<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Zhang S</submitter><pubmed_abstract>Human epidermal growth factor receptor 2 (HER2) possesses tyrosine kinase activity and participates in cell growth, differentiation and migration, and survival. Its alterations, mainly including mutations, amplifications, and overexpression are associated with poor prognosis and are one of the major drivers in non-small cell lung cancer (NSCLC). Several clinical trials had been investigating on the treatments of HER2-altered NSCLC, including conventional chemotherapy, programmed death 1 (PD-1) inhibitors, tyrosine kinase inhibitors (TKIs) and antibody-drug conjugates (ADCs), however, the results were either disappointing or encouraging, but inconsistent. Trastuzumab deruxtecan (T-DXd) was recently approved by the Food and Drug Administration as the first targeted agent for treating HER2-mu</pubmed_abstract><journal>Thoracic cancer</journal><pagination>91-104</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9807451</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chinese expert consensus on the diagnosis and treatment of HER2-altered non-small cell lung cancer.</pubmed_title><pmcid>PMC9807451</pmcid><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Shi L</pubmed_authors><pubmed_authors>Wu L</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Dong X</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Lin X</pubmed_authors><pubmed_authors>Du Y</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Gao F</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Wang K</pubmed_authors><pubmed_authors>Shi X</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Zhan P</pubmed_authors><pubmed_authors>Wan B</pubmed_authors><pubmed_authors>Rao C</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Sun P</pubmed_authors><pubmed_authors>Guo H</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Kang J</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Chu Q</pubmed_authors><pubmed_authors>Xia Y</pubmed_authors><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Yang N</pubmed_authors><pubmed_authors>Xu C</pubmed_authors><pubmed_authors>Zhong W</pubmed_authors><pubmed_authors>Yao W</pubmed_authors><pubmed_authors>Yuan J</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Min L</pubmed_authors><pubmed_authors>Yuan D</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Feng H</pubmed_authors><pubmed_authors>Lin G</pubmed_authors><pubmed_authors>Xu T</pubmed_authors><pubmed_authors>Yao C</pubmed_authors><pubmed_authors>Gao W</pubmed_authors><pubmed_authors>Pu X</pubmed_authors><pubmed_authors>Pang F</pubmed_authors><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Ma S</pubmed_authors><pubmed_authors>Meng R</pubmed_authors><pubmed_authors>Zhu Z</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Tang C</pubmed_authors><pubmed_authors>Cai J</pubmed_authors><pubmed_authors>Jia H</pubmed_authors><pubmed_authors>Yu G</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Miao L</pubmed_authors><pubmed_authors>Niu X</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Yao Y</pubmed_authors><pubmed_authors>Zhou C</pubmed_authors><pubmed_authors>Yu Z</pubmed_authors><pubmed_authors>Song Z</pubmed_authors><pubmed_authors>Nie X</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors><pubmed_authors>Song Y</pubmed_authors><pubmed_authors>Pan W</pubmed_authors><pubmed_authors>Lv D</pubmed_authors><pubmed_authors>Zhou W</pubmed_authors><pubmed_authors>Ye M</pubmed_authors><pubmed_authors>Fang Y</pubmed_authors><pubmed_authors>Luo J</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Hong Z</pubmed_authors><pubmed_authors>Fang W</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Liu A</pubmed_authors><pubmed_authors>Lv T</pubmed_authors><pubmed_authors>Fang M</pubmed_authors><pubmed_authors>Cai X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chinese expert consensus on the diagnosis and treatment of HER2-altered non-small cell lung cancer.</name><description>Human epidermal growth factor receptor 2 (HER2) possesses tyrosine kinase activity and participates in cell growth, differentiation and migration, and survival. Its alterations, mainly including mutations, amplifications, and overexpression are associated with poor prognosis and are one of the major drivers in non-small cell lung cancer (NSCLC). Several clinical trials had been investigating on the treatments of HER2-altered NSCLC, including conventional chemotherapy, programmed death 1 (PD-1) inhibitors, tyrosine kinase inhibitors (TKIs) and antibody-drug conjugates (ADCs), however, the results were either disappointing or encouraging, but inconsistent. Trastuzumab deruxtecan (T-DXd) was recently approved by the Food and Drug Administration as the first targeted agent for treating HER2-mu</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-04T10:58:59.39Z</modification><creation>2025-04-04T10:58:59.39Z</creation></dates><accession>S-EPMC9807451</accession><cross_references><pubmed>36444143</pubmed><doi>10.1111/1759-7714.14743</doi></cross_references></HashMap>