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A L833V/H835L EGFR variant lung adenocarcinoma with skin metastasis: A case report and literature review
The co-occurrence of two or more rare variants, known as compound variants, is rare in non-small cell lung carcinoma with epidermal growth factor receptor (EGFR) variants, and the compound variant L833V/H835L in exon 21 of EGFR is extremely rare. There is very little evidence regarding its treatment...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747578/ https://www.ncbi.nlm.nih.gov/pubmed/36531621 http://dx.doi.org/10.1016/j.heliyon.2022.e12080 |
Sumario: | The co-occurrence of two or more rare variants, known as compound variants, is rare in non-small cell lung carcinoma with epidermal growth factor receptor (EGFR) variants, and the compound variant L833V/H835L in exon 21 of EGFR is extremely rare. There is very little evidence regarding its treatment. Herein, we report a case of an advanced lung adenocarcinoma patient with cutaneous metastases. Next generation sequencing detected a combination variant of EGFR exon 21 L833V/H835L. To our surprise, our patient had almost complete remission of skin symptoms after 1 month of oral gefitinib (250 mg/d qd) treatment with less skin toxicity. At the time of this report submission, the last CT scan confirmed that the patient had achieved partial response. To date, the patient has achieved a remarkable result with a progression-free survival of 18 + months. The presentation of this case and a literature review suggest that tailored therapeutic interventions are available for this subset of patients. |
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