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. 2000;1999(2):CD001526.
doi: 10.1002/14651858.CD001526.

Maximal androgen blockade for advanced prostate cancer

Affiliations

Maximal androgen blockade for advanced prostate cancer

B Schmitt et al. Cochrane Database Syst Rev. 2000.

Abstract

Objectives: This systematic review assessed the effect of maximal androgen blockade (MAB) on survival when compared to castration (medical or surgical) alone for patients with advanced prostate cancer.

Search strategy: Randomized controlled trials were searched in general and specialized databases (MEDLINE, EMBASE, Cancerlit, Cochrane Library, VA Cochrane Prostate Disease register) and by reviewing bibliographies.

Selection criteria: All published randomized trials were eligible for inclusion provided they (1) randomized men with advanced prostate cancer to receive a non-steroidal anti-androgen (NSAA) medication in addition to castration (medical or surgical) or to castration alone, and (2) reported overall survival, progression-free survival, cancer-specific survival, and/or adverse events. Eligibility was assessed by two independent reviewers.

Data collection and analysis: Information on patients, interventions, and outcomes were extracted by two independent reviewers using a standardized form. The main outcome measure for comparing effectiveness was overall survival at 1, 2, and 5 years. Secondary outcome measures included progression-free survival and cancer-specific survival. The relationship of specific NSAA on outcome was evaluated. Additionally, the incidence of adverse effects was measured.

Main results: Twenty trials enrolling 6,320 patients were included. The pooled OR for overall survival was 1.03 (95% CI:0.85 to 1.25), 1.16 (95% CI:1.00 to 1.33), and 1.29 (95% CI:1.11 to 1.50) at 1, 2, and 5 years respectively. Overall survival was only significant at 5 years. The risk difference at 5 years was 0.048 (95% CI:0.02 to 0.077) and NNT at 5 years 20.8. Progression-free survival was improved only at 1 year follow-up (OR=1.38) and cancer-free survival was improved only at 5 years (OR=1.22). Adverse events occurred more frequently in those assigned to MAB and resulted in withdrawal in 10%. Quality of life was measured in only one study favored orchiectomy alone (less diarrhea and better emotional functioning in the first 6 months).

Reviewer's conclusions: MAB produces a modest overall and cancer-specific survival at 5 years but is associated with increased adverse events and reduced quality of life.

PubMed Disclaimer

Conflict of interest statement

B Schmitt has co‐authored a draft manuscript with the Blue Cross/Blue Shield Technology Evaluation Center project on hormonal therapies for prostate cancer.

CL Bennett is (1) on the speaker's bureau for Schering‐Plough and ALZA; (2) has received unrestricted grant support from Schering‐Plough, AstraZeneca, and Cell Pathways; and (3) was a consultant to the Blue Cross/Blue Shield Technology Evaluation Center project on hormonal therapies for prostate cancer.

TJ Wilt was a consultant to the Blue Cross/Blue Shield Technology Evaluation Center project on hormonal therapies for prostate cancer.

Figures

1.1
1.1. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 1 Overall survival: 1 yr.
1.2
1.2. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 2 Overall survival: 2 yr.
1.3
1.3. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 3 Overall survival: 5 yr.
1.4
1.4. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 4 Overall survival (high quality): 1 yr.
1.5
1.5. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 5 Overall survival (high quality): 2 yr.
1.6
1.6. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 6 Overall survival (high quality): 5 yr.
1.7
1.7. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 7 Overall survival [> 90% M1 disease]: 1 yr.
1.8
1.8. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 8 Overall survival [> 90% M1 disease]: 2 yr.
1.9
1.9. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 9 Overall survival [> 90% M1 disease]: 5 yr.
1.10
1.10. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 10 Overall survival (by NSAA): 1 yr.
1.11
1.11. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 11 Overall survival (by NSAA): 2 yr.
1.12
1.12. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 12 Overall survival (by NSAA): 5 yr.
1.13
1.13. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 13 Overall survival (NSAA + orch): 1 yr.
1.14
1.14. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 14 Overall survival (NSAA + orch): 2 yr.
1.15
1.15. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 15 Overall survival (NSAA + orch): 5 yr.
1.16
1.16. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 16 Overall survival (flutamide): 1 yr.
1.17
1.17. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 17 Overall survival (flutamide): 2 yr.
1.18
1.18. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 18 Overall survival (flutamide): 5 yr.
1.19
1.19. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 19 Progression‐free survival: 1 yr.
1.20
1.20. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 20 Progression‐free survival: 2 yr.
1.21
1.21. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 21 Progression‐free survival: 5 yr.
1.22
1.22. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 22 Progression‐free survival (by NSAA): 1 yr.
1.23
1.23. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 23 Progression‐free survival (by NSAA): 2 yr.
1.24
1.24. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 24 Progression‐free survival (by NSAA): 5 yr.
1.25
1.25. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 25 Cancer‐specific survival: 1 yr.
1.26
1.26. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 26 Cancer‐specific survival: 2 yr.
1.27
1.27. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 27 Cancer‐specific survival: 5 yr.
1.28
1.28. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 28 Cancer‐specific survival (by NSAA): 1 yr.
1.29
1.29. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 29 Cancer‐specific survival (by NSAA): 2 yr.
1.30
1.30. Analysis
Comparison 1 Maximal androgen blockade versus monotherapy, Outcome 30 Cancer‐specific survival (by NSAA): 5 yr.
2.1
2.1. Analysis
Comparison 2 Combined Androgen Blockade with Flutamide, Outcome 1 Survival 1 year.
2.2
2.2. Analysis
Comparison 2 Combined Androgen Blockade with Flutamide, Outcome 2 Survival: 2 year.
2.3
2.3. Analysis
Comparison 2 Combined Androgen Blockade with Flutamide, Outcome 3 Survival: 5 year.
3.1
3.1. Analysis
Comparison 3 Combined Androgen Blockade with Nilutamide, Outcome 1 Survival: 1 year.
3.2
3.2. Analysis
Comparison 3 Combined Androgen Blockade with Nilutamide, Outcome 2 Survival: 2 year.
3.3
3.3. Analysis
Comparison 3 Combined Androgen Blockade with Nilutamide, Outcome 3 Survival: 5 year.

References

References to studies included in this review

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Eisenberger 1997 {published and unpublished data}
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Iversen 1990 {published data only}
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References to studies excluded from this review

de Voogt 1990 {published data only}
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Additional references

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References to other published versions of this review

Aronson 1999
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