期刊文献+

唑来膦酸钠预防来曲唑所致绝经后乳腺癌患者骨量丢失的临床观察 被引量:3

Effects of zoledronic acid on bone metabollsm in postmenopausal breat cancer patients
下载PDF
导出
摘要 目的:通过观察唑来膦酸钠对来曲唑所致绝经后乳腺癌患者骨量丢失的临床疗效,探讨唑来膦酸钠对乳腺癌患者的骨保护作用。方法:60例绝经后乳腺癌患者均采取手术治疗,且术后常规行6个疗程的化疗,无骨转移病例。对照组:30例化疗后继续服用来曲唑2.5 mg/d;治疗组:30例患者化疗后服用来曲唑2.5 mg/d+静滴唑来膦酸钠4 mg,每3个月为1个疗程,共12个月。在治疗前后分别测定两组患者骨密度(BMD)、血钙(Ca)、血磷(P)、Ⅰ型胶原羧基末端肽(β-Crosslaps)及血清骨钙素(OPG),对两组患者治疗前后各项指标进行分析比较。结果:治疗12个月后,治疗组腰椎和股骨颈的骨密度、血清OPG均较治疗前增加,β-Crosslaps较前降低,差异有统计学意义(P<0.05),两组血钙、血磷与治疗前比较,差异无统计学意义(P>0.05)。结论:唑来膦酸钠对应用来曲唑辅助治疗的乳腺癌患者有很好的骨保护作用。 Objective To investigate the effects of zoledronic acid on bone metabollsm in postmenopausal breat cancer patients. Method 60 patients with postmenopausal breat cancer received conventional chemotherapy for six cycles. They were divided into treatment group and control group randomly. Control group: 30 patients after chemotherapy continued taking Letrozole 2. 5mg/d. Treatment group: In addition to taking Letrozole 2. 5 mg/d,30 cases after chemotherapy used zoledronic 4mg injecdon,every 3 months for a course. The bone mineral density( BMD),blood calcium and phosphorus,Crossl procollagen type Ⅰ carboxytermina( β-Crosslaps),serum osteoprotegerin. were detected at starting point and after 12 months treatment. Results After 12 months treatment,the lumbar spine and femoral neck BMD,serum osteoprotegerin of two groups increased than before,The treatment group was higher than that of control group. β-Crosslaps were delined in treatment group( P 〈 0. 05). There was no significant difference between two groups in blood calcium and phosphorus( P 〉 0. 05). Conclusion Zoledronic acid has good bone protection in patients with breat cancer who are treated with letrozole.
出处 《吉林医学》 CAS 2017年第9期1674-1676,共3页 Jilin Medical Journal
关键词 唑来膦酸钠 来曲唑 乳腺癌 骨密度 Zoledronic Letrozole Breat cancer Bone mineral density
  • 相关文献

参考文献1

二级参考文献20

  • 1Shibuya K,Mathers CD,Boschi-Pinto C,et al.Global and regional estimates of cancer mortality and incidence by site:II.Results for the global burden of disease[J].BMC Cancer,2002,2:37.
  • 2Goldhirsch A,Glick JH,Gelber RD,et al.Meeting highlights:International consensus panel of the treatment of primary breast cancer:7th international conference on adjuvant therapy of primary breast cancer[J].J Clin Oncol,2001,19(18):3817-3827.
  • 3Green JR,Muller K,Jaeggi KA,et al.Precijnical pharmacology of CGP42′446,a new,potent,heterocyclic bisphosphonate compound[J].J Bone Miner Res,1994,9(5):745-751.
  • 4Pataki A,Muller K,Green JR,et al.Effects of short-term treatment with the bisphosphonates zoledronate and pamidronate on rat bone:a comparative histomorphometric study on the cancellous bone formed before,during and after treatment[J].Anat Rec,1997,249(4):458-468.
  • 5Oades GM,Senaratne SG,Clarke IA,et al.Nitrogen containing bisphosphonates induce apoptosis and inhibit the mevalonate pathway,impairing Ras membrane localization in prostate cancer cells[J].J Urol,2003,170(1):246-252.
  • 6Van der Pluijm G,Vloedgraven H,van Beek E,et al.Bisphosphonates inhibit adhesion of breast cancer cells to bone matrices in vitro[J].J Clin Invest,1996,98(3):698-701.
  • 7Jagdev S,Coleman RE,Shipman CM,et al.The bisphosphonate zoledronic acid induces apoptosis of breast cancer cells:evidence for synergy with paclitaxel[J].Br J Can-cer,2001,84(8):1126-1134.
  • 8Gnant M,Mlineritsch B,Schippinger W,et al.Endocrine therapy plus zoledronic acid in premenopausal breast cancer[J].N Engl J Med,2009,360:579-591.
  • 9Burkinshaw R,Thorpe H,Pollard S,et al.The AZURE trial-does adjuvant zoledronic acid reduce recurrence in patients with high-risk localized breast cancer[J].Bone,2006,38:70-71.
  • 10Mystakidou K,Katsouda E.Randomized,open label,prospective study on the effect of zoledronic acid on the prevention of bone metastases in patients with recurrent solid tumors that did not present with bone metastases at baseline[J].Med Oncol,2005,22(2):195-201.

同被引文献60

引证文献3

二级引证文献24

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部