Abstract
Purpose
Patients with advanced prostate cancer (PCa) benefit from intermittent maximal androgen blockade (IMAB) therapy when time-off period (TOP) is extended. A comparative study included patients who received uninterrupted finasteride (mMAB) treatment and those who did not MAB.
Methods
A randomized group of 63 patients with PCa (T3NxM1; Gl. 6-7) was prospectively examined for 5 years: group A (GrA)—31 patients receiving MAB and group B (GrB)—32—mMAB. Testosterone inactivating pharmaceuticals period (TIP) lasted until PSA was 0.2 ng/ml (group A) and 0.1 ng/ml (group B), followed by MAB (TOP) discontinuation. CR, PR, BP, and TP evaluation criteria were adopted. Tests were carried out every 3 months.
Results
After 5 years, five patients in GrA did not reach PSA concentration nadir value and were eliminated from final evaluation. TIP1 for both groups was comparable; TIP2-4 were shorter in GrB. TOP1-3 for GrB were longer than in GrA, and TOP4 was comparable in both groups. Treatment effects were, respectively, CR, 1(3.2%) and 17(53%); PR, 9(29%) and 3(9%); BP 11(35.5%) and 5(15.6%); TP, 10(32.2%) and 7(22%). Before the therapy, QoL of 63 patients was between 4 and 5 points; after 5 years for patients with CR and PR, between 1 and 2 points, but for BP, between 3 and 4 points.
Conclusions
Better therapy effects were observed in patients treated with mMAB, receiving additional finasteride. Response to the treatment improved by nearly double, and progression was two times lower. TOP after TIP was extending in time.
Similar content being viewed by others
Abbreviations
- ADT:
-
Androgen deprivation therapy
- 5AR:
-
5-Alfa-reductase
- 5ARI:
-
5-Alfa-reductase inhibitor
- BPH:
-
Benign prostatic hyperplasia
- CAB:
-
Combined androgen blockade
- CRPCa:
-
Castration-resistant prostate cancer
- DHT:
-
Dihydrotestosterone
- GrA:
-
Group of patients A
- GrB:
-
Group of patients B
- HT:
-
Hormone therapy
- IAB:
-
Intermittent androgen blockade
- IHT:
-
Intermittent hormone therapy
- IPSS:
-
International Prostate Score System
- LHRH:
-
Luteinizing-hormone-releasing hormone
- MAB:
-
Maximal androgen blockade
- mMAB:
-
More maximal androgen blockade
- PCa:
-
Prostate cancer
- PCPT:
-
Prostate Cancer Prevention Trial
- TIP:
-
Testosterone inactivating pharmaceuticals
- TOP:
-
Time-off period
- PSA:
-
Prostate-specific antigen
- QoL:
-
Quality of life
References
Boyle P, Ferlay J (2005) Cancer incidence and mortality in Europe, 2004. Ann Oncol 16:481–488
American Cancer Society (2007) Cancer facts and figures 2007. American Cancer Society, Atlanta
Heidenrich A, Aus G, Boilo M et al (2008) EAU guidelines on prostate cancer. Eur Urol 53:68–80
Huggins C (1943) Endocrine control of prostatic cancer. Science 97:541–544
Shally AV, Arimura A, Baba Y et al (1971) Isolation and properties of the FSH and LH-releasing hormone. Biochim Biophys Res Comm 43:393–399
Peets EA, Henson MF, Neri R (1974) On the mechanism of the anti-androgenic action of flutamide (alpha-trifluoro-2-methyl-4′-nitro-m-propionotolecidide) in the rat. Endocrinology 94:532–540
Labrie F, Dupont A, Belanger A et al (1982) New hormonal therapy in prostatic carcinoma combined treatment with an LHRH agonist and an antiandrogen. Clin Invest Med 5:267–275
Lukka H, Waldron T, Klotz L et al (2006) Maximal androgen blockade for the treatment of metastatic prostate cancer—a systematic review. Curr Oncol 13:81–93
Tindall DJ, Rittmaster RS (2008) The rationale for inhibiting 5 alpha-reductase isoenzymes in the prevention and treatment of prostate cancer. J Urol 179:1235–1242
Schellhammer PF, Sharifi R, Block NL et al (1997) Clinical benefits to bicalutamide compared with flutamide in combined androgen blockade for patients with advanced prostatic carcinoma: final results of multi-centre, double-blind, randomized trial. Br J Urol 80(Suppl 2):278–279
Klotz L, Schellhammer P, Carroll KA (2004) A re-assessment of the role of combined androgen blockade for advanced prostate cancer. BJU Int 93:1177–1182
Tunn U (2007) The current status of intermittent androgen deprivation (IAD) therapy for prostate cancer: putting IAD under the spotlight. BJU Int 99(Suppl 1):19–22
Klotz L, Akakura K, Gillatt D et al (2007) Advanced prostate cancer: hormones and beyond. Eur Urol Suppl 6(3):354–364
Dutkiewicz S (2004) Pilot attempt of advanced prostate cancer treatment T3NXMX-1 by intermittent more complete androgen blockade. Int Urol Nephrol 36:359–362
Miyamoto H, Messing EM, Chang C (2004) Androgen deprivation therapy for prostate cancer: current status and future prospects. Prostate 61(4):332–353
Spry NA, Kristjanson L, Hooton B et al (2006) Adverse effects to quality of life arising from treatment can recover with intermittent androgen suppression in men with prostate cancer. Eur J Cancer 42:1083–1092
Bae DC, Stein BS (2004) The diagnosis and treatment of osteoporosis in men on androgen deprivation therapy for advanced carcinoma of the prostate. J Urol 172(6 Pt 1):2137–2144
European Association of Urology (2009) Guidelines on prostate cancer. http://www.uroweb.org/nc/professionalresources/guidelines/online/
Bubley GJ (2001) Is the flare phenomenon clinically significant? Urology 58(2 Suppl 1):5–9
Zhu YS, Sun GH (2005) 5α-reductase isoenzyme in the prostate. J Med Sci 25:1–12
Redman MW, Tangen CM, Goodman PJ (2008) Finasteride does not increase the risk of high-grade prostate cancer: a—bias—adjusted modeling approach. Cancer Prev Res 1:174–181
Scholz MC, Strum SB, Jennrich RI et al (2006) Intermittent use of testosterone inactivating pharmaceuticals using finasteride prolongs the time off period. J Urol 175(5):1673–1678
Shaw G, Oliver RTD (2009) Intermittent hormone therapy and its place in the contemporary endocrine treatment of prostate cancer. Surg Oncol 18:275–282
Sato N, Akakura K, Jsaka S et al (2004) Intermittent androgen suppression for locally advanced and metastatic prostate cancer: preliminary report of a prospective multicenter study. Urology 64:341–345
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Dutkiewicz, S.A. Comparison of maximal and more maximal intermittent androgen blockade during 5-year treatment of advanced prostate cancer T3NxMx-1. Int Urol Nephrol 44, 487–492 (2012). https://doi.org/10.1007/s11255-011-0051-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11255-011-0051-6