Efficacy of Oral Supplementation With Magnesium to Reduce Febrile Neutropenia
Study Details
Study Description
Brief Summary
Clinical Trial. Open label. Parallel Groups. The purpose of the study is to determine the efficacy of oral supplementation with magnesium oxide to reduce febrile neutropenia episodes in pediatric oncology patients treated with cisplatin-based chemotherapy.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Phase 2 |
Detailed Description
Febrile neutropenia (FN) is a worrying outcome in children receiving chemotherapy because it increments the risk of major complications, reduces quality of life and increments treatment costs. Moreover, it is the most common diagnosis in pediatric oncology patients that enter emergency rooms and the second most important cause of hospitalization, just behind hospitalization for administration of chemotherapy.
In Mexico, incidence of FN is of 62% of children with solid tumors treated with cisplatin-based chemotherapy (CBC). Cisplatin is one of the most nephrotoxic drugs being used in clinical settlements. The assessment of nephrotoxicity is made with the manifestation of tubular damage that causes electrolyte losses, specially of magnesium. Recently, our investigation group reported that there is an association of hypomagnesemia and the apparition of FN. This association has a biologic explanation in the fact that magnesium is a necessary cofactor for the neutrophil's diapedesis and the activation of complement cascade. To our knowledge, the role of magnesium supplementation has not been explored. With this evidence in mind, the investigators wondered if oral supplementation with magnesium will reduce FN episodes in pediatric oncology patients treated with CBC.
Objective: Determine the efficacy of oral supplementation with magnesium to reduce FN episodes in pediatric oncology patients treated with CBC.
Hypothesis: Previous clinical trials made in adult population have reported that supplementation with magnesium salts reduce episodes of hypomagnesemia in between 13 and 50%. Thus, oral supplementation with magnesium oxide will reduce 20% of FN episodes in pediatric oncology patients treated with CBC.
Materials and Methods: Randomized Clinical Trial, open-label, parallel groups of children over the age of nine with solid tumors treated with CBC at the Haemato-Oncology Department of the Hospital Infantil de México. To prove the hypothesis, it is required to randomize 107 CBC cycles to the intervention group and 107 CBC cycles to the control group. The sample size calculation was made by using the two proportions formula. Randomize of children will be made when they receive CBC indication. Patients assigned to the intervention group will receive institutional attention protocol plus a bottle of magnesium oxide, at the moment of hospitalization discharge. Patients assigned to the control group will receive only institutional attention protocol. The follow-up of patients will be made until an episode of FN appears or until the patient comes back for another CBC cycle. FN assessment will be measured with a unique temperature >38.3°C or a sustained temperature >38°C over the course of an hour plus a count of neutrophils under 1000 cells/mm3. The efficacy of oral supplementation with magnesium oxide will be determined by a Relative Risks calculation with confidence interval of 95% (CI95%). Moreover, Absolute Risk Reduction will be calculated, as well as Necessary Number to Treat. To adjust the principal variable a multivariate analysis will be made with a multiple logistic regression. The analysis will be made by protocol and by intention to treat.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Magnesium Oxide Supplement Magnesium Oxide 250 mg tablet, daily for 30 days. |
Dietary Supplement: Magnesium Oxide Supplement
Magnesium Oxide tablet
Other Names:
|
No Intervention: No Supplement No Intervention |
Outcome Measures
Primary Outcome Measures
- Febrile Neutropenia [After randomization until day 30]
Unique temperature >38.3°C or sustained temperature >38°C over the course of an hour, and a total count of neutrophils <1000 cells/mm3.
Secondary Outcome Measures
- Time passed from cisplatin-based chemotherapy until the apparition of febrile neutropenia [After randomization until day 30]
Total of days passed from the randomization up to the apparition of febrile neutropenia
- Safety of Oral Supplementation with Magnesium [Evaluate the apparition of adverse effects of oral supplement of magnesium oxide Time Frame: After randomization until day 30]
Evaluate the apparition of adverse effects of oral supplement of magnesium oxide
- Hypomagnesemia [After randomization until day 30]
Serum magnesium <1.6 mg/mL
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Pediatric patients > 9 years old
-
Pediatric patients with solid tumors treated with cisplatin-based chemotherapy
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Signing of Informed Consent from the parents
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Signing of Informed Assent from the children
Non-inclusion Criteria:
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Patients whose parents do not sign the Informed Consent
-
Patients with magnesium losing tubulopathy
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Patients with hypomagnesemia previous to the cisplatin-based chemotherapy
Exclusion Criteria:
- Patients whose parents retire the Informed Consent
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Hospital Infantil de Mexico Dr. Federico Gomez | Cuauhtémoc | Ciudad De México | Mexico | 06720 |
Sponsors and Collaborators
- Universidad Nacional Autonoma de Mexico
- Hospital Infantil de Mexico Federico Gomez
- Centro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional
Investigators
- Principal Investigator: Osvaldo D Castelán, PhD, Universidad Nacional Autónoma de México. Facultad de Estudios Superiores Zaragoza
- Principal Investigator: Miguel A Palomo, PhD, Hospital Infantil de México Dr. Federico Gómez
Study Documents (Full-Text)
More Information
Publications
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- Freifeld AG, Pizzo PA. The outpatient management of febrile neutropenia in cancer patients. Oncology (Williston Park). 1996 Apr;10(4):599-606, 611-2; discussion 615-6. Review.
- Klaassen RJ, Goodman TR, Pham B, Doyle JJ. "Low-risk" prediction rule for pediatric oncology patients presenting with fever and neutropenia. J Clin Oncol. 2000 Mar;18(5):1012-9.
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- Willox JC, McAllister EJ, Sangster G, Kaye SB. Effects of magnesium supplementation in testicular cancer patients receiving cis-platin: a randomised trial. Br J Cancer. 1986 Jul;54(1):19-23.
- Zarif Yeganeh M, Vakili M, Shahriari-Ahmadi A, Nojomi M. Effect of Oral Magnesium Oxide Supplementation on Cisplatin-Induced Hypomagnesemia in Cancer Patients: A Randomized Controlled Trial. Iran J Public Health. 2016 Jan;45(1):54-62.
- HIM-2017-085