期刊文献+

近距离放疗联合比卡鲁胺150mg在前列腺癌治疗中的应用 被引量:6

Application of brachytherapy combined with bicalutamide 150 mg monotherapy for the treatment of prostate cancer
下载PDF
导出
摘要 目的探讨近距离放疗联合比卡鲁胺150mg单药治疗前列腺癌的可行性。方法将符合入选标准的71例前列腺癌患者按随机数字表分为单药组(34例)和联合药物组(37例)。接受近距离放疗后,单药组采用比卡鲁胺150mg单药内分泌治疗;联合药物组接受戈舍瑞林3.6mg+比卡鲁胺50mg内分泌治疗。分别观察治疗前后的前列腺特异抗原(PSA)变化情况,第一阶段用药时间,严密记录治疗过程中的不良事件,并进行安全性评价。结果单药组有2例、联合药物组有1例在治疗1年后血清PSA不能下降到术前的50%予以剔除。2组患者在接受近距离放疗联合药物治疗1个月后,PSA值均出现了“断崖式”的下降。在随后的治疗中,联合药物组和单药组不良反应发生率差异无统计学意义[(41.7%(15/36)比31.3%(10/32),P=0.37]。PSA抑制率二者差异有统计学意义[(96±24)%比(98±24)%,P〈0.01),但对于低危患者,二者差异无统计学意义[(98±24)%比(100±25)%,P〉0.05)。联合药物组用药时间短于单药组[(8.1±2.0)个月比(9.5±2.5)个月,P〈0.01],但对于低危患者,二者之间差异无统计学意义(P〉0.05)。结论前列腺癌的近距离放疗联合戈舍瑞林3.6mg+比卡鲁胺50mg双药内分泌治疗效果较好,而对于低危患者,采用比卡鲁胺150mg单药联合近距离放疗的方案,亦能达到同样效果。 Objective To assess the feasibility of brachytherapy combined with bicalntamide 150 mg mono- therapy for the treatment of prostate cancer. Methods All 71 patients who met the inclusion criteria participated in a randomized controlled study. 68 patients with prostate cancer were randomly divided into two groups after brachy- therapy. 32 cases were treated with bicalntamide 150 mg monotherapy; other 36 patients received goserelin 3.6 mg combined with bicalutamide 50 mg. Prostate specific antigen (PSA) changes were observed before and after treat- ment and during the first stage of treatment; adverse events were recorded and security was evaluated. Chi-square test and t-test were used for statistical analysis. Results Demographic characteristics and baseline data of the 2 groups of patients were similar. After one month of brachytherapy combined with drug treatment, PSA values showed a "cliff-style" decline; during the subsequent treatment, the incidence of side effects was similiar (41.7% vs 31.3%, P =0.37) while PSA changes showed statistically significant difference [ (96 ~24)% vs (98 ±24)%, P = 0. 009 ], but for low-risk patients, there was no difference [ (98 ± 24) % vs ( 100 ± 25) %, P 〉 0.05 ]. Con- clusion For prostate cancer patients, brachytherapy combined with hormonal therapy, goserelin 3.6 mg + bicalu- tamide 50 mg are recommended for low-risk cases; brachytherapy with bicalutamide 150 mg monotherapy can also a- chieve the same effect.
出处 《中国医药》 2013年第7期966-968,共3页 China Medicine
关键词 前列腺肿瘤 近距离放疗 内分泌治疗 比卡鲁胺 戈舍瑞林 Prostate cancer Brachytherapy Endocrine therapy Bicalutamide Goserelin
  • 相关文献

参考文献14

二级参考文献87

共引文献30

同被引文献72

  • 1王加强,王孟春,孙文涛.康士得治疗晚期前列腺癌的临床观察[J].中国老年学杂志,2005,25(8):972-973. 被引量:1
  • 2叶定伟.前列腺癌的流行病学和中国的发病趋势[J].中华外科杂志,2006,44(6):362-364. 被引量:168
  • 3朱华,邹峥.非甾体抗炎药临床作用及副作用研究新进展[J].江西医药,2007,42(3):268-271. 被引量:22
  • 4Parray A,Siddique HR,Nanda S,et al.Castration-resistant prostate cancer:potential targets and therapies[J].Biologics,2012,6:267-276.
  • 5Higgins GS,Mc Laren DB,Kerr GR,et al.Outcome analysis of 300prostate cancer patients treated with neoadjuvant androgen deprication and hypofractionated radiotherapy[J].Int J Radiat Oncol Biol Phys,2006,65(4):982-989.
  • 6Barqawi AB,Moul JW,Ziada A,et al.Combination of low-dose flutamide and finasteride for PSA-only recurrent prostate cancer after primary therapy[J].Urology,2003,62(5):872-876.
  • 7Klotz L,Schellhammer P,Carroll K.A re-assessment of the role of combined androgen blockade for advanced prostate cancer[J].BJU Int,2004,93:1177-1182.
  • 8VondálováBlanárováO,JelínkováI,Szor A,et al.Cisplatin and a potent platinum(Ⅳ)complex-mediated enhancement of TRAILinduced cancer cells killing is associated with modulation of upstream events in the extrinsic apoptotic pathway[J].Carcinogenesis,2011,32(1):42-51.
  • 9Petrylak DP,Tangen CM,Hussain MH,et al.Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer[J].N Engl J Med,2004,351(15):1513-1520.
  • 10Koreckij T,Nguyen H,Brown LG,et al.Dasatinib inhibits the growth of prostate cancer in bone and provides additional protection from osteolysis[J].Br J Cancer,2009,101(2):263-268.

引证文献6

二级引证文献13

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