Clinical and Cytogenetic Profiles of Rhabdomyosarcoma with Bone Marrow Involvement in Korean Children: A 15-Year Single-Institution Experience
Annals of Laboratory Medicine
; : 132-138, 2018.
Article
em En
| WPRIM
| ID: wpr-713686
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WPRO
ABSTRACT
BACKGROUND:
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children. Alveolar RMS (ARMS) is characterized by FOXO1-related chromosomal translocations that result in a poorer clinical outcome compared with embryonal RMS (ERMS). Because the chromosomal features of RMS have not been comprehensively defined, we analyzed the clinical and laboratory data of childhood RMS patients and determined the clinical significance of chromosomal abnormalities in the bone marrow.METHODS:
Fifty-one Korean patients with RMS < 18 years of age treated between 2001 and 2015 were enrolled in this study. Clinical factors, bone marrow and cytogenetic results, and overall survival (OS) were analyzed.RESULTS:
In total, 36 patients (70.6%) had ERMS and 15 (29.4%) had ARMS; 80% of the ARMS patients had stage IV disease. The incidences of bone and bone marrow metastases were 21.6% and 19.6%, respectively, and these results were higher than previously reported results. Of the 40 patients who underwent bone marrow cytogenetic investigation, five patients had chromosomal abnormalities associated with the 13q14 rearrangement. Patients with a chromosomal abnormality (15 vs 61 months, P=0.037) and bone marrow involvement (17 vs 61 months, P=0.033) had a significantly shorter median OS than those without such characteristics. Two novel rearrangements associated with the 13q14 locus were detected. One patient with concomitant MYCN amplification and PAX3/FOXO1 fusion showed an aggressive clinical course.CONCLUSIONS:
A comprehensive approach involving conventional cytogenetics and FOXO1 FISH of the bone marrow is needed to assess high-risk ARMS patients and identify novel cytogenetic findings.Palavras-chave
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Assunto principal:
Braço
/
Rabdomiossarcoma
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Sarcoma
/
Translocação Genética
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Medula Óssea
/
Incidência
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Aberrações Cromossômicas
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Citogenética
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Metástase Neoplásica
Tipo de estudo:
Incidence_studies
/
Prognostic_studies
Limite:
Child
/
Humans
Idioma:
En
Revista:
Annals of Laboratory Medicine
Ano de publicação:
2018
Tipo de documento:
Article