MORENO, L., H. CARON, B. GEOERGER, A. EGGERT, G. SCHLEIERMACHER, P. BROCK, D. VALTEAU-COUANET, L. CHESLER, J.H. SCHULTE, K. DE PRETER, J. MOLENAAR, A. SCHRAMM, M. EILERS, T. VAN MAERKEN, J.I. JOHNSEN, M. GARRETT, S.L. GEORGE, D.A. TWEDDLE, P. KOGNER, F. BERTHOLD, J. KOSTER, G. BARONE, E.R. TUCKER, L. MARSHALL, R. HEROLD, Jaroslav ŠTĚRBA, K. NORGA, G. VASSAL and A.D.J. PEARSON. Accelerating drug development for neuroblastoma - New Drug Development Strategy: an Innovative Therapies for Children with Cancer, European Network for Cancer Research in Children and Adolescents and International Society of Paediatric Oncology Europe Neuroblastoma project. EXPERT OPINION ON DRUG DISCOVERY. ABINGDON: TAYLOR & FRANCIS LTD, 2017, vol. 12, No 8, p. 801-811. ISSN 1746-0441. Available from: https://dx.doi.org/10.1080/17460441.2017.1340269.
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Basic information
Original name Accelerating drug development for neuroblastoma - New Drug Development Strategy: an Innovative Therapies for Children with Cancer, European Network for Cancer Research in Children and Adolescents and International Society of Paediatric Oncology Europe Neuroblastoma project
Authors MORENO, L. (826 United Kingdom of Great Britain and Northern Ireland), H. CARON (756 Switzerland), B. GEOERGER (250 France), A. EGGERT (276 Germany), G. SCHLEIERMACHER (250 France), P. BROCK (826 United Kingdom of Great Britain and Northern Ireland), D. VALTEAU-COUANET (276 Germany), L. CHESLER (826 United Kingdom of Great Britain and Northern Ireland), J.H. SCHULTE (276 Germany), K. DE PRETER (56 Belgium), J. MOLENAAR (528 Netherlands), A. SCHRAMM (276 Germany), M. EILERS (276 Germany), T. VAN MAERKEN (56 Belgium), J.I. JOHNSEN (752 Sweden), M. GARRETT (826 United Kingdom of Great Britain and Northern Ireland), S.L. GEORGE (826 United Kingdom of Great Britain and Northern Ireland), D.A. TWEDDLE (36 Australia), P. KOGNER (752 Sweden), F. BERTHOLD (276 Germany), J. KOSTER (528 Netherlands), G. BARONE (826 United Kingdom of Great Britain and Northern Ireland), E.R. TUCKER (826 United Kingdom of Great Britain and Northern Ireland), L. MARSHALL (826 United Kingdom of Great Britain and Northern Ireland), R. HEROLD (826 United Kingdom of Great Britain and Northern Ireland), Jaroslav ŠTĚRBA (203 Czech Republic, guarantor, belonging to the institution), K. NORGA (56 Belgium), G. VASSAL (250 France) and A.D.J. PEARSON (826 United Kingdom of Great Britain and Northern Ireland).
Edition EXPERT OPINION ON DRUG DISCOVERY, ABINGDON, TAYLOR & FRANCIS LTD, 2017, 1746-0441.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30104 Pharmacology and pharmacy
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.692
RIV identification code RIV/00216224:14110/17:00098862
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1080/17460441.2017.1340269
UT WoS 000405392700004
Keywords in English Neuroblastoma; drug development; phase I; preclinical testing; clinical trials
Tags EL OK
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 28/1/2021 11:23.
Abstract
Introduction: Neuroblastoma, the commonest paediatric extra-cranial tumour, remains a leading cause of death from cancer in children. There is an urgent need to develop new drugs to improve cure rates and reduce long-term toxicity and to incorporate molecularly targeted therapies into treatment. Many potential drugs are becoming available, but have to be prioritised for clinical trials due to the relatively small numbers of patients. Areas covered: The current drug development model has been slow, associated with significant attrition, and few new drugs have been developed for neuroblastoma. The Neuroblastoma New Drug Development Strategy (NDDS) has: 1) established a group with expertise in drug development; 2) prioritised targets and drugs according to tumour biology (target expression, dependency, pre-clinical data; potential combinations; biomarkers), identifying as priority targets ALK, MEK, CDK4/6, MDM2, MYCN (druggable by BET bromodomain, aurora kinase, mTORC1/2) BIRC5 and checkpoint kinase 1; 3) promoted clinical trials with target-prioritised drugs. Drugs showing activity can be rapidly transitioned via parallel randomised trials into front-line studies. Expert opinion: The Neuroblastoma NDDS is based on the premise that optimal drug development is reliant on knowledge of tumour biology and prioritisation. This approach will accelerate neuroblastoma drug development and other poor prognosis childhood malignancies.
Links
LM2015090, research and development projectName: Český národní uzel Evropské sítě infrastruktur klinického výzkumu (Acronym: CZECRIN)
Investor: Ministry of Education, Youth and Sports of the CR
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