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1.
Thorac Cancer ; 12(8): 1248-1251, 2021 04.
Artículo en Inglés | MEDLINE | ID: mdl-33651475

RESUMEN

In non-small cell lung cancer (NSCLC), uncommon epidermal growth factor receptor (EGFR) mutations are mutations other than Ex19 deletion and Ex21 L858R, which are common mutations highly sensitive to EGFR-tyrosine kinase inhibitors. Afatinib, a second-generation EGFR-tyrosine kinase inhibitor, has been shown to be effective in patients with uncommon mutations. Dacomitinib, another second-generation EGFR-tyrosine kinase inhibitor, has not previously been shown to be effective in patients with uncommon mutations. Here, we report the efficacy of dacomitinib for uncommon EGFR mutations in a 71-year-old woman diagnosed with metastatic lung adenocarcinoma with uncommon EGFR mutation (Ex18 G719A). Afatinib was administered as the first-line treatment, and a remarkable antitumor effect was observed. However, the tumor grew after 14 months. Pemetrexed plus carboplatin followed by pemetrexed, docetaxel, atezolizumab and S-1 were performed in sequence. Although approximately four years had passed since the start of treatment, her physical condition was good. The patient started dacomitinib as the sixth-line treatment. Lesions were markedly reduced and treatment with dacomitinib was continued for 7.8 months. Dacomitinib is a possible treatment option for NSCLC with uncommon mutations.


Asunto(s)
Carcinoma de Pulmón de Células no Pequeñas/tratamiento farmacológico , Neoplasias Pulmonares/tratamiento farmacológico , Quinazolinonas/uso terapéutico , Anciano , Carcinoma de Pulmón de Células no Pequeñas/patología , Receptores ErbB/metabolismo , Femenino , Humanos , Neoplasias Pulmonares/patología , Mutación , Quinazolinonas/farmacología
2.
Kekkaku ; 90(5): 503-6, 2015 May.
Artículo en Japonés | MEDLINE | ID: mdl-26489154

RESUMEN

We report a case of a 75-year-old man with pleural effusion and an occupational history of asbestos exposure. Fluorodeoxyglucose positron emission tomography-computed tomography (FDG-PET/CT) examination revealed FDG up-takes along his pleura, leading to an initial suspicion of pleural mesothelioma. Pathological findings of a diagnostic video-associated pleural biopsy showed epithelioid cell granuloma. Repeated sputum cultures were positive for Mycobacterium intracellulare. The patient was diagnosed with pleuritis caused by non-tuberculous mycobacteria (NTM). NTM should be considered a potential cause of pleuritis.


Asunto(s)
Amianto , Infección por Mycobacterium avium-intracellulare/diagnóstico , Exposición Profesional , Pleuresia/diagnóstico , Anciano , Humanos , Masculino
3.
Jpn J Clin Oncol ; 44(5): 493-6, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-24620028

RESUMEN

A 59-year-old man was admitted to our hospital with dyspnea and cough. A large polypoid tumor was observed in the lower trachea and bronchoscopic polypectomy was performed using a snare to relieve symptoms. The tumor was diagnosed as a high grade mucoepidermoid carcinoma mainly by the histology of piecemeal specimens obtained by bronchoscopic resection. The primary lesion involved the trachea and the main bronchus, and there were multiple metastases in the lung. The patient was treated with the combination of carboplatin and paclitaxel. After four cycles of chemotherapy, the tumors were significantly reduced. He remains well without evidence of tumor progression for 25 months. This case suggests that the combination chemotherapy of carboplatin and paclitaxel can be an option for treatment of pulmonary mucoepidermoid carcinoma.


Asunto(s)
Antineoplásicos/uso terapéutico , Neoplasias de los Bronquios/tratamiento farmacológico , Carcinoma Mucoepidermoide/tratamiento farmacológico , Neoplasias Pulmonares/tratamiento farmacológico , Neoplasias de la Tráquea/tratamiento farmacológico , Neoplasias de los Bronquios/patología , Carboplatino/administración & dosificación , Carcinoma Mucoepidermoide/secundario , Supervivencia sin Enfermedad , Humanos , Neoplasias Pulmonares/secundario , Masculino , Persona de Mediana Edad , Paclitaxel/administración & dosificación , Neoplasias de la Tráquea/patología , Resultado del Tratamiento
4.
Emerg Infect Dis ; 19(2): 289-92, 2013 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-23460988

RESUMEN

We retrospectively confirmed 2 cases of human Anaplasma phagocytophilum infection. Patient blood samples contained unique p44/msp2 for the pathogen, and antibodies bound to A. phagocytophilum antigens propagated in THP-1 rather than HL60 cells. Unless both cell lines are used for serodiagnosis of rickettsiosis-like infections, cases of human granulocytic anaplasmosis could go undetected.


Asunto(s)
Anaplasma phagocytophilum/genética , Anaplasmosis/diagnóstico , Ehrlichiosis/diagnóstico , Anciano , Anaplasmosis/sangre , Anaplasmosis/tratamiento farmacológico , Anaplasmosis/inmunología , Anticuerpos Antibacterianos/sangre , Proteínas de la Membrana Bacteriana Externa/inmunología , ADN Bacteriano/sangre , ADN Bacteriano/genética , ADN Bacteriano/aislamiento & purificación , Ehrlichiosis/sangre , Ehrlichiosis/tratamiento farmacológico , Ehrlichiosis/inmunología , Genes Bacterianos , Células HL-60 , Humanos , Japón , Masculino , Persona de Mediana Edad , Técnicas de Diagnóstico Molecular , Tipificación Molecular , Filogenia , ARN Ribosómico 16S/genética , Estudios Retrospectivos , Pruebas Serológicas
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