M.S., Columbia University, 161 Fort Washington Avenue, 10-1068, New York, New York 10032, USA.
J Clin Endocrinol Metab. 2010 Feb;95(2):559-66. doi: 10.1210/jc.2009-1366. Epub 2009 Dec 18.
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.
The aim of the study was to examine the effect on BMD of discontinuing ZA during the subsequent year.
We conducted a randomized, double-blind trial.
Premenopausal women (mean age, 42 yr) undergoing adjuvant chemotherapy for BC participated in the study.
ZA (4 mg iv every 3 months) vs. placebo was administered for 12 months.
We measured percentage change in BMD and bone turnover markers at 12 and 24 months (1 yr after last infusion).
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.
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.
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。
本研究旨在探讨在随后的 1 年内停止使用 ZA 对 BMD 的影响。
我们进行了一项随机、双盲试验。
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。
ZA(4 毫克 iv 每 3 个月)与安慰剂治疗 12 个月。
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。
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。
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。