Satoshi Mochizuki

Dr. Satoshi Mochizuki


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 May 2012 in BMC Medicine
Verified
Journal Article
Open access
PDF file
NYNobutake Yamamichi
Nobutake Yamamichi
SMSatoshi Mochizuki
Satoshi Mochizuki
IAItsuko Asada-Hirayama
Itsuko Asada-Hirayama
RMRie Mikami-Matsuda
Rie Mikami-Matsuda
TSTakeshi Shimamoto
Takeshi Shimamoto
KKKazuhiko Koike
Kazuhiko Koike
Gastroesophageal reflux disease (GERD) is a very common disorder worldwide, comprised of reflux esophagitis (RE) and non-erosive reflux disease (NERD). As more than half of GERD patients are classified into the NERD group, precise evaluation of bothersome epigastric symptoms is essential. Nevertheless, compared with many reports targeting endoscopic reflux esophagitis, large-scale studies focusing on GERD symptoms have been very scarce.

5 June 2013 in Journal of Gastroenterology
Verified
Journal Article
Closed access
PDF file
YTYu Takahashi
Yu Takahashi
NYNobutake Yamamichi
Nobutake Yamamichi
TSTakeshi Shimamoto
Takeshi Shimamoto
SMSatoshi Mochizuki
Satoshi Mochizuki
MFMitsuhiro Fujishiro
Mitsuhiro Fujishiro
KKKazuhiko Koike
Kazuhiko Koike

21 May 2010 in Japanese Journal of Clinical Oncology
Verified
Journal Article
Open access
PDF file
SMSatoshi Mochizuki
Satoshi Mochizuki
TYTakayuki Yoshino
Takayuki Yoshino
TKTakashi Kojima
Takashi Kojima
NFNozomu Fuse
Nozomu Fuse
HIHiroaki Ikematsu
Hiroaki Ikematsu
AOAtsushi Ohtsu
Atsushi Ohtsu
The risk of venous thromboembolism has been reported to increase when receiving bevacizumab. Many cancer patients are reported to have elevated D-dimer levels. It is not clear what D-dimer level might indicate an increased risk of venous thromboembolism in the colorectal cancer patients treated with bevacizumab-containing chemotherapy. The D-dimer levels and any event concurrent with an elevated D-dimer level were evaluated in patients receiving bevacizumab. The D-dimer cut-off level was determined using the receiver-operating characteristic analysis. The selection criteria were as follows: histologically proven metastatic and unresectable colorectal adenocarcinoma; no prior chemotherapy containing bevacizumab; D-dimer test performed repetitively on the baseline and during bevacizumab administration; no venous thromboembolism identified at the baseline; and enhanced computed tomographic scan performed every 2 months. Sixty-nine patients were included. The chemotherapy regimens with bevacizumab included the regimen of 5-fluorouracil, leucovorin and oxaliplatin (FOLFOX), the regimen of 5-fluorouracil, leucovorin and irinotecan (FOLFIRI), and leucovorin-modulated 5-fluorouracil. The median baseline D-dimer level was 1.2 µg/ml. The appropriate D-dimer cut-off level was 3 µg/ml with the negative predictive value of 98% and relative risk of 6.9. Twenty-one of 69 patients showed elevated D-dimer levels of >3 µg/ml, with 11 patients for unknown reasons, 6 with tumor progression, 3 with venous thromboembolism and 1 with sepsis. In the remaining 48 patients whose D-dimer levels were ≤3 µg/ml, only one patient developed a venous thromboembolism. A D-dimer cut-off level of 3 µg/ml might be a useful indicator level to exclude venous thromboembolism or show an increased risk for venous thromboembolism in colorectal cancer patients treated with bevacizumab-containing chemotherapy.

1 May 2014 in Gastrointestinal Endoscopy
Verified
Journal Article
Closed access
SASeiichiro Abe
Seiichiro Abe
SMSatoshi Mochizuki
Satoshi Mochizuki
NUNoriya Uedo
Noriya Uedo
KKKazuhiro Kaneko
Kazuhiro Kaneko
YYYorimasa Yamamoto
Yorimasa Yamamoto
KKKazuhiko Koike
Kazuhiko Koike

30 April 2010 in Gastrointestinal Endoscopy
Verified
Journal Article
Closed access
PDF file
HSHironaga Satake
Hironaga Satake
TYTomonori Yano
Tomonori Yano
KMKeiko Minashi
Keiko Minashi
TKTakashi Kojima
Takashi Kojima
DFDaisuke Fukuda
Daisuke Fukuda
MMManabu Muto
Manabu Muto