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本文引用的文献

1
Duration of first off-treatment interval is prognostic for time to castration resistance and death in men with biochemical relapse of prostate cancer treated on a prospective trial of intermittent androgen deprivation.在一项间歇性雄激素剥夺治疗前列腺癌生化复发的前瞻性试验中,首次治疗间隔时间的持续时间是预测去势抵抗和死亡时间的预后因素。
J Clin Oncol. 2010 Jun 1;28(16):2668-73. doi: 10.1200/JCO.2009.25.1330. Epub 2010 Apr 26.
2
The effect of androgen deprivation therapy on body composition in men with prostate cancer: systematic review and meta-analysis.雄激素剥夺疗法对前列腺癌男性患者身体成分的影响:系统评价和荟萃分析。
J Cancer Surviv. 2010 Jun;4(2):128-39. doi: 10.1007/s11764-009-0114-1. Epub 2010 Jan 21.
3
Denosumab in men receiving androgen-deprivation therapy for prostate cancer.地诺单抗用于接受雄激素剥夺治疗的前列腺癌男性患者。
N Engl J Med. 2009 Aug 20;361(8):745-55. doi: 10.1056/NEJMoa0809003. Epub 2009 Aug 11.
4
Alendronate decreases the fracture risk in patients with prostate cancer on androgen-deprivation therapy and with severe osteopenia or osteoporosis.阿伦膦酸盐可降低正在接受雄激素剥夺治疗且存在严重骨质疏松症或骨量减少的前列腺癌患者的骨折风险。
BJU Int. 2009 Dec;104(11):1637-40. doi: 10.1111/j.1464-410X.2009.08622.x. Epub 2009 Jun 22.
5
Long-term changes in bone mineral density and predicted fracture risk in patients receiving androgen-deprivation therapy for prostate cancer, with stratification of treatment based on presenting values.接受雄激素剥夺治疗的前列腺癌患者骨矿物质密度的长期变化及预测骨折风险,基于初始值进行治疗分层
BJU Int. 2009 Sep;104(6):800-5. doi: 10.1111/j.1464-410X.2009.08483.x. Epub 2009 Mar 11.
6
Complications of androgen deprivation therapy in prostate cancer.前列腺癌雄激素剥夺治疗的并发症
Curr Opin Urol. 2009 May;19(3):322-6. doi: 10.1097/MOU.0b013e32832a082c.
7
Long-term effects of intermittent androgen suppression on testosterone recovery and bone mineral density: results of a 33-month observational study.间歇性雄激素抑制对睾酮恢复和骨矿物质密度的长期影响:一项33个月观察性研究的结果
BJU Int. 2009 Sep;104(6):806-12. doi: 10.1111/j.1464-410X.2009.08458.x. Epub 2009 Mar 5.
8
Androgen deprivation therapy and risk for diabetes and cardiovascular disease in prostate cancer survivors.前列腺癌幸存者的雄激素剥夺治疗与糖尿病和心血管疾病风险
Curr Urol Rep. 2008 May;9(3):197-202. doi: 10.1007/s11934-008-0035-y.
9
Quality of life, morbidity, and mortality results of a prospective phase II study of intermittent androgen suppression for men with evidence of prostate-specific antigen relapse after radiation therapy for locally advanced prostate cancer.一项针对局部晚期前列腺癌放疗后前列腺特异性抗原复发证据的男性进行间歇性雄激素抑制的前瞻性II期研究的生活质量、发病率和死亡率结果
Clin Genitourin Cancer. 2008 Mar;6(1):46-52. doi: 10.3816/CGC.2008.n.008.
10
EAU guidelines on prostate cancer.欧洲泌尿外科学会前列腺癌指南。
Eur Urol. 2008 Jan;53(1):68-80. doi: 10.1016/j.eururo.2007.09.002. Epub 2007 Sep 19.

非转移性、激素敏感型前列腺癌男性接受间歇性雄激素剥夺治疗期间骨密度的长期变化。

Long-term dynamics of bone mineral density during intermittent androgen deprivation for men with nonmetastatic, hormone-sensitive prostate cancer.

机构信息

University of Washington/Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

出版信息

J Clin Oncol. 2012 May 20;30(15):1864-70. doi: 10.1200/JCO.2011.38.3745. Epub 2012 Apr 9.

DOI:10.1200/JCO.2011.38.3745
PMID:22493411
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3383183/
Abstract

PURPOSE

To investigate changes in bone mineral density (BMD) and fracture risk in men who received intermittent androgen deprivation (IAD) for nonmetastatic, hormone-sensitive prostate cancer.

PATIENTS AND METHODS

Men with prostate cancer who lacked radiographically detectable metastases were treated in a prospective trial of IAD. After 9 months of treatment with leuprolide and flutamide, androgen deprivation therapy (ADT) was stopped until prostate-specific antigen reached a threshold (1 ng/mL for radical prostatectomy; 4 ng/mL for radiation or primary ADT) for a new cycle. Dual-energy x-ray absorptiometry (DXA) scans were performed before starting ADT and subsequently with each change in therapy. At least two consecutive DXA scans were required for this analysis. Computed tomography, bone scintigraphy, and lumbar spine x-rays were performed at the beginning and end of each treatment period.

RESULTS

Fifty-six of 100 patients met criteria for this analysis. The median age at study entry was 64.5 years (range, 49.8 to 80.9 years). The average percentage change in BMD during the first on-treatment period was -3.4% (P < .001) for the spine and -1.2% (P = .001) for the left hip. During the first off-treatment period (median, 37.4 weeks; range, 13.4 weeks to 8.7+ years), BMD recovery at the spine was significant, with an average percentage change of +1.4% (P = .002). Subsequent periods had heterogeneous changes of BMD without significant average changes. After a median of 5.5 years (range, 1.1 to 13.8+) years on trial, one patient (1.8%) had a compression fracture associated with trauma.

CONCLUSION

Patients experienced the greatest average change in BMD during early treatment periods of IAD with a smaller average change thereafter. Fractures were rare.

摘要

目的

研究非转移性、激素敏感型前列腺癌患者接受间歇性雄激素剥夺(IAD)治疗后骨密度(BMD)变化和骨折风险。

方法

在一项关于 IAD 的前瞻性试验中,对缺乏影像学转移性病变的前列腺癌患者进行治疗。在接受亮丙瑞林和氟他胺治疗 9 个月后,当前列腺特异抗原(PSA)达到新周期的阈值(根治性前列腺切除术为 1ng/ml;放疗或初始 ADT 为 4ng/ml)时,停止雄激素剥夺治疗(ADT)。在开始 ADT 前以及随后每次治疗改变时进行双能 X 线吸收法(DXA)扫描。对于这项分析,至少需要两次连续的 DXA 扫描。在每个治疗期开始和结束时进行计算机断层扫描、骨扫描和腰椎 X 光检查。

结果

100 例患者中有 56 例符合这项分析的标准。研究入组时的中位年龄为 64.5 岁(范围,49.8 岁至 80.9 岁)。第一个治疗期内 BMD 的平均百分比变化为脊柱-3.4%(P<0.001),左侧髋部-1.2%(P=0.001)。在第一个停药期(中位数为 37.4 周;范围为 13.4 周至 8.7+年),脊柱的 BMD 恢复显著,平均百分比变化为+1.4%(P=0.002)。随后的时期 BMD 变化混杂,无显著平均变化。在试验中位时间 5.5 年(范围为 1.1 年至 13.8+年)后,1 例患者(1.8%)因外伤发生压缩性骨折。

结论

患者在 IAD 的早期治疗期间经历了最大的平均 BMD 变化,此后的平均变化较小。骨折罕见。