7 results match your criteria: "Osaka Medical Center for Cancer and Cardiovascular Diseases (OMCC)[Affiliation]"
Eur J Surg Oncol
June 2017
Department of Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases (OMCC), Japan.
Background: The efficacy of neoadjuvant chemoradiotherapy (NACRT) for resectable and borderline resectable pancreatic cancer is important for predicting outcomes after radical surgery, but few clinical indicators predict outcome before resection. This study examined the utility of FDG-PET in predicting the efficacy of NACRT and outcome after radical surgery.
Methods: Eighty-three pancreatic cancer patients who underwent FDG-PET before and after NACRT and had positive standard uptake values (SUVs) before NACRT were enrolled in this study.
Nihon Rinsho
January 2003
Department of Clinical Laboratory, Osaka Medical Center for Cancer and Cardiovascular Diseases (OMCC).
Nihon Rinsho
January 2003
Department of Clinical Laboratory, Osaka Medical Center for Cancer and Cardiovascular Diseases(OMCC).
Sangyo Eiseigaku Zasshi
January 2003
Department of Clinical Laboratory, Osaka Medical Center for Cancer and Cardiovascular Diseases (OMCC), 1-3-3 Nakamachi, Higashinari-ku, Osaka 537-8511, Japan.
In 1996, the need for the clinical guidelines for the management of hyperuricemia and gout was proposed of the consensus conference held at the 29th annual meeting of the Japanese Society of Purine and Pyrimidine Metabolism (president Yuji Matsuzawa). At the consensus conference, the following announcement was made. 1.
View Article and Find Full Text PDFNihon Rinsho
December 2001
Department of Clinical Laboratory, Osaka Medical Center for Cancer and Cardiovascular Diseases (OMCC).
Cancer Chemother Pharmacol
February 1999
Department of Neurosurgery, Osaka Medical Center for Cancer and Cardiovascular Diseases (OMCC), Japan.
To evaluate the possible intrathecal use of 5-fluoro-2'-deoxyuridine (FdUrd) for neoplastic meningitis, its antitumor activity and neurotoxicity in vivo were assessed. FdUrd at doses in the range 5-100 microg/animal was effective against meningeal carcinomatosis using Walker 256 carcinoma cells in rats and MM46 mammary cancer cells in mice and against meningeal gliomatosis using 203 glioma cells in mice. After four intrathecal injections, FdUrd at these doses also showed minimal neurotoxicity in the C57BL/6 mouse brain.
View Article and Find Full Text PDFNo Shinkei Geka
November 1998
Department of Neurosurgery, Osaka Medical Center for Cancer and Cardiovascular Diseases (OMCC), Japan.
A clinical trial of intrathecal chemotherapy with FdUrd was performed in sixteen patients with meningeal dissemination of malignant tumors. Twelve of the sixteen patients responded to intrathecal FdUrd chemotherapy (1-5 micrograms/dose) through an Ommaya reservoir placed in the lateral ventricle: complete response, 2; partial response, 10; progressive disease, 4. Only slight nausea was observed in two patients and dull headache in one patient.
View Article and Find Full Text PDF