دورية أكاديمية

Diagnostic assays for identification of anaplastic lymphoma kinase-positive non-small cell lung cancer.

التفاصيل البيبلوغرافية
العنوان: Diagnostic assays for identification of anaplastic lymphoma kinase-positive non-small cell lung cancer.
المؤلفون: Weickhardt, Andrew J., Aisner, Dara L., Franklin, Wilbur A., Varella‐Garcia, Marileila, Doebele, Robert C., Camidge, D. Ross
المصدر: Cancer (0008543X); Apr2013, Vol. 119 Issue 8, p1467-1477, 11p
مصطلحات موضوعية: LUNG cancer, ADENOCARCINOMA, ANAPLASTIC lymphoma kinase, PROTEIN-tyrosine kinases, IN situ hybridization, FLUORESCENCE
مستخلص: In series dominated by adenocarcinoma histology, approximately 5% of non-small cell lung cancers (NSCLCs) harbor an anaplastic lymphoma kinase ( ALK) gene rearrangement. Crizotinib, a tyrosine kinase inhibitor with significant activity against ALK, has demonstrated high response rates and prolonged progression-free survival in ALK-positive patients enrolled in phase 1/2 clinical trials. In 2011, crizotinib received accelerated approval from the US Food and Drug Administration (FDA) for the treatment of proven ALK-positive NSCLC using an FDA-approved diagnostic test. Currently, only break-apart fluorescence in situ hybridization testing is FDA approved as a companion diagnostic for crizotinib; however, many other assays are available or in development. In the current review, the authors summarize the diagnostic tests available, or likely to become available, that could be used to identify patients with ALK-positive NSCLC, highlighting the pros and cons of each. Cancer 2013. © 2012 American Cancer Society. [ABSTRACT FROM AUTHOR]
Copyright of Cancer (0008543X) is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:0008543X
DOI:10.1002/cncr.27913