafenib(160毫克/天,然后在第1-21天,然后休息7天休息)。结果中位数患者年龄为58(26-72)岁; 61.8%的患者是男性。在68名患者中,50例(73.5%)显示甲状腺功能减退症; 39(57.4%)亚临床,11(16.2%)有症状甲状腺功能亢进。总体而言,客观反应率(ORR)和疾病控制率(DCR)分别为7.4%和70.6%;患有症状或亚临床甲状腺功能亢进症患者的患者显着提高了患者(ORR 27.3%Vs.0%,P = 0.001; DCR 100%vs.76.9%,P = 0.001)。患有症状甲状腺功能减退症的患者的中位进展生存(PFS)和整体存活率(PFS)和整体存活(OS)比亚临床甲状腺功能减退症的患者(中位数PFS 9.1对3.8个月,P = 0.018;中位OS:19.2与9.4个月,P = 0.012)或用Euthyroid状态(中位数PFS 9.1对1.8个月,P <0.001;中位OS 19.2与4.7个月,P = 0.001)。症状甲状腺功能减退症是PFS的显着保护因子(危害比(HR)= 0.37,P = 0.006)和OS(HR = 0.35,P = 0.007);没有其他不良事件与存活有关。结论雄育诱导的甲状腺功能亢进症经常发生在接受令人疣的转移CRC患者中,与改善的存活相关。应在接受RegoraFenib的CRC患者中积极监测甲状腺功能状态。

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  • 来源
    《Targeted oncology》 |2019年第6期|共9页
  • 作者单位

    Univ Ulsan Coll Med Asan Med Ctr Dept Oncol 88 Olymp Ro 43 Gil Seoul 05505 South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Oncol 88 Olymp Ro 43 Gil Seoul 05505 South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Oncol 88 Olymp Ro 43 Gil Seoul 05505 South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Oncol 88 Olymp Ro 43 Gil Seoul 05505 South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Nucl Med Seoul South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Prevent Med Seoul South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Nucl Med Seoul South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Nucl Med Seoul South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Nucl Med Seoul South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Oncol 88 Olymp Ro 43 Gil Seoul 05505 South Korea;

    Univ Ulsan Coll Med Asan Med Ctr Dept Oncol 88 Olymp Ro 43 Gil Seoul 05505 South Korea;

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  • 正文语种 eng
  • 中图分类 肿瘤学;
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