Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee.
Cancer. 2021 Jun 15;127(12):2074-2082. doi: 10.1002/cncr.33465. Epub 2021 Feb 17.
A phase 1 study was conducted to determine the maximum tolerated dose of bendamustine when given in combination with clofarabine, etoposide, and dexamethasone daily for 5 days in children and adolescents with relapsed or refractory hematologic malignancies.
Patients younger than 22 years with second or greater relapsed or refractory acute leukemia or lymphoma after 2 or more prior regimens were eligible. With the rolling 6 design, participants received escalating doses of bendamustine (30, 40, or 60 mg/m /d) in combination with clofarabine (40 mg/m ), etoposide (100 mg/m ), and dexamethasone (8 mg/m ) daily for 5 days. Optional pharmacokinetic studies were performed in cycle 1 on day 1 and day 5.
Sixteen patients were enrolled. Six patients were treated at the dose level of 30 mg/m /d, 6 were treated at the dose level of 40 mg/m /d, and 4 were treated at the dose level of 60 mg/m /d. The dose-limiting toxicity was prolonged myelosuppression. The combination was otherwise well tolerated. The recommended dose of bendamustine in this combination was 30 mg/m /d for 5 days. Ten responses were observed after 1 cycle: 6 complete remissions, 1 durable minimal residual disease-negative complete remission without platelet recovery in a patient with early T-cell precursor leukemia, and 3 partial remissions. Six patients proceeded to transplantation. The event-free survival rate was 40.6% (95% confidence interval [CI], 17.5%-63.7%) at 1 year and 33.9% (95% CI, 11.9%-55.9%) at 3 years.
Bendamustine is well tolerated in combination with clofarabine, etoposide, and dexamethasone. The combination administered over 5 days is effective for multiple relapsed and refractory hematologic malignancies. This trial is registered with ClinicalTrials.gov (NCT01900509).
Improvements to the existing chemotherapy regimen are still needed for patients who relapse after targeted therapies and immunotherapies and for those who are not eligible for or have no access to such therapies. A regimen combining cyclophosphamide, clofarabine, and etoposide has been used in relapsed and refractory pediatric patients with hematologic malignancies. This study shows that substituting bendamustine for cyclophosphamide in combination with clofarabine and etoposide is safe and effective.
一项 1 期研究旨在确定在儿童和青少年中复发或难治性血液恶性肿瘤患者中,联合使用苯达莫司汀、克拉屈滨、依托泊苷和地塞米松,每日 5 天,连续 5 天,最大耐受剂量。
符合条件的患者为 22 岁以下的患者,在 2 个或更多先前的方案后患有第二次或以上复发或难治性急性白血病或淋巴瘤。采用滚动 6 设计,参与者接受递增剂量的苯达莫司汀(30、40 或 60mg/m2/d)联合克拉屈滨(40mg/m2)、依托泊苷(100mg/m2)和地塞米松(8mg/m2),每天 5 天。在第 1 周期的第 1 天和第 5 天进行可选的药代动力学研究。
共纳入 16 例患者。6 例患者接受 30mg/m2/d 剂量治疗,6 例患者接受 40mg/m2/d 剂量治疗,4 例患者接受 60mg/m2/d 剂量治疗。剂量限制毒性为骨髓抑制延长。该组合耐受性良好。该组合中苯达莫司汀的推荐剂量为 30mg/m2/d,连续 5 天。1 个周期后观察到 10 个反应:6 个完全缓解,1 个早期 T 细胞前体白血病患者在血小板恢复无持久微小残留病阴性完全缓解,3 个部分缓解。6 例患者进行了移植。1 年时无事件生存率为 40.6%(95%置信区间[CI],17.5%-63.7%),3 年时为 33.9%(95%CI,11.9%-55.9%)。
苯达莫司汀联合克拉屈滨、依托泊苷耐受性良好。5 天内给药的联合方案对多种复发和难治性血液恶性肿瘤有效。该试验在 ClinicalTrials.gov(NCT01900509)注册。
对于接受靶向治疗和免疫治疗后复发的患者,以及不适合或无法获得此类治疗的患者,仍需要改进现有化疗方案。一种联合环磷酰胺、克拉屈滨和依托泊苷的方案已用于复发和难治性儿科血液系统恶性肿瘤患者。本研究表明,用苯达莫司汀替代环磷酰胺联合克拉屈滨和依托泊苷是安全有效的。