Department of Gynecology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Br J Cancer. 2012 Sep 4;107(6):956-60. doi: 10.1038/bjc.2012.353. Epub 2012 Aug 14.
We were able to demonstrate a predictive value of serum HER2 (sHER2) in patients receiving trastuzumab in the neoadjuvant GeparQuattro trial. However, the role of sHER2 in patients receiving neoadjuvant therapy (NT) with lapatinib is still unclear.
The neoadjuvant GeparQuinto trial compared trastuzumab vs lapatinib in addition to chemotherapy in HER2-positive primary breast cancer patients. The sHER2 levels were measured by enzyme-linked immunosorbant assay in 210 patients, of whom 109 (52%) patients received trastuzumab and 101 (48%) lapatinib at three different time points.
Twenty-two percent of patients had elevated baseline sHER2 levels (>15 ng ml⁻¹). A decrease of sHER2 levels (>20%) in the trastuzumab and lapatinib-treated group during NT was seen in 44% and 24% of the patients, an increase of sHER2 levels (>20%) was seen in 6% and 41% of patients, respectively. Higher pre-chemotherapy sHER2 levels were associated with higher pathological complete remission (pCR) rates in the entire study cohort (OR 1.8, 95% CI 1.02-3.2, P=0.043). A decline of sHER2 levels (>20%) during NT was a predictor for pCR in the lapatinib-treated patient group (OR: 11.7, 95% CI 1.3-110, P=0.031).
Results of this study demonstrate that sHER2 levels change differently during NT depending on the anti-HER2 treatment strategy. Elevated baseline sHER2 levels (>15 ng ml⁻¹) and a decrease of sHER2 levels (>20%) early after therapy initiation are both relevant criteria to predict response to lapatinib-based treatment.
我们能够在接受曲妥珠单抗新辅助治疗的 GeparQuattro 试验患者中证明血清 HER2(sHER2)的预测价值。然而,sHER2 在接受曲妥珠单抗联合拉帕替尼新辅助治疗(NT)的患者中的作用仍不清楚。
GeparQuinto 试验比较了曲妥珠单抗与拉帕替尼联合化疗治疗 HER2 阳性原发性乳腺癌患者的疗效。在 210 例患者中,通过酶联免疫吸附试验测量了 sHER2 水平,其中 109 例(52%)患者接受曲妥珠单抗治疗,101 例(48%)患者接受拉帕替尼治疗,分别在三个不同时间点进行。
22%的患者基线 sHER2 水平升高(>15ng/ml)。在 NT 期间,曲妥珠单抗和拉帕替尼治疗组的 sHER2 水平下降>20%的患者分别占 44%和 24%,sHER2 水平升高>20%的患者分别占 6%和 41%。化疗前较高的 sHER2 水平与整个研究队列的较高病理完全缓解(pCR)率相关(OR 1.8,95%CI 1.02-3.2,P=0.043)。NT 期间 sHER2 水平下降>20%是拉帕替尼治疗组 pCR 的预测因素(OR:11.7,95%CI 1.3-110,P=0.031)。
这项研究的结果表明,sHER2 水平在新辅助治疗期间根据抗 HER2 治疗策略而不同。基线 sHER2 水平升高(>15ng/ml)和治疗开始后早期 sHER2 水平下降>20%均是预测拉帕替尼治疗反应的相关标准。