首页> 外文期刊>Cancer: A Journal of the American Cancer Society >The effect of interleukin 11 on thrombocytopenia associated with tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia.
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The effect of interleukin 11 on thrombocytopenia associated with tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia.

机译:白细胞介素11对慢性粒细胞白血病患者酪氨酸激酶抑制剂治疗相关的血小板减少的影响。

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BACKGROUND: During therapy with tyrosine kinase inhibitors (TKIs), approximately 20% to 50% of patients with chronic myeloid leukemia (CML) develop grade >or=3 thrombocytopenia leading to treatment interruptions and dose reductions. Interleukin 11 (IL-11) reduces the incidence and the severity of thrombocytopenia in solid tumors. METHODS: The authors investigated the efficacy and safety of low-dose IL-11 for improving thrombocytopenia associated with TKI therapy in 14 patients with CML. The starting dose of IL-11 was 10 microg/kg 3 times weekly, and the dose was escalated by 1 dose level every 2 weeks if the patients had no sustained platelet increase. RESULTS: The median patient age was 52 years. The median platelet count at the time IL-11 was started was 37 x 10(9)/L. All patients had prior TKI dose reductions. After the initiation of IL-11, 8 of 14 patients (57%) had an increase in platelet count with a median peak platelet count of 110 x 10(9)/L. One additional patient had no platelet increase but was able to tolerate an imatinib dose increase. Eleven patients had a decrease in the number of days of TKI therapy interruption secondary to thrombocytopenia after the initiation of IL-11 (6% of total treatment time vs 34% of total treatment time before IL-11). Therapy was well tolerated. CONCLUSIONS: The current results indicated that IL-11 may correct thrombocytopenia associated with TKI therapy for patients with CML and that it has a favorable toxicity profile.
机译:背景:在使用酪氨酸激酶抑制剂(TKI)进行治疗期间,约20%至50%的慢性粒细胞白血病(CML)患者发展为>或= 3级血小板减少症,导致治疗中断和剂量减少。白细胞介素11(IL-11)可降低实体瘤中血小板减少症的发生率和严重程度。方法:作者研究了低剂量IL-11在14例CML患者中改善与TKI治疗相关的血小板减少的疗效和安全性。 IL-11的起始剂量为每周3次10 microg / kg,如果患者没有持续的血小板增加,则每2周将剂量递增1个剂量水平。结果:患者平均年龄为52岁。 IL-11开始时的中位血小板计数为37 x 10(9)/ L。所有患者先前均已降低TKI剂量。在启动IL-11后,14例患者中有8例(57%)血小板计数增加,中位峰值血小板计数为110 x 10(9)/ L。另一名患者无血小板增加,但能够耐受伊马替尼剂量增加。 IL-11启动后,血小板减少引起的继发于血小板减少症的TKI治疗中断天数减少了11名患者(占总治疗时间的6%与占IL-11之前总治疗时间的34%)。治疗耐受性好。结论:目前的结果表明,IL-11可以纠正TML治疗CML患者的血小板减少症,并且具有良好的毒性。

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