Hypoalbuminemia and not undernutrition predicts high‐dose methotrexate‐induced nephrotoxicity in children with acute lymphoblastic leukemia in resource‐constrained centers. Issue 9 (21st April 2022)

• Record Type: Journal Article
• Authors: Khera, Sanjeev; Sharma, Gaurav; Negi, Vandana; Shaw, Subhash Chandra
• Is Part Of: Pediatric blood & cancer. Volume 69:Issue 9(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-04-21
• Subjects: High‐dose methotrexate -- hypoalbuminemia -- methotrexate nephrotoxicity -- undernutrition; Tumors in children -- Periodicals; Blood -- Diseases -- Periodicals; Cancer in children -- Periodicals; 618.92
• DOI: 10.1002/pbc.29738
• Languages: English
• ISSNs: 1545-5009

Abstract

Abstract: Background: The standard practice to mitigate high‐dose methotrexate (HD‐MTX)–induced nephrotoxicity (HMN) in acute lymphoblastic leukemia (ALL) is to monitor levels until serum MTX falls below a predefined threshold. It is not feasible in most resource‐constrained centers. Literature on the various factors affecting HMN in these centers is limited, retrospective, and heterogeneous. Though hypoalbuminemia has been postulated as a risk factor for HMN, the relationship of undernutrition with HMN has not been studied. Procedure: This prospective observational study consecutively enrolled children < 12 years old with ALL receiving HD‐MTX. Children with preexisting renal disease and exposed to nephrotoxic drugs two weeks preceding HD‐MTX infusion were excluded. HD‐MTX was administered over 24 hours (BFM‐2009 protocol) with 12 hours of prehydration. Solitary MTX levels at 36 hours (MTX36) were outsourced, and 6‐8 doses of leucovorin were given six‐hourly. Hydration was continued till last dose of leucovorin. Various factors affecting HMN (rise in creatinine to 1.5 times baseline) were recorded: age, sex, type of ALL, risk group of ALL, first dose of MTX, dose of MTX, undernourishment, serum protein, and albumin along with C‐reactive protein and MTX36 levels. Results: Forty‐four children who received 150 HD‐MTX cycles were analyzed. HMN was seen in 14% of cycles. On univariate analysis, undernourishment, MTX36 levels, hypoproteinemia, and hypoalbuminemia were significantly associated with HMN. On multivariate analysis, hypoalbuminemia and MTX36 levels significantly predicted the development of HMN with odds ratios of 4.71 and 1.45. Conclusion: Hypoalbuminemia and solitary serum MTX levels predict HMN in centers where serial MTX level monitoring is not feasible.