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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.
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