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Dive into the research topics where Akihiro Haga is active.

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Featured researches published by Akihiro Haga.


Applied Physics Letters | 2004

A miniature x-ray tube

Akihiro Haga; S. Senda; Y. Sakai; Y. Mizuta; S. Kita; F. Okuyama

A miniature x-ray tube is described. The tube is made of Kovar, inside which a grounded target is located close to a field-electron emitter consisting of aligned carbon nanofibers, which continues to work for around 100 h in the 10−6 Pa region unless arcing is induced between the electrodes. The resolution of the contact x-ray images provided by the tube would be impossible using the existing techniques of conventional x-ray radiography, whether the sample is biological or nonbiological.


Radiation Oncology | 2010

Prescreening based on the presence of CT-scan abnormalities and biomarkers (KL-6 and SP-D) may reduce severe radiation pneumonitis after stereotactic radiotherapy

Hideomi Yamashita; Shino Kobayashi-Shibata; Atsuro Terahara; Kae Okuma; Akihiro Haga; Reiko Wakui; Kuni Ohtomo; Keiichi Nakagawa

PurposeTo determine the risk factors of severe radiation pneumonitis (RP) after stereotactic body radiation therapy (SBRT) for primary or secondary lung tumors.Materials and methodsFrom January 2003 to March 2009, SBRT was performed on 117 patients (32 patients before 2005 and 85 patients after 2006) with lung tumors (primary = 74 patients and metastatic/recurrent = 43 patients) in our institution. In the current study, the results on cases with severe RP (grades 4-5) were evaluated. Serum Krebs von den Lungen-6 (KL-6) and serum Surfactant protein-D (SP-D) were used to predict the incidence of RP. A shadow of interstitial pneumonitis (IP) on the CT image before performing SBRT was also used as an indicator for RP. Since 2006, patients have been prescreened for biological markers (KL-6 & SP-D) as well as checking for an IP-shadow in CT.ResultsGrades 4-5 RP was observed in nine patients (7.7%) after SBRT and seven of these cases (6.0%) were grade 5 in our institution. A correlation was found between the incidence of RP and higher serum KL-6 & SP-D levels. IP-shadow in patients CT was also found to correlate well with the severe RP. Severe RP was reduced from 18.8% before 2005 to 3.5% after 2006 (p = 0.042). There was no correlation between the dose volume histogram parameters and these severe RP patients.ConclusionPatients presenting with an IP shadow in the CT and a high value of the serum KL-6 & SP-D before SBRT treatment developed severe radiation pneumonitis at a high rate. The reduction of RP incidence in patients treated after 2006 may have been attributed to prescreening of the patients. Therefore, pre-screening before SBRT for an IP shadow in CT and serum KL-6 & SP-D is recommended in the management and treatment of patients with primary or secondary lung tumors.


International Journal of Radiation Oncology Biology Physics | 2011

Four-Dimensional Measurement of the Displacement of Internal Fiducial Markers During 320-Multislice Computed Tomography Scanning of Thoracic Esophageal Cancer

Hideomi Yamashita; Satoshi Kida; A. Sakumi; Akihiro Haga; Saori Ito; Tsuyoshi Onoe; Kae Okuma; Kenji Ino; Masaaki Akahane; Kuni Ohtomo; Keiichi Nakagawa

PURPOSE To investigate the three-dimensional movement of internal fiducial markers placed near esophageal cancers using 320-multislice CT. METHODS AND MATERIALS This study examined 22 metal markers in the esophageal wall near the primary tumors of 12 patients treated with external-beam photon radiotherapy. Motion assessment was analyzed in 41 respiratory phases during 20 s of cine CT in the radiotherapy position. RESULTS Motion in the cranial-caudal (CC) direction showed a strong correlation (R(2) > 0.4) with the respiratory curve in most markers (73%). The average absolute amplitude of the marker movement was 1.5 ± 1.6 mm, 1.6 ± 1.7 mm, and 3.3 ± 3.3 mm in the left-right (LR), anterior-posterior (AP), and CC directions, respectively. The average marker displacements in the CC direction between peak exhalation and inhalation for the 22 clips were 1.1 mm (maximum, 5.5 mm), 3.0 mm (14.5 mm), and 5.1 mm (16.3 mm) for the upper, middle, and lower thoracic esophagus, respectively. CONCLUSIONS Motion in primary esophagus tumor was evaluated with 320-multislice CT. According to this study, 4.3 mm CC, 1.5 mm AP, and 2.0 mm LR in the upper, 7.4 mm CC, 3.0 mm AP, and 2.4 mm LR in the middle, and 13.8 mm CC, 6.6 mm AP, and 6.8 mm LR in the lower thoracic esophagus provided coverage of tumor motion in 95% of the cases in our study population.


Acta Oncologica | 2009

Quality assurance of volumetric modulated arc therapy using Elekta Synergy

Akihiro Haga; Keiichi Nakagawa; Kenshiro Shiraishi; S Itoh; Atsuro Terahara; Hideomi Yamashita; Kuni Ohtomo; Shigeki Saegusa; Toshikazu Imae; Kiyoshi Yoda; Roberto Pellegrini

Purpose. Recently, Elekta has supplied volumetric modulated arc therapy (VMAT) in which multi-leaf collimator (MLC) shape, jaw position, collimator angle, and gantry speed vary continuously during gantry rotation. A quality assurance procedure for VMAT delivery is described. Methods and materials. A single-arc VMAT plan with 73 control points (CPs) and 5-degree gantry angle spacing for a prostate cancer patient has been created by ERGO + + treatment planning system (TPS), where MLC shapes are given by anatomic relationship between a target and organs at risk and the monitor unit for each CP is optimized based on given dose prescriptions. Actual leaf and jaw positions, gantry angles and dose rates during prostate VMAT delivery were recorded in every 0.25 seconds, and the errors between planned and actual values were evaluated. The dose re-calculation using these recorded data has been performed and compared with the original TPS plan using the gamma index. Results. Typical peak errors of gantry angles, leaf positions, and jaw positions were 3 degrees, 0.6 mm, and 1 mm, respectively. The dose distribution obtained by the TPS plan and the recalculated one agreed well under 2%-2 mm gamma index criteria. Conclusions. Quality assurance for prostate VMAT delivery has been performed with a satisfied result.


Review of Scientific Instruments | 2004

New field-emission x-ray radiography system

S. Senda; Masaki Tanemura; Y. Sakai; Y. Ichikawa; S. Kita; T. Otsuka; Akihiro Haga; F. Okuyama

A new field-emission x-ray radiography system based on our design is described. The key component of the system is a triode-type x-ray source with a built-in nanostructured electron source. The electron source is comprised of palladium-induced carbon nanofibers, which continue to field-emit electrons for more than 10 h at 2×10−7 Torr with a fluctuation of ±8%. Feedback control of the potential of the electron-extracting electrode, or the gate, reduces the current fluctuation to ±0.5%, but this current regulation does little to improve the image resolution. Our system provides sharp x-ray images of both biological and nonbiological samples.


Radiation Oncology | 2012

Evaluation of heterogeneity dose distributions for Stereotactic Radiotherapy (SRT): comparison of commercially available Monte Carlo dose calculation with other algorithms

Wataru Takahashi; Hideomi Yamashita; Naoya Saotome; Y. Iwai; A. Sakumi; Akihiro Haga; Keiichi Nakagawa

BackgroundThe purpose of this study was to compare dose distributions from three different algorithms with the x-ray Voxel Monte Carlo (XVMC) calculations, in actual computed tomography (CT) scans for use in stereotactic radiotherapy (SRT) of small lung cancers.MethodsSlow CT scan of 20 patients was performed and the internal target volume (ITV) was delineated on Pinnacle3. All plans were first calculated with a scatter homogeneous mode (SHM) which is compatible with Clarkson algorithm using Pinnacle3 treatment planning system (TPS). The planned dose was 48 Gy in 4 fractions. In a second step, the CT images, structures and beam data were exported to other treatment planning systems (TPSs). Collapsed cone convolution (CCC) from Pinnacle3, superposition (SP) from XiO, and XVMC from Monaco were used for recalculating. The dose distributions and the Dose Volume Histograms (DVHs) were compared with each other.ResultsThe phantom test revealed that all algorithms could reproduce the measured data within 1% except for the SHM with inhomogeneous phantom. For the patient study, the SHM greatly overestimated the isocenter (IC) doses and the minimal dose received by 95% of the PTV (PTV95) compared to XVMC. The differences in mean doses were 2.96 Gy (6.17%) for IC and 5.02 Gy (11.18%) for PTV95. The DVHs and dose distributions with CCC and SP were in agreement with those obtained by XVMC. The average differences in IC doses between CCC and XVMC, and SP and XVMC were -1.14% (p = 0.17), and -2.67% (p = 0.0036), respectively.ConclusionsOur work clearly confirms that the actual practice of relying solely on a Clarkson algorithm may be inappropriate for SRT planning. Meanwhile, CCC and SP were close to XVMC simulations and actual dose distributions obtained in lung SRT.


World Journal of Radiology | 2014

Radiation pneumonitis after stereotactic radiation therapy for lung cancer

Hideomi Yamashita; Wataru Takahashi; Akihiro Haga; Keiichi Nakagawa

Stereotactic body radiation therapy (SBRT) has a local control rate of 95% at 2 years for non-small cell lung cancer (NSCLC) and should improve the prognosis of inoperable patients, elderly patients, and patients with significant comorbidities who have early-stage NSCLC. The safety of SBRT is being confirmed in international, multi-institutional Phase II trials for peripheral lung cancer in both inoperable and operable patients, but reports so far have found that SBRT is a safe and effective treatment for early-stage NSCLC and early metastatic lung cancer. Radiation pneumonitis (RP) is one of the most common toxicities of SBRT. Although most post-treatment RP is Grade 1 or 2 and either asymptomatic or manageable, a few cases are severe, symptomatic, and there is a risk for mortality. The reported rates of symptomatic RP after SBRT range from 9% to 28%. Being able to predict the risk of RP after SBRT is extremely useful in treatment planning. A dose-effect relationship has been demonstrated, but suggested dose-volume factors like mean lung dose, lung V20, and/or lung V2.5 differed among the reports. We found that patients who present with an interstitial pneumonitis shadow on computed tomography scan and high levels of serum Krebs von den Lungen-6 and surfactant protein D have a high rate of severe radiation pneumonitis after SBRT. At our institution, lung cancer patients with these risk factors have not received SBRT since 2006, and our rate of severe RP after SBRT has decreased significantly since then.


Review of Scientific Instruments | 2007

Electron gun using carbon-nanofiber field emitter

Y. Sakai; Akihiro Haga; S. Sugita; S. Kita; S.-I. Tanaka; F. Okuyama; N. Kobayashi

An electron gun constructed using carbon-nanofiber (CNF) emitters and an electrostatic Einzel lens system has been characterized for the development of a high-resolution x-ray source. The CNFs used were grown on tungsten and palladium tips by plasma-enhanced chemical-vapor deposition. Electron beams with the energies of 10<E<20 keV were focused by the electrostatic lens and impinged on a W target for x-ray radiography. Analyzing the recorded x-ray radiographs, the focal spot size of the electron beam extracted from the CNFs was estimated to be D<50 microm in diameter. Superior performance was realized by using CNFs with larger fiber radii (100-500 nm) grown sparsely on the metal tips, which were installed in a holder at the short length L=0.5 mm.


Journal of Radiation Research | 2013

4D registration and 4D verification of lung tumor position for stereotactic volumetric modulated arc therapy using respiratory-correlated cone-beam CT

Keiichi Nakagawa; Akihiro Haga; Satoshi Kida; Yoshitaka Masutani; Hideomi Yamashita; Wataru Takahashi; A. Sakumi; Naoya Saotome; Takashi Shiraki; Kuni Ohtomo; Y. Iwai; Kiyoshi Yoda

We propose a clinical workflow of stereotactic volumetric modulated arc therapy (VMAT) for a lung tumor from planning to tumor position verification using 4D planning computed tomography (CT) and 4D cone-beam CT (CBCT). A 4D CT scanner, an Anzai belt and a BodyFix were employed to obtain 10-phase respiratory-correlated CT data for a lung patient under constrained breathing conditions. A planning target volume (PTV) was defined by adding a 5-mm margin to an internal target volume created from 10 clinical target volumes, each of which was delineated on each of the 10-phase planning CT data. A single-arc VMAT plan was created with a D95 prescription dose of 50 Gy in four fractions on the maximum exhalation phase CT images. The PTV contours were exported to a kilovoltage CBCT X-ray Volume Imaging (XVI) equipped with a linear accelerator (linac). Immediately before treatment, 10-phase 4D CBCT images were reconstructed leading to animated lung tumor imaging. Initial bone matching was performed between frame-averaged 4D planning CT and frame-averaged 4D CBCT datasets. Subsequently, the imported PTV contours and the animated moving tumor were simultaneously displayed on the XVI monitor, and a manual 4D registration was interactively performed on the monitor until the moving tumor was symmetrically positioned inside the PTV. A VMAT beam was delivered to the patient and during the delivery further 4D CBCT projection data were acquired to verify the tumor position. The entire process was repeated for each fraction. It was confirmed that the moving tumor was positioned inside the PTV during the VMAT delivery.


Radiotherapy and Oncology | 2011

4D-CBCT reconstruction using MV portal imaging during volumetric modulated arc therapy

Satoshi Kida; Naoya Saotome; Yoshitaka Masutani; Hideomi Yamashita; Kuni Ohtomo; Keiichi Nakagawa; A. Sakumi; Akihiro Haga

BACKGROUND Recording target motion during treatment is important for verifying the irradiated region. Recently, cone-beam computed tomography (CBCT) reconstruction from portal images acquired during volumetric modulated arc therapy (VMAT), known as VMAT-CBCT, has been investigated. In this study, we developed a four-dimensional (4D) version of the VMAT-CBCT. MATERIALS AND METHODS The MV portal images were sequentially acquired from an electronic portal imaging device. The flex, background, monitor unit, field size, and multi-leaf collimator masking corrections were considered during image reconstruction. A 4D VMAT-CBCT requires a respiratory signal during image acquisition. An image-based phase recognition (IBPR) method was performed using normalised cross correlation to extract a respiratory signal from the series of portal images. RESULTS Our original IBPR method enabled us to reconstruct 4D VMAT-CBCT with no external devices. We confirmed that 4D VMAT-CBCT was feasible for two patients and in good agreement with in-treatment 4D kV-CBCT. CONCLUSION The visibility of the anatomy in 4D VMAT-CBCT reconstruction for lung cancer patients has the potential of using 4D VMAT-CBCT as a tool for verifying relative positions of tumour for each respiratory phase.

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Satoshi Kida

Tokyo University of Agriculture

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Naoya Saotome

National Institute of Radiological Sciences

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