Frontiers in Oncology (Dec 2022)

Prognostic significance of steroid response in pediatric acute lymphoblastic leukemia: The CCCG-ALL-2015 study

  • Jinhua Chu,
  • Huaju Cai,
  • Jiaoyang Cai,
  • Xinni Bian,
  • Yumei Cheng,
  • Xianmin Guan,
  • Xiaoqian Chen,
  • Hua Jiang,
  • Xiaowen Zhai,
  • Yongjun Fang,
  • Lei Zhang,
  • Xin Tian,
  • Fen Zhou,
  • Yaqin Wang,
  • Lingzhen Wang,
  • Hong Li,
  • Leung Wing Kwan Alex,
  • Minghua Yang,
  • Hanfang Yang,
  • Aijun Zhan,
  • Ningling Wang,
  • Shaoyan Hu

DOI
https://doi.org/10.3389/fonc.2022.1062065
Journal volume & issue
Vol. 12

Abstract

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IntroductionWhether steroid response is an independent risk factor for acute lymphoblastic leukemia (ALL) is controversial. This study aimed to investigate the relationship between response to dexamethasone and prognosis in children with ALL.MethodsWe analyzed the data of 5,161 children with ALL who received treatment in accordance with the Chinese Children’s Cancer Group ALL-2015 protocol between January 1, 2015, and December 31, 2018, in China. All patients received dexamethasone for 4 days as upfront window therapy. Based on the peripheral lymphoblast count on day 5, these patients were classified into the dexamethasone good response (DGR) and dexamethasone poor response (DPR) groups. A peripheral lymphoblast count ≥1× 109/L indicated poor response to dexamethasone.ResultsThe age, white blood cell counts, prevalence of the BCR/ABL1 and TCF3/PBX1 fusion genes, and rates of recurrence in the central nervous system were higher in the DPR than in the DGR group (P<0.001). Compared to the DPR group, the DGR group had a lower recurrence rate (18.6% vs. 11%) and higher 6-year event-free survival (73% vs. 83%) and overall survival (86% vs. 92%) rates; nevertheless, subgroup analysis only showed significant difference in the intermediate-risk group (P<0.001).DiscussionResponse to dexamethasone was associated with an early treatment response in our study. In the intermediate-risk group, dexamethasone response added a prognostic value in addition to minimal residual disease, which may direct early intervention to reduce the relapse rate.

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