Efficacy and safety of oral magnesium supplementation in reducing febrile neutropenia episodes in children with solid tumors treated with cisplatin-based chemotherapy: randomized clinical trial
Autor: | Luis E. Juárez-Villegas, Karla M Silva-Jivaja, Victoria E. Barrios-López, Miguel Ángel Palomo-Colli, Martha A. Sánchez-Rodríguez, Osvaldo D Castelán-Martínez, Gilberto Castañeda-Hernández |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Cancer Research medicine.medical_specialty medicine.medical_treatment Neutropenia Toxicology Hypomagnesemia law.invention 03 medical and health sciences 0302 clinical medicine Randomized controlled trial law Internal medicine Medicine Pharmacology (medical) Adverse effect Pharmacology Chemotherapy Intention-to-treat analysis business.industry medicine.disease 030104 developmental biology Oncology 030220 oncology & carcinogenesis Number needed to treat business Febrile neutropenia |
Zdroj: | Cancer Chemotherapy and Pharmacology. 86:673-679 |
ISSN: | 1432-0843 0344-5704 |
DOI: | 10.1007/s00280-020-04155-4 |
Popis: | Hypomagnesemia has been associated with febrile neutropenia (FN) in pediatric patients receiving cisplatin-based chemotherapy (CDDPBC). The primary aim was to determine whether oral magnesium supplementation reduces FN episodes in pediatric patients with solid tumors treated with CDDPBC. This randomized clinical trial, with open-label, single-center, parallel group and superiority design was conducted in Hospital Infantil de Mexico Federico Gomez at Mexico City. Children ≥ 9 years with solid tumors that were to receive a CDDPBC cycle were invited to participate. Each chemotherapy cycle with CDDPBC was randomly assigned to receive oral magnesium supplementation (250 mg/day) or not receive magnesium supplementation (control group). Efficacy was determined by relative risks (RR) with 95% confidence intervals (95% CI) as well as with numbers needed to treat (NNT). Active surveillance was conducted to assess safety in both groups. Analyses were carried out by intention to treat. ClinicalTrials.gov number NCT03449693. One hundred and one chemotherapy cycles with CDDPBC were analyzed (50 in the magnesium supplement arm and 51 in control group). Baseline clinical characteristics were similar comparing both groups. Oral magnesium supplementation reduces FN episodes compared to control group [RR 0.53, (95% CI 0.32–0.89), NNT = 4]. In the supplemented group, patients had fewer episodes of septic shock secondary to FN [RR 0.43, (95% CI 0.02–0.94), NNT = 6] and FN appeared on average 5 days later (p = 0.031). Hypomagnesemia episodes and adverse events were similar across both groups. Oral supplementation with magnesium reduces FN episodes neutropenia in pediatric patients with solid tumors treated with CDDPBC. |
Databáze: | OpenAIRE |
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