Giacchetti Sylvie, Hamy Anne-Sophie, Delaloge Suzette, Brain Etienne, Berger Frédérique, Sigal-Zafrani Brigitte, Mathieu Marie-Christine, Bertheau Philippe, Guinebretière Jean Marc, Saghatchian Mahasti, Lerebours Florence, Mazouni Chafouny, Tembo Olivier, Espié Marc, Reyal Fabien, Marty Michel, Asselain Bernard, Pierga Jean-Yves
AP-HP, Hôpital Saint-Louis, Breast Disease Unit, University Paris Diderot, 75475 Paris, France.
Institut Curie, PSL Research University, Translational Research Department, INSERM, U932 Immunity and Cancer, Residual Tumor & Response to Treatment Laboratory (RT2Lab), Paris, France.
Eur J Cancer. 2017 Apr;75:323-332. doi: 10.1016/j.ejca.2017.01.008. Epub 2017 Mar 7.
The REMAGUS-02 multicenter randomised phase II trial showed that the addition to neoadjuvant chemotherapy (NAC) of trastuzumab in patients with localised HER2-positive breast cancer (BC) increased the pathological complete response (pCR) rate and that the addition of celecoxib in HER2-negative cases did not increase the pCR rate. We report here the long-term follow-up results for disease-free survival (DFS) and overall survival (OS).
From 2004 to 2007, 340 stage II-III BC patients were randomly assigned to receive neoadjuvant EC-T (four cycles of epirubicin-cyclophosphamide followed by four cycles of docetaxel) +/- celecoxib in HER2-negative cases (n = 220) and ± trastuzumab in HER2-positive cases (n = 120). From September 2005, all patients with HER2-positive BC received adjuvant T (n = 106).
Median follow-up was nearly 8 years (94.4 months, 20-127 m). In the HER2-negative subgroup, addition of celecoxib was not associated with a DFS benefit. Favourable factors were smaller tumour size, expression of progesterone receptor status (PgR) and pCR. In the HER2-positive population, neoadjuvant trastuzumab was not associated with a DFS benefit. Axillary pCR was the only prognostic factor associated with DFS in this group [HR = 0.44, 95% CI = 0.2-0.97], p = 0.035]. To note, DFS and OS were significantly higher in the HER2-positive than in HER2-negative BC patients (HR = 0.58 [0.36-0.92], p = 0.021).
Celecoxib combined with NAC provided neither pCR nor survival benefit in patients with HER2-negative BC. Absence of PgR is a major prognostic factor. Neoadjuvant trastuzumab increased pCR rates without translation into a DFS or OS benefit compared with adjuvant trastuzumab only. Axillary pCR could be a more relevant surrogate of survival than in the breast in HER2-positive population. A retrospective comparison shows that patients with HER2-positive tumours have a better outcome than HER2-negative BC patients showing the impact of trastuzumab on the natural history of BC.
REMAGUS-02多中心随机II期试验表明,在局部HER2阳性乳腺癌(BC)患者的新辅助化疗(NAC)中加入曲妥珠单抗可提高病理完全缓解(pCR)率,而在HER2阴性病例中加入塞来昔布并未提高pCR率。我们在此报告无病生存期(DFS)和总生存期(OS)的长期随访结果。
2004年至2007年,340例II-III期BC患者被随机分配接受新辅助EC-T(四个周期表柔比星-环磷酰胺,随后四个周期多西他赛),HER2阴性病例(n = 220)±塞来昔布,HER2阳性病例(n = 120)±曲妥珠单抗。从2005年9月起,所有HER2阳性BC患者接受辅助T治疗(n = 106)。
中位随访时间近8年(94.4个月,20 - 127个月)。在HER2阴性亚组中,添加塞来昔布与DFS获益无关。有利因素为肿瘤较小、孕激素受体状态(PgR)表达和pCR。在HER2阳性人群中,新辅助曲妥珠单抗与DFS获益无关。腋窝pCR是该组中与DFS相关的唯一预后因素[HR = 0.44,95%CI = 0.2 - 0.97],p = 0.035]。值得注意的是,HER2阳性BC患者的DFS和OS显著高于HER2阴性患者(HR = 0.58 [0.36 - 0.92],p = 0.021)。
塞来昔布联合NAC对HER2阴性BC患者既未提供pCR也未带来生存获益。PgR缺失是主要预后因素。与仅辅助使用曲妥珠单抗相比,新辅助曲妥珠单抗提高了pCR率,但未转化为DFS或OS获益。在HER阳性人群中,腋窝pCR可能比乳腺pCR更能代表生存情况。一项回顾性比较显示,HER2阳性肿瘤患者的预后优于HER2阴性BC患者,表明曲妥珠单抗对BC自然病程有影响。