摘要:肿瘤中叶酸相关基因的表达与晚期结直肠癌患者的无进展生存相关

Y. Wettergren, E. Odin, G. Carlsson, Pushpa Saksena, A. Edsjö, A. Cara, R. Tell, B. Gustavsson
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引用次数: 0

摘要

背景- 5-氟尿嘧啶(5-FU)联合叶酸亚叶酸钙(LV)已经形成了几十年来晚期结直肠癌化疗的支柱。许多基因编码的蛋白质参与LV进入细胞的运输,以及随后的代谢作用。我们之前报道过,在北欧单药方案中,5-FU + LV (FLV)单独治疗或与奥沙利铂(FLOX)联合治疗的III期结直肠癌患者中,参与叶酸转运、多谷氨酸化和代谢的高肿瘤基因表达与疾病复发风险降低相关。本研究的目的是确定叶酸相关基因ABCC3、MTHFD2、SLC19A1、SLC25A32、SLC46A1和TYMS的表达与转移性结直肠癌患者姑息性化疗的预后之间的关系。患者和方法:共纳入290例接受FLV (n = 113)、FLOX (n = 102)或FLV +伊立替康(FLIRI, n = 75)治疗的患者。基于RECIST标准和3年无进展生存期(PFS),通过定量PCR检测原发肿瘤中的相对基因表达(ΔCt),并分析其与临床获益的关系。对整个研究组进行分析,并根据原发性手术时肿瘤分期进行亚组分析(亚组1,I-III期;亚组2,IV期)。采用方差分析检验评估表达与临床获益之间的关系。应用多变量Cox比例风险模型评估遗传标记、临床变量与PFS之间的潜在关联。采用逐步模型选择来确定与PFS相关的最小变量集。结果-在整个组中,TYMS和MTHFD2的低表达以及ABCC3的高表达与临床获益显著相关(p结论-在整个组中,5-FU的靶酶TYMS的表达与临床获益密切相关,而TYMS和叶酸转运体SLC25A32以及ABCC3的表达分别与亚组(I-III期和IV期)的PFS相关。全球前瞻性III期研究AGENT目前正在晚期结直肠癌患者中进行,以确定这些基因的表达是否可以预测对包括LV或新型叶酸arfolitixorin在内的5- fu化疗的反应。引文格式:Yvonne Wettergren, Elisabeth Odin, Goran Carlsson, Pushpa Saksena, Anders Edsjo, Alessandro Di Cara, Roger Tell, Bengt Gustavsson。肿瘤中叶酸相关基因的表达与晚期结直肠癌患者的无进展生存期相关[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nr 346。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 346: Tumoral expression of folate-associated genes is associated with progression-free survival of patients with advanced colorectal cancer
Background - 5-fluorouracil (5-FU) in combination with the folate leucovorin (LV) has formed the backbone of chemotherapy for advanced colorectal cancer for several decades. A number of genes encode proteins that participate in transportation of LV into the cells, as well as in subsequent metabolic action. We previously reported that high tumoral expression of genes involved in folate transport, polyglutamation, and metabolism was associated with decreased risk of recurrent disease in patients with stage III colorectal cancer treated with 5-FU + LV (FLV) alone, or in combination with oxaliplatin (FLOX) according to the Nordic bolus regimen. The aim of the present study was to determine the association between expression of the folate-associated genes ABCC3, MTHFD2, SLC19A1, SLC25A32, SLC46A1, and TYMS and outcome of patients with metastatic colorectal cancer subjected to palliative chemotherapy. Patients and Methods - A total of 290 patients treated with FLV (n = 113), FLOX (n = 102) or FLV + irinotecan (FLIRI, n = 75) were included. Relative gene expression (ΔCt) was determined in primary tumors by quantitative PCR and analyzed in relation to clinical benefit, based on RECIST criteria and 3-year progression-free survival (PFS). Analyses were conducted on the whole study group, and on subgroups based on tumor stage at primary surgery (subgroup 1, stage I-III; subgroup 2, stage IV). An ANOVA test was used to assess the relationship between expression and clinical benefit. A multivariate Cox proportional hazard model was applied to assess potential associations between genetic markers, clinical variables and PFS. A Stepwise model selection was used to identify a minimal set of variables associated with PFS. Results - Low expression of TYMS and MTHFD2, and high expression of ABCC3 was significantly associated with a clinical benefit in the whole group (p Conclusion - Expression of TYMS, the target enzyme of 5-FU, was strongly associated with clinical benefit in the whole group, whereas expression of TYMS and the folate transporters SLC25A32, and ABCC3 was associated with PFS in the subgroups (stage I-III and stage IV), respectively. The prospective global phase III study AGENT is presently conducted on patients with advanced colorectal cancer, to determine whether expression of these genes can predict response to 5-FU-based chemotherapy that includes LV or the novel folate arfolitixorin. Citation Format: Yvonne Wettergren, Elisabeth Odin, Goran Carlsson, Pushpa Saksena, Anders Edsjo, Alessandro Di Cara, Roger Tell, Bengt Gustavsson. Tumoral expression of folate-associated genes is associated with progression-free survival of patients with advanced colorectal 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 346.
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