| Literature DB >> 30772656 |
Andrew D J Pearson1, Nicole Scobie2, Koenraad Norga3, Franca Ligas4, Davy Chiodin5, Amos Burke6, Veronique Minard-Colin7, Peter Adamson8, Lynley V Marshall9, Arun Balakumaran10, Bouchra Benettaib11, Pankaj Bhargava12, Catherine M Bollard13, Ellen Bolotin14, Simon Bomken15, Jochen Buechner16, Birgit Burkhardt17, Hubert Caron18, Christopher Copland19, Pierre Demolis20, Anton Egorov21, Mahdi Farhan22, Gerhard Zugmaier23, Thomas Gross24, Danielle Horton-Taylor25, Wolfram Klapper26, Giovanni Lesa4, Robert Marcus27, Rodney R Miles28, Kerri Nottage29, Lida Pacaud30, Rosanna Ricafort31, Martin Schrappe32, Jaroslav Sterba33, Remus Vezan34, Susan Weiner35, Su Young Kim36, Gregory Reaman37, Gilles Vassal38.
Abstract
Paediatric Strategy Forums have been created by the multistakeholder organisation, ACCELERATE, and the European Medicines Agency to facilitate dialogue between all relevant stakeholders and suggest strategies in critical areas of paediatric oncology drug development. As there are many medicines being developed for B-cell malignancies in adults but comparatively few in children with these malignancies, a Paediatric Strategy Forum was held to discuss the best approach to develop these products for children. It was concluded that as current frontline therapy is highly successful, despite associated acute toxicity, de-escalation of this or substitution of presently used drugs with new medicines can only be undertaken when there is an effective salvage regimen, which is currently not available. Therefore priority should be given to developing treatment for patients with relapsed and refractory mature B-cell lymphomas. The consensus of the clinicians attending the meeting was that CAR T-cells, T-cell engagers and antibody drug conjugates (excluding those with a vinca alkaloid-like drug) presently have the greatest probability of providing benefit in relapse in view of their mechanism of action. However, as producing autologous CAR T-cells currently takes at least 4 weeks, they are not products which could be quickly employed initially at relapse in rapidly progressing mature B-cell malignancies but only for the consolidation phase of the treatment. Global, industry-supported, academic-sponsored studies testing compounds from different pharmaceutical companies simultaneously should be considered in rare populations, and it was proposed that an international working group be formed to develop an overarching clinical trials strategy for these disease groups. Future Forums are planned for other relevant paediatric oncologic diseases with a high unmet medical need and relevant molecular targets.Entities:
Keywords: Mature B-cell malignancies; Medicinal product development; Paediatric oncology
Year: 2019 PMID: 30772656 DOI: 10.1016/j.ejca.2019.01.013
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162