Combination therapy with flutamide and [D-Trp6]LHRH ethylamide for stage C prostatic carcinoma
- PMID: 3289945
- DOI: 10.1016/0277-5379(88)90296-9
Combination therapy with flutamide and [D-Trp6]LHRH ethylamide for stage C prostatic carcinoma
Abstract
Sixty-seven previously untreated patients presenting with clinical stage C prostatic carcinoma with no evidence of distant metastases received combination therapy using the antiandrogen Flutamide and the LHRH agonist [D-Trp6]LHRH ethylamide for an average duration of treatment of 23.5 months. Only five patients have so far shown treatment failure with 91.8% of the patients still in remission at 2 years. Three patients have died from prostate cancer while three have died from other causes, 93.5% of the patients being alive at 2 years. Local control was achieved rapidly in all except one patient. Urinary obstruction and hydronephrosis were corrected in all cases. When comparing to recent data obtained after single endocrine therapy (orchiectomy or estrogens), or radiotherapy, the rate of treatment failure at 2 years is 3.5-fold lower after combination therapy (8.2%) than monotherapy (28.4%). The death rate at 2 years following start of the combination therapy is 6.5% while it is on average 22.2% (3.4-fold higher) in the studies using monotherapy (orchiectomy or estrogens) or radiotherapy. The present data suggest that treatment of prostate cancer with combination therapy before clinical evidence of dissemination of the disease permits a better response which is possibly explained, at least in part, by the lower degree of dedifferentiation and heterogeneity of the tumors.
Similar articles
-
Combination therapy with flutamide and the LHRH agonist [D-Trp6, des-Gly-NH(2)10]LHRH ethylamide in stage C prostatic carcinoma.Br J Urol. 1993 Nov;72(5 Pt 1):629-34. doi: 10.1111/j.1464-410x.1993.tb16223.x. Br J Urol. 1993. PMID: 10071551
-
Combination therapy with flutamide and castration (LHRH agonist or orchiectomy) in previously untreated patients with clinical stage D2 prostate cancer: today's therapy of choice.J Steroid Biochem. 1988;30(1-6):107-17. doi: 10.1016/0022-4731(88)90083-0. J Steroid Biochem. 1988. PMID: 3290578 Clinical Trial.
-
Advantages of the combination therapy in previously untreated and treated patients with advanced prostate cancer.J Steroid Biochem. 1986 Nov;25(5B):877-83. doi: 10.1016/0022-4731(86)90319-5. J Steroid Biochem. 1986. PMID: 3100871 Clinical Trial.
-
Combination therapy with flutamide and [D-Trp6, des-Gly-NH2(10)]LHRH ethylamide in stage C and D prostate cancer: today's therapy of choice--rationale and 5-year clinical experience.Prog Clin Biol Res. 1988;262:11-63. Prog Clin Biol Res. 1988. PMID: 3287388 Review. No abstract available.
-
Combination therapy in stage C and D prostatic cancer: rationale and five year clinical experience.Cancer Metastasis Rev. 1987;6(4):615-36. doi: 10.1007/BF00047470. Cancer Metastasis Rev. 1987. PMID: 3327635 Review.
Cited by
-
Active cell death in hormone-dependent tissues.Cancer Metastasis Rev. 1992 Sep;11(2):197-220. doi: 10.1007/BF00048064. Cancer Metastasis Rev. 1992. PMID: 1356648 Review.
-
Blockade of testicular and adrenal androgens in prostate cancer treatment.Nat Rev Urol. 2011 Feb;8(2):73-85. doi: 10.1038/nrurol.2010.231. Epub 2011 Jan 18. Nat Rev Urol. 2011. PMID: 21243019 Review.
-
In vivo biodistribution of an androgen receptor avid PET imaging agent 7-alpha-fluoro-17 alpha-methyl-5-alpha-dihydrotestosterone ([(18)F]FMDHT) in rats pretreated with cetrorelix, a GnRH antagonist.Eur J Nucl Med Mol Imaging. 2008 Feb;35(2):379-85. doi: 10.1007/s00259-007-0610-3. Epub 2007 Oct 13. Eur J Nucl Med Mol Imaging. 2008. PMID: 17934727
MeSH terms
Substances
LinkOut - more resources
Medical