A Risk Scoring Model for High-Dose Methotrexate-Induced Liver Injury in Children With Acute Lymphoblastic Leukemia Based on Gene Polymorphism Study

被引:1
|
作者
He, Xia [1 ,2 ]
Yao, Pingli [3 ]
Li, Mengting [1 ,2 ]
Liang, Hong [1 ,2 ]
Liu, Yilong [2 ]
Du, Shan [1 ,2 ]
Zhang, Min [4 ]
Sun, Wenzhuo [5 ]
Wang, Zeyuan [6 ]
Hao, Xin [7 ]
Yu, Ze [6 ]
Gao, Fei [6 ]
Liu, Xinxia [1 ,2 ]
Tong, Rongsheng [1 ,2 ]
机构
[1] Sichuan Acad Med Sci & Sichuan Prov Peoples Hosp, Dept Pharm, Chengdu, Peoples R China
[2] Univ Elect Sci & Technol China, Sch Med, Personalized Drug Therapy Key Lab Sichuan Prov, Chengdu, Peoples R China
[3] Yaan Polytech Coll, Yaan, Peoples R China
[4] Hosp Chengdu Univ Tradit Chinese Med, Chengdu, Peoples R China
[5] Xian Jiaotong Liverpool Univ, Xian, Peoples R China
[6] Beijing Medicinovo Technol Co Ltd, Beijing, Peoples R China
[7] Dalian Medicinovo Technol Co Ltd, Dalian, Peoples R China
关键词
acute lymphoblastic leukemia; high-dose methotrexate; liver injury; gene polymorphism; ridge regression model; children; ADVERSE EVENTS; TOXICITY; PHARMACOKINETICS; PATHWAY;
D O I
10.3389/fphar.2021.726229
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A study on 70 acute lymphoblastic leukemia (ALL) children (age <= 16 years) treated with high-dose methotrexate (HD-MTX) in Sichuan Provincial People's Hospital was conducted. The aim of the study was to establish a risk-scoring model to predict HD-MTX-induced liver injury, considering gene polymorphisms' effects. Data screening was performed through t-test, chi-square test, and ridge regression, and six predictors were identified: age, MTRR_AA, MTRR_AG, SLCO1B1_11045879_CC, albumin_1 day before MTX administration, and IBIL_1 day before MTX administration (p < 0.1). Then, the risk-scoring model was established by ridge regression and evaluated the prediction performance. In a training cohort (n = 49), the area under the curve (AUC) was 0.76, and metrics including accuracy, precision, sensitivity, specificity, positive predictive value, and negative predictive value were promising (0.86, 0.81, 0.76, 0.91, 0.81, 0.88, respectively). In a test cohort (n = 21), the AUC was 0.62 and negative predictive value was 0.80; other evaluation metrics were not satisfactory, possibly due to the limited sample size. Ultimately, the risk scores were stratified into three groups based on their distributions: low- (<= 48), medium- (49-89), and high-risk (> 89) groups. This study could provide knowledge for the prediction of HD-MTX-induced liver injury and reference for the clinical medication.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] Identifying risk factors for high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia
    Li, Xiao
    Sui, Zhongguo
    Jing, Fanbo
    Xu, Wen
    Li, Xiangpeng
    Guo, Qie
    Sun, Shuhong
    Bi, Xiaolin
    [J]. CANCER MANAGEMENT AND RESEARCH, 2019, 11 : 6265 - 6274
  • [2] Identification of Risk Factors in High-Dose Methotrexate-Induced Acute Kidney Injury in Childhood Acute Lymphoblastic Leukemia
    Cheng, Dao-Hai
    Lu, Hua
    Liu, Tao-Tao
    Zou, Xiao-Qin
    Pang, Hui-Mei
    [J]. CHEMOTHERAPY, 2018, 63 (02) : 100 - 106
  • [3] Medium and high-dose methotrexate-induced toxicity in children with acute lymphoblastic leukemia (ALL)
    Hedavatiasl, Amirabas
    Darbandi, Bahram
    Vossough, Parvaneh
    Faranoush, Mohammad
    Golpayegani, Mohammad Reza
    Zangooie, Rokhsaneh
    Yazdi, Fatemeh
    Rafsanjani, Khadijeh Arjmandi
    Ansari, Shahla
    Zarrabi, Mohammad
    [J]. PEDIATRIC BLOOD & CANCER, 2007, 49 (04) : 490 - 491
  • [4] High-Dose Methotrexate-Induced Idiopathic Intracranial Hypertension in Infant Acute Lymphoblastic Leukemia
    Zhang, Yazhi
    Qiu, Yining
    Wang, Zhujun
    Wang, Ran
    Jin, Runming
    Hinkle, Louis Edward
    Wu, Xiaoyan
    [J]. FRONTIERS IN PHARMACOLOGY, 2020, 11
  • [5] Clinical and pharmacokinetic risk factors for high-dose methotrexate-induced toxicity in children with acute lymphoblastic leukemia -: A logistic regression analysis
    Rask, C
    Albertioni, F
    Bentzen, SM
    Schroeder, H
    Peterson, C
    [J]. ACTA ONCOLOGICA, 1998, 37 (03) : 277 - 284
  • [6] High-dose methotrexate for the treatment of acute lymphoblastic leukemia in children (a pharmacokinetic study)
    Slany, J
    Grundmann, M
    Brozmanova, H
    Blazek, B
    Sterba, J
    [J]. DRUG RESISTANCE IN LEUKEMIA AND LYMPHOMA II, 1997, 3 : 183 - 188
  • [7] METHOTREXATE-INDUCED MALABSORPTION IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA
    CRAFT, AW
    KAY, HEM
    LAWSON, DN
    MCELWAIN, TJ
    [J]. BRITISH MEDICAL JOURNAL, 1977, 2 (6101): : 1511 - 1512
  • [8] Is hypoalbuminemia a risk factor for high-dose methotrexate toxicity in children with acute lymphoblastic leukemia?
    Barakat, Shaimaa
    Assem, Hala
    Salama, Mostafa
    Mikhael, Neveen
    El Chazli, Yasmine
    [J]. JOURNAL OF THE EGYPTIAN NATIONAL CANCER INSTITUTE, 2022, 34 (01)
  • [9] Is hypoalbuminemia a risk factor for high-dose methotrexate toxicity in children with acute lymphoblastic leukemia?
    Shaimaa Barakat
    Hala Assem
    Mostafa Salama
    Neveen Mikhael
    Yasmine El Chazli
    [J]. Journal of the Egyptian National Cancer Institute, 34
  • [10] Association between high-dose methotrexate-induced toxicity and polymorphisms within methotrexate pathway genes in acute lymphoblastic leukemia
    Xu, Meng
    Wu, Shuangshuang
    Wang, Yue
    Zhao, Yundong
    Wang, Ximin
    Wei, Changhong
    Liu, Xueying
    Hao, Feng
    Hu, Cheng
    [J]. FRONTIERS IN PHARMACOLOGY, 2022, 13