Improving the safety of high‐dose methotrexate for children with hematologic cancers in settings without access to MTX levels using extended hydration and additional leucovorin. Issue 12 (16th May 2018)

• Record Type: Journal Article
• Authors: Vaishnavi, Kalthi; Bansal, Deepak; Trehan, Amita; Jain, Richa; Attri, Savita Verma
• Is Part Of: Pediatric blood & cancer. Volume 65:Issue 12(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-05-16
• Subjects: folinic acid -- high‐dose methotrexate -- leukemia -- low–middle income country -- renal toxicity; Tumors in children -- Periodicals; Blood -- Diseases -- Periodicals; Cancer in children -- Periodicals; 618.92
• DOI: 10.1002/pbc.27241
• Languages: English
• ISSNs: 1545-5009

Abstract

Abstract: Background: A lack of access to methotrexate levels is common in low‐ and middle‐income countries (LMIC), relevant for 80% of children with cancer worldwide. We evaluated whether high‐dose methotrexate (HD‐MTX) can be administered safely with extended hydration and leucovorin rescue, with monitoring of serum creatinine and urine pH. Methods: The prospective study was conducted at a single centre in Chandigarh, India in 2015. Patients with B‐cell acute lymphoblastic leukemia (ALL) or with T‐cell ALL or non‐Hodgkin lymphoma (T‐NHL) were administered 3 and 5 gm/m 2 of MTX (24 hr infusion), respectively. Six doses of leucovorin (15 mg/m 2 /dose), instead of recommended three (for optimally reduced levels) at standard timing (42 hr from start of HD‐MTX) were administered. Hydration (125 ml/m 2 /hr) was continued for 72 hr, instead of the recommended 30 hr. Hydration fluid consisted of 0.45% sodium chloride, 5% dextrose, 7.5% sodium bicarbonate (50 mmol/l) and potassium chloride (20 mmol/l). Serum creatinine and urine pH were measured at baseline, 24 and 48 hr. The volume of hydration was increased (200 ml/m 2 /hr) for a serum creatinine > 1.25 times the baseline. Results: The study included 100 cycles of HD‐MTX in 53 patients: B‐ALL 25 patients (51 cycles), T‐ALL 16 patients (28 cycles), T‐NHL 10 patients (18 cycles), and relapsed ALL 2 patients (3 cycles). The mean age was 6.8 ± 3.2 years. Patients were underweight in 15 (15%) cycles. Patients in 23% of cycles had a rise in creatinine to >1.25 times the baseline. Toxicities (NCI CTCAE v4.0) included mucositis (32%), diarrhoea (10%), and febrile neutropenia (9%). One patient died from dengue shock syndrome. Conclusions: It is safe to administer 3 or 5 gm/m 2 of MTX (24 hr infusion) without measuring MTX levels, with extended hydration, additional doses of leucovorin, and monitoring of serum creatinine and urine pH.