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Erschienen in: Current Treatment Options in Oncology 1-2/2010

01.06.2010 | Lung Cancer

Exciting New Targets in Lung Cancer Therapy: ALK, IGF-1R, HDAC, and Hh

verfasst von: Joel W. Neal, MD, PhD, Lecia V. Sequist, MD, MPH

Erschienen in: Current Treatment Options in Oncology | Ausgabe 1-2/2010

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Opinion statement

The anaplastic lymphoma kinase (ALK) inhibitor crizotinib will become an integral addition to the treatment of patients with non-small cell lung cancer (NSCLC) harboring genetic ALK translocations. The insulin-like growth factor receptor (IGF-1R) monoclonal antibody figitumumab, while initially promising, appears to increase toxicity and death in combination with chemotherapy in the treatment of patients with NSCLC of squamous histology; therefore, clinical development of this class of agents will need to proceed with caution. The histone deacetylation (HDAC) inhibitor vorinostat did not demonstrate an improvement in overall survival (OS) compared with placebo in a large randomized trial, but other agents in this class may have greater selectivity and efficacy. Inhibitors of the hedgehog (Hh) signaling pathways have some early clinical promise in both NSCLC and small cell lung cancer (SCLC), and larger studies using these agents are eagerly anticipated.
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Metadaten
Titel
Exciting New Targets in Lung Cancer Therapy: ALK, IGF-1R, HDAC, and Hh
verfasst von
Joel W. Neal, MD, PhD
Lecia V. Sequist, MD, MPH
Publikationsdatum
01.06.2010
Verlag
Springer US
Erschienen in
Current Treatment Options in Oncology / Ausgabe 1-2/2010
Print ISSN: 1527-2729
Elektronische ISSN: 1534-6277
DOI
https://doi.org/10.1007/s11864-010-0120-6

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