Early therapeutic drug monitoring of methotrexate and its association with acute kidney injury: A retrospective cohort study

Author:

Tentoni Nicolás12ORCID,Hwang Miriam2ORCID,Villanueva Gabriela2ORCID,Combs Ryan2,Lowe Jennifer2,Ramsey Laura B.34ORCID,Taylor Zachary L.567ORCID,Carrillo Thais Murciano8ORCID,Aumente María Dolores9ORCID,López‐Viñau López Teresa9ORCID,Rizzari Carmelo10ORCID,Howard Scott C.21112ORCID

Affiliation:

1. Laboratory of Applied Statistics in the Health Sciences, School of Medicine University of Buenos Aires Buenos Aires Argentina

2. Resonance Memphis Tennessee USA

3. Division of Clinical Pharmacology, Toxicology & Therapeutic Innovation Children's Mercy Hospital Kansas City Missouri USA

4. Department of Pediatrics University of Missouri – Kansas City School of Medicine Kansas City Missouri USA

5. Division of Translational and Clinical Pharmacology Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

6. Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

7. Department of Pediatrics University of Cincinnati College of Medicine Cincinnati Ohio USA

8. Pediatric Oncology and Hematology Service Vall d'Hebron University Hospital Barcelona Spain

9. Pharmacy Service Reina Sofía University Hospital/Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC)/University of Córdoba Córdoba Spain

10. Department of Pediatrics, Pediatric Hematology Oncology Unit University of Milano‐Bicocca, IRCCS San Gerardo dei Tintori Monza Italy

11. Sant Joan de Déu Hospital Barcelona Barcelona Spain

12. Yeolyan National Hematology Center Yerevan Armenia

Abstract

AbstractIntroductionHigh‐dose methotrexate (HDMTX) use can be limited by the development of acute kidney injury (AKI). Early AKI detection is paramount to prevent further renal injury and irreversible toxicities. This study sought to determine whether early elimination patterns of MTX would be useful as a biomarker of AKI in HDMTX treatment.MethodsThis retrospective cohort study included two sites that collected ≥2 MTX levels within 16 h from completion of MTX infusion. Early levels were tagged and MTX elimination half‐life (t½) were calculated from combinations of two of three different early time periods. Receiver operating characteristic (ROC) curves were synthesized for each elimination t½ (biomarker) with respect to AKI and delayed methotrexate elimination (DME); the biomarker with the highest area under the ROC curve (AUC) was tested in a multiple variable logistic regression model.ResultsData from 169 patients who received a total of 556 courses of HDMTX were analyzed. ROC analysis revealed MTX elimination t½ calculated from the second and third time periods had the highest AUC for AKI at 0.62 (interquartile range [IQR] 0.56–0.69) and DME at 0.86 (IQR 0.73–1.00). After adjusting for age, sex, dose (mg/m2), infusion duration, HDMTX course, and baseline estimated glomerular filtration rate, it remained significant for AKI with an OR of 1.29 and 95% confidence interval of 1.03–1.65.ConclusionEarly MTX elimination t½ measured within 16 h of infusion completion was significantly associated with the development of AKI and serves as an early clearance biomarker that may identify patients who benefit from increased hydration, augmented leucovorin rescue, and glucarpidase administration.

Publisher

Wiley

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