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Publication
Featured researches published by Tomofumi Miura.
Journal of Cachexia, Sarcopenia and Muscle | 2017
Koji Amano; Isseki Maeda; Tatsuya Morita; Mika Baba; Tomofumi Miura; Takashi Hama; Ichiro Mori; Nobuhisa Nakajima; Tomohiro Nishi; Hiroki Sakurai; Satofumi Shimoyama; Takuya Shinjo; Hiroto Shirayama; Takeshi Yamada; Shigeki Ono; Taketoshi Ozawa; Ryo Yamamoto; Naoki Yamamoto; Hideki Shishido; Hiroya Kinoshita
The association between C‐reactive protein (CRP) level, symptoms, and activities of daily living (ADL) in advanced cancer patients is unclear.
Japanese Journal of Clinical Oncology | 2014
Tomofumi Miura; Yoshihisa Matsumoto; Shinya Motonaga; Hideaki Hasuo; Keiko Abe; Hiroya Kinoshita
OBJECTIVE Most cancer patients become increasingly anxious toward the end of their life. The objective of this study was to identify predictors of increased opioid dosage in the last week of a terminal cancer patients life. METHODS We retrospectively reviewed charts of patients who died in our palliative care unit. We assigned the patients to increased group or decreased group according to changes in oral morphine equivalent dosage in their last 7 days. Logistic regression analysis was used to identify predictors of increased oral morphine equivalent dosage. RESULTS We analyzed data of 158 patients (female: 43.7%, median age: 64 years). The median oral morphine equivalent dosages on Days 7 and 1 before death were 50 mg (interquartile range: 24-122) and 61 mg (28-129), respectively. Independent predictors of increased oral morphine equivalent dosage included dyspnea (odds ratio: 11.5, 95% confidence interval: 4.98-28.83, P < 0.01), age <65 years (odds ratio: 2.3, 95% confidence interval: 1.04-5.26, P = 0.04) and oral morphine equivalent dosage <50 mg on Day 7 before death (odds ratio: 3.7, 95% confidence interval: 1.68-8.89, P < 0.01). The median oral morphine equivalent dosages on Days 7 and 1 before death were 48 mg (interquartile range: 20-126) and 75 mg (36-170) in patients with dyspnea, and 50 mg (25-120) and 57 mg (25-124) in patients with pain, respectively. CONCLUSIONS Dyspnea, relative youth and oral morphine equivalent dosage <50 mg on Day 7 before death were predictive of increased oral morphine equivalent dosage in the last 7 days. Our findings may help oncologists to more accurately inform patients about expected opioid requirements and thus relieve their end-of-life anxiety.
Supportive Care in Cancer | 2018
Tomofumi Miura; Shuichi Mitsunaga; Masafumi Ikeda; Izumi Ohno; Hideaki Takahashi; Hidetaka Suzuki; Ai Irisawa; Takeshi Kuwata; Atsushi Ochiai
PurposeAcyl ghrelin is an orexigenic peptide. Active ghrelin ratio, the ratio of acyl ghrelin to total ghrelin, has an important role in physiological functions and gastrointestinal symptoms. However, low active ghrelin ratio-related characteristics, gastrointestinal symptoms, and chemotherapy-induced gastrointestinal toxicity in patients with advanced pancreatic cancer have not been previously evaluated. The goal of this study was to identify low active ghrelin ratio-related factors in treatment-naïve advanced pancreatic cancer patients.MethodsPatients with treatment-naïve advanced pancreatic cancer were eligible for inclusion in this study. Active ghrelin ratio and clinical parameters of patients were prospectively recorded. Factors correlated with low active ghrelin ratio and survival were analyzed.ResultsIn total, 92 patients were analyzed. Low active ghrelin ratio-related factors were advanced age (P < 0.01), severe appetite loss (P < 0.01), and decreased cholinesterase (P < 0.01). The adverse events of grade 2 or higher anorexia tended to increase in patients with low active ghrelin ratio. However, no differences were found in survival and body composition between low and high active ghrelin ratio groups.ConclusionsLow active ghrelin ratio was related to lack of appetite and low cholinesterase and tended to be related to anorexia grade 2 or higher in patients with treatment-naïve advanced pancreatic cancer.
American Journal of Hospice and Palliative Medicine | 2018
Jun Kako; Masamitsu Kobayashi; Yusuke Kanno; Asao Ogawa; Tomofumi Miura; Yoshihisa Matsumoto
Context: Terminally ill patients with cancer experience various physical and emotional symptoms that have a negative impact on quality of life and activities of daily living. Recently, revised Edmonton Symptom Assessment System (ESAS-r) scores have been proposed for assessing symptoms in terminally ill patients with cancer. Objective: To determine the optimal cutoff point for expressing ESAS-r scores as binary data, indicating the presence or absence of symptoms. Methods: We conducted a retrospective study of patients hospitalized in the palliative care unit of our hospital between September 1, 2014 and May 31, 2015. To determine the optimal cutoff point for expressing ESAS-r scores as binary data, indicating the presence or absence of 6 physical symptoms (“pain,” “tiredness,” “drowsiness,” “nausea,” “lack of appetite,” and “dyspnea”), the sensitivity and specificity of each measurement were calculated. Cutoff points were estimated using receiver operating characteristic curve analysis. Results: Data from 157 patients who performed the self-assessment in ESAS-r scores were analyzed. The mean age was 66.5 years. Approximately 60.0% of patients were male. The optimal cutoff point for pain, tiredness, drowsiness, nausea, lack of appetite, and dyspnea was 4, 4, 4, 2, 5, and 4, respectively. The area under the curve for tiredness, nausea, and dyspnea was >0.70, followed in order by pain, lack of appetite, and drowsiness. The area under the curve for drowsiness was 0.55. Conclusion: Our results suggest that physical symptoms other than drowsiness could potentially predict ESAS-r score severity.
Supportive Care in Cancer | 2015
Tomofumi Miura; Yoshihisa Matsumoto; Takashi Hama; Koji Amano; Yo Tei; Ayako Kikuchi; Akihiko Suga; Takayuki Hisanaga; Tatsuhiko Ishihara; Mutsumi Abe; Keisuke Kaneishi; Shohei Kawagoe; Toshiyuki Kuriyama; Takashi Maeda; Ichiro Mori; Nobuhisa Nakajima; Tomohiro Nishi; Hiroki Sakurai; Tatsuya Morita; Hiroya Kinoshita
Journal of Pain and Symptom Management | 2016
Koji Amano; Isseki Maeda; Tatsuya Morita; Tomofumi Miura; Satoshi Inoue; Masayuki Ikenaga; Yoshihisa Matsumoto; Mika Baba; Ryuichi Sekine; Takashi Yamaguchi; Takeshi Hirohashi; Tsukasa Tajima; Ryohei Tatara; Hiroaki Watanabe; Hiroyuki Otani; Chizuko Takigawa; Yoshinobu Matsuda; Hiroka Nagaoka; Masanori Mori; Hiroya Kinoshita
Journal of Palliative Medicine | 2015
Takashi Igarashi; Kentaro Abe; Tomofumi Miura; Keita Tagami; Shinya Motonaga; Yasuhiko Ichida; Hideaki Hasuo; Yoshihisa Matsumoto; Shinichiro Saito; Hiroya Kinoshita
Psycho-oncology | 2018
Kayo Hirooka; Hiroyuki Otani; Tatsuya Morita; Tomofumi Miura; Hiroki Fukahori; Maho Aoyama; Yoshiyuki Kizawa; Yasuo Shima; Satoru Tsuneto; Mitsunori Miyashita
Journal of Pain and Symptom Management | 2017
Yuki Sumazaki Watanabe; Tomofumi Miura; Ayumi Okizaki; Keita Tagami; Yoshihisa Matsumoto; Maiko Fujimori; Tatsuya Morita; Hiroya Kinoshita
Journal of Palliative Medicine | 2016
Keita Tagami; Tomofumi Miura; Masami Suzuki; Motohiro Matoba