2016, Number 3
<< Back Next >>
Rev Hematol Mex 2016; 17 (3)
Incidence and severity of drug adverse events to methotrexate and its relationship with the dietary intake of folates in children with acute lymphoblastic leukemia
Marqués-Maldonado AP, Pérez-Armendáriz B, Romero-Plata FE, Espinosa-Arreola M, Ruiz-Argüelles GJ
Language: Spanish
References: 55
Page: 175-186
PDF size: 487.68 Kb.
ABSTRACT
Background:Acute lymphoblastic leukemia is the most common
cancer among the pediatric population and the most frequent cause
of death from cancer before 20 years of age. Treatment includes
methotrexate, a folate antimetabolite that can cause changes of the
nutritional status and therapeutic abandonment linked to relapse and
a poor prognosis, due to adverse drug reactions.
Objetive: To determine the role of methotrexate dosis, nutrition
status and dietary folate intake on the incidence of afverse reactions
to drug.
Material and Method: A transversal and observational study was
made in a group of 30 patients whit diagnosis of acute lymphoblastic
leukemia receiving methotrexate from the Hematology and Intern
Medicine Center of the Ruiz Clinic and from the Hospital para el Niño
Poblano; the nutritional status was analyzed by anthropometry and
also the dietary folate intake which was related to the incidence and
severity of adverse drug reactions.
Results:Anthropometric data was obtained from 30 patients with
acute lymphoblastic leukemia receiving methotrexate, finding 67%
of the patients on an adequate nutritional status, 23% overweighed
and 10% with minor malnutrition. About the folate intake, 20% of
the patients have an adequate folate intake, 43% consumes less than
the recommended dietary intake and 37% consumes a bigger amount
of folates than recommended. In relation with the occurrence of adverse
drug reactions, no dependency was found between the dose of
methotrexate and the incidence or severity of the reactions (p=0.1088
and p=0.1644). The dietary adequacy of the folate intake did not show
dependency with the incidence of adverse reactions to methotrexate
(p=0.1083), the most common adverse drug reactions were nausea,
diarrhea and mucositis (p=0.3673, p=0.2360, p=0.6914). It was found
significant relation between the nutritional status and the incidence
of adverse reactions to methotrexate (p=0.0224), but this relation
was not maintained on the severity of nausea, diarrhea and mucositis
(p=0.3576, p=0.5836, p=0.5338).
Conclusions: These data are consistent with those observed in
other populations on the relationship between the nutritional status
and the incidence of the adverse reactions to methotrexate. The relationship
between the dietary intake of folates and the incidence and
severity of the adverse drug reactions may suggest an independence
that could be linked to the folate vitamer that is dietary consumed.
REFERENCES
Ortega MA, Osnaya ML, Rosas JR. Leucemia linfoblástica aguda. Med Int Mex. 2007;23:26-33.
Ruiz A, Ruiz D. Fundamentos de Hematología. 5ª ed. México: Editorial Médica Panamericana; 2014.
Chiaretti S, Gianfelic V, Ceglie G, Foà R. Genomic characterization of acute leukemias. Med Princ Pract 2014;23:487- 506.
Tasian SK, Mignon ML, Hunger SP. Childhood acute lymphoblastic leukemia: integrating genomics into therapy. Cancer 2015;121:3577-3590.
Hunger S, Mullighan C. Acute lymphoblastic leukemia in children. N Engl J Med 2015;373:1541-1552.
Rogers PC. Nutritional status as a prognostic indicator for pediatric malignancies. J Clin Oncol 2014;32:1293-1294.
Lansiaux A. Les antimétabolites. Bull Cancer 2011;98:1263- 1274.
Farber S, Diamond LK, Mercer R, Sylvester R, Wolff J. Temporary remissions in acute leukemia in children produced by folic acid antagonist, 4-aminopteroyl-gutamic acid (aminopterine). N Engl J Med 1948;238:787-793.
Farber S. Some observations on the effect of folic acid antagonists on acute leukemia and other forms of incurable cancer. Blood 1949;4:160-167.
Thiersch JB. Bone-marrow changes in man after treatment with aminopterin, amethopterin, and aminoanfol. Cancer 1949;2:877-883.
Bennette J. Amethopterin: a toxic tumour growth inhibitor. Br J Cancer 1952;6:377-388.
Dresner E, White JC. The biological action and clinical application of folic acid antagonists. Acta Haematol 1952;7:117-127.
Rihácek M, Pilatova K, Sterba J, Pilny R, Valík D. Indings in methotrexate pharmacology- diagnostic possibilities and impact on clinical care. Klin Onkol 2015;28:163-170.
Scaglione F, Panzavolta G. Folate, folic acid and 5- methyltetrahydrofolate are not the same thing. Xenobiotica 2014;44:480-488.
American Society of Health System Pharmacist. Drug Information. Washington: ASHP, 2015.
Irving J. Towards an understanding of the biology and targeted treatment of paediatric relapsed acute lymphoblastic leukaemia. Br J Haematol 2015;172:655-66. doi: 10.1111/bjh.13852.
Khalek ER, Sherif LM, Kamal NM, Gharib AF, Shawky HM. Acute lymphoblastic leukemia: are Egyptian children adherent to maintenance therapy? J Cáncer Res Ther 2015;11:54-58.
Suarez A, Piña M, Nochols-Vinueza D, Lopera J, et al. A strategy to improve treatment-related mortality and abandonment of therapy for childhood ALL in a developing country reveals the impact of treatment delays. Pediatr Blood Cáncer 2015;62:1395-1402.
Li E, Jin R. Letter to the editor. Leuk Res 20132;36:193-194.
Klünder M, Miranda A, Dorantes E, Zapata M, et al. Frecuencia de abandono del tratamiento en pacientes pediátricos con leucemia linfoblástica aguda. Bol Med Hosp Infant Mex 2012;69:226-232.
Rivera GK, Ribeiro RC. Improving treatment of children with acute lymphoblastic leukemia in developing countries through technology sharing, collaboration, and partnerships. Expert Rev Hematol 2014;7:649-657.
Hernández A, Rodríguez A, Ferrusco M. Poletti E. Estomatitis por metotrexato y sus efectos orales a bajas dosis. Dermatol Rev Mex 2014;58:458-464.
Taketomo C, Hoodding J, Kraus D. Pediatric dosage handbook. 22a Ed. Ohio: Lexi-Comp & American Pharmacists Association, 2015.
Ferreira A, Aquino A, Pereira C, Weege C, et al. Frequency of oral mucositis and microbiological analysis in children with acute lymphoblastic leukemia treated with 0.12% chlorhexidine gluconate. Braz Dent J 2011;22:312-316.
Moe P. Methotrexate and oral mucositis. Pediatr Hematol Oncol 1996;13:313-314.
Lowal KA, Alaizari NA, Tarakji B, Petro W, et al. Dental considerations for leukemic pediatric patients: an updated review for general dental practitioner. Mater Sociomed 2015;27:359-362.
Holmboe L, Andersen A, Mørkrid L, Slørdal5 L, Hall KS. High dose methotrexate chemotherapy: pharmacokinetics, folate and toxicity in osteosarcoma patients. Br J Clin Pharmacol 2011;73:106-114. doi:10.1111/j.1365- 2125.2011.04054.x
Mena J, Salazar M, Dávalos I. Farmacogenómica del metotrexato: estrategia para una terapéutica más individualizada en pacientes con artritis reumatoide. Gac Méd Méx 2008;144:449-451.
Guéant RM, Guéant JL, Debard R, Thirion S, et al. Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: a comparative study in Mexican, West African, and European populations. Am J Clin Nutr 2006;83:701-707.
den Hoed M, Lopez E, Winkel M, Tissing W, et al. Genetic and metabolic determinants of methotrexate-induced mucositis in pediatric acute lymphoblastic leukemia. Pharmacogenomics J 2015;15:248-254.
Ruiz Argüelles GJ, Coconi L, Garcés J, Reyes V. Methotrexate- induced mucositis in acute leukemia patients is not associated with the MTHFR 677T allele in Mexico. Hematology 2007;12:387-391.
Drazen J. Drug-induced megaloblastic anemia. N Engl J Med 2015;373:1649-1658.
Brito A, Hertrampfl E, Olivares M, Gaitán D, et al. Folatos y vitamina B12 en la salud humana. Rev Med Chil 2012;140:1464-1475.
Arabelovic S, Sam G, Dallal G, Jacques P, et al. Preliminary evidence shows that folic acid fortification of the food supply is associated with higher methotrexate dosing in patients with rheumatoid arthritis. J Am Coll Nutr 2007;26:453-455.
Schmiegelow K, Nielsen S, Frandsen T, Nersting J. Mercaptopurine/ methotrexate maintenance therapy of childhood acute lymphoblastic leukemia: clinical facts and fiction. J Pediatr Hematol Oncol 2014;36:503-517.
Tandon S, Moulik N, Kumar A, Mahdi A, Kumar A. Effect of pre-treatment nutritional status, folate and vitamin B12 levels on induction chemotherapy in children with acute lymphoblastic leukemia. Indian Pediatr 2015;52:385-389.
Moulik NR, Kumar A. Are concerns about folic acid supplementation in children with acute lymphoblastic leukemia justified? Indian Pediatr 2014;51:754-755.
Malihi Z, Kandiah M, Chan YM, Hosseinzadeh M, et al. Nutritional status and quality of life in patients with acute leukaemia prior to and after induction chemotherapy in three hospitals in Tehran, Iran: a prospective study. J Hum Nutr Diet 2013;26:123-131.
Linga V, Shreedhara A, Rau AT, Rau A. Nutritional assessment of children with hematological malignancies and their subsequent tolerance to chemotherapy. Ochsner J 2012;12:197-201.
Centers for Disease Control and Prevention. Atlanta: Growth Charts [actualizado el 9 de septiembre de 2010; citado el 1 de marzo de 2016]. Growth Charts; disponible en: http://www.cdc.gov/growthcharts/
Organización Panamericana de la Salud–Organización Mundial de la Salud. [Monografía de Internet]. Bolivia: los nuevos patrones de crecimiento de la OMS. [Consultado el 5 de enero de 2016]. Disponible en: http://www.ops. org.bo/textocompleto/naiepi-patrones-crecimiento.pdf
National Nutrient Database for Standard Reference [Base de datos en Internet]. United States Department of Agriculture, Agricultural Research Service. C2007. [Citado de agosto de 2015 al 15 de enero de 2016]. DIsponible en: https://ndb.nal.usda.gov/ndb/search/li
Pérez A, Palacios B, Castro A, Flores I. Sistema Mexicano de Alimentos Equivalentes. 4ª ed. Ciudad de México: Fomento de Nutrición y Salud, 2014.
Vásquez E, Romero E, Larrosa A. Nutrición clínica en pediatría: un enfoque práctico. México: Intersistemas, 2011.
Escott-Stump S. Nutrición, Diagnóstico y tratamiento. 6ª ed. New York: Lippincott Williams & Wilkins, 2012.
Kaufer M, Pérez A, Arroyo P. Nutriología médica. 4ª ed. Ciudad de México: Editorial Médica Panamericana, 2015.
National Cancer Institute [Monografía de Internet]. US. Common Terminology Criteria for Adverse Events. [Consultado el 3 de junio de 2015]. Disponible en: http:// evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_ QuickReference_5x7.pdf
Tan SY, Poh BK, Nadrah MH, Jannah NA, et al. Nutritional status and dietary intake of children with acute leukaemia during induction or consolidation chemotherapy. J Hum Nutr Diet 2013;26:23-33.
Gómez-Almaguer D, Ruiz-Argüelles GJ, Ponce-de-León S. Nutritional status and socio-economic conditions as prognostic factors in the outcome of therapy in childhood acute lymphoblastic leukemia. Int J Cancer 1998;11:52-55.
Kim H, Kim G, Jang W, Kim SY, Chang N. Association between intake of B vitamins and cognitive function in elderly Koreans with cognitive impairment. Nutr J 2014;13:118.
Martín F, Batis C, González L, Rojas E, et al. Dietary micronutrient intake in peritoneal dialysis patients: relationship with nutrition and inflammation status. Perit Dial Int 2012;32:183-191.
Jani R, Salian N, Udipi S, Ghugre P, et al. Folate status and intake of tribal Indian adolescents aged 10 to 17 years. Food Nutr Bull 2015;36:14-23.
Schmiegelow K. Advances in individual prediction of methotrexate toxicity: a review. Br J Haematol 2009;146:489-503.
Moe P, Holen A. High-Dose Methotrexate in Childhood ALL. Pediatr Hematol Oncol. 2000; 17(8):615-22.
Gil A. Tratado de nutrición. 2ª ed. Madrid: Editorial Médica Panamericana, 2010.