循环hsa-miR-29c-3p和VEGF-A水平预测老年转移性结直肠癌患者对FOLFIRI加阿非利西普的反应。

IF 3.6 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Marta Toledano-Fonseca, María Teresa Cano-Osuna, Elena Élez, Javier Soto-Alsar, David Páez, Ana Fernández-Montes, Begoña Graña, Antonieta Salud, Alfonso Yubero, Ismael Macías, Guillermo Quintero, Carlos López-López, Teresa Fernández-Rodríguez, María Victoria García-Ortiz, Javier Sastre, Pilar García-Alfonso, Antonio Rodríguez-Ariza, Enrique Aranda
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引用次数: 0

摘要

背景:转移性结直肠癌(mCRC)患者在奥沙利铂为基础的化疗进展中受益于FOLFIRI加抗血管生成药物阿非利西普的二线治疗。然而,缺乏有效的抗血管生成治疗生物标志物仍然是一个挑战。在此背景下,我们之前报道了结合血浆VEGF-A水平,循环microRNA谱和患者临床特征预测FOLFIRI加阿非利赛普治疗的结果。在目前的研究中,我们报告了一线奥沙利铂化疗后进展的老年mCRC患者对FOLFIRI加阿非利西普的生物标志物反应。方法:该研究纳入了154例70岁以上的mCRC患者,他们参加了临床II期试验AFEMA。在FOLFIRI加阿非利西普治疗前获得血浆样本,分析循环VEGF-A和13种mirna的水平。结果:VEGF-A和这13种mirna中的5种(miR-193-3b, miR-432-5p, miR-29c-3p, miR-93-5p, miR-30a-3p)的水平可以根据无进展生存期和治疗失败时间对患者进行分层。具体而言,miR-29c-3p与VEGF-A联合可提高预后准确性。结论:我们的研究强调了将miR-29c-3p分析与VEGF-A结合作为一种生物标志物策略的价值,可以推进老年mCRC患者接受FOLFIRI +阿非利西普的管理,改善结果预测并实现更个性化的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circulating hsa-miR-29c-3p and VEGF-A levels predict the response to FOLFIRI plus aflibercept in elderly metastatic colorectal cancer patients.

Background: Metastatic colorectal cancer (mCRC) patients who progress on oxaliplatin-based chemotherapy benefit from second-line treatment with FOLFIRI plus the antiangiogenic drug aflibercept. However, the absence of validated biomarkers for antiangiogenic therapies remains a challenge. In this context, we previously reported that combining plasma VEGF-A levels, a circulating microRNA profile, and patient clinical characteristics predicts outcomes in FOLFIRI plus aflibercept treatment. In the present study, we now report biomarkers of response to FOLFIRI plus aflibercept in elderly mCRC patients who progressed after first-line oxaliplatin-based chemotherapy.

Methods: The study included 154 mCRC patients over 70 years of age enrolled in the clinical phase II trial AFEMA. Plasma samples were obtained before FOLFIRI plus aflibercept treatment, and circulating levels of VEGF-A and 13 miRNAs were analysed.

Results: The levels of VEGF-A and five of these 13 miRNAs (miR-193-3b, miR-432-5p, miR-29c-3p, miR-93-5p, miR-30a-3p) enabled the stratification of patients based on progression-free survival and time-to-treatment failure. Specifically, combining miR-29c-3p with VEGF-A improved prognostic accuracy.

Conclusion: Our study underscores the value of integrating miR-29c-3p analysis with VEGF-A as a biomarker strategy to advance the management of elderly mCRC patients receiving FOLFIRI plus aflibercept, improving outcome predictions and enabling more personalised therapeutic strategies.

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来源期刊
CiteScore
9.50
自引率
3.60%
发文量
192
审稿时长
1 months
期刊介绍: EJCI considers any original contribution from the most sophisticated basic molecular sciences to applied clinical and translational research and evidence-based medicine across a broad range of subspecialties. The EJCI publishes reports of high-quality research that pertain to the genetic, molecular, cellular, or physiological basis of human biology and disease, as well as research that addresses prevalence, diagnosis, course, treatment, and prevention of disease. We are primarily interested in studies directly pertinent to humans, but submission of robust in vitro and animal work is also encouraged. Interdisciplinary work and research using innovative methods and combinations of laboratory, clinical, and epidemiological methodologies and techniques is of great interest to the journal. Several categories of manuscripts (for detailed description see below) are considered: editorials, original articles (also including randomized clinical trials, systematic reviews and meta-analyses), reviews (narrative reviews), opinion articles (including debates, perspectives and commentaries); and letters to the Editor.
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