Autologous hematopoietic cell transplantation for the treatment of relapsed/refractory pediatric, adolescent, and young adult Hodgkin lymphoma: a single institutional experience

被引:7
作者
Talleur, Aimee C. [1 ]
Flerlage, Jamie E. [2 ]
Shook, David R. [1 ]
Chilsen, Abigail M. [3 ]
Hudson, Melissa M. [2 ]
Cheng, Cheng [4 ]
Huang, Sujuan [4 ]
Triplett, Brandon M. [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Bone Marrow Transplantat & Cellular Therapy, 332 N Lauderdale St, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Oncol, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] Univ Wisconsin, Sch Med & Publ Hlth, Madison, WI USA
[4] St Jude Childrens Res Hosp, Dept Biostat, 332 N Lauderdale St, Memphis, TN 38105 USA
关键词
BONE-MARROW-TRANSPLANTATION; BRENTUXIMAB VEDOTIN; 5-YEAR SURVIVORS; SALVAGE THERAPY; LATE MORTALITY; DISEASE; CHILDREN; OUTCOMES; CANCER; CHEMOTHERAPY;
D O I
10.1038/s41409-020-0879-4
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Pediatric, adolescent, and young adult patients with relapsed or refractory Hodgkin lymphoma receive multimodal therapy, including autologous hematopoietic cell transplantation (AutoHCT). Despite aggressive therapy, historical outcomes for this patient population have been poor. This paper describes a single institutional experience utilizing AutoHCT in 74 patients treated from 1988-2015. Our results demonstrate significantly improved outcomes over time. Compared with patients treated in the earlier era (1988-2001), 5-year overall survival improved from 62.5 +/- 9.6% to 91.8 +/- 4.4% (p < 0.001) and event free survival improved from 41.7 +/- 9.6% to 87.7 +/- 5.3% (I < 0.001) for patients treated in a later era (2002-2015). Improvements in survival are multifactorial, including reductions in both relapse and nonrelapse mortality. Further investigation is needed to determine the role of AutoHCT in a modern treatment cohort that includes frequent use of targeted immunotherapies. In addition, as the use and availability of effective novel therapeutics increases for this patient population there may be an opportunity for the reduction of standard cytotoxic therapies, including in AutoHCT preparative regimens, thereby mitigating late effects.
引用
收藏
页码:1357 / 1366
页数:10
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