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本文引用的文献

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Endocrine therapy plus zoledronic acid in premenopausal breast cancer.绝经前乳腺癌的内分泌治疗加唑来膦酸
N Engl J Med. 2009 Feb 12;360(7):679-91. doi: 10.1056/NEJMoa0806285.
2
Phase III randomized, placebo-controlled, double-blind trial of risedronate for the prevention of bone loss in premenopausal women undergoing chemotherapy for primary breast cancer.利塞膦酸盐预防原发性乳腺癌化疗绝经前女性骨质流失的III期随机、安慰剂对照、双盲试验。
J Clin Oncol. 2009 Mar 1;27(7):1047-53. doi: 10.1200/JCO.2008.19.1783. Epub 2008 Dec 15.
3
Adjuvant endocrine therapy plus zoledronic acid in premenopausal women with early-stage breast cancer: 5-year follow-up of the ABCSG-12 bone-mineral density substudy.绝经前早期乳腺癌患者辅助内分泌治疗联合唑来膦酸:ABCSG-12骨密度亚研究的5年随访
Lancet Oncol. 2008 Sep;9(9):840-9. doi: 10.1016/S1470-2045(08)70204-3. Epub 2008 Aug 19.
4
Zoledronic acid prevents bone loss in premenopausal women undergoing adjuvant chemotherapy for early-stage breast cancer.唑来膦酸可预防早期乳腺癌绝经前女性在接受辅助化疗时出现骨质流失。
J Clin Oncol. 2008 Oct 10;26(29):4739-45. doi: 10.1200/JCO.2008.16.4707. Epub 2008 Aug 18.
5
Zoledronic acid and clinical fractures and mortality after hip fracture.唑来膦酸与髋部骨折后的临床骨折及死亡率
N Engl J Med. 2007 Nov 1;357(18):1799-809. doi: 10.1056/NEJMoa074941. Epub 2007 Sep 17.
6
Bisphosphonate-associated osteonecrosis of the jaw: report of a task force of the American Society for Bone and Mineral Research.双膦酸盐相关颌骨骨坏死:美国骨与矿物质研究学会特别工作组报告
J Bone Miner Res. 2007 Oct;22(10):1479-91. doi: 10.1359/jbmr.0707onj.
7
Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis.每年一次唑来膦酸用于治疗绝经后骨质疏松症。
N Engl J Med. 2007 May 3;356(18):1809-22. doi: 10.1056/NEJMoa067312.
8
Clinical features of metastatic bone disease and risk of skeletal morbidity.转移性骨病的临床特征与骨骼并发症风险
Clin Cancer Res. 2006 Oct 15;12(20 Pt 2):6243s-6249s. doi: 10.1158/1078-0432.CCR-06-0931.
9
Comparison of weekly treatment of postmenopausal osteoporosis with alendronate versus risedronate over two years.阿仑膦酸钠与利塞膦酸钠治疗绝经后骨质疏松症两年的每周治疗方案比较。
J Clin Endocrinol Metab. 2006 Jul;91(7):2631-7. doi: 10.1210/jc.2005-2602. Epub 2006 Apr 24.
10
Comparison of a single infusion of zoledronic acid with risedronate for Paget's disease.唑来膦酸单次输注与利塞膦酸钠治疗佩吉特病的比较。
N Engl J Med. 2005 Sep 1;353(9):898-908. doi: 10.1056/NEJMoa044241.

唑来膦酸可预防绝经前接受辅助化疗的女性在停止治疗后 1 年内发生骨丢失。

Prevention of bone loss by zoledronic acid in premenopausal women undergoing adjuvant chemotherapy persist up to one year following discontinuing treatment.

机构信息

M.S., Columbia University, 161 Fort Washington Avenue, 10-1068, New York, New York 10032, USA.

出版信息

J Clin Endocrinol Metab. 2010 Feb;95(2):559-66. doi: 10.1210/jc.2009-1366. Epub 2009 Dec 18.

DOI:10.1210/jc.2009-1366
PMID:20022990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2840866/
Abstract

CONTEXT

Adjuvant chemotherapy is associated with significant reductions in bone mineral density (BMD) in premenopausal women with breast cancer (BC) that is prevented with zoledronic acid (ZA) every 3 months for 1 yr.

OBJECTIVE

The aim of the study was to examine the effect on BMD of discontinuing ZA during the subsequent year.

DESIGN

We conducted a randomized, double-blind trial.

PATIENTS

Premenopausal women (mean age, 42 yr) undergoing adjuvant chemotherapy for BC participated in the study.

INTERVENTION

ZA (4 mg iv every 3 months) vs. placebo was administered for 12 months.

OUTCOME MEASURES

We measured percentage change in BMD and bone turnover markers at 12 and 24 months (1 yr after last infusion).

RESULTS

Of 101 women randomized, 85 completed 12-month and 62 completed 24-month evaluations. In the placebo group, serum C-telopeptide (CTX) increased progressively over the first 12 months, returned toward baseline but remained significantly above baseline by 24 months. Lumbar spine BMD decreased from baseline by 5.5% at 12 and 6.3% at 24 months. Similarly, by 24 months, total hip and femoral neck BMD declined by 2.6 and 2.4%, respectively. In ZA patients, BMD remained stable (P < 0.0001 compared to placebo). Serum CTX declined significantly by 6 months, but returned to baseline by 12 months, remaining there at 24 months.

CONCLUSIONS

Premenopausal women receiving chemotherapy for BC sustained significant bone loss during the first year, without recovery during the second year. ZA effectively prevented bone loss during the first year of chemotherapy. BMD remained stable 1 yr after completion of ZA. Serum CTX increased significantly by 12 and 24 months. More frequent administration may be required to suppress bone resorption in this patient population.

摘要

背景

辅助化疗与乳腺癌(BC)绝经前妇女的骨密度(BMD)显著降低有关,而每 3 个月用唑来膦酸(ZA)治疗 1 年可预防这种情况。

目的

本研究旨在探讨在随后的 1 年内停止使用 ZA 对 BMD 的影响。

设计

我们进行了一项随机、双盲试验。

患者

接受 BC 辅助化疗的绝经前妇女(平均年龄 42 岁)参加了这项研究。

干预

ZA(4 毫克 iv 每 3 个月)与安慰剂治疗 12 个月。

观察指标

我们在 12 个月和 24 个月(最后一次输注后 1 年)时测量 BMD 和骨转换标志物的百分比变化。

结果

在 101 名随机分组的妇女中,85 名完成了 12 个月的评估,62 名完成了 24 个月的评估。在安慰剂组中,血清 C 端肽(CTX)在最初的 12 个月内逐渐增加,在 12 个月时恢复到基线水平,但仍明显高于基线水平。腰椎 BMD 在 12 个月时从基线下降 5.5%,在 24 个月时下降 6.3%。同样,到 24 个月时,全髋和股骨颈 BMD 分别下降 2.6%和 2.4%。在 ZA 患者中,BMD 保持稳定(与安慰剂相比,P < 0.0001)。血清 CTX 在 6 个月时显著下降,但在 12 个月时恢复到基线,在 24 个月时仍保持在那里。

结论

接受 BC 化疗的绝经前妇女在第一年期间持续发生显著的骨丢失,第二年没有恢复。ZA 在化疗的第一年有效地预防了骨丢失。ZA 完成后 1 年 BMD 保持稳定。血清 CTX 在 12 个月和 24 个月时显著增加。在该患者人群中,可能需要更频繁的给药来抑制骨吸收。