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First-line treatment with hepatic arterial infusion plus capecitabine vs capecitabine alone for elderly patients with unresectable colorectal liver metastases

机译:一线治疗肝动脉灌注加卡培他滨vs卡培他滨单独治疗老年无法切除的结直肠肝转移患者

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摘要

This study aimed to compare the efficacy and safety of HAI fluoropyrimidine (FUDR)/capecitabine or single capecitabine as first-line treatment for elderly patients with unresectable colorectal liver metastases (CLMs). Fifty-one elderly patients with liver-only CLMs were eligible for enrollment. Patients were divided into HAI FUDR /capecitabine group and single capecitabine group randomly. The primary endpoint was median survival time (MST), defined as the time from the date of catheter implantation to the date of death or the date of the last follow-up. The secondary endpoint was objective antitumor response and adverse events. The HAI pump was implanted before chemotherapy. All patients received a 3-week cycle of oral capecitabin. In Group A, the RR and DCR were both 95.8%. In Group B, the RR and DCR were 48.1% and 81.5%, respectively. There was significant difference between the RRs of the 2 groups (P < 0.001). But there was no significant difference between the DCRs of the 2 groups (P = 0.053). There was a statistical difference between the MSTs of the 2 groups (18.5 vs.13 months, P = 0.0312). HAI FUDR combined with oral capecitabine as the first-line treatment for elderly patients with CLMs has promising efficacy and safety.
机译:这项研究旨在比较HAI氟嘧啶(FUDR)/卡培他滨或单用卡培他滨作为一线治疗老年不可切除结直肠肝转移(CLM)患者的疗效和安全性。五十一名仅患有肝脏CLM的老年患者符合入组条件。将患者随机分为HAI FUDR /卡培他滨组和单卡培他滨组。主要终点为中位生存时间(MST),定义为从导管植入日期至死亡日期或最后一次随访日期之间的时间。次要终点是客观的抗肿瘤反应和不良事件。 HAI泵是在化疗前植入的。所有患者均接受了为期3周的口服卡培他滨治疗。在A组中,RR和DCR均为95.8%。 B组的RR和DCR分别为48.1%和81.5%。两组的RR之间有显着差异(P <0.001)。但两组的DCR之间无显着差异(P = 0.053)。两组的MST之间存在统计学差异(18.5 vs.13个月,P = 0.0312)。 HAI FUDR联合口服卡培他滨作为老年CLM患者的一线治疗具有良好的疗效和安全性。

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