Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX;
Blood. 2014 Feb 27;123(9):1309-18. doi: 10.1182/blood-2013-07-513937. Epub 2013 Dec 17.
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).
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)。