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舒尼替尼诱导的甲状腺功能减退症是否在舒尼替尼治疗转移性肾细胞癌的活性中起作用?

Does sunitinib-induced hypothyroidism play a role in the activity of sunitinib in metastatic renal cell carcinoma?

机构信息

Department of Oncology, Assaf Harofeh Medical Center, Zerifin, Israel.

出版信息

Chemotherapy. 2012;58(3):200-5. doi: 10.1159/000337079. Epub 2012 Jun 29.

Abstract

BACKGROUND

The objective of this study was to evaluate if hypothyroidism developing during sunitib therapy in patients with metastatic renal cell carcinoma (mRCC) is associated with a better outcome.

METHODS

Thirty-one consecutive patients with clear cell mRCC were retrospectively analyzed. Thyroid function was assessed prior to therapy, every 6 weeks during the first 6 months and every 2-4 months thereafter. Hypothyroidism was considered present if thyroid-stimulating hormone (TSH) exceeded the upper normal limit (UNL) with normal triiodothyronine (T3) and thyroxine (T4).

RESULTS

Hypothyroidism occurred in 16 patients (52%) within 3 months (range 0.7-22.9) of treatment initiation. Thyroid replacement corrected TSH below the UNL in 10 patients (63%). The distribution according to Motzer prognostic criteria revealed good prognosis in 16 patients (52%), intermediate in 9 (29%) and poor in 6 (19%). The hypothyroid patients tended to have longer progression-free survival (PFS; median 12.2 vs. 9.4 months; p = 0.234) and longer survival (median 22.4 vs. 13.9 months; p = 0.234) than the euthyroid patients. Clinical benefits were similar in both groups.

CONCLUSIONS

Hypothyroidism that develops in mRCC patients treated with sunitinib is associated with a trend toward prolonged PFS and survival, with a similar clinical benefit rate.

摘要

背景

本研究旨在评估转移性肾细胞癌(mRCC)患者接受舒尼替尼治疗期间发生的甲状腺功能减退是否与更好的预后相关。

方法

回顾性分析了 31 例接受舒尼替尼治疗的 clear cell mRCC 患者。在治疗前、治疗的前 6 个月每 6 周以及此后每 2-4 个月评估甲状腺功能。如果促甲状腺激素(TSH)超过正常上限(UNL),同时三碘甲状腺原氨酸(T3)和甲状腺素(T4)正常,则认为存在甲状腺功能减退。

结果

在治疗开始后 3 个月内(范围 0.7-22.9),16 例患者(52%)发生甲状腺功能减退。10 例患者(63%)的甲状腺素替代治疗将 TSH 校正至 UNL 以下。根据 Motzer 预后标准的分布,16 例患者(52%)的预后良好,9 例(29%)的预后中等,6 例(19%)的预后不良。甲状腺功能减退患者的无进展生存期(PFS;中位数 12.2 个月 vs. 9.4 个月;p = 0.234)和总生存期(中位数 22.4 个月 vs. 13.9 个月;p = 0.234)均长于甲状腺功能正常患者。两组的临床获益相似。

结论

接受舒尼替尼治疗的 mRCC 患者发生的甲状腺功能减退与 PFS 和生存时间延长趋势相关,且临床获益率相似。

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