Acquisition matters - how do scan parameters affect apparent diffusion coefficient estimates in pediatric rhabdomyosarcoma.

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作者:Chatziantoniou Cyrano, van Ewijk Roelof, Adams Madeleine, Bertolini Patrizia, Bisogno Gianni, Bouhamama Amine, Caro-Dominguez Pablo, Charon Valérie, Coma Ana, Dandis Rana, Devalck Christine, De Donno Giulia, Ferrari Andrea, Fiocco Marta, Gallego Soledad, Giraudo Chiara, Glosli Heidi, Ter Horst Simone A J, Jenney Meriel, Klein Willemijn M, Leemans Alexander, Leseur Julie, Mandeville Henry C, McHugh Kieran, Merks Johannes H M, Minard-Colin Veronique, Moalla Salma, Morosi Carlo, Orbach Daniel, Ording Müller Lil-Sofie, Pace Erika, Di Paolo Pier Luigi, Perruccio Katia, Quaglietta Lucia, Renard Marleen, van Rijn Rick R, Ruggiero Antonio, Sirvent Sara I, Schoot Reineke A, De Luca Alberto
BACKGROUND: The apparent diffusion coefficient (ADC) derived from diffusion-weighted imaging (DWI) is a potential biomarker for treatment response in pediatric rhabdomyosarcoma. Due to its rarity, investigations into this marker require multicenter approaches, which can result in variability in acquisition parameters. OBJECTIVE: To evaluate the impact of different acquisition parameters on ADC estimates in a multicenter dataset of rhabdomyosarcoma patients. MATERIALS AND METHODS: We included 114 pediatric and adolescent rhabdomyosarcoma patients from 22 treatment centers (195 scans). Median age: 6.0 years (0.3-21.8). We evaluated the impact of voxel size, (number of) b-values, and echo time on tumor ADC values. The effect of the highest b-value was separately investigated on a subset of scans with five or more b-values. RESULTS: We observed a large variability in key acquisition parameters in the overall cohort, and for individual imaging centers. No parameter showed a significant effect on ADC estimates of the whole cohort when corrected for multiple-comparisons. Decreasing the highest b-value within the same acquisition caused ADC to decrease on average by 2.8% per 100 s mm(-2). Differing b-values between scans at diagnosis and treatment response yielded significant changes in the longitudinal ADC for each patient (P<0.05). CONCLUSION: While we observed wide variation of acquisition parameters within a multicenter cohort, this did not lead to significant cross-sectional differences of tumor ADC. However, we found that modifying the highest b-value between baseline and follow-up can impact longitudinal ADC estimates. As such, we recommend the highest b-value to remain constant. This retrospective study was reviewed and approved by the Internal Review Board (UMC Utrecht, reference ID: 18-412).

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