...
首页> 外文期刊>Breast Cancer Research and Treatment >Effects of dose-intensive chemotherapy and radiotherapy on serum n-terminal proatrial natriuretic peptide in high-risk breast cancer patients
【24h】

Effects of dose-intensive chemotherapy and radiotherapy on serum n-terminal proatrial natriuretic peptide in high-risk breast cancer patients

机译:剂量密集化学疗法和放射疗法对高危乳腺癌患者血清n端原发性钠尿肽的影响

获取原文
获取原文并翻译 | 示例
           

摘要

By using N-terminal proatrial natriuretic peptide (proANP) in serum as a marker of cardiac function, we compared the cardiac side effects of two intensive adjuvant treatment regimens for breast cancer. Patients received either 9 cycles of FEC (5-fluorouracil, epirubicin and cyclophosphamide) where the doses of epirubicin and cyclophosphamide were escalated according to the leucocyte nadir (n=49, FEC-group) or three cycles of FEC followed by high-dose chemotherapy with alkylating agents (n=56, CTCb-group) given with the support of peripheral blood stem cells support. Both groups received adjuvant radiotherapy. Serial measurements of proANP were performed up to three years after treatment. Mean proANP values in the FEC-group was on average 19% higher than in the CTCb-group (p=0.002). The proANP levels showed a significant association with the cumulative dose of epirubicin (p<0.001) but not with cyclophosphamide (p=0.151) and 5-FU (p=0.160). The pharmacokinetics of epirubicin was studied at the first and third chemotherapy course. The proANP levels after treatment were significantly related to the AUC (p=0.034) and Cmax(p=0.037) of epirubicin. Left-sided chest irradiation was associated with on average 12% higher proANP values than right-sided (p=0.031). We conclude that dose-escalated FEC causes a stronger increase in proANP than 3 FEC followed by high-dose CTCb-treatment. Increase of proANP levels might represent an early sign of cardiotoxicity secondary to chemotherapy and radiation treatment. Long-time follow-up is necessary to determine the clinical significance of these findings.
机译:通过使用血清中的N末端原发性钠尿肽(proANP)作为心脏功能的标志物,我们比较了两种强化辅助治疗方案对乳腺癌的心脏副作用。患者接受9个周期的FEC(5-氟尿嘧啶,表柔比星和环磷酰胺),根据白细胞最低点(n = 49,FEC组)增加表柔比星和环磷酰胺的剂量,或三个周期的FEC,然后进行大剂量化疗用烷基化剂(n = 56,CTCb-基)在外周血干细胞支持下给予。两组均接受辅助放疗。治疗前长达三年对proANP进行连续测量。 FEC组的平均proANP值平均比CTCb组高19%(p = 0.002)。 proANP水平显示与表柔比星的累积剂量显着相关(p <0.001),但与环磷酰胺(p = 0.151)和5-FU(p = 0.160)无关。在第一和第三疗程中研究了表柔比星的药代动力学。治疗后proANP水平与表柔比星的AUC(p = 0.034)和Cmax (p = 0.037)显着相关。左侧胸部放疗的proANP值平均比右侧高12%(p = 0.031)。我们得出结论,与大剂量CTCb治疗相比,剂量递增的FEC引起的proANP升高比3个FEC强。 proANP水平升高可能代表继化学疗法和放射治疗后心脏毒性的早期迹象。长期随访对于确定这些发现的临床意义是必要的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号