Wang Chun, Mu Zhaomei, Ye Zhong, Zhang Zhenchao, Abu-Khalaf Maysa M, Silver Daniel P, Palazzo Juan P, Jagannathan Geetha, Fellin Frederick M, Bhattacharya Saveri, Jaslow Rebecca J, Tsangaris Theodore N, Berger Adam, Neupane Manish, Cescon Terrence P, Lopez AnaMaria, Yao Kaelan, Chong Weelic, Lu Brian, Myers Ronald E, Hou Lifang, Wei Qiang, Li Bingshan, Cristofanilli Massimo, Yang Hushan
Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, 19107, USA.
Division of Hematology and Oncology, Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, 60611, USA.
Breast Cancer Res Treat. 2020 Jun;181(3):679-689. doi: 10.1007/s10549-020-05662-x. Epub 2020 May 4.
Discordance between HER2 expression in tumor tissue (tHER2) and HER2 status on circulating tumor cells (cHER2) has been reported. It remains largely underexplored whether patients with tHER2/cHER2 can benefit from anti-HER2 targeted therapies.
cHER2 status was determined in 105 advanced-stage patients with tHER2 breast tumors. Association between cHER2 status and progression-free survival (PFS) was analyzed by univariate and multivariate Cox models and survival differences were compared by Kaplan-Meier method.
Compared to the patients with low-risk cHER2 (cHER2 < 2), those with high-risk cHER2 (cHER2 ≥ 2) had shorter survival time and an increased risk for disease progression (hazard ratio [HR] 2.16, 95% confidence interval [CI] 1.20-3.88, P = 0.010). Among the patients with high-risk cHER2, those who received anti-HER2 targeted therapies had improved PFS compared with those who did not (HR 0.30, 95% CI 0.10-0.92, P = 0.035). In comparison, anti-HER2 targeted therapy did not affect PFS among those with low-risk cHER2 (HR 0.70, 95% CI 0.36-1.38, P = 0.306). Similar results were obtained after adjusting covariates. A longitudinal analysis of 67 patients with cHER2 detected during follow-ups found that those whose cHER2 status changed from high-risk at baseline to low-risk at first follow-up exhibited a significantly improved survival compared to those whose cHER2 remained high-risk (median PFS: 11.7 weeks vs. 2.0 weeks, log-rank P = 0.001).
In advanced-stage breast cancer patients with tHER2 tumors, cHER2 status has the potential to guide the use of anti-HER2 targeted therapy in patients with high-risk cHER2.
已有报道称肿瘤组织中HER2表达(tHER2)与循环肿瘤细胞上的HER2状态(cHER2)存在不一致。tHER2/cHER2患者是否能从抗HER2靶向治疗中获益在很大程度上仍未得到充分研究。
在105例晚期tHER2乳腺癌患者中确定cHER2状态。通过单因素和多因素Cox模型分析cHER2状态与无进展生存期(PFS)之间的关联,并采用Kaplan-Meier法比较生存差异。
与低风险cHER2(cHER2 <2)患者相比,高风险cHER2(cHER2 ≥2)患者的生存时间较短,疾病进展风险增加(风险比[HR] 2.16,95%置信区间[CI] 1.20 - 3.88,P = 0.010)。在高风险cHER2患者中,接受抗HER2靶向治疗的患者与未接受治疗的患者相比,PFS有所改善(HR 0.30,95% CI 0.10 - 0.92,P = 0.035)。相比之下,抗HER2靶向治疗对低风险cHER2患者的PFS没有影响(HR 0.70,95% CI 0.36 - 1.38,P = 0.306)。调整协变量后得到了类似结果。对随访期间检测到cHER2的67例患者进行的纵向分析发现,与cHER2仍为高风险的患者相比,那些cHER2状态从基线时的高风险变为首次随访时的低风险的患者生存情况有显著改善(中位PFS:11.7周对2.0周,对数秩检验P = 0.001)。
在晚期tHER2肿瘤的乳腺癌患者中,cHER2状态有可能指导高风险cHER2患者使用抗HER2靶向治疗。