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博舒替尼治疗对伊马替尼和其他酪氨酸激酶抑制剂耐药或不耐受的白血病患者的安全性和毒性管理。

Bosutinib safety and management of toxicity in leukemia patients with resistance or intolerance to imatinib and other tyrosine kinase inhibitors.

机构信息

Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX;

出版信息

Blood. 2014 Feb 27;123(9):1309-18. doi: 10.1182/blood-2013-07-513937. Epub 2013 Dec 17.

Abstract

Bosutinib is an oral, dual SRC/ABL tyrosine kinase inhibitor (TKI) with clinical activity in Philadelphia chromosome-positive (Ph(+)) leukemia. We assessed the safety and tolerability of bosutinib 500 mg per day in a phase 1/2 study in chronic-phase (CP) chronic myeloid leukemia (CML) or advanced Ph(+) leukemia following resistance/intolerance to imatinib and possibly other TKIs. Patient cohorts included second-line CP CML (n = 286), third-/fourth-line CP CML (n = 118), and advanced leukemia (n = 166). Median bosutinib duration was 11.1 (range, 0.03-83.4) months. Treatment-emergent adverse events (TEAEs) in each cohort were primarily gastrointestinal (diarrhea [86%/83%/74%], nausea [46%/48%/48%], and vomiting [37%/38%/43%]). Diarrhea presented early, with few (8%) patients experiencing grade 3/4 events; dose reduction due to diarrhea occurred in 6% of affected patients. Grade 3/4 myelosuppression TEAEs were reported in 41% of patients; among affected patients, 46% were managed with bosutinib interruption and 32% with dose reduction. Alanine aminotransferase elevation TEAEs occurred in 17% of patients (grade 3/4, 7%); among patients managed with dose interruption, bosutinib rechallenge was successful in 74%. Bosutinib demonstrated acceptable safety with manageable toxicities in Ph(+) leukemia. This trial (NCT00261846) was registered at www.ClinicalTrials.gov (this manuscript is based on a different data snapshot from that in ClinicalTrials.gov).

摘要

博舒替尼是一种口服的 SRC/ABL 双重酪氨酸激酶抑制剂(TKI),在费城染色体阳性(Ph(+))白血病中具有临床活性。我们在一项 1/2 期研究中评估了每天 500 毫克博舒替尼在慢性期(CP)慢性髓性白血病(CML)或对伊马替尼和可能其他 TKI 耐药/不耐受的晚期 Ph(+)白血病患者中的安全性和耐受性。患者队列包括二线 CP CML(n = 286)、三线/四线 CP CML(n = 118)和晚期白血病(n = 166)。博舒替尼中位持续时间为 11.1 个月(范围,0.03-83.4)。每个队列的治疗中出现的不良事件(TEAEs)主要是胃肠道(腹泻[86%/83%/74%]、恶心[46%/48%/48%]和呕吐[37%/38%/43%])。腹泻出现较早,仅有少数(8%)患者出现 3/4 级事件;腹泻导致的剂量减少发生在 6%的受影响患者中。41%的患者发生 3/4 级骨髓抑制 TEAEs;在受影响的患者中,46%的患者接受博舒替尼中断治疗,32%的患者接受剂量减少。17%的患者发生丙氨酸氨基转移酶升高 TEAEs(3/4 级,7%);在接受剂量中断的患者中,博舒替尼再挑战成功的比例为 74%。博舒替尼在 Ph(+)白血病中具有可接受的安全性和可管理的毒性。该试验(NCT00261846)在 www.ClinicalTrials.gov 注册(本文基于与 ClinicalTrials.gov 不同的数据快照)。

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