摘要
目的:观察氯化锶(89Sr Cl2)联合唑来膦酸治疗前列腺癌骨转移的临床效果与安全性。方法:选择183例前列腺癌骨转移伴骨痛病例,随机分为89Sr Cl2联合唑来膦酸组(A组,68例)、89Sr Cl2联合锝-99-亚甲基二膦酸盐(99Tc-MDP)组(B组,64例)及99Tc-MDP组(C组,51例),观察各组缓解骨痛、骨转移、生活质量改善和不良反应情况。结果:治疗后A组骨痛缓解有效率(88.23%)高于B组(75.00%,P=0.049)和C组(68.63%,P=0.008);A组骨转移减少率为48.53%,高于C组(29.41%,P=0.035);A组生活质量改善率为61.76%,高于C组(41.18%,P=0.004);B组和C组的骨痛缓解有效率、骨转移减少率、生活质量比较,差异均无统计学意义;3组不良反应比较,差异无统计学意义。结论:89Sr Cl2联合唑来膦酸治疗前列腺癌骨转移在骨痛缓解、骨转移减少及生活质量改善等方面均优于89Sr Cl2,较89Sr Cl2联合99Tc-MDP治疗方式简捷,安全性良好,值得临床推广。
Objective:To observe the clinical efficacy and safety of 89 SrCl2 combined with zoledronic in treatment of prostate cancer with bone metastasis. Methods: One hundred and eighty-three cases of prostate cancer with bone metastasis were randomly divided into 3 groups:89SrCl2 combined with zoledronic acid group (group A ,68 cases), 89SrCl2 combined with99Tc-MDP group (group B,64 cases) and 89SrCl2 alone group (group C,51 cases). The oc- currence of bone pain,bone metastasis, quality of life improvement and adverse reactions of the 3 groups were ob- served. Results:After treatment, the remission rate of bone pain in group A (88.23%) was higher than that in group B (75.00% ,P =0.049) and group C (68.63% ,P = 0.008). The reduction rate of bone metastasis in group A was 48.53% ,significantly higher than that in group C (29.41%, P =0.035) ;the quality of life improved rate in group A was 61.76% ,significantly higher than that in group C (41.18%, P = 0. 004) ;there were no statistically significantdifferences for the remission rate of bone pain, rate of decrease of bone metastasis, and quality of life improvement between the group B and group C and there was no significant difference in the adverse reactions in the 3 groups. Conclusion:89srCl2 combined with zoledronic acid therapy can relieve bone pain and bone metastasis, and improve quality of life without additional adverse reactions ,and it's worth clinical promotion.
出处
《东南大学学报(医学版)》
CAS
北大核心
2017年第1期82-85,共4页
Journal of Southeast University(Medical Science Edition)
关键词
氯化锶
唑来膦酸
锝-99-亚甲基二膦酸盐
前列腺癌
骨转移
strontium chloride
zoledronic acid
technetium-99- methylenediphosphonate
prostate cancer
bone metastasis