Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden von Peneder, Peter, Stütz, Adrian M., Surdez, Didier, Krumbholz, Manuela, Semper, Sabine, Chicard, Mathieu, Sheffield, Nathan C., Pierron, Gaelle, Lapouble, Eve, Tötzl, Marcus, Ergüner, Bekir, Barreca, Daniele, Rendeiro, André F., Agaimy, Abbas, Boztug, Heidrun, Engstler, Gernot, Dworzak, Michael, Bernkopf, Marie, Taschner-Mandl, Sabine, Ambros, Inge M., Myklebost, Ola, Marec-Bérard, Perrine, Burchill, Susan Ann, Brennan, Bernadette, Strauss, Sandra J., Whelan, Jeremy, Schleiermacher, Gudrun, Schaefer, Christiane, Dirksen, Uta, Hutter, Caroline, Boye, Kjetil, Ambros, Peter F., Delattre, Olivier, Metzler, Markus, Bock, Christoph, Tomazou, Eleni M.

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First-in-child phase I/II study of the dual mTORC1/2 inhibitor vistusertib (AZD2014) as monotherapy and in combination with topotecan-temozolomide in children with advanced maligna... von Morscher, Raphael J., Brard, Caroline, Berlanga, Pablo, Marshall, Lynley V., André, Nicolas, Rubino, Jonathan, Aerts, Isabelle, De Carli, Emilie, Corradini, Nadège, Nebchi, Souad, Paoletti, Xavier, Mortimer, Peter, Lacroix, Ludovic, Pierron, Gaelle, Schleiermacher, Gudrun, Vassal, Gilles, Geoerger, Birgit

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Base-excision repair pathway shapes 5-methylcytosine deamination signatures in pan-cancer genomes von Silveira, André Bortolini, Houy, Alexandre, Ganier, Olivier, Özemek, Begüm, Vanhuele, Sandra, Vincent-Salomon, Anne, Cassoux, Nathalie, Mariani, Pascale, Pierron, Gaelle, Leyvraz, Serge, Rieke, Damian, Picca, Alberto, Bielle, Franck, Yaspo, Marie-Laure, Rodrigues, Manuel, Stern, Marc-Henri

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The occurrence of intracranial rhabdoid tumours in mice depends on temporal control of Smarcb1 inactivation von Han, Zhi-Yan, Richer, Wilfrid, Fréneaux, Paul, Chauvin, Céline, Lucchesi, Carlo, Guillemot, Delphine, Grison, Camille, Lequin, Delphine, Pierron, Gaelle, Masliah-Planchon, Julien, Nicolas, André, Ranchère-Vince, Dominique, Varlet, Pascale, Puget, Stéphanie, Janoueix-Lerosey, Isabelle, Ayrault, Olivier, Surdez, Didier, Delattre, Olivier, Bourdeaut, Franck

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Balanced Translocations Disrupting SMARCB1 Are Hallmark Recurrent Genetic Alterations in Renal Medullary Carcinomas von Calderaro, Julien, Masliah-Planchon, Julien, Richer, Wilfrid, Maillot, Laetitia, Maille, Pascale, Mansuy, Ludovic, Bastien, Claire, de la Taille, Alexandre, Boussion, Hélène, Charpy, Cécile, Jourdain, Anne, Bléchet, Claire, Pierron, Gaelle, Gentien, David, Choudat, Laurence, Tournigand, Christophe, Delattre, Olivier, Allory, Yves, Bourdeaut, Franck

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Circulating tumor DNA as a Prognostic Factor in Patients with Resectable Hepatic Metastases of Uveal Melanoma von Mariani, Pascale, Bidard, François-Clément, Rampanou, Aurore, Houy, Alexandre, Servois, Vincent, Ramtohul, Toulsie, Pierron, Gaelle, Chevrier, Marion, Renouf, Benjamin, Lantz, Olivier, Gardrat, Sophie, Vincent-Salomon, Anne, Sergio-Roman, Sergio, Rodrigues, Manuel, Piperno-Neumann, Sophie, Cassoux, Nathalie, Stern, Marc-Henri, Renault, Shufang

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Radiogenomics of neuroblastomas: Relationships between imaging phenotypes, tumor genomic profile and survival von Brisse, Hervé J, Blanc, Thomas, Schleiermacher, Gudrun, Mosseri, Véronique, Philippe-Chomette, Pascale, Janoueix-Lerosey, Isabelle, Pierron, Gaelle, Lapouble, Eve, Peuchmaur, Michel, Fréneaux, Paul, Galmiche, Louise, Algret, Nathalie, Peycelon, Matthieu, Michon, Jean, Delattre, Olivier, Sarnacki, Sabine

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MDM2 amplification and fusion gene ss18-ssx in a poorly differentiated synovial sarcoma: A rare but puzzling conjunction von Di Mauro, Ilaria, Mescam-Mancini, Lénaïg, Chetaille, Bruno, Lae, Marick, Pierron, Gaelle, Dadone-Montaudie, Bérengère, Bazin, Audrey, Bouvier, Corinne, Michiels, Jean-François, Pedeutour, Florence

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Frequent hSNF5/INI1 Germline Mutations in Patients with Rhabdoid Tumor von BOURDEAUT, Franck, LEQUIN, Delphine, ORBACH, Daniel, BERGERON, Christophe, RIALLAND, Xavier, FRENEAUX, Paul, RANCHERE, Dominique, FIGARELLA-BRANGER, Dominique, AUDRY, Georges, PUGET, Stéphanie, GARETH EVANS, D, FERRERES PINAS, Joan Carles, BRUGIERES, Laurence, CAPRA, Valeria, MOSSERI, Véronique, COUPIER, Isabelle, GAUTHIER-VILLARS, Marion, PIERRON, Gaëlle, DELATTRE, Olivier, REYNAUD, Stéphanie, DUFOUR, Christelle, DOZ, François, ANDRE, Nicolas, STEPHAN, Jean-Louis, PEREL, Yves, OBERLIN, Odile

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Impact of EWS-ETS Fusion Type on Disease Progression in Ewing's Sarcoma/Peripheral Primitive Neuroectodermal Tumor: Prospective Results From the Cooperative Euro-E.W.I.N.G. 99 Tria... von Le Deley, Marie-Cecile, Delattre, Olivier, Schaefer, Karl-Ludwig, Burchill, Sue A, Koehler, Gabriele, Hogendoorn, Pancras C W, Lion, Thomas, Poremba, Christopher, Marandet, Julien, Ballet, Stelly, Pierron, Gaelle, Brownhill, Samantha C, Nesslböck, Michaela, Ranft, Andreas, Dirksen, Uta, Oberlin, Odile, Lewis, Ian J, Craft, Alan W, Jürgens, Heribert, Kovar, Heinrich

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Clinical characteristics and outcomes for children, adolescents and young adults with “CIC‐fused” or “BCOR‐rearranged” soft tissue sarcomas: A multi‐institutional European retrospe... von Sparber‐Sauer, Monika, Corradini, Nadège, Affinita, Maria Carmen, Milano, Giuseppe Maria, Pierron, Gaelle, Carton, Matthieu, Tirode, Franck, Pissaloux, Daniel, Alaggio, Rita, Vokuhl, Christian, Bisogno, Gianni, Berlanga, Pablo, Ferrari, Andrea, Orbach, Daniel

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A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion von Pierron, Gaëlle, Tirode, Franck, Lucchesi, Carlo, Reynaud, Stéphanie, Ballet, Stelly, Cohen-Gogo, Sarah, Perrin, Virginie, Coindre, Jean-Michel, Delattre, Olivier

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Integrative clinical and biopathology analyses to understand the clinical heterogeneity of infantile rhabdomyosarcoma: A report from the French MMT committee von Butel, Thibault, Karanian, Marie, Pierron, Gaelle, Orbach, Daniel, Ranchere, Dominique, Cozic, Nathalie, Galmiche, Louise, Coulomb, Aurore, Corradini, Nadège, Lacour, Brigitte, Proust, Stéphanie, Guerin, Florent, Boutroux, Hélène, Rome, Angélique, Mansuy, Ludovic, Vérité, Cécile, Defachelles, Anne‐Sophie, Tirode, Franck, Minard‐Colin, Veronique

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Clinical effect of molecular methods in sarcoma diagnosis (GENSARC): a prospective, multicentre, observational study von Italiano, Antoine, Dr, Di Mauro, Ilaria, MSc, Rapp, Jocelyn, MSc, Pierron, Gaëlle, PhD, Auger, Nathalie, MD, Alberti, Laurent, PhD, Chibon, Frédéric, PhD, Escande, Fabienne, PhD, Voegeli, Anne-Claire, MD, Ghnassia, Jean-Pierre, MD, Keslair, Frédérique, MSc, Laé, Marick, MD, Ranchère-Vince, Dominique, MD, Terrier, Philippe, MD, Baffert, Sandrine, PhD, Coindre, Jean-Michel, Prof, Pedeutour, Florence, Prof

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PAX3/FOXO1 Fusion Gene Status Is the Key Prognostic Molecular Marker in Rhabdomyosarcoma and Significantly Improves Current Risk Stratification von Missiaglia, Edoardo, Williamson, Dan, Chisholm, Julia, Wirapati, Pratyaksha, Pierron, Gaëlle, Petel, Fabien, Concordet, Jean-Paul, Thway, Khin, Oberlin, Odile, Pritchard-Jones, Kathy, Delattre, Olivier, Delorenzi, Mauro, Shipley, Janet

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Germline MBD4 Mutations and Predisposition to Uveal Melanoma von Derrien, Anne-Céline, Rodrigues, Manuel, Eeckhoutte, Alexandre, Dayot, Stéphane, Houy, Alexandre, Mobuchon, Lenha, Gardrat, Sophie, Lequin, Delphine, Ballet, Stelly, Pierron, Gaëlle, Alsafadi, Samar, Mariani, Odette, El-Marjou, Ahmed, Matet, Alexandre, Colas, Chrystelle, Cassoux, Nathalie, Stern, Marc-Henri

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Sequential genomic analysis using a multisample/multiplatform approach to better define rhabdomyosarcoma progression and relapse von de Traux de Wardin, Henry, Dermawan, Josephine K., Merlin, Marie-Sophie, Wexler, Leonard H., Orbach, Daniel, Vanoli, Fabio, Schleiermacher, Gudrun, Geoerger, Birgit, Ballet, Stelly, Guillemot, Delphine, Frouin, Eléonore, Cyrille, Stacy, Delattre, Olivier, Pierron, Gaelle, Antonescu, Cristina R.

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Reply to: Unravelling the mysteries of Alveolar soft part sarcomas in young patients von Genevois, Anne-Laure, Dufresne, Armelle, Pierron, Gaëlle, Toulmonde, Maud, Blay, Jean-Yves, Orbach, Daniel

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A subset of epithelioid and spindle cell rhabdomyosarcomas is associated with TFCP2 fusions and common ALK upregulation von Le Loarer, François, Cleven, Arjen H. G., Bouvier, Corinne, Castex, Marie-Pierre, Romagosa, Cleofe, Moreau, Anne, Salas, Sébastien, Bonhomme, Benjamin, Gomez-Brouchet, Anne, Laurent, Camille, Le Guellec, Sophie, Audard, Virginie, Giraud, Antoine, Ramos-Oliver, Irma, Cleton-Jansen, Anne-Marie, Savci-Heijink, Dilara C., Kroon, Herman M., Baud, Jessica, Pissaloux, Daniel, Pierron, Gaëlle, Sherwood, Anand, Coindre, Jean Michel, Bovée, Judith V. M. G., Larousserie, Frédérique, Tirode, Franck

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Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma von de Pontual, Loïc, Raynal, Virginie, Combaret, Valérie, Pierron, Gaëlle, Amiel, Jeanne, Ribeiro, Agnès, Michon, Jean, Lyonnet, Stanislas, Janoueix-Lerosey, Isabelle, Brugières, Laurence, Lequin, Delphine, Schleiermacher, Gudrun, Delattre, Olivier, Puisieux, Alain, Valteau-Couanet, Dominique, Frebourg, Thierry

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