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血清HER2/neu在接受曲妥珠单抗治疗的转移性乳腺癌患者无进展生存期监测及预测中的临床应用

Clinical utility of serum HER2/neu in monitoring and prediction of progression-free survival in metastatic breast cancer patients treated with trastuzumab-based therapies.

作者信息

Esteva Francisco J, Cheli Carol D, Fritsche Herbert, Fornier Monica, Slamon Dennis, Thiel Robert P, Luftner Diana, Ghani Farooq

机构信息

The University of Texas, MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Breast Cancer Res. 2005;7(4):R436-43. doi: 10.1186/bcr1020. Epub 2005 Apr 8.

Abstract

INTRODUCTION

The purpose of this retrospective study was to determine the clinical utility of serum HER2/neu in monitoring metastatic breast cancer patients undergoing trastuzumab-based therapy and to compare these results with those obtained using cancer antigen (CA) 15-3. We also sought to determine whether early changes in serum HER2/neu concentrations could be a predictor of progression-free survival.

METHODS

Sera were obtained retrospectively from 103 women at four medical institutions. Patients eligible for participation were women with metastatic breast cancer who had HER2/neu tissue overexpression and were scheduled to be treated with trastuzumab with or without additional therapies as per the established practices of the treating physicians. A baseline serum sample for each patient was taken before trastuzumab-based therapy was started. Patients were subsequently monitored over 12 to 20 months and serum samples were taken at the time of clinical assessment and tested with Bayer's HER2/neu and CA15-3 assays.

RESULTS

Concordance between clinical status in patients undergoing trastuzumab-based treatment and HER2/neu and CA15-3 used as single tests was 0.793 and 0.627, respectively, and increased to 0.829 when the tests were used in combination. Progression-free survival times did not differ significantly in patients with elevated baseline HER2/neu concentrations (> or = 15 ng/mL) and those with normal concentrations (<15 ng/mL). However, progression-free survival differed significantly (P = 0.043) according to whether the patient's HER2/neu concentration at 2 to 4 weeks after the start of therapy was >77% or < or = 77% of her baseline concentration. The median progression-free survival times for these two groups were 217 and 587 days, respectively. A similar trend was observed for a subcohort of patients treated specifically with a combination of trastuzumab and taxane.

CONCLUSION

These findings indicate that serum HER2/neu testing is clinically valuable in monitoring metastatic breast cancer patients undergoing trastuzumab-based treatment and provides additional value over the commonly used CA15-3 test. The percentage of baseline HER2/neu concentrations in the early weeks after the start of therapy may be an early predictor of progression-free-survival.

摘要

引言

本回顾性研究的目的是确定血清HER2/neu在监测接受曲妥珠单抗治疗的转移性乳腺癌患者中的临床效用,并将这些结果与使用癌抗原(CA)15-3获得的结果进行比较。我们还试图确定血清HER2/neu浓度的早期变化是否可以作为无进展生存期的预测指标。

方法

回顾性收集了四家医疗机构103名女性患者的血清。符合参与条件的患者为HER2/neu组织过表达的转移性乳腺癌女性,根据治疗医生的既定做法,她们计划接受曲妥珠单抗治疗,可联合或不联合其他治疗。在基于曲妥珠单抗的治疗开始前,为每位患者采集一份基线血清样本。随后对患者进行12至20个月的监测,并在临床评估时采集血清样本,用拜耳公司的HER2/neu和CA15-3检测方法进行检测。

结果

接受曲妥珠单抗治疗的患者的临床状态与单独使用HER2/neu和CA15-3检测结果的一致性分别为0.793和0.627,联合使用这两种检测时一致性提高到0.829。基线HER2/neu浓度升高(≥15 ng/mL)的患者和浓度正常(<15 ng/mL)的患者的无进展生存期无显著差异。然而,根据治疗开始后2至4周患者的HER2/neu浓度是高于基线浓度的77%还是低于或等于77%,无进展生存期有显著差异(P = 0.043)。这两组患者的中位无进展生存期分别为217天和587天。在专门接受曲妥珠单抗和紫杉烷联合治疗的患者亚组中也观察到了类似趋势。

结论

这些发现表明,血清HER2/neu检测在监测接受曲妥珠单抗治疗的转移性乳腺癌患者中具有临床价值,并且比常用的CA15-3检测提供了更多价值。治疗开始后早期几周内基线HER2/neu浓度的百分比可能是无进展生存期的早期预测指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d954/1175054/cd4bd63b8e62/bcr1020-1.jpg

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