Laurenz Schmitt, Tamara Schumann, Christoph Löser, Edgar Dippel
{"title":"Vemurafenib-induced pulmonary injury.","authors":"Laurenz Schmitt, Tamara Schumann, Christoph Löser, Edgar Dippel","doi":"10.1159/000355643","DOIUrl":null,"url":null,"abstract":"a nearly complete remission of the infiltrations 6 days after discontinuation of vemurafenib therapy (fig. 1B). Vemurafenib was administered again at the standard dose (960 mg twice daily) for 2 weeks after withdrawal. 3 weeks after re-initiation of vemurafenib the lung infiltrations worsened again. Because of 2 surgical interventions (uterine metastatic bleeding and non-responding axillar lymph node metastasis) administration of vemurafenib had to be stopped, twice for 3 days in each case. During these, albeit short, treatment pauses the lung infiltrates regressed once again, confirming a causative correlation to vemurafenib treatment. Because of the good response of the target lesions, we decided to continue vemurafenib treatment but at a reduced dose of 720 mg twice daily. Under this regimen, pulmonary infiltrates were no longer observed (fig. 2).","PeriodicalId":19684,"journal":{"name":"Onkologie","volume":"36 11","pages":"685-6"},"PeriodicalIF":0.3000,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000355643","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Onkologie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000355643","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/10/14 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 5
Abstract
a nearly complete remission of the infiltrations 6 days after discontinuation of vemurafenib therapy (fig. 1B). Vemurafenib was administered again at the standard dose (960 mg twice daily) for 2 weeks after withdrawal. 3 weeks after re-initiation of vemurafenib the lung infiltrations worsened again. Because of 2 surgical interventions (uterine metastatic bleeding and non-responding axillar lymph node metastasis) administration of vemurafenib had to be stopped, twice for 3 days in each case. During these, albeit short, treatment pauses the lung infiltrates regressed once again, confirming a causative correlation to vemurafenib treatment. Because of the good response of the target lesions, we decided to continue vemurafenib treatment but at a reduced dose of 720 mg twice daily. Under this regimen, pulmonary infiltrates were no longer observed (fig. 2).