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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Relevance of liver-limited disease in metastatic colorectal cancer: Subgroup findings of the FIRE-3/AIO KRK0306 trial
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Relevance of liver-limited disease in metastatic colorectal cancer: Subgroup findings of the FIRE-3/AIO KRK0306 trial

机译:转移性结直肠癌中肝有限疾病的相关性:Fire-3 / AiO KRK0306试验的亚组结果

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In metastatic colorectal cancer (mCRC), liver-limited disease (LLD) is associated with a higher chance of metastectomy leading to long-term survival. However, limited data describes the prognostic and predictive relevance of initially unresectable LLD with regard to targeted first-line therapy. The present analysis investigated the relevance of initially unresectable LLD in mCRC patients treated with targeted therapy against either the epidermal growth factor receptor (EGFR) or vascular epithelial growth factor (VEGF). The analysis was performed based on FIRE-3, a randomized phase III trial comparing first-line chemotherapy with FOLFIRI plus either cetuximab (anti-EGFR) or bevacizumab (anti-VEGF) in RAS wild-type (WT) mCRC. Of 400 patients, 133 (33.3%) had LLD and 267 (66.8%) had non-LLD. Median overall survival (OS) was significantly longer in LLD compared to non-LLD patients (36.0 vs. 25.4 months; hazard ratio [HR] = 0.66; 95% confidence interval [CI]: 0.51-0.87; p = 0.002). In a multivariate analysis also including secondary hepatic resection as time-dependent variable, LLD status was independently prognostic for OS (HR = 0.67; 95% CI: 0.50-0.91; p = 0.01). As assessed by interaction tests, treatment benefit from FOLFIRI plus cetuximab compared to FOLFIRI plus bevacizumab was independent of LLD status with regard to objective response rate (ORR), early tumour shrinkage 20% (ETS), depth of response (DpR) and OS (all p 0.05). In conclusion, LLD could be identified as a prognostic factor in RAS-WT mCRC, which was independent of hepatic resection in patients treated with targeted therapy. LLD had no predictive relevance since benefit from FOLFIRI plus cetuximab over bevacizumab was independent of LLD status.
机译:在转移性结肠直肠癌(MCRC)中,肝脏有限的疾病(LLD)与导致长期存活的血液切除术的可能性有关。然而,有限的数据描述了初始不可切除的LLD关于靶向的一线治疗的预测和预测相关性。本分析研究了初始不可切除的LLD与靶向治疗治疗对表皮生长因子受体(EGFR)或血管上皮生长因子(VEGF)治疗的MCRC患者的相关性。该分析是基于Fire-3进行的,随机相III试验将第一线化学疗法与RAS野生型(WT)MCRC中的RAS野生型(WT)MCRC中的抗琥珀(抗EGFR)或Bevacizumab(抗VEGF)进行比较。 400例患者中,133名(33.3%)LLD和267(66.8%)有非LLD。与非LLD患者相比,LLD中位数总存活(OS)在LLD中显着更长(36.0与25.4个月;危害比[HR] = 0.66; 95%置信区间[CI]:0.51-0.87; p = 0.002)。在多变量分析中,还包括次级肝切除作为时间依赖变量,LLD状态是OS的独立预后(HR = 0.67; 95%CI:0.50-0.91; P = 0.01)。如通过相互作用试验评估,与Folfiri加贝伐单抗相比,治疗益处与Folfiri加贝伐单抗与LLD状态相对于客观反应率(ORR),早期肿瘤收缩率20%(ETS),响应深度(DPR)和OS(所有p& 0.05)。总之,LLD可以被鉴定为RAS-WT MCRC中的预后因素,其与靶向治疗治疗的患者的肝切除无关。由于来自Folfiri加入的贝伐单抗,LLD没有预测相关性,因为Bevacizumab上的Cetuximab是独立于LLD地位。

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