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Featured researches published by Tetsuya Okano.


Lung Cancer | 2018

Prognostic impact of the integration of volumetric quantification of the solid part of the tumor on 3DCT and FDG-PET imaging in clinical stage IA adenocarcinoma of the lung

Hideyuki Furumoto; Yoshihisa Shimada; Kentaro Imai; Sachio Maehara; Junichi Maeda; Masaru Hagiwara; Tetsuya Okano; Ryuhei Masuno; Masatoshi Kakihana; Naohiro Kajiwara; Tatsuo Ohira; Norihiko Ikeda

OBJECTIVES The aim of this study was to conduct comparative analyses of the biological malignant potential of clinical stage IA adenocarcinoma using positron emission tomography/computed tomography (PET/CT), high-resolution CT (HRCT), and three-dimensional CT (3DCT). The predictive performance of these parameters was evaluated in terms of clinical outcomes and pathological invasiveness (positive lymphatic permeation, blood-vessel invasion, pleural invasion, and lymph-node metastasis). MATERIALS AND METHODS We enrolled 170 patients with c-IA adenocarcinoma who underwent PET/CT, HRCT, and 3D reconstruction of lung structures using the Synapse Vincent system (Fujifilm Corporation, Tokyo, Japan) followed by complete resection. Maximum standardized uptake values (SUVmax) of F18-fluorodeoxyglucose and the size and volume of the solid part of the tumor were quantified and analyzed in relation to surgical outcomes. RESULTS Univariate analysis demonstrated that all the three parameters and whole-tumor volume were associated with unfavorable disease-free survival (DFS), while the volume of the solid part was the independent predictor on multivariate analysis (p < .001). The receiver operating characteristic curves for pathological invasiveness, determined using the variables dichotomized at each cut-off level (SUVmax 2.4; solid-part size 1.23 cm; solid-part volume 779 mm3), showed that all were significantly correlated with pathological invasiveness and prognosis, whereas the combination of SUVmax and the solid-part volume was the most powerful predictor of survival and pathological invasiveness compared to any other parameters: the 4-year DFS and proportion of pathological invasiveness in patients with SUVmax > 2.4 and solid-part volume > 779 mm3 versus those with SUVmax ≤ 2.4 or solid-part volume ≤779 mm3 were 81.2% versus 98.3% (p < .001) and 84.3% versus 15.1% (p < .001), respectively. CONCLUSION In c-IA adenocarcinoma, the volume of the solid part of the tumor was the independent predictor for unfavorable DFS, and the integration of the volume of the solid part and SUVmax was highly beneficial for the prediction of survival and pathological invasiveness.


The Japanese Journal of Thoracic and Cardiovascular Surgery | 2018

Granulocyte colony stimulating factor-producing lung cancer with severe anemia of inflammation

Koutaro Murakami; Yujin Kudo; Masatoshi Kakihana; Jun Matsubayashi; Tetsuya Okano; Yoshihisa Shimada; Toshitaka Nagao; Naohiro Kajiwara; Tatsuo Ohira; Norihiko Ikeda

Granulocyte colony stimulating factor (G-CSF)-producing lung cancer occasionally induces severe inflammation with an abnormally high white blood cell count. Herein, we report a 49-year-old man who suffered from resectable G-CSF-producing non-small cell lung cancer with continuous fever and severe anemia. Red blood cell transfusion was necessary for the anemia of inflammation. The patient underwent complete surgical tumor resection. The histopathological diagnosis was a pleomorphic carcinoma at pathological stage IIB. This is apparently the first successful case of surgical resection of G-CSF-producing lung cancer in a patient with severe anemia and uncontrollable fever.


Lung Cancer | 2018

Predictive accuracy of lepidic growth subtypes in early-stage adenocarcinoma of the lung by quantitative CT histogram and FDG-PET

Daisuke Eriguchi; Yoshihisa Shimada; Kentaro Imai; Hideyuki Furumoto; Tetsuya Okano; Ryuhei Masuno; Jun Matsubayashi; Naohiro Kajiwara; Tatsuo Ohira; Norihiko Ikeda

OBJECTIVES The aim of this study was to analyze the accuracy of computed tomography (CT) and F-18 fluorodeoxyglucose-positron emission tomography/CT (FDG-PET/CT) to distinguish lepidic growth adenocarcinoma (LGA), including adenocarcinoma in situ (AIS), minimally invasive adenocarcinoma (MIA), and lepidic-predominant adenocarcinoma, all of which have favorable survival outcomes, from the more aggressive and invasive non-LGA subtypes. MATERIALS AND METHODS We identified 225 patients with c-0/I adenocarcinoma of the lung who underwent PET/CT and 3DCT followed by complete resection. Maximum standardized uptake values (SUVmax) of FDG and several histogram parameters were analyzed. Histological grades were classified according to the predominant subtype (G1: lepidic; G3: micropapillary or solid; and G2: subtypes other than G1/G3). RESULTS The proportion of pathological invasive factors (lymphatic vessel involvement/blood vessel invasion/pleural invasion/lymph node metastasis) of patients with preinvasive adenocarcinoma, G1, G2, and G3 tumors were 0%, 3.6%, 48.0%, and 100%, respectively; p <  0.001). Multivariate analysis with CT-related parameters demonstrated that 75th percentile CT attenuation value (75th%, p <  0.001) and maximum CT attenuation value (maxCT, p =  0.009) were associated with incidence of non-LGA, whereas the value of SUVmax demonstrated a significant correlation (p <  0.001). When all patients were dichotomized according to ground-glass opacities (GGO)/solid-dominancy for CT maximum diameter, a significant correlation with non-LGA was shown in patients with solid-dominant tumor on SUVmax (p <  0.001) and with GGO-dominant tumor on 75th% (p =  0.006) and maxCT (p =  0.007). The combination of one of the two significant histogram parameters and SUVmax revealed higher predictive performance for pathological high malignant features (positive pathological invasive factors, non-LGA, and the highly malignant subtype covering G2 with moderately or poorly-differentiated carcinoma and G3) than the individual use of either factor. CONCLUSION The 75th%, maxCT, and SUVmax were highly useful in distinguishing LGA from non-LGA in c-0/I adenocarcinoma.


Journal of Thoracic Disease | 2018

Prognostic factors for surgically resected non-small cell lung cancer with cavity formation

Shunsuke Shigefuku; Yujin Kudo; Daisuke Yunaiyama; Jun Matsubayashi; Jinho Park; Toshitaka Nagao; Yoshihisa Shimada; Hisashi Saji; Masaru Hagiwara; Tetsuya Okano; Masatoshi Kakihana; Naohiro Kajiwara; Tatsuo Ohira; Norihiko Ikeda

Background Small pulmonary nodules have been detected frequently by computed tomography (CT). Lung cancers with cavity formation are also easily detected. There are a few reports focused on the cavity wall, although cancer cells exist along the cavity wall, not inside. We evaluated the impact of cavity wall thickness on prognosis and assessed the clinicopathological features in non-small cell lung cancer (NSCLC) with cavity formation. Methods Between 2005 and 2011, 1,313 patients underwent complete resection for NSCLC. Of these cases, we reviewed 65 patients (5.0%) diagnosed with NSCLC with cavity formation by chest CT. We classified the patients into three groups based on the maximum cavity wall thickness, namely, ≤4 mm (Group 1, 8 patients), >4 and ≤15 mm (Group 2, 33 patients), and >15 mm (Group 3, 24 patients). Results The number of patients with pathological whole tumor size >3 cm was 2 (25%) in Group 1, 17 (52%) in Group 2, and 23 (96%) in Group 3 (P<0.001). Cases with lymph node metastasis were 0 (0%) in Group 1, 5 (15%) in Group 2, and 10 (42%) in Group 3 (P=0.016). The 5-year overall survival (OS) rates were 100% in Group 1, 84.0% in Group 2, and 52.0% in Group 3, with significant differences between Group 1 and Group 3 (P=0.044) and between Group 2 and Group 3 (P=0.034). In univariate analysis, neither whole tumor size nor lymph node metastasis was a prognostic factor for OS (P=0.51, P=0.27). Only cavity wall thickness was a significant prognostic factor by multivariate analysis (P=0.009). Conclusions Maximum cavity wall thickness was an important prognostic factor in NSCLCs with cavity formation, comparable with other established prognostic factors.


Journal of Thoracic Disease | 2018

Clinical applications of virtual navigation bronchial intervention

Naohiro Kajiwara; Sachio Maehara; Junichi Maeda; Masaru Hagiwara; Tetsuya Okano; Masatoshi Kakihana; Tatsuo Ohira; Norihiko Kawate; Norihiko Ikeda

Background In patients with bronchial tumors, we frequently consider endoscopic treatment as the first treatment of choice. All computed tomography (CT) must satisfy several conditions necessary to analyze images by Synapse Vincent. To select safer and more precise approaches for patients with bronchial tumors, we determined the indications and efficacy of virtual navigation intervention for the treatment of bronchial tumors. Methods We examined the efficacy of virtual navigation bronchial intervention for the treatment of bronchial tumors located at a variety of sites in the tracheobronchial tree using a high-speed 3-dimensional (3D) image analysis system, Synapse Vincent. Constructed images can be utilized to decide on the simulation and interventional strategy as well as for navigation during interventional manipulation in two cases. Results Synapse Vincent was used to determine the optimal planning of virtual navigation bronchial intervention. Moreover, this system can detect tumor location and alsodepict surrounding tissues, quickly, accurately, and safely. The feasibility and safety of Synapse Vincent in performing useful preoperative simulation and navigation of surgical procedures can lead to safer, more precise, and less invasion for the patient, and makes it easy to construct an image, depending on the purpose, in 5-10 minutes using Synapse Vincent. Moreover, if the lesion is in the parenchyma or sub-bronchial lumen, it helps to perform simulation with virtual skeletal subtraction to estimate potential lesion movement. By using virtual navigation system for simulation, bronchial intervention was performed with no complications safely and precisely. Conclusions Preoperative simulation using virtual navigation bronchial intervention reduces the surgeons stress levels, particularly when highly skilled techniques are needed to operate on lesions. This task, including both preoperative simulation and intraoperative navigation, leads to greater safety and precision. These technological instruments are helpful for bronchial intervention procedures, and are also excellent devices for educational training.


Annals of Cancer Research and Therapy | 2015

Carcinomatous meningitis and EGFR mutation

Rinako Ishikawa; Susumu Yamazaki; Tomohiko Mio; Akiko Kawashima; Ai Masumoto; Ayako Shiono; Hisayoshi Daito; Ou Yamaguchi; Yuri Maeno; Tetsuya Okano; Hirozo Sakaguchi; Yoshitake Murayama; Hironori Ishida; Singo Kato; Koichi Hagiwara; Kunihiko Kobayashi


Journal of Thoracic Oncology | 2018

P2.11-12 Metabolomic Analysis in Lung Cancer for Screening and Early Detection

Naohiro Kajiwara; Sachio Maehara; H. Shimada; Junichi Maeda; Masaru Hagiwara; Tetsuya Okano; Masatoshi Kakihana; Tatsuo Ohira; M. Sugimoto; Norihiko Ikeda


Journal of Thoracic Oncology | 2018

P3.01-78 The Cytology Samples and Plasma Specimens were Feasible for the EGFR Molecular Testing.

Tatsuo Ohira; W. Hamanaka; Yoshihisa Shimada; Sachio Maehara; Junichi Maeda; Masaru Hagiwara; Masatoshi Kakihana; Tetsuya Okano; Naohiro Kajiwara; Norihiko Ikeda


Journal of Thoracic Oncology | 2018

P3.01-24 The Importance to Switch from EGFR-TKI to Cytotoxic Chemotherapy for EGFR Mutation-Positive Adenocarcinoma

Daisuke Eriguchi; Tetsuya Okano; Yohei Kawaguchi; Junichi Maeda; Masaru Hagiwara; Masatoshi Kakihana; Naohiro Kajiwara; Tatsuo Ohira; Norihiko Ikeda


Journal of Thoracic Oncology | 2018

P1.16-17 The Role of Quantitative Metabolic Metrics on FDG-PET/CT in Predicting Pathological Invasive Factors in cN0 Lung Adenocarcinoma

T. Tanaka; Yoshihisa Shimada; Yojiro Makino; Junichi Maeda; Masaru Hagiwara; Tetsuya Okano; Masatoshi Kakihana; Naohiro Kajiwara; Tatsuo Ohira; Jun Matsubayashi; Norihiko Ikeda

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Norihiko Ikeda

Tokyo Medical University

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Tatsuo Ohira

Tokyo Medical University

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Junichi Maeda

Tokyo Medical University

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Sachio Maehara

Tokyo Medical University

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