A comprehensive review of 30 years of pediatric clinical trial radiotherapy dose constraints

Author:

Vassantachart April1ORCID,Olch Arthur J.23,Jones Marjorie45,Marques Christophe6,Ronckers Cécile78,Constine Louis S.9,Maduro John H.710,de Boer Charlotte11,Wong Kenneth23ORCID

Affiliation:

1. Department of Radiation Oncology LAC+USC Medical Center Los Angeles California USA

2. Department of Radiation Oncology Keck School of Medicine, University of Southern California Los Angeles California USA

3. Radiation Oncology Program Children's Hospital Los Angeles Los Angeles California USA

4. USC/CHLA Summer Oncology, Research Fellowship Children's Hospital Los Angeles Los Angeles California USA

5. University of South Alabama College of Medicine Mobile Alabama USA

6. Department of Radiation Oncology The Gayle and Tom Benson Cancer Center, Ochsner Health System New Orleans Louisiana USA

7. Princess Máxima Utrecht The Netherlands

8. Department of Health Services Research Carl von Ossietzky University of Oldenburg Oldenburg Germany

9. Departments of Radiation Oncology and Pediatrics University of Rochester Medical Center Rochester New York USA

10. Department of Radiation Oncology University of Groningen University Medical Centre Groningen Groningen The Netherlands

11. Department of Pediatric Oncology Emma Children's Hospital Amsterdam University Medical Center University of Amsterdam Amsterdam The Netherlands

Abstract

AbstractBackgroundRadiation therapy normal tissue dose constraints are critical when treating pediatric patients. However, there is limited evidence supporting proposed constraints, which has led to variations in constraints over the years. In this study, we identify these variations in dose constraints within pediatric trials both in the United States and in Europe used in the past 30 years.ProcedureAll pediatric trials from the Children's Oncology Group website were queried from inception until January 2022 and a sampling of European studies was included. Dose constraints were identified and built into an organ‐based interactive web application with filters to display data by organs at risk (OAR), protocol, start date, dose, volume, and fractionation scheme. Dose constraints were evaluated for consistency over time and compared between pediatric US and European trialsResultsOne hundred five closed trials were included—93 US trials and 12 European trials. Thirty‐eight separate OAR were found with high‐dose constraint variability. Across all trials, nine organs had greater than 10 different constraints (median 16, range 11–26), including serial organs. When comparing US versus European dose tolerances, the United States constraints were higher for seven OAR, lower for one, and identical for five. No OAR had constraints change systematically over the last 30 years.ConclusionReview of pediatric dose‐volume constraints in clinical trials showed substantial variability for all OAR. Continued efforts focused on standardization of OAR dose constraints and risk profiles are essential to increase consistency of protocol outcomes and ultimately to reduce radiation toxicities in the pediatric population.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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