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Screening for asymptomatic diabetes and metabolic comorbidities in pediatric patients during therapy for acute lymphoblastic leukemia

  • Valerie Larouche ORCID logo EMAIL logo , Caroline Bellavance , Pauline Tibout , Sebastien Bergeron , David Simonyan and Julie Gagné
Published/Copyright: April 12, 2021

Abstract

Objectives

Chronic metabolic disturbances related to cancer treatment are well reported among survivors of pediatric acute lymphoblastic leukemia (ALL). However, few studies have investigated the incidence of these complications during the phase of chemotherapy. We evaluated the incidence of acute metabolic complications occurring during therapy in our cohort of patients diagnosed with ALL.

Methods

A prospective study involving 50 ALL pediatric patients diagnosed and treated between 2012 and 2016 in our oncology unit. We collected weight, blood pressure, fasting plasma glucose and hemoglobin A1C (HBA1c) levels during the two years of therapy.

Results

Obesity and overweight occurred in 43 and 25%, respectively among patients and have been reached at 12 months of chemotherapy. About 26% of the patients developed high blood pressure and 14% experienced hyperglycemias without meeting diabetes criteria. There was a significant decrease of HBA1c levels between the beginning and the end of therapy (p<0.0001).

Conclusions

Increase of body mass index in our ALL pediatric patients occurred during the first months of therapy and plateaued after a year of treatment. We should target this population for early obesity prevention. HbA1c levels measured during therapy did not reveal diabetes criteria. Hence, fasting blood glucose levels are sufficient to monitor ALL pediatric patients’ glycemia.


Corresponding author: Dr. Valérie Larouche, Department of Pediatrics, Centre Mère-enfant Soleil du CHU de Québec-Université Laval, Quebec, Canada, Phone: +418 525 4444 #40121, Fax: +418 654 2158, E-mail:

Acknowledgments

The authors want to thank Dr Bruno Michon and Dr Lamia Naccache working as pediatric oncologists at CHU de Quebec-Université Laval for their support to realize this prospective study. We are also grateful for the revision of this manuscript by Panagiota Giannakouros.

  1. Research funding: None declared.

  2. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  3. Conflict of interest: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: This study has been approved by the institutional ethic review board. Patients and their family were approached during the first month following their diagnosis to participate in this prospective study. The therapeutic protocol used for the treatment of this cohort of pediatric ALL in our institution was the Boston protocol the Dana-Farber Cancer Institute (DFCI 05-001).

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Received: 2020-08-05
Accepted: 2021-01-19
Published Online: 2021-04-12
Published in Print: 2021-05-26

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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