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Changes in CT morphology can be an independent response marker for patients receiving regorafenib for colorectal liver metastases: retrospective pilot study

机译:回顾性初步研究表明,对于接受瑞格非尼治疗结直肠肝转移的患者,CT形态的变化可能是其独立的反应指标

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Regorafenib is a multi-kinase inhibitor, which was shown to be effective for patients with metastatic colorectal cancer refractory to standard therapies. However, its patterns of response has not yet been fully understood. Clinical records of 10 patients who received regorafenib for evaluable colorectal liver metastases were reviewed. Response to chemotherapy was evaluated with the RECIST and morphologic response criteria, and its clinical relevance was analyzed. All patients received multiple lines of fluorouracil-based chemotherapy before regorafenib. The median follow-up duration after introduction of regorafenib was 4.9?months (range, 2 to 12.5?months). Median number of chemotherapy cycles was 2 (range, 1 to 15). In size-based response evaluation, 4 patients presented SD and 6 patients showed PD according to the RECIST. In non-size-based response evaluation, 3 patients were classified as optimal morphologic response and 7 patients were categorized as suboptimal morphologic response. Patients who presented optimal morphologic response showed significantly longer progression-free survival compared with those presented suboptimal response (median, 4.9?months vs. 0.7?months; P?=?0.028), while size-based response evaluation could not well stratify patient prognosis. Non-size-based CT morphologic response could be a potential alternative response marker for patients treated with regorafenib.
机译:Regorafenib是一种多激酶抑制剂,已显示对标准疗法难以治疗的转移性结直肠癌患者有效。但是,其响应方式尚未完全了解。回顾了接受瑞戈非尼可评估的大肠肝转移的10例患者的临床记录。用RECIST和形态学反应标准评估对化疗的反应,并分析其临床相关性。所有患者在雷戈非尼之前接受了多行基于氟尿嘧啶的化疗。引入雷戈非尼后的中位随访时间为4.9个月(2至12.5个月)。化疗周期的中位数为2(范围为1至15)。根据RECIST,在基于大小的反应评估中,有4例患者出现SD,6例患者出现PD。在非基于大小的反应评估中,将3例患者分类为最佳形态学反应,将7例患者分类为次佳形态学反应。表现出最佳形态学反应的患者与未表现出最佳反应的患者相比,无进展生存期显着延长(中位,4.9个月vs. 0.7个月; P = 0.028),而基于大小的反应评估不能很好地分层患者的预后。对于瑞格非尼治疗的患者,非基于大小的CT形态学反应可能是潜在的替代反应标记。

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