Department of Pathology, Magee-Womens Hospital, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.
Mod Pathol. 2011 Mar;24(3):367-74. doi: 10.1038/modpathol.2010.209. Epub 2010 Nov 19.
Pathologic complete response to neoadjuvant chemotherapy without trastuzumab in hormone receptor-negative/HER2+ tumors is seen in 27-45% of cases. In contrast, estrogen receptor (ER)+/HER2+ tumors demonstrate pathologic complete response in ∼ 8% of cases and is generally limited to weak-to-moderate ER+/HER2+ tumors. It is speculated that addition of trastuzumab to neoadjuvant chemotherapy regimen will increase the pathologic complete response rates in all HER2+ tumors. A list of HER2+ patients who received neoadjuvant chemotherapy (with trastuzumab) in the years 2007-2010 was obtained from our hospital database. The 104 HER2+ tumors were classified into three groups based on semiquantitative hormone receptor and HER2 results as follows: ERBB2 (ER-/PR-[H-score ≤10]/HER2+), Luminal B-HER2 Hybrid (LBHH; weak to moderate ER+ [H-score 11-199]/HER2+), and Luminal A-HER2 Hybrid (LAHH; strong ER+[H-score ≥200]/HER2+). Pathologic complete response was defined as absence of invasive carcinoma in the resection specimen and in the lymph nodes. Percentage tumor volume reduction was also calculated based on pretherapy size and detailed evaluation of the resection specimen. In all, 52% (25 of 48 cases) of ERBB2 tumors showed pathologic complete response, which was significantly higher than the pathologic complete response rate in LBHH (33%; 10 of 30) and LAHH (8%; 2 of 26) tumors. Average percentage tumor volume reduction was also highest in ERBB2 tumors (86%), followed by LBHH (74%) and LAHH (64%) tumors. We conclude that addition of trastuzumab to neoadjuvant chemotherapy regimen significantly increases the pathologic complete response rates in all HER2+ tumors. However, the benefit of trastuzumab is highest in ER-negative tumors and progressively decreases with increase in tumor ER expression. This information can be utilized to counsel patients considered for neoadjuvant chemotherapy and the same principle could be applied in the adjuvant setting.
新辅助化疗中不加曲妥珠单抗时,激素受体阴性/HER2+肿瘤的病理完全缓解率为 27-45%。相比之下,雌激素受体(ER)+/HER2+肿瘤的病理完全缓解率约为 8%,且通常仅限于弱至中度 ER+/HER2+肿瘤。据推测,在新辅助化疗方案中加入曲妥珠单抗将提高所有 HER2+肿瘤的病理完全缓解率。从我院数据库中获得了 2007-2010 年接受新辅助化疗(含曲妥珠单抗)的 HER2+患者名单。根据半定量激素受体和 HER2 结果,将 104 例 HER2+肿瘤分为三组:ERBB2(ER-/PR-[H 评分≤10]/HER2+)、Luminal B-HER2 混合型(LBHH;弱至中度 ER+[H 评分 11-199]/HER2+)和 Luminal A-HER2 混合型(LAHH;强 ER+[H 评分≥200]/HER2+)。病理完全缓解定义为切除标本和淋巴结中无浸润性癌。还根据治疗前的大小和切除标本的详细评估计算了肿瘤体积减少的百分比。总的来说,52%(48 例中的 25 例)的 ERBB2 肿瘤出现病理完全缓解,明显高于 LBHH(33%;30 例中的 10 例)和 LAHH(8%;26 例中的 2 例)肿瘤的病理完全缓解率。ERBB2 肿瘤的平均肿瘤体积减少百分比也最高(86%),其次是 LBHH(74%)和 LAHH(64%)肿瘤。我们得出结论,在新辅助化疗方案中加入曲妥珠单抗可显著提高所有 HER2+肿瘤的病理完全缓解率。然而,曲妥珠单抗的获益在 ER 阴性肿瘤中最高,随着肿瘤 ER 表达的增加而逐渐降低。这些信息可用于为考虑新辅助化疗的患者提供咨询,同样的原则也可应用于辅助治疗。