2016
DOI: 10.1016/s1470-2045(16)30123-1
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Novel therapeutic targets on the horizon for lung cancer

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Cited by 161 publications
(130 citation statements)
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“…As these agents move quickly to treat early-stage lung cancers through clinical studies, other agents that target different aspects of the tumor-immune system milieu are being developed. Figure 2 demonstrates different strategies being utilized to enhance tumor recognition and elimination by the immune system [66]. …”
Section: Immunotherapiesmentioning
confidence: 99%
“…As these agents move quickly to treat early-stage lung cancers through clinical studies, other agents that target different aspects of the tumor-immune system milieu are being developed. Figure 2 demonstrates different strategies being utilized to enhance tumor recognition and elimination by the immune system [66]. …”
Section: Immunotherapiesmentioning
confidence: 99%
“…Non-small-cell lung cancer (NSCLC) is by far the most common type of lung cancer, making up ~85% of all diagnosed lung cancers. 1 Although intensive efforts have been devoted to developing novel combinational therapeutic options based on molecular targets for NSCLC, the outcome of patients with NSCLC remains poor due to chemoresistance. 2 Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), a member of the TNF family of ligands, is capable of initiating apoptosis by interacting with two death-inducing receptors, death receptor 4 (DR4) and death receptor 5 (DR5).…”
Section: Introductionmentioning
confidence: 99%
“…In 2004, the seminal discovery of activating epidermal growth factor receptor (EGFR) mutations that confer sensitivity to tyrosine kinase inhibitors (TKIs) in adenocarcinomas of NSCLCs heralded the beginning of the era of precision medicine that was based on the molecular diagnoses of NSCLCs [7,8]. In the following studies, researchers have demonstrated that besides EGFR mutations, anaplastic lymphoma kinase (ALK) rearrangements, Kirsten rat sarcoma viral oncogene (KRAS) mutations, human epidermal growth factor receptor-2 mutations and amplifications, v-Raf murine sarcoma viral oncogene homolog B mutations, rat c-ros oncogene 1 rearrangements, transfection oncogene rearrangements, encoding the proto-oncogene tyrosine kinase c-mesenchymal epithelial transition factor amplifications and exon 14 skipping serve as therapeutic targets [9,10]. According to the latest National Comprehensive Cancer Network (NCCN) guidelines (Version 2.2017), EGFR mutations and ALK rearrangements should be evaluated routinely (category 1) in patients with advanced nonsquamous NSCLCs and in patients with squamous NSCLCs that exhibit atypical clinical features (e.g.…”
Section: Introductionmentioning
confidence: 99%