Fumihiro Yamaguchi
Showa University
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Featured researches published by Fumihiro Yamaguchi.
Journal of Infection and Chemotherapy | 2014
Makoto Hayashi; Takuya Iwasaki; Yohei Yamazaki; Hiromi Takayasu; Hidetsugu Tateno; Sakiko Tazawa; Eisuke Kato; Aya Wakabayashi; Fumihiro Yamaguchi; Yutaka Tsuchiya; Jun Yamashita; Norikazu Takeda; Satoshi Matsukura; Fumio Kokubu
Pneumonia is a leading cause of death among elderly patients. Although aspiration pneumonia (AP) commonly occurs with aging, its clinical features and outcomes are still uncertain. The aims of this study were to describe the clinical features and outcomes of AP and to assess whether presence of AP affects clinical outcomes in patients with community-acquired pneumonia (CAP) and healthcare-associated pneumonia (HCAP). We retrospectively analyzed patients with CAP and HCAP hospitalized in our institution in Japan from October 2010 to March 2012. We compared clinical features and outcomes between AP and non-AP, and investigated risk factors for recurrence of pneumonia and death. Of 214 consecutive patients, 100 (46.7%) were diagnosed as having aspiration pneumonia. These patients were older and had lower body mass index, more comorbidities, and poorer Eastern Cooperative Oncology Group performance status (ECOG PS) than the patients with non-AP. Patients with AP had more severe disease, required longer hospital stays, and had a frequent recurrence rate of pneumonia and higher mortality. In multivariate analyses, AP, age, and ECOG PS were related to recurrence of pneumonia, and the prognostic factors were CURB-65 score and ECOG PS. AP was not a significant indicator for prognosis but was the strongest risk factor for recurrence of pneumonia. Clinical background and outcomes including recurrence and mortality of AP were obviously different from those of non-AP; therefore AP should be considered as a distinct subtype of pneumonia, and it is important to prevent the recurrence of pneumonia in the patients with AP.
Lung Cancer | 2012
Fumihiro Yamaguchi; Satoshi Kugawa; Hidetsugu Tateno; Fumio Kokubu; Kunihiko Fukuchi
Histopathological samples are commonly used for molecular testing to detect both oncogenes and tumor-suppressor genes in lung cancer. The purpose of this study was to determine the efficacy of using curette lavage fluid for molecular testing to detect EGFR, KRAS and P53 mutations in lung cancer patients. Samples were obtained from 77 lung cancer patients by bronchoscopy at the time of diagnosis, collected by scraping the site of the primary tumor lesion with a curette. DNA was extracted from cells in the curette lavage fluid, and PCRs were performed to amplify mutation hot spot regions in the EGFR, KRAS and P53 genes. The PCR products were direct-sequenced to detect mutations of each gene. The reference sequence of each gene was obtained from GenBank. Overall, 27% (21 of 77) were found with EGFR mutations, 1% (1 of 77) with KRAS mutations, and 36% (28 of 77) with P53 mutations. KRAS mutations were not detected in patients harboring mutations in either EGFR or P53. P53 mutations were identified in 38% (8 of 21) of the patients with EGFR mutations, all of who had advanced lung cancer. Of these patients, a 62-year-old female current smoker was given EGFR-TKI as third-line therapy, with no improvement in clinical symptoms or results of radiographic examination. Multivariate analysis indicated that P53 mutation rates in advanced-stage lung cancer were significantly higher than those in early-stage lung cancer (P=.017). In contrast, EGFR mutation rates were not significantly associated with staging. L747S in EGFR, described as a mutation associated with secondary resistance to EGFR-TKI, was detected in three patients who had never received EGFR-TKI, including one SCLC patient. It is possible to analyze EGFR, KRAS and P53 mutations using curette lavage fluid collected from lung cancer patients. This is useful when sufficient amounts of tumor samples cannot be obtained. Data from the current study suggest that EGFR mutations in concert with P53 mutations accelerate cancer development and lead to evolution of therapeutic resistance.
Oncology Letters | 2014
Fumihiro Yamaguchi; Kunihiko Fukuchi; Yohei Yamazaki; Hiromi Takayasu; Sakiko Tazawa; Hidetsugu Tateno; Eisuke Kato; Aya Wakabayashi; Mami Fujimori; Takuya Iwasaki; Makoto Hayashi; Yutaka Tsuchiya; Jun Yamashita; Norikazu Takeda; Fumio Kokubu
The purpose of the present study was to report cases of epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI)-naïve patients carrying a mutation associated with acquired resistance to the drug. Gene alterations in 77 lung carcinoma patients were analyzed by collecting and studying curette lavage fluid at the time of diagnosis. PCRs were performed to amplify mutation hotspot regions in EGFR genes. The PCR products were direct-sequenced and the mutations confirmed by resequencing using different primers. Case 1 was a 78-year-old Japanese male diagnosed with stage IB lung adenocarcinoma who was found to have two EGFR mutations, G719S and L747S. Case 2 was a 73-year-old Japanese male diagnosed with stage IV squamous cell lung carcinoma and bone metastasis who had the EGFR mutation, L747S. Case 3 was an 82-year-old Japanese male diagnosed with hyponatremia due to inappropriate secretion of antidiuretic hormone and stage IIIB small cell lung carcinoma (SCLC) who had the EGFR mutation, L747S. Thus, the EGFR mutation L747S associated with acquired EGFR-TKI resistance was detected in two non-small cell lung carcinoma (NSCLC) patients and one SCLC patient, none of whom had ever received EGFR-TKI. The patients were current smokers with stages at diagnosis ranging from IB to IV, and their initial tumors contained resistant clones carrying L747S. L747S may be associated with primary resistance. To the best of our knowledge, this study is the first report of an EGFR mutation associated with resistance to EGFR-TKI in SCLC patients. The early detection of EGFR-TKI resistance mutations may be beneficial in making treatment decisions for lung carcinoma patients, including those with SCLC.
Case reports in pulmonology | 2017
Yusuke Kakiuchi; Fumihiro Yamaguchi; Makoto Hayashi; Yusuke Shikama
The purpose of this article is to report a case of hemoptysis occurring in combination with secondary spontaneous pneumothorax following chemical pleurodesis by talc. A Japanese male with cancer of renal pelvis was found with the left pneumothorax and multiple lung metastases. A computed-tomography scan revealed severe emphysema throughout the lungs. Talc pleurodesis was employed to arrest air leakage. The patient developed hemoptysis 45 minutes after talc injection into the thorax. This is the first report of hemoptysis following talc pleurodesis. The agent could induce severe inflammation in capillary vessels of the lung following visceral pleura infiltration.
The Japanese Journal of Thoracic and Cardiovascular Surgery | 2011
Ryosuke Usuda; Fumihiro Yamaguchi; Shugo Uematsu; Atsuko Masunaga; Makoto Nonaka; Takashi Suzuki
A 69-year-old man was hospitalized for fever and cough. He was diagnosed with and treated for an abscess in the left lower jaw and pneumonia by an otolaryngologist, but the pneumonia persisted with no improvement. Chest computed tomography revealed the presence of a heterogeneous torose lesion in the inlet of the left upper bronchus, and bronchoscopy revealed an endobronchial tumor with a smooth surface. An episode of sudden dyspnea occurred and was resolved after the patient changed his sitting position. We concluded that this symptom occurred because the tumor was incarcerated in the left lower lobe bronchus. The tumor was excised by bronchofi berscopic snare resection under tracheal intubation. It was found to be a pleomorphic carcinoma, and left upper lobectomy was performed. There has been no recurrence during the 3 years since the operation.
Allergology International | 2016
Satoshi Matsukura; Yuki Osakabe; Ayaka Sekiguchi; Daisuke Inoue; Yusuke Kakiuchi; Toshitaka Funaki; Yohei Yamazaki; Hiromi Takayasu; Hidetsugu Tateno; Eisuke Kato; Aya Wakabayashi; Makoto Hayashi; Gen Ishii; Fumihiro Yamaguchi; Yutaka Tsuchiya; Keita Kasahara; Hironori Sagara; Fumio Kokubu
The Japanese journal of clinical pathology | 2010
Takahashi N; Fumihiro Yamaguchi; Chen G; Yasuhara T; Ito R; Wakuta R; Kunihiko Fukuchi
The Japanese journal of clinical pathology | 2012
Kazuhide Gomi; Nanako Takahashi; Fumihiro Yamaguchi; Yuko Tateishi; Katsuhiko Yoshida; Kunihiko Fukuchi
The Showa University Journal of Medical Sciences | 2016
Yutaka Tsuchiya; Aya Wakabayashi; Satoshi Matsukura; Yuki Osakabe; Ayaka Sekiguchi; Daisuke Inoue; Yusuke Kakiuchi; Toshitaka Funaki; Yohei Yamazaki; Hiromi Takayasu; Hidetsugu Tateno; Eisuke Kato; Makoto Hayashi; Gen Ishii; Fumihiro Yamaguchi; Fumio Kokubu
European Respiratory Journal | 2011
Fumihiro Yamaguchi; Kunihiko Fukuchi; Sakiko Tazawa; Hidethugu Tateno; Eisuke Kato; Aya Wakabayashi; Asami Tada; Takuya Iwasaki; Makoto Hayashi; Yutaka Thuchiya; Jun Yamashita; Norikazu Takeda; Shogo Tomita; Fumio Kokubu