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Please use this identifier to cite or link to this item:
https://ir.csmu.edu.tw:8080/ir/handle/310902500/24855
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Title: | ALK variants, PD-L1 expression, and their association with outcomes in ALK-positive NSCLC patients |
Authors: | Chang, GC;Yang, TY;Chen, KC;Hsu, KH;Huang, YH;Su, KY;Yu, SL;Tseng, JS |
Date: | 2020 |
Issue Date: | 2022-08-09T08:09:05Z (UTC)
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Publisher: | NATURE RESEARCH |
ISSN: | 2045-2322 |
Abstract: | It remains unclear how programmed death-ligand 1 ( PD-L1) expression interacts with anaplastic lymphoma kinase (ALK) mutation, its variants, and the outcome of treatment. One hundred and twenty four out of 1255 patients (9.9%) were deemed ALK-positive by the Ventana IHC assay. PD-L1 status and ALK variants were available in 100 and 59 patients, respectively. PD-L1 positive (TPS >= 1%) and strong positive (TPS >= 50%) rate was 50% and 16%, respectively. A total of 64 variant types were detected in 59 patients. V1 ( 32.8%) and V3a/b (28.1%) were the most common variants. There was no significant association between ALK variants and the PD-L1 expression. The presence of V3a/b subtype independently predicted a worse overall survival in patients receiving ALK inhibitor(s) (aHR 5.10 [95% CI 1.22-21.25], P = 0.025) and platinum plus pemetrexed (aHR 9.62 [95% CI 1.90-48.80], P = 0.006). While incorporating ALK variants and PD-L1 expression together, patients with non-V3a/b/positive PD-L1 showed a trend towards longer OS. In conclusion, ALK-positive NSCLC patients possess a high PD-L1 expression rate. Although there was no significant association between PD-L1 expression and ALK variants, the outcome of ALK- positive patients could be sorted by these two biomarkers. |
URI: | http://dx.doi.org/10.1038/s41598-020-78152-1 https://www.webofscience.com/wos/woscc/full-record/WOS:000615394300063 https://ir.csmu.edu.tw:8080/handle/310902500/24855 |
Relation: | SCIENTIFIC REPORTS ,2020 ,v10 ,issue 1 |
Appears in Collections: | [中山醫學大學研究成果] 期刊論文
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