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日本前列腺癌患者骨密度与雄激素剥夺治疗的关系。

Relationship between bone mineral density and androgen-deprivation therapy in Japanese prostate cancer patients.

机构信息

Department of Medical Oncology and Genitourinary Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.

出版信息

Urology. 2010 May;75(5):1131-7. doi: 10.1016/j.urology.2009.10.075. Epub 2010 Feb 16.

Abstract

OBJECTIVES

To examine Japanese patients who had received androgen-deprivation therapy (ADT) for longer periods, as it is known that ADT of patients with prostate cancer reduces their bone mineral density (BMD). However, our previous cross-sectional study revealed that short-term ADT (average, 23.5 months) does not significantly increase the prevalence of osteoporosis in Japanese patients.

METHODS

The subjects consisted of 201 native Japanese patients with prostate cancer. They comprised 113 ADT-treated and 88 hormone-naive patients. Lumbar spine, total hip, and femoral neck BMDs were measured by dual-energy x-ray absorptiometry and expressed in standard deviation units relative to the scores of young adult men (T-score) or age-matched men (Z-score). Serum levels of bone metabolism markers were also measured.

RESULTS

The ADT-treated patients had significantly lower BMD values, T-scores, and even Z-scores than the hormone-naive patients (P <.001). For patients who were hormone-naive, ADT-treated for less than 2 years, and ADT-treated for more than 2 years, the osteoporosis prevalence was 4.5% (4/88), 12.1% (4/33), and 10.8% (4/37), respectively. The ADT-treated patients had significantly higher serum amino-terminal telopeptide levels than the hormone-naive patients (P = .014), but significantly lower serum carboxy-terminal telopeptide of type-I collagen levels than the ADT-treated patients with bone metastasis (P <.001).

CONCLUSIONS

Our cross-sectional study confirmed that both ADT-treated and hormone-naive Japanese patients with prostate cancer have low rates of osteoporosis. These findings are different from those of studies in western countries. Genetic and hormonal or other environmental factors may result in population differences in the characteristics of prostate cancer and BMD.

摘要

目的

研究接受雄激素剥夺疗法(ADT)时间较长的日本患者,因为已知前列腺癌患者的 ADT 会降低其骨密度(BMD)。然而,我们之前的横断面研究显示,短期 ADT(平均 23.5 个月)不会显著增加日本患者骨质疏松症的患病率。

方法

研究对象包括 201 名日本原发性前列腺癌患者。他们包括 113 名接受 ADT 治疗的患者和 88 名激素未治疗的患者。通过双能 X 射线吸收法测量腰椎、全髋关节和股骨颈 BMD,并以年轻成年男性(T 评分)或年龄匹配男性(Z 评分)的分数表示相对标准偏差单位。还测量了血清骨代谢标志物的水平。

结果

ADT 治疗组患者的 BMD 值、T 评分甚至 Z 评分均显著低于激素未治疗组(P<.001)。对于激素未治疗、ADT 治疗时间少于 2 年和 ADT 治疗时间超过 2 年的患者,骨质疏松症的患病率分别为 4.5%(4/88)、12.1%(4/33)和 10.8%(4/37)。ADT 治疗组患者的血清氨基末端肽水平明显高于激素未治疗组(P=0.014),但血清 I 型胶原羧基末端肽水平明显低于 ADT 治疗伴骨转移的患者(P<.001)。

结论

我们的横断面研究证实,接受 ADT 治疗和激素未治疗的日本前列腺癌患者均有较低的骨质疏松症发生率。这些发现与西方国家的研究结果不同。遗传和激素或其他环境因素可能导致人群在前列腺癌和 BMD 特征上存在差异。

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