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
  • [31] High Dose Methotrexate-Induced Acute Kidney Injury: Incidence, Risk Factors, and Recovery
    Latcha, Sheron
    Gupta, Mohit
    Lin, I-Hsin
    Jaimes, Edgar A.
    [J]. KIDNEY INTERNATIONAL REPORTS, 2023, 8 (02): : 360 - 364
  • [32] Pharmacokinetics of High-Dose Methotrexate in Infants Treated for Acute Lymphoblastic Leukemia
    Lonnerholm, Gudmar
    Valsecchi, Maria Grazia
    De Lorenzo, Paola
    Schrappe, Martin
    Hovi, Liisa
    Campbell, Myriam
    Mann, Georg
    Janka-Schaub, Gritta
    Li, Chi-Kong
    Stary, Jan
    Hann, Ian
    Pieters, Rob
    [J]. PEDIATRIC BLOOD & CANCER, 2009, 52 (05) : 596 - 601
  • [33] Hepatoxicity in a Patient with Acute Lymphoblastic Leukemia Receiving High-Dose Methotrexate
    Kalakota, Neeharika
    Sharma, Ashish
    Bhakta, Dimpal
    Gould, Milena
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2016, 111 : S1346 - S1346
  • [34] RELATIONSHIP BETWEEN MTHFR POLYMORPHISM AND SIDE EFFECTS OF HIGH-DOSE METHOTREXATE IN PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA
    Ragab, S. M.
    El-Rashedy, F. H.
    Dawood, A. A.
    El-Hawy, M. A.
    [J]. HAEMATOLOGICA, 2014, 99 : 279 - 279
  • [35] Neurotoxicity in children with acute lymphoblastic leukemia treated in the FRALLE 93 study is not restricted to high-dose methotrexate.
    Landman-Parker, J
    Leblanc, T
    Tabone, MD
    Schmitt, C
    Perel, Y
    Auclerc, MF
    Cornu, G
    Edan, C
    Michel, G
    De Lumley, L
    Demeocq, F
    Stephan, JL
    Schaison, G
    Leverger, G
    Mahmoud, HH
    Baruchel, A
    [J]. BLOOD, 1999, 94 (10) : 288A - 288A
  • [36] Comparison of pharmacokinetics and toxicity after high-dose methotrexate treatments in children with acute lymphoblastic leukemia
    Csordas, Katalin
    Hegyi, Marta
    Eipel, Oliver T.
    Muller, Judit
    Erdelyi, Daniel J.
    Kovacs, Gabor T.
    [J]. ANTI-CANCER DRUGS, 2013, 24 (02) : 189 - 197
  • [37] Assessment of Renal Function During High-Dose Methotrexate Treatment in Children With Acute Lymphoblastic Leukemia
    Ylinen, Elisa
    Jahnukainen, Kirsi
    Saarinen-Pihkala, Ulla M.
    Jahnukainen, Timo
    [J]. PEDIATRIC BLOOD & CANCER, 2014, 61 (12) : 2199 - 2202
  • [38] Risk Factors of Delayed Elimination of High-dose Methotrexate in Childhood Acute Lymphoblastic Leukemia or Lymphoma
    Nakano, Takaaki
    Kobayashi, Ryouji
    Matsushima, Satoru
    Hori, Daiki
    Yanagi, Masato
    Suzuki, Daisuke
    Kobayashi, Kunihiko
    [J]. PEDIATRIC BLOOD & CANCER, 2019, 66 : S29 - S29
  • [39] Risk factors for delayed elimination of high-dose methotrexate in childhood acute lymphoblastic leukemia and lymphoma
    Takaaki Nakano
    Ryoji Kobayashi
    Satoru Matsushima
    Daiki Hori
    Masato Yanagi
    Daisuke Suzuki
    Kunihiko Kobayashi
    [J]. International Journal of Hematology, 2021, 113 : 744 - 750
  • [40] Risk factors for delayed elimination of high-dose methotrexate in childhood acute lymphoblastic leukemia and lymphoma
    Nakano, Takaaki
    Kobayashi, Ryoji
    Matsushima, Satoru
    Hori, Daiki
    Yanagi, Masato
    Suzuki, Daisuke
    Kobayashi, Kunihiko
    [J]. INTERNATIONAL JOURNAL OF HEMATOLOGY, 2021, 113 (05) : 744 - 750