Targeting NTRK fusion in non-small cell lung cancer: rationale and clinical evidence

被引:41
作者
Ricciuti, Biagio [1 ]
Brambilla, Marta [1 ]
Metro, Giulio [1 ]
Baglivo, Sara [1 ]
Matocci, Roberta [1 ]
Pirro, Matteo [2 ]
Chiari, Rita [1 ]
机构
[1] Azienda Osped Perugia, Santa Maria della Misericordia Hosp, Dept Med Oncol, Via Dottori 1, I-06156 Perugia, Italy
[2] Univ Perugia, Dept Med, Perugia, Italy
关键词
NSCLC; NTRK mutations; Entrectinib; LOXO-101; ADVANCED SOLID TUMORS; ORAL PAN-TRK; ALK-INHIBITOR; OPEN-LABEL; CHEMOTHERAPY; RECEPTOR; ADENOCARCINOMA; ENTRECTINIB; EGFR; EXPRESSION;
D O I
10.1007/s12032-017-0967-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the era of personalized medicine, the identification of targetable genetic alterations represented a major step forward in anticancer therapy. NTRK rearrangements represent the molecular driver of a subset of solid tumors, including 3% of non-small-cell lung cancers (NSCLCs). Preliminary data indicate that molecularly selected NSCLC patients harboring NTRK fusions derive an unprecedented clinical benefit from Trk-directed targeted therapies. The aim of this review is to describe the molecular biology of NTRK signaling pathway and to summarize the preclinical data on novel Trk inhibitors, touching upon the clinical development of these inhibitors for the treatment of advanced NSCLC, which have already shown encouraging anticancer activity and acceptable safety profile in early phase I clinical trials.
引用
收藏
页数:8
相关论文
共 41 条
[1]  
*AM CANC SOC, NONSM CELL LUNG CANC
[2]   NTRK gene fusions as novel targets of cancer therapy across multiple tumour types [J].
Amatu, Alessio ;
Sartore-Bianchi, Andrea ;
Siena, Salvatore .
ESMO OPEN, 2016, 1 (02)
[3]   Inhibition of Irk-driven tumors by the pan-Trk inhibitor RXDX-101 [J].
Anderson, D. ;
Ciomei, M. ;
Banfi, P. ;
Cribioli, S. ;
Ardini, E. ;
Galvani, A. ;
Li, G. .
EUROPEAN JOURNAL OF CANCER, 2014, 50 :101-101
[4]  
[Anonymous], J THORAC ONCOL
[5]  
Ardini E, 2009, MOL CANC THER, V8, pA244
[6]   Long-term follow-up of the PI3Kb inhibitor TGR-1202 to demonstrate a differentiated safety profile and high response rates in CLL and NHL: Integrated analysis of TGR-1202 monotherapy and combined with ublituximab. [J].
Burris, Howard A. ;
Flinn, Ian ;
Lunning, Matthew Alexander ;
Vose, Julie ;
Fowler, Nathan Hale ;
Nastoupil, Loretta J. ;
O'Brien, Susan Mary ;
Schreeder, Marshall T. ;
Patel, Manish R. ;
Fenske, Timothy ;
Brander, Danielle M. ;
Siddiqi, Tanya ;
Flowers, Christopher ;
Burger, Jan Andreas ;
Wierda, William G. ;
Kuhn, John G. ;
Sportelli, Peter ;
Miskin, Hari P. ;
Weiss, Michael S. ;
O'Connor, Owen A. .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
[7]   Beyond EGFR and ALK inhibition: Unravelling and exploiting novel genetic alterations in advanced non small-cell lung cancer [J].
Califano, Raffaele ;
Abidin, Aidalena ;
Tariq, Noor-ul-Ain ;
Economopoulou, Panagiota ;
Metro, Giulio ;
Mountzios, Giannis .
CANCER TREATMENT REVIEWS, 2015, 41 (05) :401-411
[8]   Alka-372-001: First-in-human, phase I study of entrectinib - an oral pan-trk, ROS1, and ALK inhibitor - in patients with advanced solid tumors with relevant molecular alterations. [J].
De Braud, Filippo G. ;
Niger, Monica ;
Damian, Silvia ;
Bardazza, Benedetta ;
Martinetti, Antonia ;
Pelosi, Giuseppe ;
Marrapese, Giovanna ;
Palmeri, Laura ;
Cerea, Giulio ;
Valtorta, Emanuele ;
Veronese, Silvio ;
Sartore-Bianchi, Andrea ;
Ardini, Elena ;
Isachi, Antonella ;
Martignoni, Marcella ;
Galvani, Arturo ;
Luo, David ;
Yeh, Litain ;
Senderowicz, Adrian Mario ;
Siena, Salvatore .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15)
[9]   An Oncogenic NTRK Fusion in a Patient with Soft-Tissue Sarcoma with Response to the Tropomyosin-Related Kinase Inhibitor LOXO-101 [J].
Doebele, Robert C. ;
Davis, Lara E. ;
Vaishnavi, Aria ;
Le, Anh T. ;
Estrada-Bernal, Adriana ;
Keysar, Stephen ;
Jimeno, Antonio ;
Varella-Garcia, Marileila ;
Aisner, Dara L. ;
Li, Yali ;
Stephens, J. ;
Morosini, Deborah ;
Tuch, Brian B. ;
Fernandes, Michele ;
Nanda, Nisha ;
Low, Jennifer A. .
CANCER DISCOVERY, 2015, 5 (10) :1049-1057
[10]   An in vivo functional genetic screen reveals a role for the TRK-T3 oncogene in tumor progression [J].
Edel, MJ ;
Shvarts, A ;
Medema, JP ;
Bernards, R .
ONCOGENE, 2004, 23 (29) :4959-4965