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Published on: September 30, 2021
Proactive enteral tube feeding in pediatric patients undergoing chemotherapy
Nancy Sacks1, Wei-Ting Hwang, Beverly J Lange
1Department of Clinical Nutrition, Division of Oncology, Center for Childhood Cancer Research, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Insights
Proactive enteral tube feeding (ETF) is feasible for pediatric cancer patients, improving nutritional status by the end of therapy. Further research is needed to understand infection risks associated with proactive ETF.
Area of Science:
- Pediatric Oncology
- Clinical Nutrition
- Cancer Care
Background:
- Assessing the feasibility and safety of proactive enteral tube feeding (ETF) in pediatric oncology.
- Evaluating nutritional support strategies for children undergoing cancer treatment.
Purpose of the Study:
- To determine if proactive ETF is feasible and safe in pediatric cancer patients.
- To compare nutritional outcomes between proactive ETF and standard care.
Main Methods:
- Enrolled pediatric patients with newly diagnosed brain tumors, leukemia, or high-risk solid tumors.
- Compared proactive ETF participants (PPs) with controls receiving standard nutritional care.
- Assessed nutritional status via anthropometry and documented infection/toxicity episodes.
Main Results:
- Proactive ETF was feasible, though enrollment barriers existed.
- Minimal ETF toxicity was observed; proactive group had more infections.
- Proactive ETF patients had less weight loss and improved nutritional status by study end.
Conclusions:
- Proactive ETF is feasible in pediatric cancer patients, leading to better nutritional status.
- Infection episodes in the proactive group warrant further investigation in larger trials.
- Improved nutritional status may mitigate some treatment toxicities.
Background:
To determine feasibility and safety of proactive enteral tube feeding (ETF) in pediatric oncology patients.
Methods:
Pediatric patients with newly diagnosed brain tumors, myeloid leukemia or high-risk solid tumors were eligible. Subjects agreeing to start ETF before cycle 2 chemotherapy were considered proactive participants (PPs). Those who declined could enroll as chart collection receiving nutritional standard of care. Nutritional status was assessed using standard anthropometric measurements. Episodes of infection and toxicity related to ETF were documented from diagnosis to end of therapy. A descriptive comparison between PPs and controls was conducted.
Results:
One hundred four eligible patients were identified; 69 enrolled (20 PPs and 49 controls). At diagnosis, 17% of all subjects were underweight and 26% overweight. Barriers to enrollment included physician, subject and/or family refusal, and inability to initiate ETF prior to cycle 2 of chemotherapy. Toxicity of ETF was minimal, but higher percentage of subjects in the proactive group had episodes of infection than controls. Thirty-nine percent of controls eventually started ETF and were twice as likely to receive parenteral nutrition. PPs experienced less weight loss at ETF initiation than controls receiving ETF and were the only group to demonstrate improved nutritional status at end of study.
Conclusions:
Proactive ETF is feasible in children with cancer and results in improved nutritional status at end of therapy. Episodes of infection in this study are concerning; therefore, a larger randomized trial is required to further delineate infectious risks and toxicities that may be mitigated by improved nutritional status.
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