404:一种新的4基因评分预测胰腺癌患者的生存和病理完全切除(R0)

M. Oshi, L. Le, Y. Tokumaru, A. Patel, R. Matsuyama, I. Endo, Li Yan, M. Katz, K. Takabe
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METHODS: The 4-gene score is derived from tumor expression of DOK4, HCCS, PGF, and SHCBP1 genes, which were identified based on differential mRNA expression analysis of a human breast cell line, its metastatic variant cells, and clinical outcome data of breast cancer patient cohorts, as previously reported. A total of 954 pancreatic cancer patients were analyzed for both discovery and validation of the 4-gene score from publicly available datasets to investigate the relationship between the score with clinical features such as metastasis, cancer aggressiveness, immune cell infiltration, patient survival, and resectability. RESULTS: We found that the 4-gene score correlation in pancreatic cancer was higher than in breast cancer cohorts, specifically in clinically aggressive parameters such as pathological grade and MKI67 expression. 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引用次数: 0

摘要

背景:胰腺癌是最具侵袭性的癌症之一,5年生存率低于10%。手术是治疗胰腺癌的唯一方法,但大多数患者在诊断时已出现转移性疾病。全身化疗仍然是主要的治疗选择。鉴于隐匿的临床表现和不良的治疗反应,迫切需要发现一种预测性的生物标志物,以适当地选择患者。我们假设反映肿瘤细胞增殖的4基因评分是胰腺癌的预后和预测性生物标志物。方法:4基因评分来源于肿瘤中DOK4、HCCS、PGF和SHCBP1基因的表达,这些基因是根据人类乳腺细胞系及其转移变异细胞的差异mRNA表达分析和乳腺癌患者队列的临床结局数据确定的,如先前报道的那样。我们对954例胰腺癌患者进行了分析,从公开数据集中发现并验证了4基因评分,以探讨该评分与转移、肿瘤侵袭性、免疫细胞浸润、患者生存和可切除性等临床特征之间的关系。结果:我们发现胰腺癌的4基因评分相关性高于乳腺癌队列,特别是在临床侵袭性参数如病理分级和MKI67表达方面。此外,转移性肿瘤组的评分高于原发癌组(p结论:4基因评分可识别胰腺癌患者的不良生存率,并有可能作为转移性胰腺癌R0切除术和治疗反应的预测性生物标志物。评估4基因评分的程度可能是一种有价值的潜在预后工具。引文格式:Masanori Oshi, Lan Le, Yoshihisa Tokumaru, Ankit Patel, Ryusei Matsuyama, Itaru Endo, Li Yan, Matthew H.G. Katz, Kazuaki Takabe。一种新的4基因评分预测胰腺癌患者的生存和病理完全切除(R0)[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要第404页。
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Abstract 404: A novel 4-gene score predict patient survival as well as pathologically complete (R0) resection in pancreatic cancer
BACKGROUND: Pancreatic cancer is one of the most aggressive cancers with a 5-year survival of less than 10%. Surgery is the only cure for pancreatic cancer but the majority of patients present with metastatic disease at the time of diagnosis. Systemic chemotherapy remains the primary treatment option. Given the insidious clinical presentation and poor treatment response, there is an urgent need to discover a predictive biomarker for appropriate patient selection. We hypothesized that the 4-gene score, which reflects tumor cell proliferation, is both a prognostic and predictive biomarker for pancreatic cancer. METHODS: The 4-gene score is derived from tumor expression of DOK4, HCCS, PGF, and SHCBP1 genes, which were identified based on differential mRNA expression analysis of a human breast cell line, its metastatic variant cells, and clinical outcome data of breast cancer patient cohorts, as previously reported. A total of 954 pancreatic cancer patients were analyzed for both discovery and validation of the 4-gene score from publicly available datasets to investigate the relationship between the score with clinical features such as metastasis, cancer aggressiveness, immune cell infiltration, patient survival, and resectability. RESULTS: We found that the 4-gene score correlation in pancreatic cancer was higher than in breast cancer cohorts, specifically in clinically aggressive parameters such as pathological grade and MKI67 expression. Also, the score in metastatic tumor cohorts was higher than in primary cancer cohorts (p CONCLUSION: The 4-gene score identified poor survival in pancreatic cancer and has potential as a predictive biomarker for R0 resection and treatment response in metastatic pancreatic cancer. Evaluating the degree of the 4-gene score could be a valuable potential prognostic tool. Citation Format: Masanori Oshi, Lan Le, Yoshihisa Tokumaru, Ankit Patel, Ryusei Matsuyama, Itaru Endo, Li Yan, Matthew H.G. Katz, Kazuaki Takabe. A novel 4-gene score predict patient survival as well as pathologically complete (R0) resection in pancreatic cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 404.
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