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Clinical Trial
. 2014 Apr 10;32(11):1143-50.
doi: 10.1200/JCO.2013.51.6500. Epub 2014 Mar 3.

Randomized controlled trial of early zoledronic acid in men with castration-sensitive prostate cancer and bone metastases: results of CALGB 90202 (alliance)

Affiliations
Clinical Trial

Randomized controlled trial of early zoledronic acid in men with castration-sensitive prostate cancer and bone metastases: results of CALGB 90202 (alliance)

Matthew R Smith et al. J Clin Oncol. .

Abstract

Purpose: Zoledronic acid decreases the risk for skeletal-related events (SREs) in men with castration-resistant prostate cancer and bone metastases but its role earlier in the natural history of the disease is unknown. This phase III study evaluated the efficacy and safety of earlier treatment with zoledronic acid in men with castration-sensitive metastatic prostate cancer.

Patients and methods: Men with castration-sensitive prostate cancer and bone metastases whose androgen-deprivation therapy was initiated within 6 months of study entry were randomly assigned in a blinded 1:1 ratio to receive zoledronic acid (4 mg intravenously every 4 weeks) or a placebo. After their disease progressed to castration-resistant status, all patients received open-label treatment with zoledronic acid. The primary end point was time to first SRE, defined as radiation to bone, clinical fracture, spinal cord compression, surgery to bone, or death as a result of prostate cancer. Target accrual was 680 patients. Primary analysis was planned after 470 SREs. The study was discontinued prematurely (645 patients; 299 SREs) after the corporate supporter withdrew study drug supply.

Results: Early zoledronic acid was not associated with increased time to first SRE. The median time to first SRE was 31.9 months in the zoledronic acid group (95% CI, 24.2 to 40.3) and 29.8 months in the placebo group (95% CI, 25.3 to 37.2; hazard ratio, 0.97; 95% CI, 0 to 1.17; one-sided stratified log-rank P = .39). Overall survival was similar between the groups (hazard ratio, 0.88; 95% CI, 0.70 to 1.12; P = .29). Rates of adverse events were similar between the groups.

Conclusion: In men with castration-sensitive prostate cancer and bone metastases, early treatment with zoledronic acid was not associated with lower risk for SREs.

Trial registration: ClinicalTrials.gov NCT00079001.

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Conflict of interest statement

Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article.

Figures

Fig 1.
Fig 1.
CONSORT diagram. SRE, skeletal-related events.
Fig 2.
Fig 2.
(A) Kaplan-Meier plot for skeletal-related events (SRE) –free survival by treatment arm. (B) Kaplan-Meier plot for progression-free survival by treatment arm. (C) Kaplan-Meier plot for overall survival by treatment arm. ZA, zoledronic acid.
Fig 3.
Fig 3.
Forest plot of skeletal-related events (SRE) in select subgroups. (*) One-sided test. Alk Phos, alkaline phosphatase; HR, hazard ratio; NR, not reached; PS, performance status; ULN, upper limit of normal; ZA, zoledronic acid.

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