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Dive into the research topics where Nobuyoshi Tajiri is active.

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Featured researches published by Nobuyoshi Tajiri.


Liver International | 2007

Serum C‐reactive protein levels predict survival in hepatocellular carcinoma

Sakae Nagaoka; Takafumi Yoshida; Junji Akiyoshi; Jun Akiba; Takuji Torimura; Hisashi Adachi; Junichi Kurogi; Nobuyoshi Tajiri; Kinya Inoue; Takashi Niizeki; Hironori Koga; Tsutomu Imaizumi; Masamichi Kojiro; Michio Sata

Background/Aims: C‐reactive protein (CRP) was recently identified as a prognostic factor for patients with hepatocellular carcinoma (HCC) after surgical resection. We investigated the relationship between the serum levels of high sensitivity CRP (H‐CRP) and the prognosis of HCC patients.


Liver International | 2006

Value of fusing PET plus CT images in hepatocellular carcinoma and combined hepatocellular and cholangiocarcinoma patients with extrahepatic metastases: preliminary findings.

Sakae Nagaoka; Satoshi Itano; Masatoshi Ishibashi; Takuji Torimura; Kenkichi Baba; Junji Akiyoshi; Junichi Kurogi; Satoru Matsugaki; Kinya Inoue; Nobuyoshi Tajiri; Akio Takada; Eiji Ando; Ryoko Kuromatsu; Hayato Kaida; Mina Kurogi; Hironori Koga; Ryukichi Kumashiro; Naofumi Hayabuchi; Masamichi Kojiro; Michio Sata

Abstract: Background/Aims: This study aimed to evaluate the usefulness of 18F‐fluoro‐2‐deoxy‐d‐glucose positron emission tomography (PET) and PET plus computed tomography (CT) fusion images for the detection of extrahepatic metastases of hepatocellular carcinoma (HCC) and combined hepatocellular and cholangiocarcinoma (combined HCC/CC).


The American Journal of Gastroenterology | 2004

Prophylactic Lamivudine Administration Prevents Exacerbation of Liver Damage in HBe Antigen Positive Patients with Hepatocellular Carcinoma Undergoing Transhepatic Arterial Infusion Chemotherapy

Hiroaki Nagamatsu; Satoshi Itano; Sakae Nagaoka; Junji Akiyoshi; Satoru Matsugaki; Junichi Kurogi; Nobuyoshi Tajiri; Sanki Yamasaki; Hironori Koga; Takuji Torimura; Ryukichi Kumashiro; Michio Sata

BACKGROUND AND AIMS:Exacerbation of liver damage during transhepatic arterial infusion chemotherapy (THAIC) is a critical complication in patients with hepatitis B virus (HBV) related hepatocellular carcinoma (HCC). We previously reported that HBe antigen positivity was the associating factor for the exacerbation of liver damage. In the present study, we investigated the effect of lamivudine administration for exacerbation of liver damage in such patients.PATIENTS AND METHODS:Seventeen patients with HBV-related hepatocellular carcinoma who received THAIC were reviewed. Eight of these patients received lamivudine administration. Nine patients did not receive lamivudine administration. All patients were HBe antigen positive. Liver function tests, liver enzymes, HBV-DNA levels, HBe antigen, HBe antibody, and mutation in the precore and core-promoter regions of HBV DNA were evaluated.RESULTS:In the lamivudine-treated group, HBV-DNA levels were significantly reduced and did not increase throughout chemotherapy. Lamivudine did not induce any changes in precore or core-promoter regions. Although levels of alanine aminotransferase (ALT), asparate aminotransferase (AST), total bilirubin, and prothrombin time (PT) in the lamivudine-treated group did not change, levels of ALT, AST and total bilirubin increased, and PT were prolonged in the untreated group by chemotherapy. No patients receiving lamivudine administration showed exacerbation of liver damage. Exacerbation of liver damage was detected in six patients without lamivudine administration. Of these, three patients died of progressive liver failure due to reactivation of HBV.CONCLUSION:These results indicate that prophylactic lamivudine administration reduces HBV-DNA levels and prevents exacerbation of liver damage throughout the period of chemotherapy in HBe antigen positive patients with hepatocellular carcinoma.


Oncology | 2013

Efficacy, Safety, and Survival Factors for Sorafenib Treatment in Japanese Patients with Advanced Hepatocellular Carcinoma

Masahito Nakano; Masatoshi Tanaka; Ryoko Kuromatsu; Hiroaki Nagamatsu; Kenji Sakata; Satoru Matsugaki; Masahiko Kajiwara; Kunitaka Fukuizumi; Nobuyoshi Tajiri; Norito Matsukuma; Terufumi Sakai; Noriyuki Ono; Yoichi Yano; Hironori Koga; Junichi Kurogi; Akio Takata; Shuji Sumie; Manabu Satani; Shingo Yamada; Takashi Niizeki; Hajime Aino; Hideki Iwamoto; Takuji Torimura; Michio Sata

Background: Sorafenib, an oral multikinase inhibitor, was approved for the treatment of advanced hepatocellular carcinoma (HCC), but has not been adequately evaluated for safety and effectiveness in Japanese patients with advanced HCC. Aims: The purpose of this study was to prospectively assess the efficacy, safety, and risk factors for survival in patients with advanced HCC treated with sorafenib. Methods: Between May 2009 and December 2010, 96 Japanese patients with advanced HCC (76 male, 20 female, mean age: 70.4 years) were treated with sorafenib. Eighty-eight patients had Child-Pugh class A, and 8 patients had Child-Pugh class B liver cirrhosis. Barcelona Clinic Liver Cancer stage B and C were found in 64 and 32 patients, respectively. Results: Twelve patients demonstrated partial response to sorafenib therapy, 43 patients had stable disease, and 33 patients had progressive disease at the first radiologic assessment. The most frequent adverse events leading to discontinuation of sorafenib treatment were liver dysfunction (n = 8), hand-foot skin reaction (n = 7), and diarrhea (n = 4). The median survival time and time to progression were 11.6 and 3.2 months, respectively. By multivariate analysis, des-γ-carboxy prothrombin serum levels and duration of treatment were identified as independent risk factors for survival. Conclusions: This study showed that sorafenib was safe and useful in Japanese patients with advanced HCC. In addition, this study demonstrated that sorafenib should be administered as a long-term treatment for advanced HCC regardless of therapeutic effect and dosage.


Cancer Medicine | 2015

Sorafenib for the treatment of advanced hepatocellular carcinoma with extrahepatic metastasis: a prospective multicenter cohort study

Masahito Nakano; Masatoshi Tanaka; Ryoko Kuromatsu; Hiroaki Nagamatsu; Nobuyoshi Tajiri; Manabu Satani; Takashi Niizeki; Hajime Aino; Shusuke Okamura; Hideki Iwamoto; Shigeo Shimose; Tomotake Shirono; Hironori Koga; Takuji Torimura

Sorafenib, an oral multikinase inhibitor, is approved for advanced hepatocellular carcinoma (HCC) treatment. However, its therapeutic effect in advanced HCC patients with extrahepatic metastasis remains uncertain. This study aimed to prospectively assess the efficacy, safety, and survival risk factors and evaluate the prognostic impact of sorafenib treatment in advanced HCC patients with or without extrahepatic metastasis. Between May 2009 and March 2014, 312 consecutive advanced HCC patients who received sorafenib were enrolled in this study. We evaluated their characteristics and compared the clinical outcomes of those with and without extrahepatic metastasis. Of the enrolled patients, 245 (81%) received sorafenib treatment for more than 1 month, with a median duration of 3.6 months. Eighteen patients demonstrated partial response to sorafenib therapy, 127 had stable disease, and 134 had progressive disease at the first radiologic assessment. The median survival time (MST) and progression‐free survival (PFS) were 10.3 and 3.6 months, respectively. Multivariate analysis identified gender, Child‐Pugh class, baseline serum des‐gamma‐carboxy prothrombin level, and treatment duration as independent risk factors for survival. Extrahepatic metastasis was detected in 178 patients. However, the MST, PFS, and therapeutic effect were comparable between patients with and without extrahepatic metastasis. The independent risk factors for decreased overall survival in patients with extrahepatic metastasis were similar to those affecting all patients. Our results indicated that sorafenib could be administered for hepatic reserve and as long‐term treatment for advanced HCC patients regardless of their extrahepatic metastasis status.


Digestive and Liver Disease | 2016

Diffusion-weighted magnetic resonance imaging predicts malignant potential in small hepatocellular carcinoma

Shusuke Okamura; Shuji Sumie; Tatsuyuki Tonan; Masahito Nakano; Manabu Satani; Shigeo Shimose; Tomotake Shirono; Hideki Iwamoto; Hajime Aino; Takashi Niizeki; Nobuyoshi Tajiri; Ryoko Kuromatsu; Koji Okuda; Osamu Nakashima; Takuji Torimura

BACKGROUND Poor differentiation and microvascular invasion are indicators of poor outcome after hepatectomy for patients with small hepatocellular carcinoma (HCC). AIMS We investigated whether gadoxetic acid-enhanced and diffusion-weighted magnetic resonance imaging (MRI) could predict these factors before hepatectomy. METHODS Between July 2008 and April 2012, 75 patients who underwent hepatectomy for small HCCs (diameter: ≤3cm, tumor number: ≤3) were consecutively enrolled. In gadoxetic acid-enhanced MRI, the signal intensity in the tumor was corrected to that in the paraspinous muscles, and the relative enhancement was calculated. In diffusion-weighted imaging, we measured the apparent diffusion coefficient (ADC). We then investigated the correlations between relative enhancement or ADC and histological grade, microvascular invasion and recurrence-free survival. RESULTS Poorly differentiated HCCs showed significantly lower ADC than well-differentiated and moderately differentiated HCCs. There was no significant difference in the hepatobiliary phase. Only ADC was an independent predictor of microvascular invasion, and the best cut-off point of its prediction was 1.175×10(-3)mm(2)/s. Additionally, the recurrence-free survival was significantly shorter in low-ADC group than in high-ADC group. CONCLUSION ADC is useful for predicting poorly differentiated HCCs and microvascular invasion, and low ADC is associated with increased recurrence risk for small HCCs after hepatectomy.


American Journal of Roentgenology | 2007

Temporary indwelling catheter system via the left brachial artery: evaluation in 83 patients with hepatic tumors.

Sakae Nagaoka; Satoshi Itano; Hiroaki Nagamatsu; Junji Akiyoshi; Junichi Kurogi; Nobuyoshi Tajiri; Masahiko Kajiwara; Michio Sata

OBJECTIVE The purpose of our study was to evaluate retrospectively the usefulness and complications associated with a temporary indwelling catheter system through the brachial artery for patients with liver tumors. CONCLUSION The temporary indwelling catheter system via the left brachial artery can be used not only for CO2-enhanced sonographically guided aspiration biopsy, radiofrequency ablation, and percutaneous ethanol injection, but also for short-term hepatic arterial infusion chemotherapy and transcatheter arterial chemoembolization.


Molecular and Clinical Oncology | 2014

Clinical characteristics and prognostic factors for advanced hepatocellular carcinoma with extrahepatic metastasis

Hajime Aino; Shuji Sumie; Takashi Niizeki; Ryoko Kuromatsu; Nobuyoshi Tajiri; Masahito Nakano; Manabu Satani; Shingo Yamada; Shusuke Okamura; Shigeo Shimose; Hiroaki Sumie; Takuji Torimura; Michio Sata


Molecular and Clinical Oncology | 2016

The systemic inflammatory response as a prognostic factor for advanced hepatocellular carcinoma with extrahepatic metastasis

Hajime Aino; Shuji Sumie; Takashi Niizeki; Ryoko Kuromatsu; Nobuyoshi Tajiri; Masahito Nakano; Manabu Satani; Shusuke Okamura; Shigeo Shimose; Kensuke Miyahara; Takuji Torimura


Cancer Chemotherapy and Pharmacology | 2016

Hepatic arterial infusion chemoembolization therapy for advanced hepatocellular carcinoma: multicenter phase II study

Hiroaki Nagamatsu; Shuji Sumie; Takashi Niizeki; Nobuyoshi Tajiri; Hideki Iwamoto; Hajime Aino; Masahito Nakano; Shigeo Shimose; Manabu Satani; Shusuke Okamura; Ryoko Kuromatsu; Satoshi Matsugaki; Junichi Kurogi; Masahiko Kajiwara; Hironori Koga; Takuji Torimura

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