Expanded activated autologous lymphocyte infusions improve outcomes of low- and intermediate-risk childhood acute myeloid leukemia with low level of minimal residual disease.


Journal

Cancer letters
ISSN: 1872-7980
Titre abrégé: Cancer Lett
Pays: Ireland
ID NLM: 7600053

Informations de publication

Date de publication:
28 11 2020
Historique:
received: 25 02 2020
revised: 31 07 2020
accepted: 05 08 2020
pubmed: 24 8 2020
medline: 26 3 2021
entrez: 24 8 2020
Statut: ppublish

Résumé

The presence of minimal residual disease (MRD) is a risk factor for relapse among children with acute myeloid leukemia (AML), and eliminating MRD can usually improve survival rates. To investigate the effect of expanded activated autologous lymphocytes (EAALs) combined with chemotherapy on eliminating MRD and improving survival rates of children with AML, we retrospectively analyzed the results of 115 children with low- or intermediate-risk AML with MRD treated at the Pediatric Hematological Center, Peking University People's Hospital, between January 2010 and January 2016. The patients were assigned to the chemotherapy plus EAAL (combined therapy) group (n = 61) and chemotherapy group (n = 54). The MRD-negativity rates were 95.1% (58/61) in the combined therapy group and 63.0% (34/54) in the chemotherapy group (P < 0.0001) during consolidation treatment. The 5-year event-free survival rate was higher in the combined therapy group than in the chemotherapy group (86.3 ± 4.6% vs. 72.1 ± 6.1%, P = 0.025). No severe adverse event was observed after EAAL infusion. The present study showed that EAAL combined with chemotherapy could improve the MRD-negativity rate and event-free survival rate among children with AML with low level MRD-positive status.

Identifiants

pubmed: 32829005
pii: S0304-3835(20)30415-8
doi: 10.1016/j.canlet.2020.08.003
pii:
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

128-132

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Le-Ping Zhang (LP)

Department of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China. Electronic address: zlppeking@163.com.

Ai-Dong Lu (AD)

Department of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.

Jun Wu (J)

Department of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.

Yue-Ping Jia (YP)

Department of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.

Ying-Xi Zuo (YX)

Department of Pediatrics, Peking University People's Hospital, Peking University, Beijing, China.

Yong-Hua Zhang (YH)

Immunotech Applied Science Limited, Beijing, China.

Yong-Hong Zhao (YH)

Immunotech Applied Science Limited, Beijing, China.

Wei Shang (W)

Immunotech Applied Science Limited, Beijing, China.

Dong-Feng Xie (DF)

Immunotech Applied Science Limited, Beijing, China.

Ying-Chun Li (YC)

Immunotech Applied Science Limited, Beijing, China.

Zhao Sun (Z)

Peking Union Medical College Hospital, Beijing, China.

Shui-Qing Ma (SQ)

Peking Union Medical College Hospital, Beijing, China. Electronic address: mashuiqing1964@163.com.

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