Toyofusa Tobe
Chiba University
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Publication
Featured researches published by Toyofusa Tobe.
The Journal of Urology | 2001
Tatsuo Igarashi; Toyofusa Tobe; Hiroomi Nakatsu; Noriyuki Suzuki; Shino Murakami; Masaaki Hamano; Masayuki Maruoka; Tadao Nagayama; Osamu Matsuzaki; Haruo Ito
PURPOSE The 1997 TNM classification defines T1 tumors as those smaller than 7 cm. Recently, a cutoff point of 4 cm. has been proposed to create a subclass of T1 tumors. We evaluated the validity of this cutoff point by assessing the pathological findings and prognoses of patients with T1N0M0 renal cell carcinoma following radical nephrectomy. MATERIALS AND METHODS We reviewed the hospital charts of 333 patients with T1N0M0 tumors, followed as long as 282 months (median 63) after radical nephrectomy. The validity of tumor size cutoff point for predicting survival outcome was tested in relation to other prognostic factors, including patient age, tumor position, nuclear grade, tumor histopathology and degree of microscopic venous invasion. RESULTS During followup 32 patients (9.6%) had tumor recurrence and 21 (6.3%) died of renal cell carcinoma. A 5 cm. cutoff point maximized the differences in cancer specific survival rates and a 4 cm. cutoff point maximized the differences in disease-free survival rates. Tumor size was directly related to microscopic venous invasion and nuclear grade, which are significant prognostic factors, and a 4 cm. cutoff point enhanced these relationships. CONCLUSIONS Tumor size is an important prognostic factor for patients with T1N0M0 renal cell carcinoma. A cutoff point of 4 cm. is practical for dividing the T1N0M0 classification into T1a and T1b subclasses.
International Journal of Urology | 2005
Yukio Naya; Hiroyoshi Suzuki; Akira Komiya; Maki Nagata; Toyofusa Tobe; Takeshi Ueda; Tomohiko Ichikawa; Tatsuo Igarashi; Kunio Yamaguchi; Haruo Ito
Objectives: The maximum size of adrenal tumors that should be removed by laparoscopic adrenalectomy is controversial. We conducted a retrospective comparison of the results of laparoscopic adrenalectomy between patients with adrenal tumors ≥6 cm (‘large tumors’) and patients with adrenal tumors <6 cm (‘small tumors’).
International Journal of Urology | 2005
Shuichi Kamijima; Toyofusa Tobe; Takahito Suyama; Takeshi Ueda; Tatsuo Igarashi; Tomohiko Ichikawa; Haruo Ito
Aim: To investigate the prognostic and predictive relevance of p53 protein, Ki‐67 antigen, MMP‐2 and MMP‐9 in patients with transitional cell carcinoma (TCC) of the upper urinary tract.
Pathology International | 2003
Shigeo Kawai; Kenzo Hiroshima; Yoshiaki Tsukamoto; Toyofusa Tobe; Hiroyoshi Suzuki; Haruo Ito; Hidemi Ohwada; Hisao Ito
An autopsy case of primary small cell carcinoma (SCC) of the prostate in a 68‐year‐old man is reported. The patient was admitted to hospital because of a bloody stool and suspected rectal cancer. However, a diagnosis of prostate cancer was made on the basis of a digital rectal examination, the serum level of prostate‐specific antigen, and a needle biopsy of the prostate. The patient also experienced a syndrome of inappropriate secretion of antidiuretic hormone. He died 29 days after admission. At autopsy, the tumor had invaded the rectum, bladder and pelvic peritoneum. Metastases to the heart, vertebrae and lymph nodes were observed. Microscopically, the tumor was composed of small round cells that showed a solid growth pattern. Rosette formations were observed. Immunohistochemically, the tumor cells were positive for a prostatic epithelial marker and neuroendocrine markers. A high level of antidiuretic hormone was detected in the tumor tissue. To our knowledge, this is the first reported case of SCC of the prostate in which both a prostatic epithelial marker and neuroendocrine markers have been found in the same tumor. This finding supports the hypothesis that SCC of the prostate originates from a multipotential stem cell of the prostatic epithelium.
Urologia Internationalis | 2002
Tatsuo Igarashi; Hidenori Takahashi; Toyofusa Tobe; Hiroyoshi Suzuki; Kenichi Mizoguchi; Hiroomi Nakatsu; Haruo Ito
Introduction: Immunotherapy effectively treats advanced renal cell carcinoma in only a limited number of patients. However, the predicted prognosis for each patient in relation to immune status and response to immunotherapy remains problematic. We analyzed tumor-infiltrating lymphocyte (TIL) subsets to determine whether these correlated with the prognoses for the patients and the response to α-interferon therapy. Materials and Methods: TIL subsets from resected specimens of 79 patients were analyzed by two-color flow cytometry and then compared with the patients’ long-term clinical courses and responses to interferon therapy. Results: In patients with stages III and IV, an increased infiltration of CD4+ cells and decreased CD8+ cells constituted a fair prognostic factor. In 17 patients with metastatic lesions, 8 of 10 patients who had disease progression after interferon therapy showed an increase in CD8+ cells above 25%, whereas 2 responders and 5 patients who had stable disease showed infiltration of CD8+ cells below 25%. Conclusions: The TIL subset is a prognostic factor for advanced renal cell carcinoma, and its analysis provides a method to predict the susceptibility to interferon therapy.
International Journal of Urology | 2006
Masaharu Ishihara; Hiroyoshi Suzuki; Koichiro Akakura; Akira Komiya; Takashi Imamoto; Toyofusa Tobe; Tomohiko Ichikawa
Objectives: The purpose of this study was to clarify characteristics of baseline health‐related quality of life (HRQOL) during the diagnostic process of prostate cancer.
International Journal of Urology | 2003
Kazuya Sekiyama; Koichiro Akakura; Kazuo Mikami; Ken-ichi Mizoguchi; Toyofusa Tobe; Koichi Nakano; Tsutomu Numata; Akiyoshi Konno; Haruo Ito
Background : In patients with primary hyperparathyroidism, prevention of urinary stone recurrence can be achieved by surgical removal of the enlarged parathyroid gland. To ensure the efficacy of surgery for primary hyperparathyroidism, preoperative localization of the enlarged gland is important. In the present study, usefulness of diagnostic imaging for localization of the enlarged gland was investigated in primary hyperparathyroidism.
International Journal of Urology | 2001
Takako Yamazaki; Hiroyoshi Suzuki; Toyofusa Tobe; Nobuyuki Sekita; Hiroki Kito; Tomohiko Ichikawa; Koichiro Akakura; Tatsuo Igarashi; Haruo Ito
Abstract The syndrome of inappropriate secretion of antidiuretic hormone (ADH) was recognized in a 68‐year‐old man with a poorly differentiated metastatic adenocarcinoma of the prostate. Elevated levels of ADH were found in the tissues of the primary tumor and lymph node metastasis. The patients clinical course is detailed and the pathophysiology of this syndrome is discussed. To our knowledge, this case is the ninth reported case of syndrome of inappropriate secretion of ADH with adenocarcinoma of the prostate. Antidiuretic hormone activity was proven in only three cases including this case.
The Journal of Urology | 2002
Hiroki Kito; Hiroyoshi Suzuki; Tatsuo Igarashi; Toyofusa Tobe; Ken Ichi Mizoguchi; Naoto Kamiya; Tomohiko Ichikawa; Haruo Ito
PURPOSE Bilateral renal cell carcinoma has been reported to occur in 1% to 4% of patients with renal cancer. However, whether bilateral renal cell carcinoma involves metastatic lesions of the contralateral kidney or develops as simultaneous primary tumors remains unclear to date. Thus, we investigated chromosomal losses and von Hippel-Lindau (VHL) gene abnormalities in bilateral tumors from patients with nonfamilial bilateral renal cell carcinoma. MATERIALS AND METHODS Genomic DNA was exacted from 2 tumors in 8 patients each with nonfamilial bilateral renal cell carcinoma, including clinically asynchronous and synchronous disease in 5 and 3, respectively. The DNA was then subjected to microsatellite analysis on 13 chromosomal loci. In addition, polymerase chain reaction-single nucleotide specific conformation polymorphism analysis and direct sequencing of 3 exons of the VHL gene were performed. RESULTS All 5 asynchronous cases showed loss of the same allele in bilateral tumors, indicating a common clonal origin. In contrast, 2 of the 3 synchronous cases showed different patterns of chromosomal loss in the right and left renal tumors, suggesting bilateral primary origins. The other synchronous case with loss of the same allele in each tumor involved right stage T3b and left stage T1a neoplasms. No VHL gene mutations were detected in any case. CONCLUSIONS Except for a small number of cases synchronous and asynchronous bilateral renal cell carcinoma may represent the simultaneous appearance of separate primary tumors and metastatic progression from the contralateral kidney, respectively.
International Journal of Urology | 2007
Yukio Naya; Toyofusa Tobe; Takahito Suyama; Kazuhiro Araki; Akira Komiya; Hiroyoshi Suzuki; Tatsuo Igarashi; Tomohiko Ichikawa
Objectives: Laparoscopic surgery for kidney treatment is a common procedure. However, the efficacy of this procedure in patients with several comorbidities has not been well investigated. We conducted a retrospective comparison of results of laparoscopic surgery between patients with several comorbidities and patients with no comorbidity to access the efficacy and safety of this procedure.