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Erschienen in: Clinical and Translational Oncology 12/2021

01.07.2021 | Clinical Guides in Oncology

GEIS-SEHOP clinical practice guidelines for the treatment of rhabdomyosarcoma

verfasst von: S. Gallego, D. Bernabeu, M. Garrido-Pontnou, G. Guillen, N. Hindi, A. Juan-Ribelles, C. Márquez, C. Mata, J. Orcajo, G. Ramírez, M. Ramos, C. Romagosa, D. Ruano, P. Rubio, R. Vergés, C. Valverde, GEIS (Grupo Español de Investigación en Sarcomas), SEHOP (Sociedad Española de Hematología y Oncología Pediátrica)

Erschienen in: Clinical and Translational Oncology | Ausgabe 12/2021

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Abstract

Rhabdomyosarcoma (RMS) is the most frequent soft tissue sarcoma (STS) in children and adolescents. In Spain the annual incidence is 4.4 cases per million children < 14 years. It is an uncommon neoplasm in adults, but 40% of RMS are diagnosed in patients over 20 years of age, representing 1% of all STS in this age group. RMS can appear anywhere in the body, with some sites more frequently affected including head and neck, genitourinary system and limbs. Assessment of a patient with suspicion of RMS includes imaging studies (MRI, CT, PET-CT) and biopsy. All patients with RMS should receive chemotherapy, either at diagnosis in advanced or metastatic stages, or after initial resection in early local stages. Local control includes surgery and/or radiotherapy depending on site, stage, histology and response to chemotherapy. This guide provides recommendations for diagnosis, staging and treatment of this neoplasm.
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Metadaten
Titel
GEIS-SEHOP clinical practice guidelines for the treatment of rhabdomyosarcoma
verfasst von
S. Gallego
D. Bernabeu
M. Garrido-Pontnou
G. Guillen
N. Hindi
A. Juan-Ribelles
C. Márquez
C. Mata
J. Orcajo
G. Ramírez
M. Ramos
C. Romagosa
D. Ruano
P. Rubio
R. Vergés
C. Valverde
GEIS (Grupo Español de Investigación en Sarcomas), SEHOP (Sociedad Española de Hematología y Oncología Pediátrica)
Publikationsdatum
01.07.2021
Verlag
Springer International Publishing
Erschienen in
Clinical and Translational Oncology / Ausgabe 12/2021
Print ISSN: 1699-048X
Elektronische ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-021-02654-1

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