A 2035 Clinical Research Vision and Roadmap for High-Risk Neuroblastoma

被引:0
作者
Moreno, Lucas [1 ,2 ,3 ]
Dubois, Steven G. [4 ]
Bird, Nicholas [5 ]
Knox, Leona [5 ]
Ludwinski, Donna [5 ,6 ]
Pearson, Andrew D. J. [7 ]
Beck-Popovic, Maja [8 ]
Bagatell, Rochelle [9 ]
机构
[1] Hosp Univ Vall dHebron, Vall dHebron Comprehens Canc Ctr, Barcelona, Spain
[2] Vall dHebron Inst Res VHIR, Barcelona, Spain
[3] Univ Autonoma Barcelona UAB, Barcelona, Spain
[4] Dana Farber Boston Childrens Canc & Blood Disorder, Boston, MA USA
[5] Solving Kids Canc UK, London, England
[6] Solving Kids Canc US, New York, NY USA
[7] Inst Canc Res, Dept Paediat Oncol, London, England
[8] CHU Vaudois, Unite Hematooncol Pediat, Lausanne, Switzerland
[9] Univ Penn, Childrens Hosp Philadelphia, Abramson Canc Ctr, Philadelphia, PA USA
关键词
anti-GD2; immunotherapy; neuroblastoma; new agents; ANTI-GD2; MONOCLONAL-ANTIBODY; PHASE-II; TELOMERE MAINTENANCE; FREE SURVIVAL; OPEN-LABEL; CHILDREN; TRIAL; CHEMOTHERAPY; IMPACT; INTERLEUKIN-2;
D O I
10.1002/pbc.31660
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite the introduction of anti-GD2 antibody therapy, outcomes for children with high-risk neuroblastoma remain poor, with low cure rates and a high proportion of survivors facing long-term sequelae. In this report, leaders from international cooperative groups and patient advocacy organizations review lessons learnt, identify current challenges, and provide a vision to bring new agents into frontline therapy to increase cure rates and reduce long-term toxicities over the next decade. The implementation of this vision requires improved global collaboration, incorporation of novel biomarkers, and a strengthened interaction with the regulatory landscape.
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页数:9
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