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Quantitative diffusion-weighted MRI response assessment in rhabdomyosarcoma: an international retrospective study on behalf of the European paediatric Soft tissue sarcoma Study Group Imaging Committee

Objective To investigate the feasibility of diffusion-weighted magnetic resonance imaging (DW-MRI) as a predictive imaging marker after neoadjuvant chemotherapy in patients with rhabdomyosarcoma. Material and methods We performed a multicenter retrospective study including pediatric, adolescent and...

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Published in:Pediatric radiology 2023-11, Vol.53 (12), p.2539-2551
Main Authors: van Ewijk, Roelof, Chatziantoniou, Cyrano, Adams, Madeleine, Bertolini, Patrizia, Bisogno, Gianni, Bouhamama, Amine, Caro-Dominguez, Pablo, Charon, Valerie, 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 Muller, Lil-Sofie, Pace, Erika, Di Paolo, Pier Luigi, Perruccio, Katia, Quaglietta, Lucia, Renard, Marleen, van Rijn, Rick R., Ruggiero, Antonio, Sirvent, Sara I., De Luca, Alberto, Schoot, Reineke A.
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container_end_page 2551
container_issue 12
container_start_page 2539
container_title Pediatric radiology
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creator van Ewijk, Roelof
Chatziantoniou, Cyrano
Adams, Madeleine
Bertolini, Patrizia
Bisogno, Gianni
Bouhamama, Amine
Caro-Dominguez, Pablo
Charon, Valerie
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 Muller, Lil-Sofie
Pace, Erika
Di Paolo, Pier Luigi
Perruccio, Katia
Quaglietta, Lucia
Renard, Marleen
van Rijn, Rick R.
Ruggiero, Antonio
Sirvent, Sara I.
De Luca, Alberto
Schoot, Reineke A.
description Objective To investigate the feasibility of diffusion-weighted magnetic resonance imaging (DW-MRI) as a predictive imaging marker after neoadjuvant chemotherapy in patients with rhabdomyosarcoma. Material and methods We performed a multicenter retrospective study including pediatric, adolescent and young adult patients with rhabdomyosarcoma, Intergroup Rhabdomyosarcoma Study group III/IV, treated according to the European paediatric Soft tissue sarcoma Study Group (E p SSG) RMS2005 or MTS2008 studies. DW-MRI was performed according to institutional protocols. We performed two-dimensional single-slice tumor delineation. Areas of necrosis or hemorrhage were delineated to be excluded in the primary analysis. Mean, median and 5th and 95th apparent diffusion coefficient (ADC) were extracted. Results Of 134 included patients, 82 had measurable tumor at diagnosis and response and DW-MRI scans of adequate quality and were included in the analysis. Technical heterogeneity in scan acquisition protocols and scanners was observed. Mean ADC at diagnosis was 1.1 (95% confidence interval [CI]: 1.1–1.2) (all ADC expressed in * 10 −3 mm 2 /s), versus 1.6 (1.5–1.6) at response assessment. The 5th percentile ADC was 0.8 (0.7–0.9) at diagnosis and 1.1 (1.0–1.2) at response. Absolute change in mean ADC after neoadjuvant chemotherapy was 0.4 (0.3–0.5). Exploratory analyses for association between ADC and clinical parameters showed a significant difference in mean ADC at diagnosis for alveolar versus embryonal histology. Landmark analysis at nine weeks after the date of diagnosis showed no significant association (hazard ratio 1.3 [0.6–3.2]) between the mean ADC change and event-free survival. Conclusion A significant change in the 5th percentile and the mean ADC after chemotherapy was observed. Strong heterogeneity was identified in DW-MRI acquisition protocols between centers and in individual patients. Graphical Abstract
doi_str_mv 10.1007/s00247-023-05745-z
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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 Muller, Lil-Sofie ; Pace, Erika ; Di Paolo, Pier Luigi ; Perruccio, Katia ; Quaglietta, Lucia ; Renard, Marleen ; van Rijn, Rick R. ; Ruggiero, Antonio ; Sirvent, Sara I. ; De Luca, Alberto ; Schoot, Reineke A.</creator><creatorcontrib>van Ewijk, Roelof ; Chatziantoniou, Cyrano ; Adams, Madeleine ; Bertolini, Patrizia ; Bisogno, Gianni ; Bouhamama, Amine ; Caro-Dominguez, Pablo ; Charon, Valerie ; 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 Muller, Lil-Sofie ; Pace, Erika ; Di Paolo, Pier Luigi ; Perruccio, Katia ; Quaglietta, Lucia ; Renard, Marleen ; van Rijn, Rick R. ; Ruggiero, Antonio ; Sirvent, Sara I. ; De Luca, Alberto ; Schoot, Reineke A.</creatorcontrib><description>Objective To investigate the feasibility of diffusion-weighted magnetic resonance imaging (DW-MRI) as a predictive imaging marker after neoadjuvant chemotherapy in patients with rhabdomyosarcoma. Material and methods We performed a multicenter retrospective study including pediatric, adolescent and young adult patients with rhabdomyosarcoma, Intergroup Rhabdomyosarcoma Study group III/IV, treated according to the European paediatric Soft tissue sarcoma Study Group (E p SSG) RMS2005 or MTS2008 studies. DW-MRI was performed according to institutional protocols. We performed two-dimensional single-slice tumor delineation. Areas of necrosis or hemorrhage were delineated to be excluded in the primary analysis. Mean, median and 5th and 95th apparent diffusion coefficient (ADC) were extracted. Results Of 134 included patients, 82 had measurable tumor at diagnosis and response and DW-MRI scans of adequate quality and were included in the analysis. Technical heterogeneity in scan acquisition protocols and scanners was observed. Mean ADC at diagnosis was 1.1 (95% confidence interval [CI]: 1.1–1.2) (all ADC expressed in * 10 −3 mm 2 /s), versus 1.6 (1.5–1.6) at response assessment. The 5th percentile ADC was 0.8 (0.7–0.9) at diagnosis and 1.1 (1.0–1.2) at response. Absolute change in mean ADC after neoadjuvant chemotherapy was 0.4 (0.3–0.5). Exploratory analyses for association between ADC and clinical parameters showed a significant difference in mean ADC at diagnosis for alveolar versus embryonal histology. Landmark analysis at nine weeks after the date of diagnosis showed no significant association (hazard ratio 1.3 [0.6–3.2]) between the mean ADC change and event-free survival. Conclusion A significant change in the 5th percentile and the mean ADC after chemotherapy was observed. Strong heterogeneity was identified in DW-MRI acquisition protocols between centers and in individual patients. Graphical Abstract</description><identifier>ISSN: 1432-1998</identifier><identifier>ISSN: 0301-0449</identifier><identifier>EISSN: 1432-1998</identifier><identifier>DOI: 10.1007/s00247-023-05745-z</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescents ; Alveoli ; Chemotherapy ; Diagnosis ; Diffusion coefficient ; Hemorrhage ; Heterogeneity ; Histology ; Imaging ; Magnetic resonance imaging ; Medical imaging ; Medicine ; Medicine &amp; Public Health ; Necrosis ; Neuroradiology ; Nuclear Medicine ; Oncology ; Original Article ; Patients ; Pediatrics ; Radiology ; Rhabdomyosarcoma ; Sarcoma ; Soft tissue sarcoma ; Soft tissues ; Tumors ; Ultrasound ; Young adults</subject><ispartof>Pediatric radiology, 2023-11, Vol.53 (12), p.2539-2551</ispartof><rights>The Author(s) 2023</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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J.</creatorcontrib><creatorcontrib>Jenney, Meriel</creatorcontrib><creatorcontrib>Klein, Willemijn M.</creatorcontrib><creatorcontrib>Leemans, Alexander</creatorcontrib><creatorcontrib>Leseur, Julie</creatorcontrib><creatorcontrib>Mandeville, Henry C.</creatorcontrib><creatorcontrib>McHugh, Kieran</creatorcontrib><creatorcontrib>Merks, Johannes H. M.</creatorcontrib><creatorcontrib>Minard-Colin, Veronique</creatorcontrib><creatorcontrib>Moalla, Salma</creatorcontrib><creatorcontrib>Morosi, Carlo</creatorcontrib><creatorcontrib>Orbach, Daniel</creatorcontrib><creatorcontrib>Ording Muller, Lil-Sofie</creatorcontrib><creatorcontrib>Pace, Erika</creatorcontrib><creatorcontrib>Di Paolo, Pier Luigi</creatorcontrib><creatorcontrib>Perruccio, Katia</creatorcontrib><creatorcontrib>Quaglietta, Lucia</creatorcontrib><creatorcontrib>Renard, Marleen</creatorcontrib><creatorcontrib>van Rijn, Rick R.</creatorcontrib><creatorcontrib>Ruggiero, Antonio</creatorcontrib><creatorcontrib>Sirvent, Sara I.</creatorcontrib><creatorcontrib>De Luca, Alberto</creatorcontrib><creatorcontrib>Schoot, Reineke A.</creatorcontrib><title>Quantitative diffusion-weighted MRI response assessment in rhabdomyosarcoma: an international retrospective study on behalf of the European paediatric Soft tissue sarcoma Study Group Imaging Committee</title><title>Pediatric radiology</title><addtitle>Pediatr Radiol</addtitle><description>Objective To investigate the feasibility of diffusion-weighted magnetic resonance imaging (DW-MRI) as a predictive imaging marker after neoadjuvant chemotherapy in patients with rhabdomyosarcoma. Material and methods We performed a multicenter retrospective study including pediatric, adolescent and young adult patients with rhabdomyosarcoma, Intergroup Rhabdomyosarcoma Study group III/IV, treated according to the European paediatric Soft tissue sarcoma Study Group (E p SSG) RMS2005 or MTS2008 studies. DW-MRI was performed according to institutional protocols. We performed two-dimensional single-slice tumor delineation. Areas of necrosis or hemorrhage were delineated to be excluded in the primary analysis. Mean, median and 5th and 95th apparent diffusion coefficient (ADC) were extracted. Results Of 134 included patients, 82 had measurable tumor at diagnosis and response and DW-MRI scans of adequate quality and were included in the analysis. Technical heterogeneity in scan acquisition protocols and scanners was observed. Mean ADC at diagnosis was 1.1 (95% confidence interval [CI]: 1.1–1.2) (all ADC expressed in * 10 −3 mm 2 /s), versus 1.6 (1.5–1.6) at response assessment. The 5th percentile ADC was 0.8 (0.7–0.9) at diagnosis and 1.1 (1.0–1.2) at response. Absolute change in mean ADC after neoadjuvant chemotherapy was 0.4 (0.3–0.5). Exploratory analyses for association between ADC and clinical parameters showed a significant difference in mean ADC at diagnosis for alveolar versus embryonal histology. Landmark analysis at nine weeks after the date of diagnosis showed no significant association (hazard ratio 1.3 [0.6–3.2]) between the mean ADC change and event-free survival. Conclusion A significant change in the 5th percentile and the mean ADC after chemotherapy was observed. Strong heterogeneity was identified in DW-MRI acquisition protocols between centers and in individual patients. 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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 Muller, Lil-Sofie ; Pace, Erika ; Di Paolo, Pier Luigi ; Perruccio, Katia ; Quaglietta, Lucia ; Renard, Marleen ; van Rijn, Rick R. ; Ruggiero, Antonio ; Sirvent, Sara I. ; De Luca, Alberto ; Schoot, Reineke A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c347t-9bacf8b4ef06f0214c7cff3fdd7307a341bdfe1835c408a17150b00405bfc4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adolescents</topic><topic>Alveoli</topic><topic>Chemotherapy</topic><topic>Diagnosis</topic><topic>Diffusion coefficient</topic><topic>Hemorrhage</topic><topic>Heterogeneity</topic><topic>Histology</topic><topic>Imaging</topic><topic>Magnetic resonance imaging</topic><topic>Medical imaging</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Necrosis</topic><topic>Neuroradiology</topic><topic>Nuclear Medicine</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Radiology</topic><topic>Rhabdomyosarcoma</topic><topic>Sarcoma</topic><topic>Soft tissue sarcoma</topic><topic>Soft tissues</topic><topic>Tumors</topic><topic>Ultrasound</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van Ewijk, Roelof</creatorcontrib><creatorcontrib>Chatziantoniou, Cyrano</creatorcontrib><creatorcontrib>Adams, Madeleine</creatorcontrib><creatorcontrib>Bertolini, Patrizia</creatorcontrib><creatorcontrib>Bisogno, Gianni</creatorcontrib><creatorcontrib>Bouhamama, Amine</creatorcontrib><creatorcontrib>Caro-Dominguez, Pablo</creatorcontrib><creatorcontrib>Charon, Valerie</creatorcontrib><creatorcontrib>Coma, Ana</creatorcontrib><creatorcontrib>Dandis, Rana</creatorcontrib><creatorcontrib>Devalck, Christine</creatorcontrib><creatorcontrib>De Donno, Giulia</creatorcontrib><creatorcontrib>Ferrari, Andrea</creatorcontrib><creatorcontrib>Fiocco, Marta</creatorcontrib><creatorcontrib>Gallego, Soledad</creatorcontrib><creatorcontrib>Giraudo, Chiara</creatorcontrib><creatorcontrib>Glosli, Heidi</creatorcontrib><creatorcontrib>ter Horst, Simone A. 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J.</au><au>Jenney, Meriel</au><au>Klein, Willemijn M.</au><au>Leemans, Alexander</au><au>Leseur, Julie</au><au>Mandeville, Henry C.</au><au>McHugh, Kieran</au><au>Merks, Johannes H. M.</au><au>Minard-Colin, Veronique</au><au>Moalla, Salma</au><au>Morosi, Carlo</au><au>Orbach, Daniel</au><au>Ording Muller, Lil-Sofie</au><au>Pace, Erika</au><au>Di Paolo, Pier Luigi</au><au>Perruccio, Katia</au><au>Quaglietta, Lucia</au><au>Renard, Marleen</au><au>van Rijn, Rick R.</au><au>Ruggiero, Antonio</au><au>Sirvent, Sara I.</au><au>De Luca, Alberto</au><au>Schoot, Reineke A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative diffusion-weighted MRI response assessment in rhabdomyosarcoma: an international retrospective study on behalf of the European paediatric Soft tissue sarcoma Study Group Imaging Committee</atitle><jtitle>Pediatric radiology</jtitle><stitle>Pediatr Radiol</stitle><date>2023-11-01</date><risdate>2023</risdate><volume>53</volume><issue>12</issue><spage>2539</spage><epage>2551</epage><pages>2539-2551</pages><issn>1432-1998</issn><issn>0301-0449</issn><eissn>1432-1998</eissn><abstract>Objective To investigate the feasibility of diffusion-weighted magnetic resonance imaging (DW-MRI) as a predictive imaging marker after neoadjuvant chemotherapy in patients with rhabdomyosarcoma. Material and methods We performed a multicenter retrospective study including pediatric, adolescent and young adult patients with rhabdomyosarcoma, Intergroup Rhabdomyosarcoma Study group III/IV, treated according to the European paediatric Soft tissue sarcoma Study Group (E p SSG) RMS2005 or MTS2008 studies. DW-MRI was performed according to institutional protocols. We performed two-dimensional single-slice tumor delineation. Areas of necrosis or hemorrhage were delineated to be excluded in the primary analysis. Mean, median and 5th and 95th apparent diffusion coefficient (ADC) were extracted. Results Of 134 included patients, 82 had measurable tumor at diagnosis and response and DW-MRI scans of adequate quality and were included in the analysis. Technical heterogeneity in scan acquisition protocols and scanners was observed. Mean ADC at diagnosis was 1.1 (95% confidence interval [CI]: 1.1–1.2) (all ADC expressed in * 10 −3 mm 2 /s), versus 1.6 (1.5–1.6) at response assessment. The 5th percentile ADC was 0.8 (0.7–0.9) at diagnosis and 1.1 (1.0–1.2) at response. Absolute change in mean ADC after neoadjuvant chemotherapy was 0.4 (0.3–0.5). Exploratory analyses for association between ADC and clinical parameters showed a significant difference in mean ADC at diagnosis for alveolar versus embryonal histology. Landmark analysis at nine weeks after the date of diagnosis showed no significant association (hazard ratio 1.3 [0.6–3.2]) between the mean ADC change and event-free survival. Conclusion A significant change in the 5th percentile and the mean ADC after chemotherapy was observed. Strong heterogeneity was identified in DW-MRI acquisition protocols between centers and in individual patients. 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identifier ISSN: 1432-1998
ispartof Pediatric radiology, 2023-11, Vol.53 (12), p.2539-2551
issn 1432-1998
0301-0449
1432-1998
language eng
recordid cdi_proquest_miscellaneous_2863303654
source Springer Nature
subjects Adolescents
Alveoli
Chemotherapy
Diagnosis
Diffusion coefficient
Hemorrhage
Heterogeneity
Histology
Imaging
Magnetic resonance imaging
Medical imaging
Medicine
Medicine & Public Health
Necrosis
Neuroradiology
Nuclear Medicine
Oncology
Original Article
Patients
Pediatrics
Radiology
Rhabdomyosarcoma
Sarcoma
Soft tissue sarcoma
Soft tissues
Tumors
Ultrasound
Young adults
title Quantitative diffusion-weighted MRI response assessment in rhabdomyosarcoma: an international retrospective study on behalf of the European paediatric Soft tissue sarcoma Study Group Imaging Committee
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