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タイトル: | 尿路上皮癌に対するCisplatin(CDDP)を含む化学療法施行時の腎機能評価方法の比較検討 |
その他のタイトル: | Impact of Different Methods of Estimating Renal Function on Determining Eligibility for Cisplatin (CDDP)-Based Chemotherapy in Patients with Invasive Urothelial Carcinoma |
著者: | 後藤, 崇之 ![]() 吉村, 耕治 ![]() 松井, 喜之 ![]() 清水, 洋祐 ![]() 井上, 貴博 ![]() 大久保, 和俊 ![]() 神波, 大己 ![]() 西山, 博之 ![]() 小川, 修 ![]() |
著者名の別形: | Goto, Takayuki Yoshimura, Koji Matsui, Yoshiyuki Shimizu, Yosuke Inoue, Takahiro Okubo, Kazutoshi Kamba, Tomomi Nishiyama, Hiroyuki Ogawa, Osamu |
キーワード: | Urothelial carcinoma Renal function Side effects |
発行日: | Dec-2011 |
出版者: | 泌尿器科紀要刊行会 |
誌名: | 泌尿器科紀要 |
巻: | 57 |
号: | 12 |
開始ページ: | 671 |
終了ページ: | 676 |
抄録: | Assessment of renal function is important to determine the appropriate dose for cisplatin (CDDP)-based chemotherapy. Many previous CDDP-based chemotherapy trials for bladder cancer have required a creatinine-clearance (Ccr) ≧60 ml/min for entry. However, there is little evidence on renal function assessed by estimated glomerular filtration rate (eGFR) using the 4-variable Modification of Diet in Renal Disease Study Equation (MDRD), which has recently been introduced, to determine the eligibility for CDDP-based chemotherapy. To evaluate the proportion of patients with invasive urothelial carcinoma(UC) who would be ineligible (“unfit”) to receive CDDP-based chemotherapy based on eGFR criteria (eGFR <60 ml/min/1.73 m2), and to determine the side effects of chemotherapy in these “unfit” patients, we conducted a retrospective clinical study. Our study population consisted of 61 consecutive patients who underwent 100% dose CDDP-based chemotherapy for invasive UC with 24 h-Ccr≧50 ml/min between June 2001 and July 2009. We assessed renal function using 3 equations (eGFR, Ccr according to Cockcroft-Gault formula (C-G Ccr), and Ccr examined by 24-hour urine collection (24 h-Ccr)) as well. Mean values of eGFR, C-G Ccr, and 24 h-Ccr were 58.6, 68.9, and 82.8 ml/min, respectively (P< 0.001). In total, 29/61(48%) patients were ineligible (“unfit”) to receive chemotherapy based on eGFR criteria. However, there was no difference in the frequency of side effects between eGFR ≧60 ml/min/ 1.73 m2 and eGFR <60 ml/min/1.73 m2 groups. Our observations suggest that 24 h-Ccr≧50 ml/min would be a reasonable cutoff for CDDP-based chemotherapy even when eGFR <60 ml/min/1.73 m2. |
著作権等: | 許諾条件により本文は2013-01-01に公開 |
URI: | http://hdl.handle.net/2433/152317 |
PubMed ID: | 22240299 |
出現コレクション: | Vol.57 No.12 |

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