Treating ALK-positive lung cancer-early successes and future challenges

被引:200
作者
Camidge, D. Ross [1 ]
Doebele, Robert C. [1 ]
机构
[1] Univ Colorado, Div Med Oncol, Ctr Canc, Aurora, CO 80045 USA
关键词
ANAPLASTIC LYMPHOMA KINASE; RECEPTOR TYROSINE KINASE; GASTROINTESTINAL STROMAL TUMORS; EML4-ALK FUSION GENE; GROWTH-FACTOR; ACTIVATING MUTATIONS; CLINICAL RESISTANCE; ONCOGENIC MUTATIONS; ACQUIRED-RESISTANCE; CELL LYMPHOMA;
D O I
10.1038/nrclinonc.2012.43
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rearrangements of the anaplastic lymphoma kinase (ALK) gene occur infrequently in non-small-cell lung cancer (NSCLC), but provide an important paradigm for oncogene-directed therapy in this disease. Crizotinib, an orally bioavailable inhibitor of ALK, provides significant benefit for patients with ALK-positive (ALK+) NSCLC in association with characteristic, mostly mild, toxic effects, and this drug has been approved by the FDA for clinical use in this molecularly defined subgroup of lung cancer. Many new ALK inhibitors are being developed and understanding the challenges of determining and addressing the adverse effects that are likely to be ALK specific, while maximizing the time of benefit on targeted agents, and understanding the mechanisms that underlie drug resistance will be critical in the future for informing the optimal therapy of ALK+ NSCLC.
引用
收藏
页码:268 / 277
页数:10
相关论文
共 97 条
[91]  
Weickhardt A. J, 2012, CANCER IN PRESS
[92]  
Wong K., 2011, J. Clin. Oncol, V29, pa7500
[93]   EML4-ALK Translocation Predicts Better Outcome in Lung Adenocarcinoma Patients with Wild-Type EGFR [J].
Wu, Shang-Gin ;
Kuo, Yao-Wen ;
Chang, Yih-Leong ;
Shih, Jin-Yuan ;
Chen, Ya-Hui ;
Tsai, Meng-Feng ;
Yu, Chong-Jen ;
Yang, Chih-Hsin ;
Yang, Pan-Chyr .
JOURNAL OF THORACIC ONCOLOGY, 2012, 7 (01) :98-104
[94]   Worse Disease-Free Survival in Never-Smokers with ALK plus Lung Adenocarcinoma [J].
Yang, Ping ;
Kulig, Kimary ;
Boland, Jennifer M. ;
Erickson-Johnson, Michele R. ;
Oliveira, Andre M. ;
Wampfler, Jason ;
Jatoi, Aminah ;
Deschamps, Claude ;
Marks, Randolph ;
Fortner, Connie ;
Stoddard, Shawn ;
Nichols, Francis ;
Molina, Julian ;
Aubry, Marie-Christine ;
Tang, Hui ;
Yi, Eunhee S. .
JOURNAL OF THORACIC ONCOLOGY, 2012, 7 (01) :90-97
[95]   The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP [J].
Yun, Cai-Hong ;
Mengwasser, Kristen E. ;
Toms, Angela V. ;
Woo, Michele S. ;
Greulich, Heidi ;
Wong, Kwok-Kin ;
Meyerson, Matthew ;
Eck, Michael J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (06) :2070-2075
[96]   Crizotinib-Resistant Mutants of EML4-ALK Identified Through an Accelerated Mutagenesis Screen [J].
Zhang, Sen ;
Wang, Frank ;
Keats, Jeffrey ;
Zhu, Xiaotian ;
Ning, Yaoyu ;
Wardwell, Scott D. ;
Moran, Lauren ;
Mohemmad, Qurish K. ;
Anjum, Rana ;
Wang, Yihan ;
Narasimhan, Narayana I. ;
Dalgarno, David ;
Shakespeare, William C. ;
Miret, Juan J. ;
Clackson, Tim ;
Rivera, Victor M. .
CHEMICAL BIOLOGY & DRUG DESIGN, 2011, 78 (06) :999-1005
[97]   Fusion of EML4 and ALK is associated with development of lung adenocarcinomas lacking EGFR and KRAS mutations and is correlated with ALK expression [J].
Zhang, Xuchao ;
Zhang, Shirley ;
Yang, Xuening ;
Yang, Jinji ;
Zhou, Qing ;
Yin, Lucy ;
An, Shejuan ;
Lin, Jiaying ;
Chen, Shiliang ;
Xie, Zhi ;
Zhu, Mike ;
Zhang, Xiaolin ;
Wu, Yi-Long .
MOLECULAR CANCER, 2010, 9