Improved risk-stratification for posterior fossa ependymoma of childhood considering clinical, histological and genetic features – a retrospective analysis of the HIT ependymoma trial cohort
Autor: | André O. von Bueren, Martin Mynarek, Stefan Rutkowski, Ludger Klein-Hitpass, Inken Wohlers, Torsten Pietsch, Stephanie T Jünger, Sven Rahmann, Beate Timmermann, Natalia Velez-Char, Monika Warmuth-Metz, Katja von Hoff, Rolf-Dieter Kortmann, Evelyn Dörner, Anja zur Mühlen |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Ependymoma
Oncology Male medicine.medical_specialty Multivariate statistics Neurology Adolescent Medizin Infratentorial Neoplasms Molecular Inversion Probe Infratentorial Neoplasms / pathology Ependymoma / epidemiology Risk Assessment lcsh:RC346-429 Pathology and Forensic Medicine Cohort Studies Cellular and Molecular Neuroscience Posterior fossa Infratentorial Neoplasms / genetics Internal medicine Germany Genetics Medicine Humans Risk Assessment / standards Child Survival analysis Risk stratification Neuropathology lcsh:Neurology. Diseases of the nervous system Retrospective Studies ddc:618 business.industry Proportional hazards model Research Ependymoma / pathology Germany / epidemiology Infant medicine.disease Log-rank test Child Preschool Cohort Ependymoma / genetics Female Neurology (clinical) Infratentorial Neoplasms / epidemiology business Follow-Up Studies |
Zdroj: | Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-12 (2019) Acta Neuropathologica Communications Acta neuropathologica communications, Vol. 7, No 1 (2019) P. 181 |
ISSN: | 2051-5960 |
DOI: | 10.1186/s40478-019-0820-5 |
Popis: | Introduction Risk stratification of children with ependymomas of the posterior fossa in current therapeutic protocols is mainly based on clinical criteria. We aimed to identify independent outcome predictors for this disease entity by a systematic integrated analysis of clinical, histological and genetic information in a defined cohort of patients treated according to the German HIT protocols. Methods Tumor samples of 134 patients aged 0.2–15.9 years treated between 1999 and 2010 according to HIT protocols were analyzed for histological features including mitotic activity, necrosis and vascular proliferation and genomic alterations by SNP and molecular inversion probe analysis. Survival analysis was performed by Kaplan-Meier method with log rank test and multivariate Cox regression analysis. Results Residual tumor after surgery, chromosome 1q gain and structural genomic alterations were identified as predictors of significantly shorter event-free (EFS) and overall survival (OS). Furthermore, specific histological features including vascular proliferation, necrosis and high mitotic activity were predictive for shorter OS. Multivariate Cox regression revealed residual tumor, chromosome 1q gain and mitotic activity as independent predictors of both EFS and OS. Using these independent predictors of outcome, we were able to build a 3-tiered risk stratification model that separates patients with standard, intermediate and high risk, and which outperforms current stratification procedures. Conclusion The integration of defined clinical, histological and genetic parameters led to an improved risk-stratification model for posterior fossa ependymoma of childhood. After validation in independent cohorts this model may provide the basis for risk-adapted treatment of children with ependymomas of the posterior fossa. |
Databáze: | OpenAIRE |
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