| Literature DB >> 28604107 |
Lucas Moreno1,2,3, Hubert Caron4,5, Birgit Geoerger6, Angelika Eggert7, Gudrun Schleiermacher8, Penelope Brock9, Dominique Valteau-Couanet6, Louis Chesler3,10, Johannes H Schulte7, Katleen De Preter11, Jan Molenaar12, Alexander Schramm13, Martin Eilers14, Tom Van Maerken11, John Inge Johnsen15, Michelle Garrett16, Sally L George3,10, Deborah A Tweddle17, Per Kogner15, Frank Berthold18, Jan Koster12, Giuseppe Barone3,10, Elizabeth R Tucker3,10, Lynley Marshall3,10, Ralf Herold19, Jaroslav Sterba20,21,22, Koen Norga23, Gilles Vassal24, Andrew Dj Pearson3,10.
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.Entities:
Keywords: Neuroblastoma; clinical trials; drug development; phase I; preclinical testing
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Year: 2017 PMID: 28604107 DOI: 10.1080/17460441.2017.1340269
Source DB: PubMed Journal: Expert Opin Drug Discov ISSN: 1746-0441 Impact factor: 6.098