Ning Yi Yap, Komathi Perumal, Pathmanathan Rajadurai
{"title":"人类表皮生长因子受体 2 改变的非小细胞肺癌的发病率和治疗:回顾性分析和系统性文献综述。","authors":"Ning Yi Yap, Komathi Perumal, Pathmanathan Rajadurai","doi":"10.3332/ecancer.2024.1734","DOIUrl":null,"url":null,"abstract":"<p><p>Human epidermal growth factor receptor 2 (HER2) is known for its oncogenic activities in diverse cancers, including non-small cell lung cancer (NSCLC). However, the prevalence of <i>HER2</i> alterations in Malaysian NSCLC patients remains unreported. This study examined the prevalence and characteristics of <i>HER2</i> mutations and amplification in a Malaysian cohort. Additionally, a systematic review was conducted to evaluate the global prevalence of <i>HER2</i> alterations in NSCLC, as well as the efficacy of HER2-targeted therapies observed in clinical trials. NSCLC tumour samples received from October 2019 to December 2022 for next-generation sequencing diagnostics were included in the retrospective analysis. In this patient cohort, <i>HER2</i> alteration was present in 5.8% of patients; 3.9% had <i>HER2</i> mutations, 1.5% had <i>HER2</i> amplifications and 0.4% were both <i>HER2</i>-mutated and amplified. <i>HER2</i> exon 20 insertions were the most common <i>HER2</i> variants, detected in 47/59 (79.7%) of <i>HER2</i>-mutated patients. Among cases with <i>HER2</i> exon 20 insertions, the Y772_A775dup variant was found in 34 patient samples. <i>HER2</i>-mutated patients were significantly younger than non-<i>HER2</i>-mutants (61 versus 64 years old; <i>p</i> = 0.046) and were inclined to be female and never-smokers, albeit not statistically significant. Patients with <i>HER2</i> amplification were more likely to have progressed post-tyrosine kinase inhibitor therapy (<i>p</i> = 0.015). The systematic review highlighted a global variation in the prevalence of <i>HER2</i> alterations in NSCLC, ranging from 0.3% to 9.1% for mutations and 0.2% to 19% for amplification. Finally, phase II clinical trials involving <i>HER2-</i>altered NSCLC patients demonstrated promising treatment outcomes with trastuzumab deruxtecan, trastuzumab emtansine, pyrotinib, pyrotinib + apatinib and trastuzumab + pertuzumab + docetaxel. In conclusion, the prevalence of <i>HER2</i> alteration among Malaysian NSCLC patients falls within the global range. A systematic review of clinical trials revealed promising treatment outcomes and Malaysian NSCLC patients with <i>HER2</i> alterations are anticipated to similarly benefit from <i>HER2</i>-targeted therapies.</p>","PeriodicalId":11460,"journal":{"name":"ecancermedicalscience","volume":"18 ","pages":"1734"},"PeriodicalIF":1.2000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11484687/pdf/","citationCount":"0","resultStr":"{\"title\":\"Prevalence and treatment of human epidermal growth factor receptor 2-altered non-small cell lung cancer: a retrospective analysis and systematic literature review.\",\"authors\":\"Ning Yi Yap, Komathi Perumal, Pathmanathan Rajadurai\",\"doi\":\"10.3332/ecancer.2024.1734\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Human epidermal growth factor receptor 2 (HER2) is known for its oncogenic activities in diverse cancers, including non-small cell lung cancer (NSCLC). However, the prevalence of <i>HER2</i> alterations in Malaysian NSCLC patients remains unreported. This study examined the prevalence and characteristics of <i>HER2</i> mutations and amplification in a Malaysian cohort. Additionally, a systematic review was conducted to evaluate the global prevalence of <i>HER2</i> alterations in NSCLC, as well as the efficacy of HER2-targeted therapies observed in clinical trials. NSCLC tumour samples received from October 2019 to December 2022 for next-generation sequencing diagnostics were included in the retrospective analysis. In this patient cohort, <i>HER2</i> alteration was present in 5.8% of patients; 3.9% had <i>HER2</i> mutations, 1.5% had <i>HER2</i> amplifications and 0.4% were both <i>HER2</i>-mutated and amplified. <i>HER2</i> exon 20 insertions were the most common <i>HER2</i> variants, detected in 47/59 (79.7%) of <i>HER2</i>-mutated patients. Among cases with <i>HER2</i> exon 20 insertions, the Y772_A775dup variant was found in 34 patient samples. <i>HER2</i>-mutated patients were significantly younger than non-<i>HER2</i>-mutants (61 versus 64 years old; <i>p</i> = 0.046) and were inclined to be female and never-smokers, albeit not statistically significant. Patients with <i>HER2</i> amplification were more likely to have progressed post-tyrosine kinase inhibitor therapy (<i>p</i> = 0.015). The systematic review highlighted a global variation in the prevalence of <i>HER2</i> alterations in NSCLC, ranging from 0.3% to 9.1% for mutations and 0.2% to 19% for amplification. Finally, phase II clinical trials involving <i>HER2-</i>altered NSCLC patients demonstrated promising treatment outcomes with trastuzumab deruxtecan, trastuzumab emtansine, pyrotinib, pyrotinib + apatinib and trastuzumab + pertuzumab + docetaxel. In conclusion, the prevalence of <i>HER2</i> alteration among Malaysian NSCLC patients falls within the global range. A systematic review of clinical trials revealed promising treatment outcomes and Malaysian NSCLC patients with <i>HER2</i> alterations are anticipated to similarly benefit from <i>HER2</i>-targeted therapies.</p>\",\"PeriodicalId\":11460,\"journal\":{\"name\":\"ecancermedicalscience\",\"volume\":\"18 \",\"pages\":\"1734\"},\"PeriodicalIF\":1.2000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11484687/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ecancermedicalscience\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3332/ecancer.2024.1734\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ecancermedicalscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3332/ecancer.2024.1734","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
Prevalence and treatment of human epidermal growth factor receptor 2-altered non-small cell lung cancer: a retrospective analysis and systematic literature review.
Human epidermal growth factor receptor 2 (HER2) is known for its oncogenic activities in diverse cancers, including non-small cell lung cancer (NSCLC). However, the prevalence of HER2 alterations in Malaysian NSCLC patients remains unreported. This study examined the prevalence and characteristics of HER2 mutations and amplification in a Malaysian cohort. Additionally, a systematic review was conducted to evaluate the global prevalence of HER2 alterations in NSCLC, as well as the efficacy of HER2-targeted therapies observed in clinical trials. NSCLC tumour samples received from October 2019 to December 2022 for next-generation sequencing diagnostics were included in the retrospective analysis. In this patient cohort, HER2 alteration was present in 5.8% of patients; 3.9% had HER2 mutations, 1.5% had HER2 amplifications and 0.4% were both HER2-mutated and amplified. HER2 exon 20 insertions were the most common HER2 variants, detected in 47/59 (79.7%) of HER2-mutated patients. Among cases with HER2 exon 20 insertions, the Y772_A775dup variant was found in 34 patient samples. HER2-mutated patients were significantly younger than non-HER2-mutants (61 versus 64 years old; p = 0.046) and were inclined to be female and never-smokers, albeit not statistically significant. Patients with HER2 amplification were more likely to have progressed post-tyrosine kinase inhibitor therapy (p = 0.015). The systematic review highlighted a global variation in the prevalence of HER2 alterations in NSCLC, ranging from 0.3% to 9.1% for mutations and 0.2% to 19% for amplification. Finally, phase II clinical trials involving HER2-altered NSCLC patients demonstrated promising treatment outcomes with trastuzumab deruxtecan, trastuzumab emtansine, pyrotinib, pyrotinib + apatinib and trastuzumab + pertuzumab + docetaxel. In conclusion, the prevalence of HER2 alteration among Malaysian NSCLC patients falls within the global range. A systematic review of clinical trials revealed promising treatment outcomes and Malaysian NSCLC patients with HER2 alterations are anticipated to similarly benefit from HER2-targeted therapies.