Wang Jing, Long Xin, Tang Mingxi, Xiao Xiuli
Department of Pathology, Yaan People's Hospital, Yaan, Sichuan, China.
Department of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Front Oncol. 2025 Jun 9;15:1522460. doi: 10.3389/fonc.2025.1522460. eCollection 2025.
The expression of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) in residual lesions may be different compared with primary tumors of the breast after neoadjuvant therapy (NAT). Given the clinical implications of hormone receptor expression for breast cancer management, we assessed conversions in ER, PR, and HER2 in breast cancer patients after NAT.
Our study comprised 589 individuals with aggressive breast cancer who underwent NAT. We examined the ER, PR, and HER2 statuses in primary and residual breast cancers and investigated the relationship between receptor conversion and clinicopathological variables.
The pathologic complete response (pCR) rate for the overall cohort was 38.7%, with pCR rates of 57.0%, 13.1%, and 33.3% for HER2-positive, Luminal, and triple-negative breast cancer (TNBC), respectively. Cases with negative hormone receptor expression were more likely to achieve pCR than positive cases. The highest pCR rates were seen in HER2-positive breast cancers, followed by HER2-zero and HER2-low tumors. After NAT, there were 26 (7.8%) cases of ER status conversion and 53 (16.0%) cases of PR status conversion. The conversion of hormone receptors was mainly from positive to negative. When cases were categorized as HER2-negative or positive, 15 (5.1%) cases had a conversion of HER2 status, predominantly positive to negative. When cases were classified as HER2-zero, -low, or -positive, HER2 status conversion happened in 54 (18.6%) cases and was mostly happened between HER2-zero and HER2-low. HER2 status before NAT correlated with ER and HER2 conversion.
Some breast cancer patients may show ER, PR, or HER2 status conversion after NAT. Residual lesions need to be immunohistochemically re-tested to reassess the patient's receptor expression status and to adjust the subsequent treatment regimen.
与新辅助治疗(NAT)后的原发性乳腺癌相比,残余病灶中雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体2(HER2)的表达可能有所不同。鉴于激素受体表达对乳腺癌治疗的临床意义,我们评估了NAT后乳腺癌患者ER、PR和HER2的转变情况。
我们的研究纳入了589例接受NAT的侵袭性乳腺癌患者。我们检测了原发性和残余乳腺癌中的ER、PR和HER2状态,并研究了受体转变与临床病理变量之间的关系。
整个队列的病理完全缓解(pCR)率为38.7%,HER2阳性、Luminal和三阴性乳腺癌(TNBC)的pCR率分别为57.0%、13.1%和33.3%。激素受体表达阴性的病例比阳性病例更有可能实现pCR。pCR率最高的是HER2阳性乳腺癌,其次是HER2阴性和HER2低表达肿瘤。NAT后,有26例(7.8%)ER状态转变,53例(16.0%)PR状态转变。激素受体的转变主要是从阳性转为阴性。当病例分为HER2阴性或阳性时,有15例(5.1%)HER2状态转变,主要是从阳性转为阴性。当病例分为HER2阴性、低表达或阳性时,54例(18.6%)发生HER2状态转变,且大多发生在HER2阴性和HER2低表达之间。NAT前的HER2状态与ER和HER2转变相关。
一些乳腺癌患者在NAT后可能出现ER、PR或HER2状态转变。需要对残余病灶进行免疫组化重新检测,以重新评估患者的受体表达状态,并调整后续治疗方案。