An implant releasing the gonadotropin hormone-releasing hormone agonist histrelin maintains medical castration for up to 30 months in metastatic prostate cancer

被引:25
作者
Chertin, B
Spitz, IM
Lindenberg, T
Algur, N
Zer, T
Kuzma, P
Young, AJM
Catane, R
Farkas, A
机构
[1] Shaare Zedek Med Ctr, Dept Urol, IL-91031 Jerusalem, Israel
[2] Shaare Zedek Med Ctr, Dept Biochem, IL-91031 Jerusalem, Israel
[3] Shaare Zedek Med Ctr, Hormone Res Inst, IL-91031 Jerusalem, Israel
[4] Shaare Zedek Med Ctr, Inst Oncol, IL-91031 Jerusalem, Israel
[5] Natl Patenet Dev, New Brunswick, NJ USA
[6] Zer Labs, Jerusalem, Israel
[7] Biomed Res Ctr, Populat Council, New York, NY USA
关键词
prostate; prostatic neoplasms; neoplasm metastasis; drug implants; castration; male;
D O I
10.1016/S0022-5347(05)67816-0
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: The administration of gonadotropin hormone-releasing hormone agonists is well established for treating metastatic prostate cancer. In an ongoing study we evaluated the effect of a long acting implant that releases the gonadotropin hormone-releasing hormone agonist histrelin ([ImBzl]D-His6,Pro9-Net) in 15 patients with disseminated prostate cancer. Materials and Methods: The 2.6 cm. implant releasing 60 mu g, histrelin daily is inserted subcutaneously into the upper arm using local anesthesia. Of the patients 8 received 1 and the remainder received 2 implants. Treatment with the antiandrogen flutamide or cyproterone acetate began 2 weeks before implant insertion and continued for up to 12 weeks. Testosterone, luteinizing hormone (LH) and prostate specific antigen were determined monthly, and a metastatic evaluation was performed every 6 months. Results: LH and testosterone increased after flutamide administration and decreased after implant insertion. By day 28 LH and testosterone were completely suppressed. LH and testosterone decreased immediately after cyproterone acetate administration. Prostate specific antigen began to decrease during antiandrogen therapy and decreased further after implant insertion. One patient requested implant removal after 1 year for personal reasons and 1 died of an unrelated cause 18 months after insertion. Escape was demonstrated in 4 cases at 5, 10, 12 and 19 months, although LH and testosterone remained suppressed. Duration of treatment in the remaining 9 patients was between 21 and 30 months. LH and testosterone remained completely suppressed and prostate specific antigen levels were in the normal range. The clinical and biochemical response was identical in those who received 1 or 2 implants. At 12 months 8 patients were challenged at intermittent intervals for up to 24 months with a bolus of 100 mu g. gonadotropin hormone-releasing hormone followed by 2 weeks of flutamide. The response was compared with that in untreated controls recently diagnosed with prostate cancer. Unlike controls there was complete LH suppression in the 8 challenged patients. Conclusions: A histrelin implant suppresses LH and testosterone in prostate cancer for up to 30 months. This finding represents a significant improvement over existing preparations, which must be administered at 1 to S-month intervals.
引用
收藏
页码:838 / 844
页数:7
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