Wayne Alan S, Shah Nirali N, Bhojwani Deepa, Silverman Lewis B, Whitlock James A, Stetler-Stevenson Maryalice, Sun Weili, Liang Meina, Yang Jie, Kreitman Robert J, Lanasa Mark C, Pastan Ira
Children's Center for Cancer and Blood Diseases, Division of Hematology, Oncology, and Blood and Marrow Transplantation, Children's Hospital Los Angeles, USC Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Pediatric Oncology Branch, Center for Cancer Research (CCR), National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD.
Blood. 2017 Oct 5;130(14):1620-1627. doi: 10.1182/blood-2017-02-749101. Epub 2017 Aug 9.
Novel therapies are needed to overcome chemotherapy resistance for children with relapsed/refractory acute lymphoblastic leukemia (ALL). Moxetumomab pasudotox is a recombinant anti-CD22 immunotoxin. A multicenter phase 1 study was conducted to determine the maximum-tolerated cumulative dose (MTCD) and evaluate safety, activity, pharmacokinetics, and immunogenicity of moxetumomab pasudotox in children, adolescents, and young adults with ALL (N = 55). Moxetumomab pasudotox was administered as a 30-minute IV infusion at doses of 5 to 50 µg/kg every other day for 6 (cohorts A and B) or 10 (cohort C) doses in 21-day cycles. Cohorts B and C received dexamethasone prophylaxis against capillary leak syndrome (CLS). The most common treatment-related adverse events were reversible weight gain, hepatic transaminase elevation, and hypoalbuminemia. Dose-limiting CLS occurred in 2 of 4 patients receiving 30 µg/kg of moxetumomab pasudotox every other day for 6 doses. Incorporation of dexamethasone prevented further dose-limiting CLS. Six of 14 patients receiving 50 µg/kg of moxetumomab pasudotox for 10 doses developed hemolytic uremic syndrome (HUS), thrombotic microangiopathy (TMA), or HUS-like events, exceeding the MTCD. Treatment expansion at 40 µg/kg for 10 doses (n = 11) exceeded the MTCD because of 2 HUS/TMA/HUS-like events. Dose level 6B (ie, 50 µg/kg × 6 doses) was the MTCD, selected as the recommended phase 2 dose. Among 47 evaluable patients, an objective response rate of 32% was observed, including 11 (23%) composite complete responses, 5 of which were minimal residual disease negative by flow cytometry. Moxetumomab pasudotox showed a manageable safety profile and evidence of activity in relapsed or refractory childhood ALL. This trial was registered at www.clinicaltrials.gov as #NCT00659425.
对于复发/难治性急性淋巴细胞白血病(ALL)患儿,需要新的疗法来克服化疗耐药性。莫昔妥珠单抗是一种重组抗CD22免疫毒素。开展了一项多中心1期研究,以确定最大耐受累积剂量(MTCD),并评估莫昔妥珠单抗在ALL患儿、青少年和年轻成人(N = 55)中的安全性、活性、药代动力学和免疫原性。莫昔妥珠单抗通过静脉输注30分钟给药,剂量为5至50 μg/kg,每隔一天给药一次,共给药6次(A组和B组)或10次(C组),每21天为一个周期。B组和C组接受地塞米松预防毛细血管渗漏综合征(CLS)。最常见的治疗相关不良事件为可逆性体重增加、肝转氨酶升高和低白蛋白血症。4例接受30 μg/kg莫昔妥珠单抗每隔一天给药一次共6次的患者中有2例发生了剂量限制性CLS。加入地塞米松可预防进一步的剂量限制性CLS。14例接受50 μg/kg莫昔妥珠单抗给药10次的患者中有6例发生了溶血性尿毒症综合征(HUS)、血栓性微血管病(TMA)或类HUS事件,超过了MTCD。以40 μg/kg给药10次(n = 11)进行治疗扩展时,由于发生了2例HUS/TMA/类HUS事件,超过了MTCD。6B剂量水平(即50 μg/kg×6次剂量)为MTCD,被选为推荐的2期剂量。在47例可评估患者中,观察到客观缓解率为32%,包括11例(23%)完全缓解,其中5例通过流式细胞术检测微小残留病呈阴性。莫昔妥珠单抗显示出可控的安全性,并有证据表明其对复发或难治性儿童ALL有活性。该试验已在www.clinicaltrials.gov注册,编号为#NCT00659425。