Literature DB >> 30280786

The therapeutic efficacy of pediatric ALL patients with MLL gene rearrangement treated with CCLG-ALL2008 protocol.

Y-N Sun1, Y-X Hu, L Gao, P-F Xiao, J Lu, S-Y Wu, M Wang, X-J Shao, C-Y Zhou, J Ling, J-Q Li, J Pan, J Gao, S-Y Hu.   

Abstract

OBJECTIVE: In this study, we retrospectively evaluated the therapeutic efficacy of China Children Leukemia Group-ALL2008 (CCLG-ALL 2008) protocol in pediatric patients with mixed-lineage leukaemia (MLL) gene rearrangement of acute lymphoblastic leukemia (ALL) to identify the prognostic factors. PATIENTS AND METHODS: Six hundred and thirty-four patients with ALL were enrolled in this study between June 2008 and Dec 2014. High-risk group (HR) consisted of 217 cases, of which 28 cases were MLL related positive (first group), 22 cases were BCR/ABL positive (second group), and 167 cases were negative with MLL related or BCR/ABL (third group). The therapeutic efficacy was evaluated at the time points of day 8 (TP1), day 15 (TP2), day 33 (TP3) and 12th week (TP4) with the protocol, respectively. Overall-survival (OS) and relapse-free-survival (RFS) and treatment-related mortality (TRD) were analyzed as well.
RESULTS: The first group accounted for 4.4% of all patients. Compared with the second and third group, the first group had more cases younger than 2 years, with initial leukocytes ≥50×109/L, and poor response on TP2. Moreover, patients older than 2 years old had a good 5 years OS (84% ± 9% vs. 37% ± 20%, p<0.05) and RFS (84% ± 9% vs. 29% ± 17%, p<0.05). There were no significant differences in the recurrence rate, TRD, 5 years OS and RFS among three groups. For the first group, compared with good response to prednisone, patients with poor response to prednisone had a poor 5 years RFS (41% ± 17% vs. 81% ± 10%, p<0.05). Multivariate Cox regression analysis identified that RFS and OS were influenced by such factors as age, MLL fusion partners, and prednisone response (p<0.05).
CONCLUSIONS: Such factors as younger age than 2 years old, MLL/AF4 fusion gene, poor response to prednisone, or no complete remission (CR) on TP3 were poor prognostic parameters in predicting the outcome in childhood ALL with MLL gene rearrangement treated with CCLG-ALL 2008 protocol.

Entities:  

Year:  2018        PMID: 30280786     DOI: 10.26355/eurrev_201809_15938

Source DB:  PubMed          Journal:  Eur Rev Med Pharmacol Sci        ISSN: 1128-3602            Impact factor:   3.507


  4 in total

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Authors:  Yu-Juan Xue; Ai-Dong Lu; Yu Wang; Yue-Ping Jia; Ying-Xi Zuo; Le-Ping Zhang
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2020-12

2.  Rationale for targeting BCL6 in MLL-rearranged acute lymphoblastic leukemia.

Authors:  Christian Hurtz; Lai N Chan; Huimin Geng; Erica Ballabio; Gang Xiao; Gauri Deb; Haytham Khoury; Chun-Wei Chen; Scott A Armstrong; Jianjun Chen; Patricia Ernst; Ari Melnick; Thomas Milne; Markus Müschen
Journal:  Genes Dev       Date:  2019-08-08       Impact factor: 12.890

3.  Surface Proteomics Reveals CD72 as a Target for In Vitro-Evolved Nanobody-Based CAR-T Cells in KMT2A/MLL1-Rearranged B-ALL.

Authors:  Matthew A Nix; Kamal Mandal; Huimin Geng; Neha Paranjape; Yu-Hsiu T Lin; Jose M Rivera; Makeba Marcoulis; Kristie L White; Jeffrey D Whitman; Sagar P Bapat; Kevin R Parker; Jonathan Ramirez; Anne Deucher; Paul Phojanokong; Veronica Steri; Faranak Fattahi; Byron C Hann; Ansuman T Satpathy; Aashish Manglik; Elliot Stieglitz; Arun P Wiita
Journal:  Cancer Discov       Date:  2021-03-16       Impact factor: 39.397

4.  Treatment outcomes in children with Acute lymphoblastic leukemia with versus without coexisting Down's syndrome: A systematic review and meta-analysis.

Authors:  Wenjun Liao; Ying Liu
Journal:  Medicine (Baltimore)       Date:  2020-07-17       Impact factor: 1.817

  4 in total

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