Differentiating MYCN-amplified RB1 wild-type retinoblastoma from biallelic RB1 mutant retinoblastoma using MR-based radiomics: a retrospective multicenter case–control study

Autor: Christiaan M. de Bloeme, Robin W. Jansen, Liesbeth Cardoen, Sophia Göricke, Sabien van Elst, Jaime Lyn Jessen, Aparna Ramasubramanian, Alison H. Skalet, Audra K. Miller, Philippe Maeder, Ogul E. Uner, G. Baker Hubbard, Hans Grossniklaus, H. Culver Boldt, Kim E. Nichols, Rachel C. Brennan, Saugata Sen, Mériam Koob, Selma Sirin, Hervé J. Brisse, Paolo Galluzzi, Charlotte J. Dommering, Matthijs Cysouw, Ronald Boellaard, Josephine C. Dorsman, Annette C. Moll, Marcus C. de Jong, Pim de Graaf, European Retinoblastoma Imaging Collaboration

Publikováno v: Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)

Abstract MYCN-amplified RB1 wild-type (MYCN amp RB1 +/+) retinoblastoma is a rare and aggressive subtype, often resistant to standard therapies. Identifying unique MRI features is crucial for diagnosing this subtype, as biopsy is not recommended. Thi

Externí odkaz: https://doaj.org/article/06040e955dd1422f9077c75ea93b9aaf

Risk factors in pediatric Malignant Peripheral Nerve Sheath Tumors (MPNST): Results from the French Pediatric Oncology Society (SFCE) cohort

Autor: Jordane Chaix, Marie Karanian, Nadège Corradini, Maria Merched, Frédérique Larousserie, Louise Galmiche, Brigitte Lacour, Aude Marie-Cardine, Anne-Sophie Defachelles, Pablo Berlanga, Angélique Rome, Estelle Thébaud, Valérie Bernier-Chastagner, Hervé J. Brisse, Frédéric Hameury, Pierre Wolkenstein, Stéphane Ducassou, Daniel Orbach, Cécile Vérité

Publikováno v: EJC Paediatric Oncology, Vol 1, Iss , Pp 100013- (2023)

Introduction: Malignant Peripheral Nerve Sheath Tumors (MPNST) are very rare and aggressive tumors, which can affect children, adolescents, and young adults. These tumors are frequently associated with type 1 neurofibromatosis (NF1). This study aims

Externí odkaz: https://doaj.org/article/f3151756ad4b4376942cc0267aae768d

MRI Features for Identifying MYCN-amplified RB1 Wild-type Retinoblastoma

Autor: Robin W. Jansen, Christiaan M. de Bloeme, Liesbeth Cardoen, Sophia Göricke, Sabien van Elst, Jaime Lyn Jessen, Aparna Ramasubramanian, Alison H. Skalet, Audra K. Miller, Philippe Maeder, Ogul E. Uner, G. Baker Hubbard, Hans Grossniklaus, H. Culver Boldt, Kim E. Nichols, Rachel C. Brennan, Saugata Sen, Selma Sirin, Hervé J. Brisse, Paolo Galluzzi, Charlotte J. Dommering, Jonas A. Castelijns, Paul van der Valk, Ronald Boellaard, Josephine Dorsman, Annette C. Moll, Marcus C. de Jong, Pim de Graaf

Publikováno v: Jansen, R W, de Bloeme, C M, Cardoen, L, Göricke, S, van Elst, S, Jessen, J L, Ramasubramanian, A, Skalet, A H, Miller, A K, Maeder, P, Uner, O E, Hubbard, G B, Grossniklaus, H, Boldt, H C, Nichols, K E, Brennan, R C, Sen, S, Sirin, S, Brisse, H J, Galluzzi, P, Dommering, C J, Castelijns, J A, van der Valk, P, Boellaard, R, Dorsman, J, Moll, A C, de Jong, M C & de Graaf, P 2023, ' MRI Features for Identifying MYCN-amplified RB1 Wild-type Retinoblastoma ', Radiology, vol. 307, no. 5, pp. e222264 . https://doi.org/10.1148/radiol.222264
Radiology. Radiological Society of North America Inc.

Background MYCN-amplified RB1 wild-type (MYCNARB1+/+) retinoblastoma is a rare but clinically important subtype of retinoblastoma due to its aggressive character and relative resistance to typical therapeutic approaches. Because biopsy is not indicat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9dc60d381d5b8e90dd136736f233da9
https://research.vumc.nl/en/publications/a546c773-92ef-4214-b15b-49f2ba6e37ba

Metastatic Malignant Perivascular Epithelioid Cell Tumors With Microsatellite Instability Within Lynch Syndrome Successfully Treated With Anti-PD1 Pembrolizumab

Autor: Lounes Djerroudi, Julien Masliah-Planchon, Hervé J. Brisse, Sophie El Zein, Sylvie Helfre, Dimitri Tzanis, Nadim Hamzaoui, Clément Bonnet, Valérie Laurence, Sylvie Bonvalot, Sarah Watson

Publikováno v: JCO Precision Oncology.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0852daa68c4db59a602a0f3c1537ec5a
https://doi.org/10.1200/po.22.00627

Oral vinorelbine in young patients with desmoid-type fibromatosis

Autor: Laure Kornreich, Daniel Orbach, Nayla Nicolas, Hervé J Brisse, Pablo Berlanga, Anne-Sophie Defachelles, Ludovic Mansuy, Cécile Verite, Laure Saumet, Marie Karanian, Nadège Corradini

Publikováno v: Tumori Journal. :030089162311698

Background: Desmoid-type fibromatosis are rare intermediate tumors in children and adolescents. Owing to local aggressiveness and relapse, systemic treatment for symptomatic advanced or progressive forms is recommended. Following promising results in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d5eb30632ea70623a1485b47c4bb60e9
https://doi.org/10.1177/03008916231169806