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Hepatic Arterial Infusion Chemotherapy with Cisplatin for TACE-Refractory or -Ineligible Hepatocellular Carcinoma with Child-Pugh Score of 8 or Above

机译:顺铂肝动脉灌注化疗治疗Child-Pugh得分≥8的TACE难治性或不合格肝细胞癌

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Background: This study aimed to retrospectively assess the safety and usefulness of hepatic arterial infusion chemotherapy (HAIC) with cisplatin in patients with hepatocellular carcinoma (HCC) and Child-Pugh (C-P) score ≥ 8, who were refractory to or ineligible for transcatheter arterial chemoembolization (TACE). Methods: In this study, 28 cisplatin-na?ve patients with HCC, C-P score ≥ 8, and no evidence of extrahepatic lesions were treated using HAIC with cisplatin between July 2004 and July 2013. Results: Of 28 patients, 10 were refractory to TACE and 18 ineligible for TACE. In terms of C-P score, 17 patients had a score of 8, 6 a score of 9, and 5 a score of 10. The injected dose of cisplatin was reduced in 64.3% of cases. The overall response rate was 10.7%, with a disease control rate of 35.7%. Overall, median survival time (MST) and progression-free survival were 186 and 80 days, respectively. In patients with macroscopic vascular invasion (MVI-positive; n = 9), these values decreased to 161 and 72 days, respectively; while they increased to 341 and 87 days, respectively, in MVI-negative patients (n = 19). Patients achieving partial response (PR) and stable disease (SD) status as well as those achieving SD status showed significantly better survival than patients with progressive disease (PD status): PR + SD vs. PD: MST = 447 vs. 123 days, P < 0.001; SD vs. PD: MST = 447 vs. 123 days, P = 0.001). No serious adverse event or treatment-related death occurred. Conclusions: HAIC with cisplatin can be safely administered in patients with HCC and C-P score ≥ 8, who are TACE-refractory or -ineligible. An extended survival time is expected when the treatment outcome is either SD or more favorable.
机译:背景:本研究旨在回顾性评估顺铂治疗肝细胞癌(HCC)和Child-Pugh(CP)得分≥8,难治性或不适合经导管动脉的肝动脉灌注化疗(HAIC)的安全性和有效性。化学栓塞(TACE)。方法:在本研究中,2004年7月至2013年7月之间,采用HAIC联合顺铂治疗了28例初次行HCC,CP评分≥8,无肝外病变证据的顺铂患者。结果:28例患者中,有10例难治TACE和18个不符合TACE资格的人。就C-P评分而言,有17例患者的评分为8、6、9和5为10。在64.3%的病例中,顺铂的注射剂量降低了。总体缓解率为10.7%,疾病控制率为35.7%。总体而言,中位生存时间(MST)和无进展生存期分别为186天和80天。在具有宏观血管侵犯(MVI阳性; n = 9)的患者中,这些值分别降至161天和72天;而MVI阴性的患者分别增加到341天和87天(n = 19)。达到部分反应(PR)和稳定疾病(SD)状态的患者以及达到SD状态的患者,其生存率明显优于进行性疾病(PD状态)的患者:PR + SD与PD:MST = 447 vs. 123天, P <0.001; SD vs.PD:MST = 447 vs. 123天,P = 0.001)。没有发生严重的不良事件或与治疗有关的死亡。结论:HIC和C-P评分≥8的TACE难治或不合格的患者可以安全地使用顺铂的HAIC。当治疗结果为SD或更有利时,可以延长生存时间。

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