Suppr超能文献

分析分子预处理肿瘤特征作为预测生物标志物,预测摩洛哥人群直肠癌新辅助治疗后治疗反应和生存结局。

Analysis of Molecular Pretreated Tumor Profiles as Predictive Biomarkers of Therapeutic Response and Survival Outcomes after Neoadjuvant Therapy for Rectal Cancer in Moroccan Population.

机构信息

Laboratory of Biomedical and Translational Research, University of Medicine and Pharmacy of Fez, Morocco.

Laboratory of Anatomic Pathology and Molecular Pathology, University Hospital Hassan II, 30070 Fes, Morocco.

出版信息

Dis Markers. 2020 Jan 11;2020:8459303. doi: 10.1155/2020/8459303. eCollection 2020.

Abstract

Pathologic features depending on tumor response to preoperative chemoradiotherapy are important to determine the outcomes in patients with rectal cancer. Evaluating the potential predictive roles of biomarker expression and their prognostic impact is a promising challenge. We reported here the immunohistochemical staining of a panel marker of mismatch repair protein (MMR), Ki67, HER-2, and p53. Additionally, identification of somatic mutations of KRAS, NRAS, and BRAF genes were performed by direct sequencing and pyrosequencing in pretreated biopsy tissues from 57 patients diagnosed for rectal cancer. Clinical features and pathological criteria for postneoadjuvant treatment surgical resection specimen's data were collected. Immunohistochemical expression and mutational status were correlated with therapeutic response, overall survival, and disease progression. The mean age of patients was 56 years. Seven (12.3%) out of 57 patients had a complete therapeutic response. Our analysis showed that when using complete therapeutic response (Dworak 4) and incomplete therapeutic response (Dworak 3, 2, and 1) as grouping factor, high p53 expression at the pretreatment biopsy was significantly associated to an incomplete response ( = 0.002). For 20 and 2 out of 57, KRAS and NRAS mutations were detected, respectively. The majority of these mutations affected codon 12. KRAS mutations detected at codon 146 (A146T, A146V) was associated with the appearance of recurrence and distant metastasis ( = 0.019). A high expression of HER-2 corresponding to score 3+ was observed in 3 pretreatment biopsy specimens. This class was significantly associated with a short relapse-free survival ( = 0.002). Furthermore, the high expression of Ki67 was moderately correlated with an older age ( = 0.016, = 0.319). In addition, this shows that high p53 expression in the pretreatment biopsy was associated with an incomplete response in surgical resection specimens after neoadjuvant treatment, and a HER-2 score 3+ can be a predictive factor of distant metastasis and local recurrence. Larger, prospective, and more studies are needed.

摘要

术前放化疗后肿瘤反应的病理特征对直肠癌患者的预后至关重要。评估生物标志物表达的潜在预测作用及其预后影响是一项具有挑战性的工作。我们在此报告了错配修复蛋白(MMR)、Ki67、HER-2 和 p53 标志物的免疫组化染色。此外,在 57 例直肠癌患者的预处理活检组织中,通过直接测序和焦磷酸测序,鉴定了 KRAS、NRAS 和 BRAF 基因的体细胞突变。收集了新辅助治疗后手术切除标本的临床特征和病理标准数据。免疫组化表达和突变状态与治疗反应、总生存和疾病进展相关。患者的平均年龄为 56 岁。57 例患者中有 7 例(12.3%)有完全的治疗反应。我们的分析表明,当使用完全治疗反应(Dworak 4)和不完全治疗反应(Dworak 3、2 和 1)作为分组因素时,预处理活检中高 p53 表达与不完全反应显著相关( = 0.002)。在 57 例中,分别检测到 20 例和 2 例 KRAS 和 NRAS 突变。这些突变大多数影响密码子 12。在密码子 146 检测到的 KRAS 突变(A146T、A146V)与复发和远处转移有关( = 0.019)。在 3 例预处理活检中观察到高 HER-2 表达,对应评分 3+。这一类别与无复发生存时间短显著相关( = 0.002)。此外,Ki67 的高表达与年龄较大呈中度相关( = 0.016, = 0.319)。此外,这表明预处理活检中高 p53 表达与新辅助治疗后手术切除标本的不完全反应相关,HER-2 评分 3+可能是远处转移和局部复发的预测因子。需要更大规模、前瞻性和更多的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2097/6977322/cb0bd80ec457/DM2020-8459303.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验