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A long duration of the prediagnostic symptomatic interval is not associated with an unfavourable prognosis in childhood medulloblastoma
Authors:Gerber Nicolas U  von Hoff Katja  von Bueren André O  Treulieb Wiebke  Deinlein Frank  Benesch Martin  Zwiener Isabella  Soerensen Niels  Warmuth-Metz Monika  Pietsch Torsten  Mittler Uwe  Kuehl Joachim  Kortmann Rolf-Dieter  Grotzer Michael A  Rutkowski Stefan
Affiliation:Department of Oncology, University Children's Hospital, CH-8032 Zurich, Switzerland. nicolas.gerber@kispi.uzh.ch
Abstract:BackgroundDue to the lacking specificity of symptoms making a correct diagnosis can be a challenge in children with medulloblastoma. This can lead to prediagnostic symptomatic intervals (PSIs) of several weeks to months. It is unknown whether the length of the PSI is associated with an inferior survival outcome in this population.MethodsTo study the association of PSI with disease stage at diagnosis, tumour control and survival in children with medulloblastoma, prospectively collected data on PSI, clinical, and biological features were analysed in 224 patients diagnosed at the age of 3–18 years and treated within the prospective randomised multicentre trial HIT’91.ResultsPatients with lower-stage disease tended towards a longer median PSI than those with higher-stage disease (M0 stage, 2.0 months; M1 stage, 2.0 months; M2/M3 stage, 1 month; p = 0.094. M0/1 stage versus M2/3 stage; p = 0.025). The patient group with the longest PSI had the best survival outcome (PSI ⩾4.0 months: 10-year overall survival rate (OS), 71%; PSI <4.0 months, 10-year OS, 61%; p = 0.056). Age at diagnosis was positively correlated with PSI (p = 0.027). No associations were found between PSI and sex histological subtype, presence of postoperative residual tumour, or c-myc and TrkC mRNA expression.ConclusionContrary to a common belief that a longer PSI may adversely affect prognosis, a longer PSI was associated with a trend towards lower metastatic stage and better survival probabilities. Nevertheless these findings do not obviate the importance of a timely diagnosis in paediatric patients with medulloblastoma.
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