Maintenance Metronomic Chemotherapy in Treatment of Metastatic Colorectal Cancer

О. V. Streltsova, А. V. Prokharau, А. S. Portyanko, Е. I. Suboch, Y. Baranau
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Abstract

Treatment of metastatic colorectal cancer (mCRC) is one of the most challenging and important problems in oncology at present moment. This article presents the interim results of treatment of patients with colorectal cancer, who were enrolled from 2016 till 2019 (n=60) with the use of maintenance metronomic chemotherapy. Metronomic regimen consisted of oral capecitabine 500 mg 3 times a day and oral cyclophosphane 50 mg daily. The control arm consisted of mCRC patients who received the same induction chemotherapy without maintenance from 2011 till 2015 (n=70). Median follow-up time was 18.5 months. Median progression-free survival (PFS) was 9.0 and 7.4 months in the maintenance and control arms respectively. Median overall survival (OS), counted from the beginning of induction chemotherapy, is currently 22.9 months in the maintenance arm, and 14.7 months in control. High expression levels of genes, encoding enzymes TS (thymidylate synthetase), DPD (dihydropyrimidine dehydrogenase) and receptor VEGFR1, low expression level of gene TP (thymidylate phosphorylase), as well as low levels of tumor markers CEA and СА 19-9 are the prognostic factors of sensitivity to metronomic chemotherapy given to colorectal cancer patients. Based on these data, we identified a group of patients who are recommended to use this method of treatment.
维持性计量化疗治疗转移性结直肠癌癌症
转移性癌症(mCRC)的治疗是目前肿瘤学中最具挑战性和最重要的问题之一。本文介绍了2016年至2019年(n=60)大肠癌癌症患者使用维持性节拍化疗的中期治疗结果。计量方案包括每天3次口服卡培他滨500 mg和每天口服环膦50 mg。对照组包括mCRC患者,他们在2011年至2015年期间接受了相同的诱导化疗,但没有维持(n=70)。中位随访时间为18.5个月。维持组和对照组的中位无进展生存期(PFS)分别为9.0和7.4个月。从诱导化疗开始计算的中位总生存期(OS),目前维持组为22.9个月,对照组为14.7个月。编码酶TS(胸苷酸合成酶)、DPD(二氢嘧啶脱氢酶)和受体VEGFR1的基因的高表达水平、TP(胸苷磷酸化酶)基因的低表达水平以及肿瘤标志物CEA和СА19-9的低水平是结直肠癌癌症患者对节拍化疗敏感性的预后因素。根据这些数据,我们确定了一组建议使用这种治疗方法的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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