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HER2 表达状态不确定的晚期胃食管交界部癌患者,无论 ERBB2 基因是否扩增,其治疗结局。

Outcomes of Advanced Gastroesophageal Cancer Patients with Equivocal HER2 Expression with or without ERBB2 Gene Amplification.

机构信息

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

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

出版信息

Oncology. 2020;98(12):884-888. doi: 10.1159/000509148. Epub 2020 Sep 30.

Abstract

BACKGROUND

Prior studies have shown that patients whose tumor overexpresses Her2 at 3+ level by immunohistochemistry (IHC) fare better than those whose tumor overexpresses Her2 at 2+ level (with ERBB2 amplified). Therefore, it would be important to compare the outcome of patients whose tumor expresses Her2 at 2+ level but further classify by gene amplification studies as positive or negative.

METHODS

We retrospectively identified patients with advanced gastroesophageal adenocarcinoma with low Her2 protein expression (2+ by IHC) whose tumors were evaluated for gene amplification of ERBB2 by fluorescence in situ hybridization (FISH). All patients received first-line therapy, and trastuzu-mab was added according to Her2 status. We compared overall survival (OS), progression-free survival (PFS), and overall response rate (ORR) of the entire cohort and compared Her2-positive tumor patients' outcomes with Her2-negative tumor patients' outcomes. All patients had treatment response assessments and follow-ups at our institution.

RESULTS

We identified 87 patients whose tumors expressed Her2 at 2+ level. 51 (58.6%) were Her2-negative and 36 (41.4%) were Her2-positive by FISH. For the entire cohort, the median OS was 26 months (95% confidence interval 16.6-37.6), and the median PFS was 12.2 months (95% confidence interval 9.7-19.3). Median OS, median PFS, and ORR did not differ between Her2-positive and Her2-negative patients (p = 0.70, p = 0.60, p = 0.91, respectively).

CONCLUSIONS

Our data suggest that patients with Her2 positivity or negativity when tumors have lower Her2 protein expression (2 + by IHC) have similar clinical outcomes. Further research is warranted in this cohort.

摘要

背景

先前的研究表明,肿瘤免疫组织化学(IHC)检测到 3+水平过表达 Her2 的患者比肿瘤过表达 Her2 为 2+水平(ERBB2 扩增)的患者预后更好。因此,比较那些肿瘤 Her2 表达为 2+但通过基因扩增研究进一步分类为阳性或阴性的患者的结局将非常重要。

方法

我们回顾性地确定了晚期胃食管腺癌患者,这些患者的肿瘤 Her2 蛋白表达水平较低(IHC 为 2+),并且通过荧光原位杂交(FISH)评估了 ERBB2 的基因扩增情况。所有患者均接受一线治疗,并根据 Her2 状态添加曲妥珠单抗。我们比较了整个队列的总生存期(OS)、无进展生存期(PFS)和总缓解率(ORR),并比较了 Her2 阳性肿瘤患者和 Her2 阴性肿瘤患者的结局。所有患者均在我们机构进行了治疗反应评估和随访。

结果

我们确定了 87 例肿瘤 Her2 表达为 2+的患者。51 例(58.6%)为 Her2 阴性,36 例(41.4%)为 Her2 阳性。对于整个队列,中位 OS 为 26 个月(95%置信区间 16.6-37.6),中位 PFS 为 12.2 个月(95%置信区间 9.7-19.3)。Her2 阳性和 Her2 阴性患者的中位 OS、中位 PFS 和 ORR 无差异(p=0.70、p=0.60、p=0.91)。

结论

我们的数据表明,当肿瘤 Her2 蛋白表达较低(IHC 为 2+)时,Her2 阳性或阴性患者的临床结局相似。在这一队列中需要进一步的研究。

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