Effect of pediatric- versus adult-type chemotherapy regimens on outcomes of allogeneic hematopoietic stem cell transplants for adult T-cell acute lymphoblastic leukemia in first complete remission

The optimal chemotherapy regimen pre-transplantation for adult T-cell acute lymphoblastic leukemia (T-ALL) patients remains unknown. Here, we compared the transplant outcomes in 127 subjects receiving pediatric- ( N  = 57) or adult-type ( N  = 70) regimens pre-transplant. The corresponding 3-year cu...

Full description

Saved in:
Bibliographic Details
Published inBone marrow transplantation (Basingstoke) Vol. 57; no. 11; pp. 1704 - 1711
Main Authors Qi, Han-zhou, Xu, Jun, Yang, Qian-qian, Lin, Ren, Wang, Zhi-xiang, Zhao, Ke, Wang, Qiang, Zhou, Xuan, Fan, Zhi-ping, Huang, Fen, Xu, Na, Xuan, Li, Jin, Hua, Sun, Jing, Gale, Robert Peter, Zhou, Hong-sheng, Liu, Qi-fa
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.11.2022
Nature Publishing Group
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The optimal chemotherapy regimen pre-transplantation for adult T-cell acute lymphoblastic leukemia (T-ALL) patients remains unknown. Here, we compared the transplant outcomes in 127 subjects receiving pediatric- ( N  = 57) or adult-type ( N  = 70) regimens pre-transplant. The corresponding 3-year cumulative incidences of relapse (CIR) was 7% (95% CI: 3–11%) and 29% (95% CI: 23–35%; P  = 0.02), leukemia-free survivals (LFS) was 86% (95% CI: 81–91%) and 57% (95% CI: 51–63%; P  = 0.003), overall survivals (OS) was 88% (95% CI: 84–92%) and 58% (95% CI: 52–64%; P  = 0.002), the 1-year NRM was 4% (95% CI: 1–7%) and 9% (95% CI: 4–14%; P  = 0.40). Multivariate analysis showed that pediatric-type regimen was associated with lower CIR (Hazard Ratio [HR] = 0.31 [95% CI: 0.09–1.00]; P  = 0.05), better LFS (HR = 0.34 [95% CI: 0.15–0.78]; P  = 0.01) and OS (HR = 0.30 [95% CI: 0.13–0.72]; P  = 0.01). Our results suggested that adult T-ALL patients undergoing allo-HSCT might benefit from pediatric-type chemotherapy.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:0268-3369
1476-5365
1476-5365
DOI:10.1038/s41409-022-01796-2