{"title":"非小细胞肺癌中同时存在表皮生长因子受体突变/酪氨酸癌基因 1 重排:病例报告。","authors":"Gui-Qin Peng, Hai-Chi Song, Wan-Yi Chen","doi":"10.5306/wjco.v15.i7.945","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Epidermal growth factor receptor (<i>EGFR</i>) mutation and c-ros oncogene 1 (<i>ROS1</i>) rearrangement are key genetic alterations and predictive tumor markers for non-small cell lung cancer (NSCLC) and are typically considered to be mutually exclusive. <i>EGFR/ROS1</i> co-mutation is a rare event, and the standard treatment approach for such cases is still equivocal.</p><p><strong>Case summary: </strong>Herein, we report the case of a 64-year-old woman diagnosed with lung adenocarcinoma, with concomitant <i>EGFR</i> L858R mutation and <i>ROS1</i> rearrangement. The patient received two cycles of chemotherapy after surgery, but the disease progressed. Following 1-month treatment with gefitinib, the disease progressed again. However, after switching to crizotinib, the lesion became stable. Currently, crizotinib has been administered for over 53 months with a remarkable treatment effect.</p><p><strong>Conclusion: </strong>The efficacy of <i>EGFR</i> tyrosine kinase inhibitors and crizotinib was vastly different in this NSCLC patient with <i>EGFR</i>/<i>ROS1</i> co-mutation. This report will aid future treatment of such patients.</p>","PeriodicalId":23802,"journal":{"name":"World journal of clinical oncology","volume":"15 7","pages":"945-952"},"PeriodicalIF":2.6000,"publicationDate":"2024-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11271735/pdf/","citationCount":"0","resultStr":"{\"title\":\"Concomitant epidermal growth factor receptor mutation/c-ros oncogene 1 rearrangement in non-small cell lung cancer: A case report.\",\"authors\":\"Gui-Qin Peng, Hai-Chi Song, Wan-Yi Chen\",\"doi\":\"10.5306/wjco.v15.i7.945\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Epidermal growth factor receptor (<i>EGFR</i>) mutation and c-ros oncogene 1 (<i>ROS1</i>) rearrangement are key genetic alterations and predictive tumor markers for non-small cell lung cancer (NSCLC) and are typically considered to be mutually exclusive. <i>EGFR/ROS1</i> co-mutation is a rare event, and the standard treatment approach for such cases is still equivocal.</p><p><strong>Case summary: </strong>Herein, we report the case of a 64-year-old woman diagnosed with lung adenocarcinoma, with concomitant <i>EGFR</i> L858R mutation and <i>ROS1</i> rearrangement. The patient received two cycles of chemotherapy after surgery, but the disease progressed. Following 1-month treatment with gefitinib, the disease progressed again. However, after switching to crizotinib, the lesion became stable. Currently, crizotinib has been administered for over 53 months with a remarkable treatment effect.</p><p><strong>Conclusion: </strong>The efficacy of <i>EGFR</i> tyrosine kinase inhibitors and crizotinib was vastly different in this NSCLC patient with <i>EGFR</i>/<i>ROS1</i> co-mutation. This report will aid future treatment of such patients.</p>\",\"PeriodicalId\":23802,\"journal\":{\"name\":\"World journal of clinical oncology\",\"volume\":\"15 7\",\"pages\":\"945-952\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-07-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11271735/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"World journal of clinical oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5306/wjco.v15.i7.945\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"World journal of clinical oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5306/wjco.v15.i7.945","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
Concomitant epidermal growth factor receptor mutation/c-ros oncogene 1 rearrangement in non-small cell lung cancer: A case report.
Background: Epidermal growth factor receptor (EGFR) mutation and c-ros oncogene 1 (ROS1) rearrangement are key genetic alterations and predictive tumor markers for non-small cell lung cancer (NSCLC) and are typically considered to be mutually exclusive. EGFR/ROS1 co-mutation is a rare event, and the standard treatment approach for such cases is still equivocal.
Case summary: Herein, we report the case of a 64-year-old woman diagnosed with lung adenocarcinoma, with concomitant EGFR L858R mutation and ROS1 rearrangement. The patient received two cycles of chemotherapy after surgery, but the disease progressed. Following 1-month treatment with gefitinib, the disease progressed again. However, after switching to crizotinib, the lesion became stable. Currently, crizotinib has been administered for over 53 months with a remarkable treatment effect.
Conclusion: The efficacy of EGFR tyrosine kinase inhibitors and crizotinib was vastly different in this NSCLC patient with EGFR/ROS1 co-mutation. This report will aid future treatment of such patients.
期刊介绍:
The WJCO is a high-quality, peer reviewed, open-access journal. The primary task of WJCO is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of oncology. In order to promote productive academic communication, the peer review process for the WJCO is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJCO are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in oncology. Scope: Art of Oncology, Biology of Neoplasia, Breast Cancer, Cancer Prevention and Control, Cancer-Related Complications, Diagnosis in Oncology, Gastrointestinal Cancer, Genetic Testing For Cancer, Gynecologic Cancer, Head and Neck Cancer, Hematologic Malignancy, Lung Cancer, Melanoma, Molecular Oncology, Neurooncology, Palliative and Supportive Care, Pediatric Oncology, Surgical Oncology, Translational Oncology, and Urologic Oncology.