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Early tumour response as a survival predictor in previously- treated patients receiving triplet hepatic artery infusion and intravenous cetuximab for unresectable liver metastases from wild-type KRAS colorectal cancer

机译:在接受三联肝动脉输注和西妥昔单抗静脉源性治疗的野生型KRAS结直肠癌肝转移患者中,先前接受治疗的患者的早期肿瘤反应可作为生存预测指标

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摘要

Background:udEarly tumour shrinkage has been associated with improved survival in patients receiving cetuximab-based systemic chemotherapy for liver metastases from colorectal cancer (LM-CRC). We tested this hypothesis for previously treated LM-CRC patients receiving cetuximab (500 mg/m2) and triplet hepatic artery infusion (HAI) within European trial OPTILIV.ududMethods:udIrinotecan (180 mg/m2), 5-fluorouracil (2800 mg/m2) and oxaliplatin (85 mg/m2) were given as chronomodulated or conventional delivery. Patients were retrospectively categorised as early responders (complete or partial RECIST response after three courses) or non-early responders (late or no response). Prognostic factors were determined using multivariate logistic or Cox regression models.ududResults:udResponse was assessed in 57 of 64 registered patients (89%), who had previously received one to three prior systemic chemotherapy protocols. An early response occurred at 6 weeks in 16 patients (28%; 9 men, 7 women), aged 33–76 years, with a median of 12 liver metastases (LMs) (2–50), involving five segments (1–8). Ten patients had a late response, and 31 patients had no response. Grade 3–4 fatigue selectively occurred in the non-early responders (0% versus 26%; p = 0.024). Early tumour response was jointly predicted by chronomodulation—odds ratio (OR): 6.0 (1.2–29.8; p = 0.029)—and LM diameter ≤57 mm—OR: 5.3 (1.1–25.0; p = 0.033). Early tumour response predicted for both R0-R1 liver resection—OR: 11.8 (1.4–100.2; p = 0.024) and overall survival—hazard ratio: 0.39 (0.17–0.88; p = 0.023) in multivariate analyses.ududConclusions:udEarly tumour response on triplet HAI and systemic cetuximab predicted for complete macroscopic liver resection and prolonged survival for LM-CRC patients within a multicenter conversion-to-resection medicosurgical strategy. Confirmation is warranted for early response on HAI to guide decision making.
机译:背景:早期肿瘤缩小与接受基于西妥昔单抗的系统化学疗法治疗大肠癌肝转移(LM-CRC)的患者的生存率提高相关。我们在欧洲试验OPTILIV中对接受西妥昔单抗(500 mg / m2)和三联肝动脉输注(HAI)的先前治疗过的LM-CRC患者进行了这一假设检验。 ud udMethods: udIrinotecan(180 mg / m2),5-氟尿嘧啶( 2800 mg / m2)和奥沙利铂(85 mg / m2)以计时或常规方式给药。回顾性将患者分为早期反应者(三个疗程后完全或部分RECIST反应)或非早期反应者(晚期或无反应)。预后因素使用多元logistic或Cox回归模型确定。 ud ud结果: ud对64位注册患者中的57位患者(89%)进行了反应评估,这些患者以前曾接受过一到三个先前的全身化疗方案。早期反应发生于6周的16位患者(28%; 9位男性,7位女性),年龄33-76岁,中位肝转移(LM)为12个(2-50),涉及五个部分(1-8) )。 10例患者有较晚反应,而31例患者无反应。非早期应答者有选择地发生3-4级疲劳(0%对26%; p = 0.024)。早期肿瘤反应是通过时间调制共同预测的:奇数比(OR):6.0(1.2–29.8; p = 0.029)和LM直径≤57mm–OR:5.3(1.1–25.0; p = 0.033)。在多变量分析中,预测R0-R1肝切除的早期肿瘤反应为:OR:11.8(1.4-100.2; p = 0.024)和总生存率:风险比:0.39(0.17–0.88; p = 0.023)。 ud ud结论: ud对多中心转换-切除药物治疗策略中的三联体HAI和全身西妥昔单抗的早期肿瘤反应可预测完全宏观肝切除和LM-CRC患者的生存期延长。为了确保对HAI的早期响应,可以进行确认以指导决策。

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