Tisagenlecleucel for the treatment of B-cell acute lymphoblastic leukemia

被引:30
作者
Leahy, Allison Barz [1 ,2 ]
Elgarten, Caitlin W.
Grupp, Stephan A.
Maude, Shannon L.
Teachey, David T.
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Div Pediat Hematol, Perelman Sch Med, Colket Translat Res Bldg,3501 Civ Ctr Blvd, Philadelphia, PA 19104 USA
[2] Univ Penn, Childrens Hosp Philadelphia, Div Oncol, Perelman Sch Med, Colket Translat Res Bldg,3501 Civ Ctr Blvd, Philadelphia, PA 19104 USA
关键词
Tisagenlecleucel; cytokine release syndrome; CD19; Kymriah; lymphoblastic leukemia; chimeric antigen receptor T cell; CART; immunotherapy; CAR-T-CELLS; CYTOKINE RELEASE SYNDROME; PEDIATRIC-PATIENTS; YOUNG-ADULTS; CHILDREN; THERAPY; CHEMOTHERAPY; IMMUNOTHERAPY; BLINATUMOMAB; REMISSION;
D O I
10.1080/14737140.2018.1512411
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Cure rates for pediatric and young adult patients with refractory or recurrently relapsed acute lymphoblastic leukemia (ALL) are dismal. Survival from time of relapse is typically measured in weeks to months, and standard chemotherapy and currently approved targeted therapy achieve remission in less than a third of affected patients. To date, the only definitive curative therapy has been allogeneic hematopoietic stem cell transplant (HSCT). Advances in immunotherapy, with the introduction of chimeric antigen receptor T-cell therapies and the development of tisagenlecleucel, have changed the landscape.Areas covered: This review will describe the pharmacology of tisagenlecleucel and summarize the clinical evidence for its use in the treatment of multiple-relapsed or refractory B-cell ALL (B-ALL). Also discussed are other immunotherapies for B-ALL as well as the most commonly-encountered toxicities and corresponding management strategies.Expert commentary: Early phase trials indicate that tisagenlecleucel significantly improves survival for patients with B-ALL that is refractory or in second or later relapse. In responding patients, remissions have been reported on the order of years, and thus, tisagenlecleucel may herald a dramatic shift in the treatment paradigm of this largely fatal disease.
引用
收藏
页码:959 / 971
页数:13
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