Investigational treatment options in phase I and phase II trials for relapsed or refractory acute lymphoblastic leukemia in pediatric patients

被引:3
|
作者
Asare, Julie M. [1 ,2 ]
Rabik, Cara A. [1 ,2 ]
Muller, Bradley [2 ]
Brown, Patrick A. [1 ,2 ]
Cooper, Stacy [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
关键词
B-ALL; T-ALL; blinatumomab; CAR T-cells; inotuzumab; daratumumab; venetoclax; acute lymphoblastic leukemia; CHIMERIC ANTIGEN RECEPTOR; TERM-FOLLOW-UP; T-CELLS; YOUNG-ADULTS; MONOCLONAL-ANTIBODIES; PROTEASOME INHIBITORS; BITE ANTIBODY; BLINATUMOMAB; CHILDREN; VENETOCLAX;
D O I
10.1080/13543784.2021.1916466
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Upfront treatment of pediatric patients with B-cell acute lymphoblastic leukemia (B-ALL) and T-cell acute lymphoblastic leukemia (T-ALL) results in cure rates of 60-95%, depending on risk factors. However, patients with refractory or relapsed B-ALL or T-ALL have much worse outcomes with conventional chemotherapy, hence treatment of these cohorts with novel agents is a priority. Areas Covered: This paper reviews early phase clinical trials in pediatric leukemia. Investigational antibody therapy, chimeric antigen receptor T-cell (CAR-T), and other targeted therapies are examined. The authors discuss the mechanisms of action, side effects, trial designs, and outcomes and reflect on potential research directions. PubMed and Clinicaltrials.gov were searched from 2010 to present, using keywords 'lymphoblastic leukemia' with filters for pediatric age, Phase 1 clinical trial and Phase 2 clinical trial. Expert Opinion: Pediatric patients with relapsed or refractory leukemia often do not derive additional benefit from intensified conventional chemotherapy approaches which have arguably been maximized in the upfront setting. Therefore, novel approaches, such as immunotherapy and targeted agents should be prioritized. Progress will require commitment from pharmaceutical companies regarding these orphan diagnoses and acknowledgment from regulatory bodies that outcomes are suboptimal with conventional chemotherapy.
引用
收藏
页码:611 / 620
页数:10
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