Home > Publications database > Molecular, Pathological, Radiological, and Immune Profiling of Non-brainstem Pediatric High-Grade Glioma from the HERBY Phase II Randomized Trial. > print |
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024 | 7 | _ | |a 10.1016/j.ccell.2018.04.004 |2 doi |
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100 | 1 | _ | |a Mackay, Alan |b 0 |
245 | _ | _ | |a Molecular, Pathological, Radiological, and Immune Profiling of Non-brainstem Pediatric High-Grade Glioma from the HERBY Phase II Randomized Trial. |
260 | _ | _ | |a Cambridge, Mass. |c 2018 |b Cell Press |
336 | 7 | _ | |a article |2 DRIVER |
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336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1660038281_23715 |2 PUB:(DE-HGF) |
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520 | _ | _ | |a The HERBY trial was a phase II open-label, randomized, multicenter trial evaluating bevacizumab (BEV) in addition to temozolomide/radiotherapy in patients with newly diagnosed non-brainstem high-grade glioma (HGG) between the ages of 3 and 18 years. We carried out comprehensive molecular analysis integrated with pathology, radiology, and immune profiling. In post-hoc subgroup analysis, hypermutator tumors (mismatch repair deficiency and somatic POLE/POLD1 mutations) and those biologically resembling pleomorphic xanthoastrocytoma ([PXA]-like, driven by BRAF_V600E or NF1 mutation) had significantly more CD8+ tumor-infiltrating lymphocytes, and longer survival with the addition of BEV. Histone H3 subgroups (hemispheric G34R/V and midline K27M) had a worse outcome and were immune cold. Future clinical trials will need to take into account the diversity represented by the term 'HGG' in the pediatric population. |
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700 | 1 | _ | |a Burford, Anna |b 1 |
700 | 1 | _ | |a Molinari, Valeria |b 2 |
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700 | 1 | _ | |a Izquierdo, Elisa |b 4 |
700 | 1 | _ | |a Brouwer-Visser, Jurriaan |b 5 |
700 | 1 | _ | |a Giangaspero, Felice |b 6 |
700 | 1 | _ | |a Haberler, Christine |b 7 |
700 | 1 | _ | |a Pietsch, Torsten |b 8 |
700 | 1 | _ | |a Jacques, Thomas S |b 9 |
700 | 1 | _ | |a Figarella-Branger, Dominique |b 10 |
700 | 1 | _ | |a Rodriguez, Daniel |b 11 |
700 | 1 | _ | |a Morgan, Paul S |b 12 |
700 | 1 | _ | |a Raman, Pichai |b 13 |
700 | 1 | _ | |a Waanders, Angela J |b 14 |
700 | 1 | _ | |a Resnick, Adam C |b 15 |
700 | 1 | _ | |a Massimino, Maura |b 16 |
700 | 1 | _ | |a Garrè, Maria Luisa |b 17 |
700 | 1 | _ | |a Smith, Helen |b 18 |
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700 | 1 | _ | |a Würdinger, Thomas |b 21 |
700 | 1 | _ | |a Tam, Rachel |b 22 |
700 | 1 | _ | |a Garcia, Josep |b 23 |
700 | 1 | _ | |a Thakur, Meghna Das |b 24 |
700 | 1 | _ | |a Vassal, Gilles |b 25 |
700 | 1 | _ | |a Grill, Jacques |b 26 |
700 | 1 | _ | |a Jaspan, Tim |b 27 |
700 | 1 | _ | |a Varlet, Pascale |b 28 |
700 | 1 | _ | |a Jones, Chris |b 29 |
773 | _ | _ | |a 10.1016/j.ccell.2018.04.004 |g Vol. 33, no. 5, p. 829 - 842.e5 |0 PERI:(DE-600)2074034-7 |n 5 |p 829 - 842.e5 |t Cancer cell |v 33 |y 2018 |x 1535-6108 |
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