Shiro Iraha
University of the Ryukyus
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International Journal of Radiation Oncology Biology Physics | 1999
Takafumi Toita; Yasumasa Kakinohana; Sanae Shinzato; Kazuhiko Ogawa; Masatomi Yoshinaga; Shiro Iraha; Masahiro Higashi; Kaoru Sakumoto; Koji Kanazawa; Satoshi Sawada
PURPOSE To evaluate the prognostic value of tumor diameter/volume and pelvic node status assessed by magnetic resonance imaging (MRI) in patients with uterine cervical cancer treated with radiation therapy. METHODS AND MATERIALS Forty-four patients with intact uterine cervical squamous carcinoma treated with a combination of external irradiation and high-dose-rate intracavitary therapy were analyzed. Actuarial disease-free survival (DFS), pelvic control rate (PC), and distant metastasis-free rate (DMF) were analyzed by tumor diameter, volume, and pelvic node status assessed by pretreatment MRI. RESULTS Anteroposterior (AP) and lateral (RL) tumor diameter significantly affected DFS. The 2-year DFS was 74% for patients with < 40 mm in AP diameter tumor, and 24% for > or = 40 mm tumor (p = 0.02). Whereas PC was not influenced, DMF was significantly affected by AP tumor diameter. Tumor volume did not significantly affect any endpoints. Patients with enlarged pelvic nodes had significantly poorer outcome compared to those with none on PC, DMF, and DFS. The 2-year DFS was 78% for node-negative, and 10% for node-positive patients (p = 0.0001). CONCLUSION AP tumor diameter and pelvic lymph node status assessed by MRI were the significant prognostic factors in uterine cervical cancer treated with irradiation. Prognostic value of tumor volume should be reassessed prospectively with an appropriate imaging technique. AP tumor diameter predominantly affected the incidence of distant metastasis, and lymph node status affected both pelvic control and distant metastasis.
International Journal of Radiation Oncology Biology Physics | 2008
Kazuhiko Ogawa; Yoshihiko Yoshii; Naoto Shikama; Katsumasa Nakamura; Takashi Uno; Hiroshi Onishi; Jun Itami; Yoshiyuki Shioyama; Shiro Iraha; Akio Hyodo; Takafumi Toita; Yasumasa Kakinohana; Wakana Tamaki; Hisao Ito; Sadayuki Murayama
PURPOSE To analyze retrospectively the risk factors of spinal recurrence in patients with intracranial germinoma and clinical outcomes of patients who developed spinal recurrence. METHODS AND MATERIALS Between 1980 and 2007, 165 patients with no evidence of spinal metastases at diagnosis were treated with cranial radiotherapy without spinal irradiation. The median follow-up in all 165 patients was 61.2 months (range, 1.2-260.1 months). RESULTS After the initial treatment, 15 patients (9.1%) developed spinal recurrences. Multivariate analysis revealed that large intracranial disease (>/=4 cm) and multifocal intracranial disease were independent risk factors for spinal recurrence. Radiation field, total radiation dose, and the use of chemotherapy did not affect the occurrence of spinal recurrences. Of the 15 patients who experienced spinal recurrence, the 3-year actuarial overall survival and disease-free survival (DFS) rates from the beginning of salvage treatments were 65% and 57%, respectively. In the analysis, presence of intracranial recurrence and salvage treatment modality (radiotherapy with chemotherapy vs. radiotherapy alone) had a statistically significant impact on DFS. The 3-year DFS rate in patients with no intracranial recurrence and treated with both spinal radiotherapy and chemotherapy was 100%, whereas only 17% in patients with intracranial recurrence or treated with radiotherapy alone (p = 0.001). CONCLUSION Large intracranial disease and multifocal intracranial disease were risk factors for spinal recurrence in patients with intracranial germinoma with no evidence of spinal metastases at diagnosis. For patients who developed spinal recurrence alone, salvage treatment combined with spinal radiotherapy and chemotherapy was effective in controlling the recurrent disease.
International Journal of Radiation Oncology Biology Physics | 2012
Kazuhiko Ogawa; Shogo Ishiuchi; Osamu Inoue; Yoshihiko Yoshii; Atsushi Saito; Takashi Watanabe; Shiro Iraha; Takafumi Toita; Yasumasa Kakinohana; Takuro Ariga; Goro Kasuya; Sadayuki Murayama
PURPOSE To analyze the long-term results of a Phase II trial of radiotherapy given immediately after hyperbaric oxygenation (HBO) with multiagent chemotherapy in adults with high-grade gliomas. METHODS AND MATERIALS Patients with histologically confirmed high-grade gliomas were administered radiotherapy in daily 2 Gy fractions for 5 consecutive days per week up to a total dose of 60 Gy. Each fraction was administered immediately after HBO, with the time interval from completion of decompression to start of irradiation being less than 15 minutes. Chemotherapy consisting of procarbazine, nimustine, and vincristine and was administered during and after radiotherapy. RESULTS A total of 57 patients (39 patients with glioblastoma and 18 patients with Grade 3 gliomas) were enrolled from 2000 to 2006, and the median follow-up of 12 surviving patients was 62.0 months (range, 43.2-119.1 months). All 57 patients were able to complete a total radiotherapy dose of 60 Gy immediately after HBO with one course of concurrent chemotherapy. The median overall survival times in all 57 patients, 39 patients with glioblastoma and 18 patients with Grade 3 gliomas, were 20.2 months, 17.2 months, and 113.4 months, respectively. On multivariate analysis, histologic grade alone was a significant prognostic factor for overall survival (p < 0.001). During treatments, no patients had neutropenic fever or intracranial hemorrhage, and no serious nonhematologic or late toxicities were seen in any of the 57 patients. CONCLUSIONS Radiotherapy delivered immediately after HBO with multiagent chemotherapy was safe, with virtually no late toxicities, and seemed to be effective in patients with high-grade gliomas.
Acta Radiologica | 2016
Akira Yogi; Tetsuhiro Miyara; Kazuhiko Ogawa; Shiro Iraha; Shigetaka Matori; Shusaku Haranaga; Sadayuki Murayama
Background Though a few reports have summarized the computed tomography (CT) findings of pulmonary metastases from angiosarcoma, the detailed CT findings of cysts are not well known, except for their characteristic thin walls. Purpose To retrospectively summarize the CT findings of pulmonary metastases from angiosarcoma, focusing mainly on the CT findings of cysts. Material and Methods Thirty-three patients with pulmonary metastases from angiosarcoma were selected retrospectively. Two radiologists reviewed and assessed patients’ chest CT images on a consensus basis for nodules, cysts, the CT halo sign, pneumothorax, pleural effusion, and enlarged lymph nodes. Cysts were also evaluated by wall thickness and smoothness, air-fluid levels, and vessels or bronchi penetrating the cysts. The relationship between cysts and pneumothorax was assessed using the Chi-square test. Results Nodules were found in 28 (85%) patients. Cysts were found in 19 (58%) patients; 17 had thin and smooth walls, 10 had thin and irregular walls, and four had thick and irregular walls. In addition, 12 patients showed vessels or bronchi penetrating the cysts, and six showed air-fluid levels. The CT halo sign, pneumothorax, pleural effusion, and mediastinal lymphadenopathy were seen in 19 (58%), 16 (48%), 26 (78.8%), and five (15.2%) patients, respectively. Pneumothorax occurred significantly more frequently in patients with cysts (P = 0.002). Conclusion Cysts showed variability in their walls, and air-fluid levels and vessels or bronchi penetrating the cysts appeared to be characteristic findings, which may be useful for detection and accurate diagnosis in patients with pulmonary metastases from angiosarcoma.
Journal of Neuro-oncology | 2008
Kazuhiko Ogawa; Yoshihiko Yoshii; Tadashi Nishimaki; Nobumitsu Tamaki; Takao Miyaguni; Yukihiro Tsuchida; Yoshihiko Kamada; Takafumi Toita; Yasumasa Kakinohana; Wakana Tamaki; Shiro Iraha; Genki Adachi; Akio Hyodo; Sadayuki Murayama
Neurologia Medico-chirurgica | 2008
Kazuhiko Ogawa; Yoshihiko Yoshii; Yoichi Aoki; Yutaka Nagai; Yukihiro Tsuchida; Takafumi Toita; Yasumasa Kakinohana; Wakana Tamaki; Shiro Iraha; Genki Adachi; Makoto Hirakawa; Kazuya Kamiyama; Morihiko Inamine; Akio Hyodo; Sadayuki Murayama
International Journal of Radiation Oncology Biology Physics | 2007
Shiro Iraha; Kazuhiko Ogawa; Hidehiko Moromizato; Masayuki Shiraishi; Yutaka Nagai; Hironori Samura; Takafumi Toita; Yasumasa Kakinohana; Genki Adachi; Wakana Tamaki; Makoto Hirakawa; Kazuya Kamiyama; Morihiko Inamine; Tadashi Nishimaki; Yoichi Aoki; Sadayuki Murayama
Japanese Journal of Clinical Oncology | 2001
Takafumi Toita; Kazuhiko Ogawa; Genki Adachi; Yasumasa Kakinohana; Yukiko Nishikuramori; Shiro Iraha; Takashi Utsunomiya; Sadayuki Murayama
Anticancer Research | 2012
Yuko Iraha; Sadayuki Murayama; Ayano Kamiya; Shiro Iraha; Kazuhiko Ogawa
Anticancer Research | 2013
Goro Kasuya; Kazuhiko Ogawa; Shiro Iraha; Yutaka Nagai; Makoto Hirakawa; Takafumi Toita; Yasumasa Kakinohana; Wataru Kudaka; Morihiko Inamine; Takuro Ariga; Yoichi Aoki; Sadayuki Murayama