Elsevier

Urology

Volume 70, Issue 1, July 2007, Pages 122-126
Urology

Adult urology
Lifestyle Factors and Duration of Androgen Deprivation Affect Bone Mineral Density of Patients with Prostate Cancer During First Year of Therapy

https://doi.org/10.1016/j.urology.2007.03.026Get rights and content

Objectives

Androgen deprivation therapy (ADT) is associated with loss of bone mineral density (BMD) and increased fracture risk. We sought to examine the impact of ADT and lifestyle variables on BMD in 120 patients with prostate cancer without bone metastases entering a randomized clinical trial.

Methods

A total of 120 patients with prostate cancer and without bone metastases who had been treated with ADT for less than 12 months were enrolled in a clinical trial of zoledronic acid versus placebo. BMD measurements of the femoral neck, total hip, and lumbar spine were obtained before starting the study treatment by dual energy x-ray absorptiometry. The subjects answered a questionnaire regarding possible osteoporosis risk factors, including dairy product use, caffeinated beverage use, smoking history, alcohol intake, calcium/vitamin D supplementation, thyroid medication, and exercise.

Results

The median duration of ADT was 3 months (range 0 to 12). Osteopenia or osteoporosis (T score of less than −1) was detected in two thirds of the subjects at one or more measured sites. The mean baseline BMD Z scores were femoral neck −0.091 ± 0.959, total hip 0.122 ± 1.005, and lumbar spine 0.657 ± 1.789. On multiple linear regression analysis, the duration of ADT was negatively associated with the Z score at all three sites and the body mass index, calcium/vitamin D supplementation, and alcohol use were positively associated with the Z score.

Conclusions

BMD loss is a function of the duration of ADT during the first year of therapy. The body mass index, calcium/vitamin D supplementation, and alcohol use were associated with greater BMD, even after controlling for ADT exposure.

Section snippets

Material and Methods

The US05 study was a randomized, placebo-controlled study of zoledronic acid versus placebo in patients with prostate cancer without bone metastases within the first 12 months of ADT.13 Men older than 18 years of age with a histologic diagnosis of prostate cancer, no evidence of metastases on bone scan, and a life expectancy of at least 12 months were eligible. The subjects must have received ADT for 12 months or less before enrollment or were to initiate ADT within 7 days after study

Results

A total of 120 men with prostate cancer and without bone metastases were enrolled. The demographic and clinical characteristics of these men are shown in Table 1. The mean age was 71.6 years, 78% were white, 73% had Stage T1-T2 disease, and 57% had a Gleason score of 5 to 7. The median duration of ADT was 3 months (range 0 to 12); 69% had received ADT for less than 6 months (including 17.5% who were ADT naive) and 31% had received ADT for 6 to 12 months. ADT was administered by luteinizing

Comment

In this cross-sectional analysis of patients with prostate cancer, we found that the duration of ADT was significantly associated with the baseline Z scores. The relationship between the Z score and exposure to ADT was in quadratic form, suggesting that BMD may rapidly decrease in the first 6 months after the initiation of ADT, followed by some recovery. Admittedly, this observation could have been due to random fluctuation, because only 31% of the subjects had received ADT for more than 6

Conclusions

The results of our study have shown that low BMD is highly prevalent in patients with prostate cancer without bone metastases during the first year of ADT. Although advanced age was likely a major factor influencing this finding, other treatment and lifestyle factors influenced BMD in our patients with prostate cancer. The duration of ADT was associated with lower BMD, especially during the initial months of treatment. Other lifestyle factors influenced bone density and should be considered in

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    This study was funded by Novartis Oncology, East Hanover, New Jersey.

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    C.W. Ryan is a paid consultant to, and study investigator partially funded by, the sponsor.

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    D. Huo and J.W. Stallings are study investigators partially funded by the sponsor.

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