The effect of the plasma methotrexate concentration during high-dose methotrexate therapy in childhood acute lymphoblastic leukemia

被引:5
作者
Liao, Chan [1 ]
Nie, Jing [2 ,3 ]
Xu, Xiao-Jun [1 ]
Zhang, Jing-Ying [1 ]
Xu, Wei-Qun [1 ]
Song, Hua [1 ]
Shen, He-Ping [1 ]
Shen, Di-Ying [1 ]
Zhao, Fen-Ying [1 ]
Liang, Juan [1 ]
Miao, Jing [2 ,3 ,5 ,6 ]
Tang, Yong-Min [1 ,4 ]
机构
[1] Zhejiang Univ, Dept Pediat Hematol Oncol, Childrens Hosp, Sch Med,Pediat Leukemia Diagnost & Therapeut Techn, Hangzhou, Peoples R China
[2] Zhejiang Univ, Childrens Hosp, Natl Clin Res Ctr Child Hlth, Dept Pharm,Sch Med, Hangzhou, Peoples R China
[3] Zhejiang Univ, Res Ctr Clin Pharm, Hangzhou, Peoples R China
[4] Zhejiang Univ, Dept Pediat Hematol Oncol, Childrens Hosp, Sch Med,Pediat Leukemia Diagnost & Therapeut Techn, 57 Zhuganxiang Rd,Yan An St, Hangzhou 310003, Peoples R China
[5] Zhejiang Univ, Childrens Hosp, Natl Clin Res Ctr Child Hlth, Dept Pharm,Sch Med, Hangzhou 310052, Zhejiang, Peoples R China
[6] Zhejiang Univ, Res Ctr Clin Pharm, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Methotrexate; childhood; acute lymphoblastic leukemia; ACUTE LYMPHOCYTIC-LEUKEMIA; MTHFR POLYMORPHISMS; TOXICITY; PATHWAY; GENES; PHARMACOKINETICS; ASSOCIATION;
D O I
10.1080/10428194.2023.2266075
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Two hundred and thirty-one acute lymphoblastic leukemia (ALL) children with 1376 high-dose methotrexate (HD-MTX) courses (3-5 g/m2) were enrolled to analyze the influence of the plasma MTX concentration (CMTX) in ALL. The 24-h target peak CMTX (C24h) was set at 33 mu mol/l for low-risk (LR) and 65 mu mol/l for intermediate/high-risk (IR/HR) groups. The median C24h was 42.0 mu mol/l and 69.7 mu mol/l for LR and IR/HR groups, respectively. MTX excretion delay was observed in 14.6% of courses, which was more frequent in IR/HR groups (56.9% vs. LR group 40.2%, p = .014) and T-ALL patients (82.6% vs. B-ALL 47.1%, p = .001). MTX-related toxicities were more common in courses with MTX excretion delay. However, survival between the patients who failed to reach the target C24h or not, with or without MTX excretion delay, was comparable. These findings suggest that, owing to the effectiveness of risk stratification chemotherapy, CMTX does not exert an independent influence on the prognosis of childhood ALL.
引用
收藏
页码:91 / 99
页数:9
相关论文
共 36 条
[1]   INTENSIVE INTRAVENOUS METHOTREXATE AND MERCAPTOPURINE TREATMENT OF HIGHER-RISK NON-T, NON-B ACUTE LYMPHOCYTIC-LEUKEMIA - A PEDIATRIC-ONCOLOGY-GROUP STUDY [J].
CAMITTA, B ;
MAHONEY, D ;
LEVENTHAL, B ;
LAUER, SJ ;
SHUSTER, JJ ;
ADAIR, S ;
CIVIN, C ;
MUNOZ, L ;
STEUBER, P ;
STROTHER, D ;
KAMEN, BA .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (07) :1383-1389
[2]   Polymorphisms of SLC19A1 80 G>A, MTHFR 677 C>T, and Tandem TS Repeats Influence Pharmacokinetics, Acute Liver Toxicity, and Vomiting in Children With Acute Lymphoblastic Leukemia Treated With High Doses of Methotrexate [J].
Cwiklinska, Magdalena ;
Czogala, Malgorzata ;
Kwiecinska, Kinga ;
Madetko-Talowska, Anna ;
Szafarz, Malgorzata ;
Pawinska, Katarzyna ;
Wieczorek, Aleksandra ;
Klekawka, Tomasz ;
Rej, Magdalena ;
Stepien, Konrad ;
Halubiec, Przemyslaw ;
Lazarczyk, Agnieszka ;
Miklusiak, Karol ;
Bik-Multanowski, Miroslaw ;
Balwierz, Walentyna ;
Skoczen, Szymon .
FRONTIERS IN PEDIATRICS, 2020, 8
[3]   Effect of polymorphisms in folate-related genes on in vitro methotrexate sensitivity in pediatric acute lymphoblastic leukemia [J].
de Jonge, R ;
Hooijberg, JH ;
van Zelst, BD ;
Jansen, G ;
van Zantwijk, CH ;
Kaspers, GJL ;
Peters, FGJ ;
Ravindranath, Y ;
Pieters, R ;
Lindemans, J .
BLOOD, 2005, 106 (02) :717-720
[4]   Genetic and metabolic determinants of methotrexate-induced mucositis in pediatric acute lymphoblastic leukemia [J].
den Hoed, M. A. H. ;
Lopez-Lopez, E. ;
te Winkel, M. L. ;
Tissing, W. ;
de Rooij, J. D. E. ;
Gutierrez-Camino, A. ;
Garcia-Orad, A. ;
den Boer, E. ;
Pieters, R. ;
Pluijm, S. M. F. ;
de Jonge, R. ;
van den Heuvel-Eibrink, M. M. .
PHARMACOGENOMICS JOURNAL, 2015, 15 (03) :248-254
[5]   High dose methotrexate in adult Egyptian patients with hematological malignancies: impact of ABCB1 3435C > T rs1045642 and MTHFR 677C > T rs1801133 polymorphisms on toxicities and delayed elimination [J].
Ebid, Abdel-Hameed I. M. ;
Hossam, Ahmed ;
El Gammal, Mosaad M. ;
Soror, Sameh ;
Mangoud, Nadia O. M. ;
Mahmoud, Mohamed Adel .
JOURNAL OF CHEMOTHERAPY, 2022, 34 (06) :381-390
[6]   CLINICAL PHARMACODYNAMICS OF HIGH-DOSE METHOTREXATE IN ACUTE LYMPHOCYTIC-LEUKEMIA - IDENTIFICATION OF A RELATION BETWEEN CONCENTRATION AND EFFECT [J].
EVANS, WE ;
CROM, WR ;
ABROMOWITCH, M ;
DODGE, R ;
LOOK, AT ;
BOWMAN, WP ;
GEORGE, SL ;
PUI, CH .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (08) :471-477
[7]   Involvement of C677T MTHFR variant but not A1298C in methotrexate-induced toxicity in acute lymphoblastic leukemia [J].
Frikha, Rim ;
Ben Jemaa, Maha ;
Frikha, Fakher ;
Turki, Ines ;
Elloumi, Moez ;
Keskes, Leila ;
Kamoun, Hassen ;
Rebai, Tarek .
JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2021, 27 (06) :1382-1387
[8]   Effects of genetic polymorphisms on methotrexate levels and toxicity in Chinese patients with acute lymphoblastic leukemia [J].
Hao, Qishan ;
Song, Yang ;
Fang, Qiuyun ;
Lin, Yani ;
Chen, Long ;
Wang, Xiaodan ;
Zhang, Ping ;
Wang, Zhe ;
Gong, Xiaoyuan ;
Liu, Kaiqi ;
Li, Qinghua ;
Tian, Zheng ;
Wang, Min ;
Wang, Jianxiang ;
Mi, Yingchang .
BLOOD SCIENCE, 2023, 5 (01) :32-38
[9]   Successful Outcomes of Newly Diagnosed T Lymphoblastic Lymphoma: Results From Children's Oncology Group AALL0434 [J].
Hayashi, Robert J. ;
Winter, Stuart S. ;
Dunsmore, Kimberly P. ;
Devidas, Meenakshi ;
Chen, Zhiguo ;
Wood, Brent L. ;
Hermiston, Michelle L. ;
Teachey, David T. ;
Perkins, Sherrie L. ;
Miles, Rodney R. ;
Raetz, Elizabeth A. ;
Loh, Mignon L. ;
Winick, Naomi J. ;
Carroll, William L. ;
Hunger, Stephen P. ;
Lim, Megan S. ;
Gross, Thomas G. ;
Bollard, Catherine M. .
JOURNAL OF CLINICAL ONCOLOGY, 2020, 38 (26) :3062-+
[10]   Preventing and Managing Toxicities of High-Dose Methotrexate [J].
Howard, Scott C. ;
McCormick, John ;
Pui, Ching-Hon ;
Buddington, Randall K. ;
Harvey, R. Donald .
ONCOLOGIST, 2016, 21 (12) :1471-1482