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HERA DASL队列中单个基因预测生物标志物的探索性分析表明,C8A mRNA表达可预测预后及曲妥珠单抗治疗获益情况。

Exploratory Analysis of Single-Gene Predictive Biomarkers in HERA DASL Cohort Reveals That C8A mRNA Expression Is Prognostic of Outcome and Predictive of Benefit of Trastuzumab.

作者信息

Willis Scooter, Polydoropoulou Varvara, Sun Yuliang, Young Brandon, Tsourti Zoi, Karlis Dimitris, Long Bradley, Lin Xiaoqian, Theel Stephanie, Carlson Jennifer, Győrffy Balazs, Williams Casey, Abramovitz Mark, Dafni Urania, Dowsett Mitch, Leyland-Jones Brian

机构信息

, , , , , , , , and , Avera Cancer Institute, Sioux Falls, SD; , , , and , Frontier Science Foundation-Hellas; , University of Athens, Athens, Greece; , Scripps Florida, Jupiter, FL; , MTA-TTK Lendület Cancer Biomarker Research Group, Budapest, Hungary; and , Royal Marsden Hospital, London, United Kingdom.

出版信息

JCO Precis Oncol. 2018 Nov 1;2. doi: 10.1200/PO.18.00016. eCollection 2018.

Abstract

PURPOSE

The Herceptin Adjuvant study is an international multicenter randomized trial that compared 1 or 2 years of trastuzumab given every 3 weeks with observation in women with human epidermal growth factor 2-positive (HER2+) breast cancer after chemotherapy. Identification of biomarkers predictive of a benefit from trastuzumab will minimize overtreatment and lower health care costs.

METHODS

To identify possible single-gene biomarkers, an exploratory analysis of 3,669 gene probes not expected to be expressed in normal breast tissue was conducted. Disease-free survival (DFS) was used as the end point in a Cox regression model, with the interaction term between C8A mRNA and treatment as a categorical variable split on the cohort mean.

RESULTS

A significant interaction between C8A mRNA and treatment was detected ( < .001), indicating a predictive response to trastuzumab treatment. For the C8A-low subgroup (mRNA expression lower than the cohort mean), no significant treatment benefit was observed ( = .73). In the C8A-high subgroup, patients receiving trastuzumab experienced a lower hazard of a DFS event by approximately 75% compared with those in the observation arm (hazard ratio [HR], 0.25; < .001). A significant prognostic effect of C8A mRNA also was seen ( < .001) in the observation arm, where the C8A-high group hazard of a DFS event was three times the respective hazard of the C8A-low group (HR, 3.27; < .001). C8A mRNA is highly prognostic in the Hungarian Academy of Science HER2+ gastric cancer cohort (HR, 1.72; < .001).

CONCLUSION

C8A as a single-gene biomarker prognostic of DFS and predictive of a benefit from trastuzumab has the potential to improve the standard of care in HER2+ breast cancer if validated by additional studies. Understanding the advantage of overexpression of C8A related to the innate immune response can give insight into the mechanisms that drive cancer.

摘要

目的

赫赛汀辅助治疗研究是一项国际多中心随机试验,该试验将每3周给予曲妥珠单抗治疗1年或2年与对接受化疗后的人表皮生长因子2阳性(HER2+)乳腺癌女性进行观察相比较。鉴定可预测从曲妥珠单抗治疗中获益的生物标志物将使过度治疗最小化并降低医疗成本。

方法

为了鉴定可能的单基因生物标志物,对预计在正常乳腺组织中不表达的3669个基因探针进行了探索性分析。无病生存期(DFS)被用作Cox回归模型中的终点,将C8A mRNA与治疗之间的相互作用项作为在队列均值处划分的分类变量。

结果

检测到C8A mRNA与治疗之间存在显著相互作用(P <.001),表明对曲妥珠单抗治疗有预测反应。对于C8A低亚组(mRNA表达低于队列均值),未观察到显著的治疗益处(P =.73)。在C8A高亚组中,与观察组相比,接受曲妥珠单抗治疗的患者发生DFS事件的风险降低了约75%(风险比[HR],0.25;P <.001)。在观察组中也观察到C8A mRNA具有显著的预后作用(P <.001),其中C8A高组发生DFS事件的风险是C8A低组相应风险的三倍(HR,3.27;P <.001)。C8A mRNA在匈牙利科学院HER2+胃癌队列中具有高度预后性(HR,1.72;P <.001)。

结论

如果通过进一步研究验证,C8A作为DFS的单基因生物标志物以及曲妥珠单抗治疗获益的预测指标,有可能改善HER2+乳腺癌的治疗标准。了解C8A过表达与先天免疫反应相关的优势可以深入了解驱动癌症的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bb1/7446467/e97ca6348523/PO.18.00016f1.jpg

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