Assessment of the expression pattern of HER2 and its correlation with HER2-targeting antibody-drug conjugate therapy in urothelial cancer

Huizi Lei , Yun Ling , Pei Yuan , Xieqiao Yan , Lin Wang , Yanxia Shi , Xin Yao , Hong Luo , Benkang Shi , Jiyan Liu , Zhisong He , Guohua Yu , Weiqing Han , Changlu Hu , Zhihong Chi , Chuanliang Cui , Lu Si , Jianmin Fang , Jun Guo , Xinan Sheng , Jianming Ying
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Abstract

Background

Human epidermal growth factor receptor 2 (HER2) overexpression is related to anti-HER2 therapy in many tumors. RC48- antibody-drug conjugate (ADC) has shown promising efficacy in patients with HER2-positive locally advanced or metastatic urothelial carcinoma (UC). The characteristic expression and scoring systems of HER2 are nonexistent in UC. We aimed to explore HER2 status and its correlation with the efficacy of HER2-targeting ADC therapy in UC.

Methods

A total of 137 and 43 patients were enrolled in cohort 1 and cohort 2, respectively, from March 2009 to December 2018. The patients in cohort 2 were enrolled in a phase II study of RC48-ADC. UC samples were tested for HER2 status using immunohistochemistry (IHC) and/or fluorescence in situ hybridization (FISH). The 2018 ASCO/CAP HER2 scoring system was adopted and modified to score HER2 expression in UC.

Results

The HER2-positive (IHC 2+ or 3+) rate was 24.1% (33/137). In HER2 IHC 2+ or 3+ patients, the HER2 gene amplification rate was 31% (13/42). The objective response rates (ORRs) in RC48-ADC-treated patients with IHC 3+, IHC 2+ and FISH+, IHC 2+ and FISH- were 58.8%, 66.7% and 40%, respectively. The ORR showed a trend toward a better benefit for RC48-ADC therapy in patients with HER2 amplification than in those without amplification (61.5% vs. 44.8%, P = 0.059). The heterogeneity of HER2 expression in the primary tumor was 55.5% (15/27), and the ORR was not significantly different between patients with tumor heterogeneity and homogeneity.

Conclusions

IHC testing should be performed to assess the HER2 status before the initiation of HER2-ADC therapy. There was a trend toward a better benefit for patients with HER2 amplification, and tumor heterogeneity did not influence the drug efficacy.

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尿路上皮癌中HER2表达模式的评估及其与HER2靶向抗体-药物结合治疗的相关性
人类表皮生长因子受体2 (HER2)过表达与许多肿瘤的抗HER2治疗有关。RC48-抗体-药物偶联物(ADC)在her2阳性的局部晚期或转移性尿路上皮癌(UC)患者中显示出良好的疗效。UC中没有HER2的特征性表达和评分系统。我们旨在探讨HER2状态及其与UC中HER2靶向ADC治疗疗效的相关性。方法2009年3月至2018年12月,在队列1和队列2中分别纳入137例和43例患者。队列2的患者被纳入RC48-ADC的II期研究。使用免疫组织化学(IHC)和/或荧光原位杂交(FISH)检测UC样品的HER2状态。采用2018 ASCO/CAP HER2评分系统,并对其进行修改,对UC中的HER2表达进行评分。结果her2阳性(IHC 2+或3+)率为24.1%(33/137)。在HER2 IHC 2+或3+患者中,HER2基因扩增率为31%(13/42)。经rc48 - adc治疗的IHC 3+、IHC 2+和FISH+、IHC 2+和FISH-患者的客观缓解率(ORRs)分别为58.8%、66.7%和40%。ORR显示,在HER2扩增患者中,RC48-ADC治疗的获益趋势优于无扩增患者(61.5%比44.8%,P = 0.059)。HER2在原发肿瘤中的表达异质性为55.5%(15/27),肿瘤异质性和同质性患者的ORR无显著差异。结论在开始HER2- adc治疗前应进行sihc检测以评估HER2状态。HER2扩增患者有更好获益的趋势,肿瘤异质性不影响药物疗效。
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