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Monitoring serum HER2 levels during neoadjuvant trastuzumab treatment within the GeparQuattro trial

机译:在GeparQuattro试验中监测新辅助曲妥珠单抗治疗期间的血清HER2水平

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In the context of neoadjuvant therapy (NT) for breast cancer patients, different targeted therapy approaches are currently evaluated in clinical trials. Serum markers could help to monitor and optimize such treatment strategies. We investigated human epidermal growth factor receptor 2 serum (sHER2) levels in 175 breast cancer patients participating in the GeparQuattro trial. This study incorporated NT approaches and additional trastuzumab treatment for all patients with HER2-positive tumors. Human epidermal growth factor receptor 2 serum levels were measured by enzyme-linked immunosorbent assay (ELISA) before initiation of NT and after NT (pre-surgery) in a HER2-positive (n = 90) and a HER2-negative patient cohort (n = 85). Median pre-chemotherapy sHER2 levels were higher in patients with positive HER2 status of the primary tumor than in patients with negative HER2 status (14.9 ng/ml vs. 7.7 ng/ml, P 0.05). Monitoring sHER2 levels in the presence of anti-HER2 treatment might be an adjunct to the clinical evaluation during NT.
机译:在针对乳腺癌患者的新辅助治疗(NT)的背景下,目前在临床试验中评估了不同的靶向治疗方法。血清标志物可以帮助监测和优化此类治疗策略。我们调查了参加GeparQuattro试验的175名乳腺癌患者的人表皮生长因子受体2血清(sHER2)水平。本研究为所有HER2阳性肿瘤患者合并了NT方法和其他曲妥珠单抗治疗。在HER2阳性(n = 90)和HER2阴性的患者队列(n)中,在NT发生之前和NT(手术前)之后,通过酶联免疫吸附测定(ELISA)测量人表皮生长因子受体2的血清水平。 = 85)。原发性HER2阳性患者的化疗前sHER2水平高于阴性HER2的患者(14.9 ng / ml与7.7 ng / ml,P 0.05)。在存在抗HER2治疗的情况下监测sHER2水平可能是NT期间临床评估的辅助手段。

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