Allogeneic hematopoietic stem cell transplant for relapsed and refractory non-Hodgkin lymphoma in pediatric patients

被引:10
|
作者
Naik, Swati [1 ,2 ,3 ]
Martinez, Caridad A. [1 ,2 ,3 ]
Omer, Bilal [1 ,2 ,3 ]
Sasa, Ghadir [1 ,2 ,3 ]
Yassine, Khaled [1 ,2 ,3 ]
Allen, Carl E. [1 ,2 ,3 ]
Kamdar, Kala [2 ,3 ]
Orth, Robert [3 ,4 ]
Wu, Mengfen [5 ]
Leung, Kathryn [1 ,2 ,3 ]
Gottschalk, Stephen [1 ,2 ,3 ]
Brenner, Malcolm K. [1 ,2 ,3 ,6 ]
Heslop, Helen E. [1 ,2 ,3 ,6 ]
Krance, Robert A. [1 ,2 ,3 ,6 ]
机构
[1] Texas Childrens Hosp, Baylor Coll Med, Houston Methodist Hosp, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Texas Childrens Canc Ctr, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[4] Texas Childrens Hosp, Dept Radiol, Houston, TX 77030 USA
[5] Baylor Coll Med, Dan L Duncan Ctr, Biostat Shared Resource, Houston, TX 77030 USA
[6] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
关键词
BONE-MARROW-TRANSPLANTATION; LYMPHOBLASTIC LYMPHOMA; RETROSPECTIVE ANALYSIS; CHILDHOOD; CHILDREN; DISEASE; ADOLESCENTS; RECURRENT;
D O I
10.1182/bloodadvances.2018026203
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic hematopoietic stem cell transplant (HSCT) for relapsed pediatric non-Hodgkin lymphoma (NHL) is often reserved for patients with certain NHL subtypes or high-risk disease whereas the remainder receive autologous HSCT. Given the aggressive nature of pediatric NHL, we performed allogeneic HSCTs for all patients regardless of disease risk. We report overall survival (OS) and prognostic variables in 36 pediatric patients who underwent allogeneic HSCT between 1998 and 2016. OS at 3 years was 67%. The 3-year OS varied based on NHL subtype: 100% for anaplastic large cell lymphoma (n = 14), 63% for diffuse large B-cell lymphoma (n = 8), 17% for lymphoblastic lymphoma (LL; n = 9) and 80% for other subtypes combined (n = 5). Disease status influenced outcome with 3-year OS of 100% for patients in complete remission (n = 15), 59% with partial remission (PR; n = 17), and 0% with progressive/stable disease (n = 3) (P = .004). Of the 17 patients in PR, all 6 with LL died of relapsed disease, whereas the other 11 attained remission after HSCT and remained disease-free. The cumulative incidence of relapse after HSCT for LL was 78% compared with 15% for all other NHL subtypes combined (P < .0001). Cumulative incidence of nonrelapse mortality (NRM) was low in our cohort at 6%. Hence, allogeneic HSCT is a well-tolerated and useful therapeutic option with low rates of NRM and relapse for all NHL subtypes except LL with active disease at HSCT.
引用
收藏
页码:2689 / 2695
页数:7
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