INternational Soft Tissue saRcoma ConsorTium (INSTRuCT) consensus statement: Imaging recommendations for the management of rhabdomyosarcoma

被引:2
作者
Schoot, Reineke A. [1 ]
van Ewijk, Roelof [1 ]
von Witzleben, Anna-Anais [2 ]
Kao, Simon C. [3 ]
Merks, J. H. M. [1 ]
Morosi, Carlo [4 ]
Pace, Erika [5 ]
Shulkin, Barry L. [6 ]
Ferrari, Andrea [7 ]
von Kalle, Thekla [2 ]
Rijn, Rick R. van [8 ]
Weiss, Aaron R. [9 ]
Sparber-Sauer, Monika [10 ,11 ]
ter Horst, Simone A. J. [1 ,12 ]
McCarville, M. [6 ]
机构
[1] Princess Maxima Ctr Pediat Oncol, Utrecht, Netherlands
[2] Klinikum Stuttgart, Inst Radiol Olgahospital, Zentrum Kinder Jugend & Frauenmed, Stuttgart, Germany
[3] Univ Iowa, Dept Radiol, Carver Coll Med, Iowa City, IA USA
[4] Ist Nazl Tumori, Dept Radiol, Milan, Italy
[5] Royal Marsden NHS Fdn Trust, Dept Radiol, London, England
[6] St Jude Childrens Res Hosp, Dept Diagnost Imaging, Memphis, TN 38105 USA
[7] Ist Nazl Tumori, Med Oncol & Hematol Dept, Pediat Oncol Unit, Milan, Italy
[8] Univ Amsterdam, Emma Childrens Hosp, Dept Radiol & Nucl Med, Amsterdam UMC, Amsterdam, Netherlands
[9] Maine Med Ctr, Dept Pediat, Div Pediat Hematol Oncol, Portland, ME USA
[10] Klinikum Landeshauptstadt Stuttgart gKAoR, Stuttgart Canc Ctr, Zent Kinder Jugend & Frauenmed, Olgahosp,Padiatrie Padiatr Onkol Hamatol Immunol 5, Stuttgart, Germany
[11] Univ Med Tubingen, Tubingen, Germany
[12] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, Dept Radiol & Nucl Med, Utrecht, Netherlands
关键词
Pediatric rhabdomyosarcoma; Metastatic disease; Soft-tissue neoplasm; International sarcoma consortium; Rhabdomyosarcoma imaging; RESPONSE EVALUATION CRITERIA; GROUP-III RHABDOMYOSARCOMA; SENTINEL NODE BIOPSY; INTERGROUP RHABDOMYOSARCOMA; METASTATIC RHABDOMYOSARCOMA; PEDIATRIC RHABDOMYOSARCOMA; CHILDHOOD RHABDOMYOSARCOMA; PROGNOSTIC-FACTORS; PULMONARY NODULES; TUMOR VOLUME;
D O I
10.1016/j.ejrad.2023.111012
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Rhabdomyosarcoma is the most common soft-tissue neoplasm in the pediatric population. The survival of children with rhabdomyosarcoma has only marginally improved over the past 25 years and remains poor for those with metastatic disease. A significant challenge to advances in treatment of rhabdomyosarcoma is the relative rarity of this disease, necessitating years to complete clinical trials. Progress can be accelerated by in-ternational cooperation and sharing national experiences. This necessitates agreement on a common language to describe patient cohorts and consensus standards to guide diagnosis, treatment, and response assessment. These goals formed the premise for creating the INternational Soft Tissue saRcoma ConsorTium (INSTRuCT) in 2017. Multidisciplinary members of this consortium have since developed international consensus statements on the diagnosis, treatment, and management of pediatric soft-tissue sarcomas. Herein, members of the INSTRuCT Diagnostic Imaging Working Group present international consensus recommendations for imaging of patients with rhabdomyosarcoma at diagnosis, at staging, and during and after completion of therapy. The intent is to promote a standardized imaging approach to pediatric patients with this malignancy to create more-reliable comparisons of results of clinical trials internationally, thereby accelerating progress in managing rhabdomyo-sarcoma and improving survival.
引用
收藏
页数:9
相关论文
共 50 条
  • [21] Biliary tract rhabdomyosarcoma: a report from the Soft Tissue Sarcoma Committee of the Associazione Italiana Ematologia Oncologia Pediatrica
    Perruccio, Katia
    Cecinati, Valerio
    Scagnellato, Angela
    Provenzi, Massimo
    Milano, Giuseppe Maria
    Basso, Eleonora
    Manzitti, Carla
    Cecchetto, Giovanni
    Alaggio, Rita
    Di Martino, Martina
    Schiavetti, Amalia
    Melchionda, Fraia
    Affinita, Maria Carmen
    Chiaravalli, Stefano
    Miglionico, Lucia
    Balter, Rita
    Tamburini, Angela
    Bisogno, Gianni
    Ferrari, Andrea
    TUMORI JOURNAL, 2018, 104 (03): : 232 - 237
  • [22] Is alveolar histotype a prognostic factor in paratesticular rhabdomyosarcoma? The experience of Italian and German soft tissue sarcoma cooperative group
    Ferrari, A
    Bisogno, G
    Casanova, M
    Brecht, IB
    Alaggio, R
    Cecchetto, G
    Provenzi, M
    Koscielniak, E
    Treuner, J
    Carli, M
    PEDIATRIC BLOOD & CANCER, 2004, 42 (02) : 134 - 138
  • [23] Soft-tissue sarcoma in adults: Imaging appearances, pitfalls and diagnostic algorithms
    Crombe, Amandine
    Kind, Michele
    Fadli, David
    Miceli, Marco
    Linck, Pierre-Antoine
    Bianchi, Giuseppe
    Sambri, Andrea
    Spinnato, Paolo
    DIAGNOSTIC AND INTERVENTIONAL IMAGING, 2023, 104 (05) : 207 - 220
  • [24] Topotecan/carboplatin regimen for refractory/recurrent rhabdomyosarcoma in children: Report from the AIEOP Soft Tissue Sarcoma Committee
    Compostella, Alessia
    Affinita, Maria Carmen
    Casanova, Michela
    Milano, Giuseppe Maria
    Scagnellato, Angela
    Dall'Igna, Patrizia
    Chiaravalli, Stefano
    Pierobon, Marta
    Manzitti, Carla
    Zanetti, Ilaria
    Schiavetti, Amalia
    Sorbara, Silvia
    Mura, Rosella Maria
    Ruggiero, Antonio
    Ferrari, Andrea
    Bisogno, Gianni
    TUMORI JOURNAL, 2019, 105 (02): : 138 - 143
  • [25] Rhabdomyosarcoma with isolated lung metastases: A report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group
    Vasquez, Juan C.
    Luo, Leo Y.
    Hiniker, Susan M.
    Rhee, Daniel S.
    Dasgupta, Roshni
    Chen, Sonja
    Weigel, Brenda J.
    Xue, Wei
    Venkatramani, Rajkumar
    Arndt, Carola A.
    PEDIATRIC BLOOD & CANCER, 2023, 70 (06)
  • [26] Local recurrence of soft-tissue sarcoma: issues in imaging surveillance strategy
    Ezuddin, Nisreen S.
    Pretell-Mazzini, Juan
    Yechieli, Raphael L.
    Kerr, Darcy A.
    Wilky, Breelyn A.
    Subhawong, Ty K.
    SKELETAL RADIOLOGY, 2018, 47 (12) : 1595 - 1606
  • [27] Considerations for Imaging of Malignant Pleural Mesothelioma: A Consensus Statement from the International Mesothelioma Interest Group
    Katz, Sharyn I.
    Straus, Christopher M.
    Roshkovan, Leonid
    Blyth, Kevin G.
    Frauenfelder, Thomas
    Gill, Ritu R.
    Lalezari, Ferry
    Erasmus, Jeremy
    Nowak, Anna K.
    Gerbaudo, Victor H.
    Francis, Roslyn J.
    Armato III, Samuel G.
    JOURNAL OF THORACIC ONCOLOGY, 2023, 18 (03) : 278 - 298
  • [28] Outcome of extracranial malignant rhabdoid tumours in children registered in the European Paediatric Soft Tissue Sarcoma Study Group Non-Rhabdomyosarcoma Soft Tissue Sarcoma 2005 Study-dEpSSG NRSTS 2005
    Brennan, Bernadette
    De Salvo, Gian Luca
    Orbach, Daniel
    De Paoli, Angela
    Kelsey, Anna
    Mudry, Peter
    Francotte, Nadine
    Van Noesel, Max
    Bisogno, Gianni
    Casanova, Michela
    Ferrari, Andrea
    EUROPEAN JOURNAL OF CANCER, 2016, 60 : 69 - 82
  • [29] Current concepts and future perspectives in retroperitoneal soft-tissue sarcoma management
    Thomas, David M.
    O'Sullivan, Brian
    Gronchi, Alessandro
    EXPERT REVIEW OF ANTICANCER THERAPY, 2009, 9 (08) : 1145 - 1157
  • [30] Fusion Status in Patients With Lymph Node-Positive (N1) Alveolar Rhabdomyosarcoma Is a Powerful Predictor of Prognosis: Experience of the European Paediatric Soft Tissue Sarcoma Study Group (EpSSG)
    Gallego, Soledad
    Zanetti, Ilaria
    Orbach, Daniel
    Ranchere, Dominique
    Shipley, Janet
    Zin, Angelica
    Bergeron, Christophe
    de Salvo, Gian Luca
    Chisholm, Julia
    Ferrari, Andrea
    Jenney, Meriel
    Mandeville, Henry C.
    Rogers, Timothy
    Merks, Johannes H. M.
    Mudry, Peter
    Glosli, Heidi
    Milano, Giuseppe Maria
    Ferman, Sima
    Bisogno, Gianni
    CANCER, 2018, 124 (15) : 3201 - 3209