期刊文献+

曲妥珠单抗辅助或新辅助治疗HER2阳性转移性乳腺癌的临床结果 被引量:4

Clinical Outcome of HER2-positive Metastatic Breast Cancer Managed with Adjuvant or Neoadjuvant Trastuzumab
原文传递
导出
摘要 目的:比较人表皮生长因子受体2过表达(HER2+)的患者既往接受以曲妥珠单抗为基础辅助或新辅助治疗后再次接受针曲妥珠单抗治疗的临床结果。方法:共247例(I-III期170例,IV期77例)HER2+转移性乳腺癌患者,其中首次接受曲妥珠单抗治疗患者211例(I-III期134例,IV期77例),再次接受曲妥珠单抗治疗患者36例(I-III期)。使用Cox比例风险回归和logistic回归分析首次或提前接受曲妥珠单抗治疗的患者的预后的临床结果,生存评估使用Kaplan-Meier法。结果:I-III期HER2+转移性乳腺癌患者中,未预先接受曲妥珠单抗治疗组的中位总生存期为36个月和预先接受曲妥珠单抗治疗组为28个月(危害比[HR],1.45;95%CI,1.05-2.02[P=0.012]);I-IV期HER2+转移性乳腺癌患者中,未预先使用曲妥珠单抗组的中位总生存期为37个月,客观缓解率58%;临床获益率77%;预先使用曲妥珠单抗组为25个月,客观缓解率28%;临床获益率37%;调整后的比值比为客观缓解率0.37(9%CI,0.18-0.77;P=0.010)和临床获益率0.28(95%CI,0.14-0.59;P=0.014)。单因素分析没有提前接受曲妥珠单抗治疗组中位总生存率较长(P=0.012)。多因素分析发现总生存率没有显著差异(P=0.19)。结论:当曲妥珠单抗用于转移性疾病,没有提前接受曲妥珠单抗治疗的HER2+乳腺癌患者临床结果优于提前接受曲妥珠单抗治疗的患者。 Objective: The aim of this study was to compare the outcomes of patients with human epidermal growth factor receptor 2(HER2)overexpressed(HER2+) breast cancer that were treated or not treated with trastuzumab previously for metastatic breast cancer. Methods: A total of 247 patients(170 I-III stage, 77 IV stage) with metastatic HER2+ breast cancer were selected for this study.There were 211 patients((134, I-III stage; 77, IV stage) who received trastuzumab treatment for the first time and 36 patients who received trastuzumab treatment previously. The clinical outcomes of patients who had or not received prior trastuzumab were compared using Cox proportional hazards regression and logistic regression analyses. The survival was assessed using the Kaplan-Meier method.Results: The median overall survival of HER2+ metastatic breast cancer(I-III stage) was 36 months in the group who did not receive prior trastuzumab and 28 months in the group previously treated with trastuzumab( [HR], 1.45; 95% CI, 1.05-2.02 [P=0.012]). The median overall survival of HER2+ metastatic breast cancer(I-IV stage) was 37 months, objective response rate was 58%, clinical benefit rates was 76% in the group who did not receive prior trastuzumab and 25 months, 28 %, 37 % in the group previously treated with trastuzumab, respectively. The adjusted odds ratios were 0.37(P=0.010) for objective response rates and 0.38(P=0.014) for clinical benefit rates. In the univariate analysis, the median overall survival rate was longer in the group who did not receive prior trastuzumab(P=0.012). The multivariate analysis found no significant difference in overall survival(P=0.19). Conclusions: The HER21 metastatic breast cancer patients that had not received treatment of trastuzumab had superior clinical outcomes than those with prior exposure.
出处 《现代生物医学进展》 CAS 2016年第32期6332-6335,6363,共5页 Progress in Modern Biomedicine
关键词 人表皮生长因子受体2(HER2) 曲妥珠单抗 转移乳腺癌 耐药 Human epidermal growth factor receptor 2(HER2) Trastuzumab Metastatic breast cancer Drug resistance
  • 相关文献

参考文献1

二级参考文献13

  • 1Slamon D J, Clark GM, Wong SG, et al. Human breast cancer: correlation of relapse and survival with amplification of the HER- 2/neu oncogene. Science, 1987, 235 : 177-182.
  • 2Slamon D J, Leyland-Jones B, Shak S, et al. Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. N Engl J Med, 2001, 344:783- 792.
  • 3Marry M, Cognetti F, Maraninchi D, et al. Randomized phase Ⅱ trial of the efficacy and safety of trastuzumab combined with docetaxel in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer administered as first-line treatment: the M77001 study group. J Clin Oncol, 2005, 23: 4265 -4274.
  • 4Schaller G, Fuchs I, Gonsch T, et al. Phase Ⅱ study of capecitabine plus trastuzumab in human epidermal growth factor receptor 2 overexpressing metastatic breast cancer pretreated with anthracyclines or taxanes. J Clin Oncol, 2007, 25:3246-3250.
  • 5Scaltriti M, Verma C, Guzman M, et al. Lapatinib, a HER2 tyrosine kinase inhibitor, induces stabilization and accumulation of HER2 and potentiates trastuzumab-dependent cell cytotoxicity. Oncogene, 2009, 28:803-814.
  • 6Liu L, Greger J, Shi H, et al. Novel mechanism of lapatinib resistance in HER2-positive breast tumor cells : activation of AXL. Cancer Res, 2009, 69:6871-6878.
  • 7Cancello G, Montagna E, D' Agostino D, et al. Continuing trastuzumab beyond disease progression: outcomes analysis in patients with metastatic breast cancer. Breast Cancer Res, 2008, 10 : R60.
  • 8yon Minckwitz G, du Bois A, Schmidt M, et al. Trastuzumab beyond progression in human epidermal growth factor receptor 2- positive advanced breast cancer: a german breast group 26/breast international group 03-05 study. J Clin Onco|, 2009, 27: 1999- 2006.
  • 9Extra JM, Antoine EC, Vincent-Salomon A, et al. Efficacy of trastuzumab in routine clinical practice and after progression for metastatic breast cancer patients: the observational Hermine study. Oncologist, 2010, 15:799-809.
  • 10Gori S, Montemurro F, Spazzapan S, et al. Retreatment with trastuzumab-based therapy after disease progression following lapatinib in HER2-positive metastatic breast cancer. Ann Oncol, 2012, 23:1436-1441.

共引文献10

同被引文献30

二级引证文献28

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