Evaluation of dietetic intervention in children with medulloblastoma or supratentorial primitive neuroectodermal tumors
β Scribed by Jaimie Bakish; Darren Hargrave; Nauman Tariq; Normand Laperriere; James T. Rutka; Eric Bouffet
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 130 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0008-543X
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β¦ Synopsis
Abstract
BACKGROUND
Malnutrition is a common complication of cancer treatment; it can affect energy levels and, as a consequence, quality of life. The goal of the current study was to evaluate the effect of dietetic intervention in a cohort of children treated for medulloblastoma and supratentorial primitive neuroectodermal tumors (PNET) over a 10βyear period.
METHODS
A retrospective chart review (1992β2002) of newly diagnosed cases of medulloblastoma/supratentorial PNET was performed. Hospital records were reviewed for data, including demographic characteristics, patient heights and weights, and information on treatment modalities and the use of dietetic intervention. Percent changes in body weight were calculated at time points associated with particular stages of treatment or dietetic intervention.
RESULTS
One hundred three of 112 cases were evaluable. Treatment methods included surgery only (7.8%), surgery + radiotherapy (16.5%), surgery + chemotherapy (14.5%), and surgery + radiotherapy + chemotherapy (61.2%). There was no significant change in patient weight due to surgery (median change in body weight [MCBW], β0.35%) or radiotherapy (MCBW, β0.78%). In contrast, children experienced significant weight loss (MCBW, β4.35%; P < 0.0001) 3 months after starting chemotherapy. A dietician saw 53 of the 103 children in the study cohort. There were 84 dietetic interventions (oral, 36%; parenteral, 27%; enteral, 37%) among these 53 patients. Oral diets did not result in weight gain. Parenteral nutrition was associated with significant weight gain at 1 month (MCBW, +2.7%; P = 0.03), but not at 3 months. The use of enteral feeds resulted in significant weight gain at 1 month (MCBW, +4.8%; P = 0.006) and at 3 months (MCBW, +11.8%; P < 0.0001).
CONCLUSIONS
Current multimodality treatment of intracranial PNET results in significant nutritional morbidity, primarily due to the use of intensive chemotherapy regimens. Dietetic input for pediatric patients with medulloblastoma/PNET is essential, and the implementation of enteral feeding in these children can help to reverse their nutritional morbidity. Cancer 2003;98:1014β20. Β© 2003 American Cancer Society.
DOI 10.1002/cncr.11598
π SIMILAR VOLUMES
Primitive neuroectodermal tumors/medulloblastoma (PNET/MB) are the most common posterior fossa tumors in childhood. Despite surgery and radiation therapy, 40% to 50% of children with PNET/MB will have recurrent disease. Various chemotherapeutic agents are transiently effective in recurrent PNET/MB,
## Abstract ## BACKGROUND. An openβlabel Phase II study of tipifarnib was conducted to evaluate its safety and efficacy in children with recurrent or refractory medulloblastoma (MB)/primitive neuroectodermal tumor (PNET), highβgrade glioma (HGG), and diffuse intrinsic brainstem glioma (BSG). ## M