Risk factors for disseminated intravascular coagulation in pediatric acute promyelocytic leukemia: Insights from the cclg-APL 2016 study
Abstract
Abstract Purpose: To identify early risk factors for DIC, particularly severe DIC (grade 4-5), in pediatric APL, with the aim of guiding early clinical intervention. Methods: 186 pediatric APL patients enrolled in the CCLG-APL 2016 study across 38 hospitals nationwide were grouped based on the occurrence and severity of DIC during induction therapy. Results: DIC occurred in 52.2% of patients during induction therapy, with 7.5% developing grade 4-5 DIC. Significant differences were observed between the DIC and non-DIC groups in the proportion of patients with initial WBC≥5×109/L, initial PLT≤26×109/L, and ATO use (P<0.05). Multivariate analysis identified initial PLT ≤26×109/L (P=0.002, OR=2.679, 95% CI: 1.438-4.992) as an independent risk factor, while induction therapy using RIF was a protective factor (P=0.030, OR=0.465, 95%CI: 0.232-0.929). Patients with initial WBC≥55×109/L (P=0.014) were more likely to develop grade 4-5 DIC. Further analysis revealed that FLT3 mutation (P=0.023, OR=11.742, 95% CI: 1.405-98.149), initial PLT≤26×109/L (P=0.017, OR=13.784, 95% CI: 1.598-118.905), and initial bone marrow blasts ≥90% (P=0.030, OR=5.289, 95% CI: 1.178-23.744) were significant risk factors for grade 4-5 DIC. Conclusion: Initial WBC≥5×109/L is associated with an increased risk of DIC, with PLT≤26×109/L as an independent risk factor. Compared with ATO, RIF is a protective factor of DIC during induction therapy. Additionally, initial WBC≥55×109/L is related to grade 4-5 DIC. FLT3 mutation, PLT≤26×109/L, and initial bone marrow blasts ≥90% are independent risk factors for grade 4-5 DIC. This is the largest pediatric APL cohort to date specifically focused on DIC and offers comprehensive analyses that may inform future prospective studies.
Article Details
Authors (5)
Qingyuan Xu
1Beijing Children's Hospital, Capital Medical University, Beijing, China
Linya Wang
1Peking University People's Hospital, Beijing, China
Yaguang Peng
Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Centre for Excellence in Molecular Sciences, Centre for Carbon Neutral Chemistry
Ruidong Zhang
2Hematology Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China
Huyong Zheng
1Beijing Children's Hospital, Capital Medical University, Beijing, China