| Autor: |
Veldhuijzen van Zanten, S.E.M. Baugh, J. Chaney, B. De Jongh, D. Sanchez Aliaga, E. Barkhof, F. Noltes, J. De Wolf, R. Van Dijk, J. Cannarozzo, A. Damen-Korbijn, C.M. Lieverst, J.A. Colditz, N. Hoffmann, M. Warmuth-Metz, M. Bison, B. Jones, D.T.W. Sturm, D. Gielen, G.H. Jones, C. Hulleman, E. Calmon, R. Castel, D. Varlet, P. Giraud, G. Slavc, I. Van Gool, S. Jacobs, S. Jadrijevic-Cvrlje, F. Sumerauer, D. Nysom, K. Pentikainen, V. Kivivuori, S.-M. Leblond, P. Entz-Werle, N. von Bueren, A.O. Kattamis, A. Hargrave, D.R. Hauser, P. Garami, M. Thorarinsdottir, H.K. Pears, J. Gandola, L. Rutkauskiene, G. Janssens, G.O. Torsvik, I.K. Perek-Polnik, M. Gil-da-Costa, M.J. Zheludkova, O. Shats, L. Deak, L. Kitanovski, L. Cruz, O. Morales La Madrid, A. Holm, S. Gerber, N. Kebudi, R. Grundy, R. Lopez-Aguilar, E. Zapata-Tarres, M. Emmerik, J. Hayden, T. Bailey, S. Biassoni, V. Massimino, M. Grill, J. Vandertop, W.P. Kaspers, G.J.L. Fouladi, M. Kramm, C.M. van Vuurden, D.G. on behalf of the members of the SIOPE DIPG Network |
| Jazyk: |
angličtina |
| Rok vydání: |
2017 |
| Popis: |
Diffuse intrinsic pontine glioma (DIPG) is a rare and deadly childhood malignancy. After 40 years of mostly single-center, often non-randomized trials with variable patient inclusions, there has been no improvement in survival. It is therefore time for international collaboration in DIPG research, to provide new hope for children, parents and medical professionals fighting DIPG. In a first step towards collaboration, in 2011, a network of biologists and clinicians working in the field of DIPG was established within the European Society for Paediatric Oncology (SIOPE) Brain Tumour Group: the SIOPE DIPG Network. By bringing together biomedical professionals and parents as patient representatives, several collaborative DIPG-related projects have been realized. With help from experts in the fields of information technology, and legal advisors, an international, web-based comprehensive database was developed, The SIOPE DIPG Registry and Imaging Repository, to centrally collect data of DIPG patients. As for April 2016, clinical data as well as MR-scans of 694 patients have been entered into the SIOPE DIPG Registry/Imaging Repository. The median progression free survival is 6.0 months (95% Confidence Interval (CI) 5.6–6.4 months) and the median overall survival is 11.0 months (95% CI 10.5–11.5 months). At two and five years post-diagnosis, 10 and 2% of patients are alive, respectively. The establishment of the SIOPE DIPG Network and SIOPE DIPG Registry means a paradigm shift towards collaborative research into DIPG. This is seen as an essential first step towards understanding the disease, improving care and (ultimately) cure for children with DIPG. © 2017, The Author(s). |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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