Literature DB >> 19165889

Does the time-point of relapse influence outcome in pediatric rhabdomyosarcomas?

Adrian C Mattke1, Emily J Bailey, Andreas Schuck, Tobias Dantonello, Ivo Leuschner, Thomas Klingebiel, Joern Treuner, Ewa Koscielniak.   

Abstract

BACKGROUND: Childhood rhabdomyosarcoma (RMS), a soft tissue malignant tumor of skeletal muscle origin, accounts for approximately 3.5% of the cases of cancer among children 0-14 years and 2% of the cases among adolescents and young adults 15-19 years of age. PROCEDURE: We evaluated survival (SUR) after first relapse depending on the time to relapse (TTR) in RMSs of childhood and adolescence. Early, intermediate, and late relapsing patients were evaluated for prognostic risk factors.
RESULTS: Two hundred thirty-four patients with RMS enrolled in the German sarcoma trial CWS-81, CWS-86, CWS-91, and CWS-96 met selection criteria. Of the 234 patients, 35%, 32%, and 33% relapsed within 6 (early), 6-12 (intermediate), and more than 12 (late) months respectively after the end of primary therapy. Four-year SUR was 12%, 21%, and 41% for early, intermediate, and late relapse respectively (P < 0.001). Four-year SUR after local relapse was 18% (early), 38% (intermediate), and 49% (late). Embryonal RMS showed four year SUR of 16%, 30%, and 46% (P < 0.001) whereas alveolar histology showed four year SUR of 8%, 6%, and 23% (P < 0.01) for early, intermediate, and late relapse respectively.
CONCLUSION: TTR has significant influence on prognosis in relapsed RMS. It influences SUR independent of other features such as type of relapse, histology, tumor site, primary treatment time or irradiation in primary treatment. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19165889     DOI: 10.1002/pbc.21906

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  4 in total

Review 1.  Soft tissue sarcomas in children.

Authors:  Gauri Kapoor; Kunal Das
Journal:  Indian J Pediatr       Date:  2011-09-21       Impact factor: 1.967

2.  Early treatment failure in intermediate-risk rhabdomyosarcoma: results from IRS-IV and D9803--a report from the Children's Oncology Group.

Authors:  A Yuriko Minn; Elizabeth R Lyden; James R Anderson; Lynn Million; Carola A Arndt; Kenneth Brown; Douglas S Hawkins; Sarah S Donaldson
Journal:  J Clin Oncol       Date:  2010-08-16       Impact factor: 44.544

Review 3.  Rhabdomyosarcoma of the head and neck in children.

Authors:  Joanna Radzikowska; Wojciech Kukwa; Andrzej Kukwa; Anna Czarnecka; Antoni Krzeski
Journal:  Contemp Oncol (Pozn)       Date:  2015-02-13

4.  Radiation therapy is an important factor to improve survival in pediatric patients with head and neck rhabdomyosarcoma by enhancing local control: a historical cohort study from a single center.

Authors:  Yuan Wen; Dongsheng Huang; Weiling Zhang; Yi Zhang; Huimin Hu; Jing Li
Journal:  BMC Pediatr       Date:  2020-05-29       Impact factor: 2.125

  4 in total

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