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タイトル: LH-RH analogue初回投与時のFlare-up予防に関するDiethylstilbestrol併用投与の効果について
その他のタイトル: Study on prevention of flare-up phenomenon following initial LH-RH analogue administration: combination therapy with diethylstilbestrol
著者: 竹内, 信一  KAKEN_name
吉田, 謙一郎  KAKEN_name
遠坂, 顕  KAKEN_name
小林, 信幸  KAKEN_name
東, 四雄  KAKEN_name
根岸, 壮治  KAKEN_name
著者名の別形: Takeuchi, Shin-ichi
Yoshida, Ken-ichiro
Tosaka, Akira
Kobayashi, Nobuyuki
Higashi, Yotsuo
Negishi, Takeharu
キーワード: Diethylstilbestrol
LH-RH analogue
Prostate carcinoma
Flare-up
発行日: Mar-1995
出版者: 泌尿器科紀要刊行会
誌名: 泌尿器科紀要
巻: 41
号: 3
開始ページ: 191
終了ページ: 196
抄録: 進行前立腺癌16例に対して, LH-RH analogue初回投与時のflare-upを予防する目的で, DES 500mg/dayを前投与, 同時投与などの4群に分け施行した。LH-RH analogue初回投与時のflare-up予防にはDES 500mg/dayをLH-RH analogue投与前7日から投与後3日まで投与すれば十分である
To eliminate the initial testosterone (T) surge and prevent the risk of flare-up induced by the first administration of luteinizing hormone-releasing hormone (LH-RH) analogue, we examined the effectiveness of short-term combination therapy with diethylstilbestrol (DES). Sixteen previously untreated patients with prostate carcinoma (Stage C: 4 cases, Stage D2: 12 cases) were randomly assigned to 4 groups. Each group included 4 patients. Group 1 received DES (500 mg daily injection) for 7 days, staring before the first subcutaneous injection of luteinizing hormone releasing hormone (LH-RH) analogue (3.6 mg of Zoladex depot); Group 2 received 500 mg of DES injection for 7 days prior to the initiation of therapy with the LH-RH analogue, and moreover received a DES injection for 7 days; Group 3 received 500 mg of DES injection for 7 days simultaneously with the first injection of the LH-RH analogue; Group 4 was pretreated with 500 mg of DES injection for 7 days prior to the initiation of therapy with the LH-RH analogue, with additional DES injection for 3 days. In groups 1, 2 and 4 the level of T decreased during the 7 days of DES therapy, and at 3 days after the first injection of LH-RH analogue increased again. The mean T value in groups 1, 2 and 4 decreased by 33.2 +/- 27.6% (mean +/- SE), 20.5 +/- 20.8%, 13.2 +/- 9.8%, respectively, at the day of the first injection of LH-RH analogue, and increased by 75.2 +/- 21.6%, 70.7 +/- 63.4%, 56.7 +/- 46.4%, respectively, at 3 days after the first injection of LH-RH analogue.(ABSTRACT TRUNCATED AT 250 WORDS)
URI: http://hdl.handle.net/2433/115467
PubMed ID: 7741071
出現コレクション:Vol.41 No.3

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