Department of Pathology, University Hospital of Besançon, 3 Boulevard Alexandre Fleming, Besancon, 25000, France.
Department of Oncobiology, University Hospital of Besançon, 3 Boulevard Alexandre Fleming, Besancon, 25000, France.
Diagn Pathol. 2024 Jun 22;19(1):88. doi: 10.1186/s13000-024-01508-y.
HER2-targeted therapies have recently emerged as an option in the management of metastatic colorectal cancer (mCRC) overexpressing HER2. However, data regarding HER2 status in primary CRC and its corresponding liver metastases are limited, potentially influencing clinical decisions. Therefore, the aim of this study was to compare the HER2 status in primary CRC and paired liver metastases.
Patients with mCRC who were operated from their primary colorectal cancer and their corresponding synchronous or metachronous liver metastases, in the digestive surgery department of Besançon University Hospital, between April 1999 and October 2021, were included. Tissue microarrays were constructed from matched primary CRC and liver metastastic tissue samples. HER2 status was assessed by immunohistochemistry and in situ hybridization according to Valtorta's criteria.
A series of 108 paired primary CRC and liver metastases, including a series of multiple liver metastases originating from the same patients (n = 24), were assessed. Among the primary CRC, 89 (82.4%), 17 (15.8%) and 2 (1.8%) cases were scored 0, 1 + and 2 + respectively. In liver metastases, 99 (91.7%), 7 (6.5%) and 2 (1.8%) were scored 0, 1 + and 2, respectively. Overall, there was a 19% discrepancy rate in HER2 status between primary CRC and metastases, which increased to 21% in cases with multiple synchronous or metachronous liver metastases in a given patient. No significant difference was found between metachronous and synchronous metastases regarding the HER2 status (p = 0.237).
Our study highlights the temporal and spatial heterogeneity of HER2 status between primary CRC and corresponding liver metastases. These findings raise the question of a sequential evaluation of the HER2 status during disease progression, to provide the most suitable treatment strategy.
HER2 靶向治疗最近已成为过表达 HER2 的转移性结直肠癌(mCRC)治疗的一种选择。然而,关于原发性 CRC 及其相应肝转移灶中 HER2 状态的数据有限,这可能会影响临床决策。因此,本研究旨在比较原发性 CRC 和配对肝转移灶的 HER2 状态。
纳入 1999 年 4 月至 2021 年 10 月在贝桑松大学医院消化外科部门接受过原发结直肠癌手术及其相应同步或异时性肝转移灶手术的 mCRC 患者。从匹配的原发性 CRC 和肝转移组织样本中构建组织微阵列。根据 Valtorta 标准,通过免疫组织化学和原位杂交评估 HER2 状态。
评估了 108 对原发性 CRC 和肝转移灶,包括来自同一患者的一系列多个肝转移灶(n=24)。在原发性 CRC 中,89(82.4%)、17(15.8%)和 2(1.8%)例分别被评为 0、1+和 2+。在肝转移灶中,99(91.7%)、7(6.5%)和 2(1.8%)例分别被评为 0、1+和 2+。总体而言,原发性 CRC 和转移灶之间的 HER2 状态存在 19%的差异率,在同一患者中存在多个同步或异时性肝转移灶时,这一比例增加到 21%。在 HER2 状态方面,同步和异时性转移之间没有发现显著差异(p=0.237)。
我们的研究强调了原发性 CRC 和相应肝转移灶中 HER2 状态的时间和空间异质性。这些发现提出了在疾病进展过程中对 HER2 状态进行序贯评估的问题,以提供最合适的治疗策略。