Tasian Sarah K, Gardner Rebecca A
Children's Hospital of Philadelphia, Division of Oncology and Center for Childhood Cancer Research; University of Pennsylvania Perelman School of Medicine, Department of Pediatrics and Abramson Cancer Center; 3501 Civic Center Boulevard, CTRB 3010, Philadelphia, PA 19104, USA.
Division of Hematology/Oncology and Ben Towne Center for Childhood Cancer Research/Seattle Children's Research Institute, Seattle Children's Hospital, Seattle, WA, USA and University of Washington School of Medicine, Seattle, WA, USA.
Ther Adv Hematol. 2015 Oct;6(5):228-41. doi: 10.1177/2040620715588916.
Relapsed and chemotherapy-refractory B-cell acute lymphoblastic leukemia (B-ALL) remain significant causes of cancer-associated morbidity and mortality for children and adults. Development of new molecularly targeted treatment strategies for patients with high-risk B-ALL is thus a major preclinical and clinical priority. Adoptive cellular therapy with patient-derived human T cells genetically engineered to express CD19 redirected chimeric antigen receptors (CD19 CAR T cells) is one immunotherapeutic modality that has recently demonstrated remarkable efficacy in re-inducing remission in patients with multiply relapsed B-ALL. Investigative teams at several major cancer centers are currently conducting phase I clinical trials in children and/or adults with relapsed/refractory B-ALL to assess the safety and to identify the maximally tolerated dose of each group's CD19 CAR T-cell product. All groups have reported major clinical toxicities associated with CD19 CAR T-cell treatment, including cytokine release syndrome (CRS) and macrophage activation syndrome, neurologic dysfunction and aplasia of normal B lymphocytes, while CD19 CAR T cells persist in vivo. Toxicities have generally been transient or manageable with supportive care measures. Some patients with life-threatening CD19 CAR T-cell induced sequelae have received anti-cytokine receptor antibody treatment to diminish CRS symptoms and/or corticosteroids to terminate CAR T-cell proliferation. Remarkably, 67-90% of children and adults with B-ALL treated with CD19 CAR T cells in these trials have achieved morphologic leukemia remission with many patients also in molecular remission. The duration of CD19 CAR T cell persistence in vivo has varied appreciably among treated patients and likely reflects differences in the CD19 CAR constructs utilized at each institution. CD19-positive and CD19-negative B-ALL relapses after CD19 CAR T-cell treatment have occurred in some patients. Phase II trials to assess the efficacy of CD19 CAR T-cell immunotherapy in larger cohorts of patients with relapsed/refractory B-ALL are ongoing or planned.
复发和化疗难治性B细胞急性淋巴细胞白血病(B-ALL)仍然是儿童和成人癌症相关发病和死亡的重要原因。因此,为高危B-ALL患者开发新的分子靶向治疗策略是临床前和临床的主要优先事项。采用基因工程改造的患者来源的人类T细胞进行过继性细胞治疗,使其表达CD19重定向嵌合抗原受体(CD19 CAR T细胞),是一种免疫治疗方式,最近已证明在多重复发的B-ALL患者中重新诱导缓解方面具有显著疗效。几个主要癌症中心的研究团队目前正在对复发/难治性B-ALL儿童和/或成人进行I期临床试验,以评估安全性并确定每组CD19 CAR T细胞产品的最大耐受剂量。所有研究组均报告了与CD19 CAR T细胞治疗相关的主要临床毒性,包括细胞因子释放综合征(CRS)和巨噬细胞活化综合征、神经功能障碍以及正常B淋巴细胞发育不全,而CD19 CAR T细胞在体内持续存在。毒性反应通常是短暂的,或可通过支持性护理措施进行控制。一些患有危及生命的CD19 CAR T细胞诱导后遗症的患者接受了抗细胞因子受体抗体治疗以减轻CRS症状和/或使用皮质类固醇来终止CAR T细胞增殖。值得注意的是,在这些试验中接受CD19 CAR T细胞治疗的B-ALL儿童和成人中,67%-90%实现了形态学白血病缓解,许多患者也达到了分子学缓解。CD19 CAR T细胞在体内持续存在的时间在接受治疗的患者中差异很大,这可能反映了每个机构使用的CD19 CAR构建体的差异。一些患者在CD19 CAR T细胞治疗后出现了CD19阳性和CD19阴性B-ALL复发。评估CD19 CAR T细胞免疫疗法在更大规模复发/难治性B-ALL患者队列中疗效的II期试验正在进行或计划中。