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  3. Prolonged Response to Afatinib and Crizotinib in a Rare Case of EGFR-, HER2-, MET- and ROS1-Alterated Lung Adenocarcinoma.
 

Prolonged Response to Afatinib and Crizotinib in a Rare Case of EGFR-, HER2-, MET- and ROS1-Alterated Lung Adenocarcinoma.

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BORIS DOI
10.48350/197955
Publisher DOI
10.3390/ijms25115698
PubMed ID
38891886
Description
We present the case of a 70-year-old never-smoking female patient with epidermal growth factor receptor (EGFR) p.L858R-mutated metastatic non-small cell lung cancer (NSCLC). After three months of first-line treatment with erlotinib, progression occurred and platinum/pemetrexed was initiated, followed by a response for more than two years. After the progression, the molecular testing of a vertebral metastasis revealed a ROS proto-oncogene 1 (ROS1) translocation and a human epidermal growth factor receptor 2 (HER2) p.S310F mutation, in addition to the known EGFR p.L858R mutation. Crizotinib then led to a durable response of 17 months. The molecular retesting of the tumour cells obtained from the recurrent pleural effusion revealed the absence of the ROS1 translocation, whereas the EGFR and HER2 mutations were still present. Afatinib was added to the crizotinib, and the combination treatment resulted in another durable response of more than two years. The patient died more than 7 years after the initial diagnosis of metastatic NSCLC. This case demonstrates that the repeated molecular testing of metastatic NSCLC may identify new druggable genomic alterations that can impact the patient management and improve the patient outcome.
Date of Publication
2024-05-23
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Keyword(s)
EGFR-mutated NSCLC NSCLC drug combinations molecular pathology targeted therapies
Language(s)
en
Contributor(s)
Plomer, Eva
Früh, Martin
Universitätsklinik für Medizinische Onkologie
Lauber, Arno
Demmer, Izadora
Jochum, Wolfram
Koster, Kira-Lee
Additional Credits
Universitätsklinik für Medizinische Onkologie
Series
International journal of molecular sciences
Publisher
MDPI
ISSN
1422-0067
Access(Rights)
open.access
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