2016
DOI: 10.18632/oncotarget.8130
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The comparison of outcomes from tyrosine kinase inhibitor monotherapy in second- or third-line for advanced non-small-cell lung cancer patients with wild-type or unknown EGFR status

Abstract: BackgroundSecond-line treatment for advanced non-small-cell lung cancer (NSCLC) patients includes monotherapy with a third-generation cytotoxic drug (CT) or a tyrosine kinase inhibitor (TKI). These options are the actual standard for EGFR wild-type (WT) status, as patients with EGFR mutations achieve greater benefit by the use of TKI in first-line treatment. Some clinical trials and meta-analyses investigated the comparison between CT and TKI in second-line, but data are conflicting.MethodsWe designed a retros… Show more

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Cited by 8 publications
(5 citation statements)
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“…In addition, P2Et or P2Et plus aPD-L1 treatment, also induced a high frequency of activated (CD44 + ) CD4 + and CD8 + T cells ( Figure 5D). The assessment of other immune cell populations in the tumor ( Figure 5E) showed that the three treatment strategies decreased the number of MDSC, which due to lack of functional evaluation are called myeloid-derived suppressor like cells (MDSC-LCs) ( Figure 5F) (29). However, the number of tumor-infiltrating monocytic MDSC (M-MDSC) was lower with P2Et plus aPD-L1 treatment compared to P2Et alone ( Figure 5F).…”
Section: P2et Treatment Alone or In Combination With Apd-l1 Modulatesmentioning
confidence: 99%
“…In addition, P2Et or P2Et plus aPD-L1 treatment, also induced a high frequency of activated (CD44 + ) CD4 + and CD8 + T cells ( Figure 5D). The assessment of other immune cell populations in the tumor ( Figure 5E) showed that the three treatment strategies decreased the number of MDSC, which due to lack of functional evaluation are called myeloid-derived suppressor like cells (MDSC-LCs) ( Figure 5F) (29). However, the number of tumor-infiltrating monocytic MDSC (M-MDSC) was lower with P2Et plus aPD-L1 treatment compared to P2Et alone ( Figure 5F).…”
Section: P2et Treatment Alone or In Combination With Apd-l1 Modulatesmentioning
confidence: 99%
“…The identification of susceptible oncogenic 'drivers' has hastened the development of highly effective drugs. To date these include epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs), which target activating mutations in exons 18-21 of the EGFR gene, and anaplastic lymphoma kinase (ALK) inhibitors, which target the echinoderm microtubule associated protein like 4 (EML4)-ALK or c-ros oncogene 1 (ROS1) translocation Bronte et al, 2016). When these oncogenic driver mutations are found in tumour tissue, the efficacy of their respective targeted agents is substantially higher than that of standard chemotherapy.…”
Section: Introductionmentioning
confidence: 99%
“…Specific mutations of epidermal growth factor receptor (EGFR) play a key role in the development of non-small cell lung cancer (NSCLC), primarily adenocarcinomas, and specific EGFR-targeted therapy has revolutionized the treatment of the subset of adenocarcinomas harboring an EGFR-activating mutation. 1 , 2 …”
Section: Introductionmentioning
confidence: 99%