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Dive into the research topics where Daisuke Miyaki is active.

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Featured researches published by Daisuke Miyaki.


Hepatology Research | 2012

Recent trend of clinical features in patients with hepatocellular carcinoma

Yuko Nagaoki; Hideyuki Hyogo; Mio Tanaka; Noriaki Naeshiro; Takashi Nakahara; Yoji Honda; Daisuke Miyaki; Tomokazu Kawaoka; Shintaro Takaki; Akira Hiramatsu; Koji Waki; Michio Imamura; Yoshiiku Kawakami; Shoichi Takahashi; Kazuaki Chayama

Aim:  In this study, we evaluated the clinical characteristics of hepatocellular carcinoma (HCC) because the etiology of HCC has been changing recently.


Journal of Gastroenterology and Hepatology | 2013

Stereotactic body radiation therapy combined with transcatheter arterial chemoembolization for small hepatocellular carcinoma

Yohji Honda; Tomoki Kimura; Tomoki Kobayashi; Takayuki Fukuhara; Keiichi Masaki; Takashi Nakahara; Noriaki Naeshiro; Atsushi Ono; Daisuke Miyaki; Yuko Nagaoki; Tomokazu Kawaoka; Shintaro Takaki; Akira Hiramatsu; Masaki Ishikawa; Hideaki Kakizawa; Masahiro Kenjo; Shoichi Takahashi; Kazuo Awai; Yasushi Nagata; Kazuaki Chayama

To compare the tumor control and safety of stereotactic body radiation therapy (SBRT) combined with transcatheter arterial chemoembolization (TACE) for small, solitary, and hypervascular hepatocellular carcinoma (HCC) with TACE alone.


Oncology | 2012

Evaluation of the mRECIST and α-fetoprotein ratio for stratification of the prognosis of advanced-hepatocellular-carcinoma patients treated with sorafenib.

Tomokazu Kawaoka; Eisuke Murakami; Takashi Nakahara; Noriaki Naeshiro; Mio Tanaka; Yoji Honda; Daisuke Miyaki; Yuko Nagaoki; Shintaro Takaki; Akira Hiramatsu; Koji Waki; Shoichi Takahashi; Kazuaki Chayama

Objective: To compare the assessment of response and prognosis of patients to sorafenib treatment by the Response Evaluation Criteria in Solid Tumors (RECIST), modified RECIST (mRECIST), α-fetoprotein (AFP) and des-γ-carboxy prothrombin (DCP). Methods: Sixty-six patients with advanced hepatocellular carcinoma (HCC) treated with sorafenib were enrolled in this retrospective study. The response to treatment was evaluated by RECIST, mRECIST and changes in AFP and DCP. Results: The median survival time of all patients was 8.6 months. The median time to radiological progression was 3.3 months. The response rates [complete response (CR) + partial response (PR)] by RECIST and mRECIST were 3.0 and 9.0%, respectively, while the disease control rates [CR + PR + stable disease (SD)] were 50 and 50%, respectively. Assessment by mRECIST of overall survival provided a better stratification of the patients according to the response to treatment (p = 0.009) than RECIST (p = 0.09). Assessment of overall survival by a change in AFP ratio of ≤1 at 8 weeks was better than that of >1 at 8 weeks (p = 0.002). The DCP ratio was not useful for assessment of overall survival. Multivariate analysis identified mRECIST response (CR + PR + SD; p = 0.001), AFP ratio at 8 weeks (≤1; p = 0.046) and Child-Pugh A before treatment (p = 0.012) as significant and independent determinants of survival. The combination of AFP ratio at 8 weeks, assessment by mRECIST and Child-Pugh score before treatment allows stratification of prognosis of patients treated with sorafenib. Conclusion: The combination of mRECIST and AFP ratio is useful for the assessment of prognosis of patients with advanced HCC treated with sorafenib.


Hepatology Research | 2013

Utility of controlled attenuation parameter measurement for assessing liver steatosis in Japanese patients with chronic liver diseases

Keiichi Masaki; Shintaro Takaki; Hideyuki Hyogo; Tomoki Kobayashi; Takayuki Fukuhara; Noriaki Naeshiro; Yoji Honda; Takashi Nakahara; Atsushi Ohno; Daisuke Miyaki; Eisuke Murakami; Yuko Nagaoki; Tomokazu Kawaoka; Masataka Tsuge; Nobuhiko Hiraga; Akira Hiramatsu; Michio Imamura; Yoshiiku Kawakami; Hidenori Ochi; Shoichi Takahashi; Koji Arihiro; Kazuaki Chayama

Steatosis is a common histological feature of chronic liver disease, especially alcoholic and non‐alcoholic fatty liver disease, as well as chronic hepatitis C. A recent study showed that evaluating the controlled attenuation parameter (CAP) with transient elastography was an efficient way of non‐invasively determining the severity of hepatic steatosis. The objective of this study was to prospectively evaluate the utility of CAP for diagnosing steatosis in patients with chronic liver disease.


Journal of Gastroenterology and Hepatology | 2012

Hepatic arterial infusion chemotherapy for advanced hepatocellular carcinoma according to Child-Pugh classification.

Daisuke Miyaki; Yohji Honda; Noriaki Naeshiro; Takashi Nakahara; Mio Tanaka; Yuko Nagaoki; Tomokazu Kawaoka; Shintaro Takaki; Koji Waki; Akira Hiramatsu; Shoichi Takahashi; Masaki Ishikawa; Hideaki Kakizawa; Kazuo Awai; Kazuaki Chayama

We compared the treatment response, survival, and safety to hepatic arterial infusion chemotherapy (HAIC) in patients with advanced hepatocellular carcinoma (HCC) according to Child–Pugh (CP) score.


Hepatology Research | 2015

Efficacy and safety of the anticoagulant drug, danaparoid sodium, in the treatment of portal vein thrombosis in patients with liver cirrhosis

Noriaki Naeshiro; Hideyuki Hyogo; Hiromi Kan; Hatsue Fujino; Tomoki Kobayashi; Takayuki Fukuhara; Yohji Honda; Takashi Nakahara; Atsushi Ohno; Daisuke Miyaki; Eisuke Murakami; Tomokazu Kawaoka; Masataka Tsuge; Nobuhiko Hiraga; Akira Hiramatsu; Michio Imamura; Yoshiiku Kawakami; Hidenori Ochi; Kazuaki Chayama

To assess the efficacy and safety of the anticoagulant drug, danaparoid sodium, in the treatment of portal vein thrombosis (PVT) in patients with liver cirrhosis.


Hepatology Research | 2015

Role of 3-D conformal radiotherapy for major portal vein tumor thrombosis combined with hepatic arterial infusion chemotherapy for advanced hepatocellular carcinoma

Hatsue Fujino; Tomoki Kimura; Daisuke Miyaki; Tomokazu Kawaoka; Hiromi Kan; Takayuki Fukuhara; Tomoki Kobayashi; Noriaki Naeshiro; Yohji Honda; Masataka Tsuge; Akira Hiramatsu; Michio Imamura; Yoshiiku Kawakami; Hideyuki Hyogo; Shoichi Takahashi; Rika Yoshimatsu; Takuji Yamagami; Masahiro Kenjo; Yasushi Nagata; Kazuo Awai; Kazuaki Chayama

To evaluate the response, survival and safety on 3‐D conformal radiotherapy (3D‐CRT) for major portal vein tumor thrombosis (PVTT) combined with hepatic arterial infusion chemotherapy (HAIC) for advanced hepatocellular carcinoma (HCC).


Hepatology Research | 2014

Interferon lambda 4 polymorphism affects on outcome of telaprevir, pegylated interferon and ribavirin combination therapy for chronic hepatitis C

Yuko Nagaoki; Michio Imamura; Yoshiiku Kawakami; Hiromi Kan; Hatsue Fujino; Takayuki Fukuhara; Tomoki Kobayashi; Atsushi Ono; Takashi Nakahara; Noriaki Naeshiro; Ayako Urabe; Satoe Yokoyama; Daisuke Miyaki; Eisuke Murakami; Tomokazu Kawaoka; Masataka Tsuge; Akira Hiramatsu; Shoichi Takahashi; C. Nelson Hayes; Hidenori Ochi; Kazuaki Chayama

The predictive value of the recently identified interferon‐λ (IFNL)4 polymorphism on the outcome of telaprevir (TVR), pegylated interferon (PEG IFN) plus ribavirin (RBV) combination therapy for chronic hepatitis C is unknown.


Hepatology Research | 2012

Hepatic arterial infusion chemotherapy using 5-fluorouracil and systemic interferon-α for advanced hepatocellular carcinoma in combination with or without three-dimensional conformal radiotherapy to venous tumor thrombosis in hepatic vein or inferior vena cava

Eisuke Murakami; Daisuke Miyaki; Yuko Nagaoki; Yoshio Katamura; Tomokazu Kawaoka; Shintaro Takaki; Akira Hiramatsu; Koji Waki; Shoichi Takahashi; Tomoki Kimura; Masahiro Kenjo; Yasushi Nagata; Masaki Ishikawa; Hideaki Kakizawa; Kazuo Awai; Kazuaki Chayama

Aim:  We investigated the efficacy of hepatic arterial infusion chemotherapy (HAIC) using 5‐fluorouracil (5‐FU) and systemic interferon (IFN)‐α (HAIC‐5‐FU/IFN) for advanced hepatocellular carcinoma (HCC) with venous tumor thrombosis (VTT) in the hepatic vein trunk (Vv2) or inferior vena cava (Vv3).


Journal of Digestive Diseases | 2015

Comparison of hepatic arterial infusion chemotherapy versus sorafenib monotherapy in patients with advanced hepatocellular carcinoma

Tomokazu Kawaoka; Hideyuki Hyogo; Reona Morio; Kei Morio; Masahiro Hatooka; Takayuki Fukuhara; Tomoki Kobayashi; Noriaki Naeshiro; Daisuke Miyaki; Akira Hiramatsu; Michio Imamura; Yoshiiku Kawakami; Shoichi Takahashi; Koji Waki; Keiji Tsuji; Hirotaka Kohno; Hiroshi Kohno; Takashi Moriya; Kazuaki Chayama

Sorafenib is the standard treatment for advanced hepatocellular carcinoma (HCC) with distant metastasis, unresectable HCC, and those refractory to transcatheter arterial chemoembolization (TACE) or with macroscopic vascular invasion (MVI). The application of sorafenib has been approved by the Japanese Government‐sponsored Medicare for unresectable HCC. In this retrospective cohort study we aimed to compare various aspects of HAIC with sorafenib in the treatment of Child–Pugh A patients with advanced HCC who were otherwise free of extrahepatic metastasis.

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