L
Luca Lazzari
Researcher at University of Turin
Publications - 34
Citations - 2391
Luca Lazzari is an academic researcher from University of Turin. The author has contributed to research in topics: Cetuximab & Panitumumab. The author has an hindex of 17, co-authored 29 publications receiving 1847 citations. Previous affiliations of Luca Lazzari include University of Milan.
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Journal ArticleDOI
Tumor heterogeneity and Lesion-Specific response to targeted therapy in colorectal cancer
Mariangela Russo,Giulia Siravegna,Lawrence S. Blaszkowsky,Giorgio Corti,Giovanni Crisafulli,Leanne G. Ahronian,Benedetta Mussolin,Eunice L. Kwak,Michela Buscarino,Luca Lazzari,Emanuele Valtorta,Mauro Truini,Nicholas A. Jessop,Hayley Robinson,Theodore S. Hong,Mari Mino-Kenudson,Federica Di Nicolantonio,Ashraf Thabet,Andrea Sartore-Bianchi,Salvatore Siena,A. John Iafrate,Alberto Bardelli,Ryan B. Corcoran +22 more
TL;DR: In this article, the authors studied EGFR blockade in colorectal cancer to assess whether tissue and liquid biopsies can be integrated with radiological imaging to monitor the impact of individual oncogenic alterations on lesion-specific responses.
Journal ArticleDOI
Acquired Resistance to the TRK Inhibitor Entrectinib in Colorectal Cancer
Mariangela Russo,Sandra Misale,Ge Wei,Giulia Siravegna,Giovanni Crisafulli,Luca Lazzari,Giorgio Corti,Giuseppe Rospo,Luca Novara,Benedetta Mussolin,Alice Bartolini,Nicholas Cam,R. Patel,Shunqi Yan,Robert H. Shoemaker,Robert A. Wild,Federica Di Nicolantonio,Andrea Bianchi,Gang Li,Salvatore Siena,Alberto Bardelli +20 more
TL;DR: Proof of principle that analyses of xenopatients and liquid biopsies allow the identification of drug resistance mechanisms in parallel with clinical treatment of an individual patient is provided and can be immediately exploited to design next-generation TRKA inhibitors.
Journal ArticleDOI
ALK, ROS1, and NTRK Rearrangements in Metastatic Colorectal Cancer.
Filippo Pietrantonio,Federica Di Nicolantonio,Alexa B. Schrock,Jeeyun Lee,Sabine Tejpar,Andrea Sartore-Bianchi,Jaclyn F. Hechtman,Jason Christiansen,Luca Novara,Niall C. Tebbutt,Giovanni Fucà,Carlotta Antoniotti,Seung Tae Kim,Danielle Murphy,Rosa Berenato,Federica Morano,James Sun,Bosun Min,Philip J. Stephens,Marissa Chen,Luca Lazzari,Vincent A. Miller,Robert H. Shoemaker,Alessio Amatu,Massimo Milione,Jeffrey S. Ross,Salvatore Siena,Alberto Bardelli,Siraj M. Ali,A. Falcone,Filippo de Braud,Chiara Cremolini +31 more
TL;DR: ALK, ROS1, and NTRK rearrangements define a new rare subtype of mCRC with extremely poor prognosis, and four evaluable patients with rearranged patients showed primary resistance to anti-epidermal growth factor receptor agents.
Journal ArticleDOI
Blockade of EGFR and MEK Intercepts Heterogeneous Mechanisms of Acquired Resistance to Anti-EGFR Therapies in Colorectal Cancer
Sandra Misale,Sabrina Arena,Simona Lamba,Giulia Siravegna,Alice Lallo,Sebastijan Hobor,Mariangela Russo,Michela Buscarino,Luca Lazzari,Andrea Sartore-Bianchi,Katia Bencardino,Alessio Amatu,Calogero Lauricella,Emanuele Valtorta,Salvatore Siena,Federica Di Nicolantonio,Alberto Bardelli +16 more
TL;DR: The studies from Bettegowda and Misale and their colleagues show the effectiveness of analyzing circulating DNA from a variety of tumors and highlight the potential applications of this technology for early detection, monitoring resistance, and devising treatment plans to overcome resistance.
Journal ArticleDOI
Emergence of Multiple EGFR Extracellular Mutations during Cetuximab Treatment in Colorectal Cancer
Sabrina Arena,Beatriz Bellosillo,Giulia Siravegna,Alejandro Martínez,Israel Cañadas,Luca Lazzari,Noelia Ferruz,Mariangela Russo,Sandra Misale,Iria Gonzalez,Mar Iglesias,Elena Gavilán,Giorgio Corti,Sebastijan Hobor,Giovanni Crisafulli,Marta Salido,Juan Sánchez,Alba Dalmases,Joaquim Bellmunt,Gianni De Fabritiis,Gianni De Fabritiis,Ana Rovira,Federica Di Nicolantonio,Joan Albanell,Alberto Bardelli,Clara Montagut +25 more
TL;DR: Colorectal tumors evade EGFR blockade by constitutive activation of downstream signaling effectors and through mutations affecting receptor–antibody binding through mechanisms of resistance to cetuximab, which may occur concomitantly.