Response to Cabozantinib in Patients with RET Fusion-Positive Lung Adenocarcinomas

被引:378
作者
Drilon, Alexander [1 ]
Wang, Lu [2 ]
Hasanovic, Adnan [5 ]
Suehara, Yoshiyuki [4 ]
Lipson, Doron [6 ]
Stephens, Phil [6 ]
Ross, Jeffrey [6 ]
Miller, Vincent [6 ]
Ginsberg, Michelle [3 ]
Zakowski, Maureen F. [2 ]
Kris, Mark G. [1 ]
Ladanyi, Marc [4 ]
Rizvi, Naiyer [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Thorac Oncol Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Radiol, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, New York, NY 10065 USA
[5] Lenox Hill Hosp, Dept Pathol, New York, NY 10021 USA
[6] Fdn Med, Cambridge, MA USA
关键词
TYROSINE KINASE; GENE FUSIONS; CANCER; ALK; IDENTIFICATION; REARRANGEMENTS; TUMORS; ROS1; INHIBITION; MUTATIONS;
D O I
10.1158/2159-8290.CD-13-0035
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The discovery of RET fusions in lung cancers has uncovered a new therapeutic target for patients whose tumors harbor these changes. In an unselected population of non-small cell lung carcinomas (NSCLCs), RET fusions are present in 1% to 2% of cases. This incidence increases substantially, however, in never-smokers with lung adenocarcinomas that lack other known driver oncogenes. Although preclinical data provide experimental support for the use of RET inhibitors in the treatment of RET fusion-positive tumors, clinical data on response are lacking. We report preliminary data for the first three patients treated with the RET inhibitor cabozantinib on a prospective phase II trial for patients with RET fusion-positive NSCLCs (NCT01639508). Confirmed partial responses were observed in 2 patients, including one harboring a novel TRIM33-RET fusion. A third patient with a KIF5B-RET fusion has had prolonged stable disease approaching 8 months (31 weeks). All three patients remain progression-free on treatment. SIGNIFICANCE: Driver oncogene discovery in lung cancers has dramatically changed today's therapeutic landscape. This report of the activity of cabozantinib in RET fusion-positive disease provides early clinical validation of RET fusions as drivers in lung cancers and suggests that RET inhibition may represent a new treatment paradigm in this molecular cohort.
引用
收藏
页码:630 / 635
页数:6
相关论文
共 26 条
[1]   RET and NTRK1 proto-oncogenes in human diseases [J].
Albert, L ;
Carniti, C ;
Miranda, C ;
Roccato, E ;
Pierotti, MA .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 195 (02) :168-186
[2]   ROS1 Rearrangements Define a Unique Molecular Class of Lung Cancers [J].
Bergethon, Kristin ;
Shaw, Alice T. ;
Ou, Sai-Hong Ignatius ;
Katayama, Ryohei ;
Lovly, Christine M. ;
McDonald, Nerina T. ;
Massion, Pierre P. ;
Siwak-Tapp, Christina ;
Gonzalez, Adriana ;
Fang, Rong ;
Mark, Eugene J. ;
Batten, Julie M. ;
Chen, Haiquan ;
Wilner, Keith D. ;
Kwak, Eunice L. ;
Clark, Jeffrey W. ;
Carbone, David P. ;
Ji, Hongbin ;
Engelman, Jeffrey A. ;
Mino-Kenudson, Mari ;
Pao, William ;
Iafrate, A. John .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (08) :863-870
[3]  
Bongarzone I, 1998, CLIN CANCER RES, V4, P223
[4]   High prevalence of activating ret proto-oncogene rearrangements, in thyroid tumors from patients who had received external radiation [J].
Bounacer, A ;
Wicker, R ;
Caillou, B ;
Cailleux, AF ;
Sarasin, A ;
Schlumberger, M ;
Suarez, HG .
ONCOGENE, 1997, 15 (11) :1263-1273
[5]   EML4-ALK Mutations in Lung Cancer That Confer Resistance to ALK Inhibitors [J].
Choi, Young Lim ;
Soda, Manabu ;
Yamashita, Yoshihiro ;
Ueno, Toshihide ;
Takashima, Junpei ;
Nakajima, Takahiro ;
Yatabe, Yasushi ;
Takeuchi, Kengo ;
Hamada, Toru ;
Haruta, Hidenori ;
Ishikawa, Yuichi ;
Kimura, Hideki ;
Mitsudomi, Tetsuya ;
Tanio, Yoshiro ;
Mano, Hiroyuki .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (18) :1734-1739
[6]   Immunohistochemistry is a Reliable Screening Tool for Identification of ALK Rearrangement in Non-Small-Cell Lung Carcinoma and is Antibody Dependent [J].
Conklin, Chris M. J. ;
Craddock, Kenneth J. ;
Have, Cherry ;
Laskin, Janessa ;
Couture, Christian ;
Ionescu, Diana N. .
JOURNAL OF THORACIC ONCOLOGY, 2013, 8 (01) :45-51
[7]   Identifying and Targeting ROS1 Gene Fusions in Non-Small Cell Lung Cancer [J].
Davies, Kurtis D. ;
Le, Anh T. ;
Theodoro, Mariana F. ;
Skokan, Margaret C. ;
Aisner, Dara L. ;
Berge, Eamon M. ;
Terracciano, Luigi M. ;
Cappuzzo, Federico ;
Incarbone, Matteo ;
Roncalli, Massimo ;
Alloisio, Marco ;
Santoro, Armando ;
Camidge, D. Ross ;
Varella-Garcia, Marileila ;
Doebele, Robert C. .
CLINICAL CANCER RESEARCH, 2012, 18 (17) :4570-4579
[8]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[9]   Epidermal Growth Factor Receptor Inhibition in Lung Cancer Status 2012 [J].
Hirsch, Fred R. ;
Jaenne, Pasi A. ;
Eberhardt, Wilfried E. ;
Cappuzzo, Federico ;
Thatcher, Nick ;
Pirker, Robert ;
Choy, Hak ;
Kim, Edward S. ;
Paz-Ares, Luis ;
Gandara, David R. ;
Wu, Yi-Long ;
Ahn, Myung-Ju ;
Mitsudomi, Tetsuya ;
Shepherd, Frances A. ;
Mok, Tony S. .
JOURNAL OF THORACIC ONCOLOGY, 2013, 8 (03) :373-384
[10]   EML4-ALK lung cancers are characterized by rare other mutations, a TTF-1 cell lineage, an acinar histology, and young onset [J].
Inamura, Kentaro ;
Takeuchi, Kengo ;
Togashi, Yuki ;
Hatano, Satoko ;
Ninomiya, Hironori ;
Motoi, Noriko ;
Mun, Ming-yon ;
Sakao, Yukinori ;
Okumura, Sakae ;
Nakagawa, Ken ;
Soda, Manabu ;
Choi, Young Lim ;
Mano, Hiroyuki ;
Ishikawa, Yuichi .
MODERN PATHOLOGY, 2009, 22 (04) :508-515