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CalliSpheres 载药微球栓塞剂经动脉化疗栓塞治疗巴塞罗那临床肝癌分期 C 期患者的疗效和安全性。

Efficacy and Safety of CalliSpheres Drug-Eluting Beads Transarterial Chemoembolization in Barcelona Clinic Liver Cancer Stage C Patients.

机构信息

Department of Minimally Invasive Interventional Radiology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, P.R. China.

出版信息

Oncol Res. 2019 May 7;27(5):565-573. doi: 10.3727/096504018X15313896322888. Epub 2018 Jul 13.

Abstract

This study aimed to investigate the efficacy and safety of drug-eluting beads transarterial chemoembolization (DEB-TACE) treatment in Barcelona Clinic Liver Cancer (BCLC) stage C liver cancer patients. In 39 patients with BCLC stage C liver cancer, after the first cycle of DEB-TACE, 2 (5.1%) and 24 (61.5%) patients achieved complete response (CR) and partial response (PR) to give an overall objective response rate (ORR) of 66.7%. With respect to the second cycle of therapy, the ORR was higher in patients receiving DEB-TACE compared with those receiving cTACE (57.1% vs. 11.1%). After the first cycle of DEB-TACE treatment, the percentages of abnormal albumin (ALB), total protein (TP), total bilirubin (TBIL), and alanine aminotransferase (ALT) worsened at 1 week and recovered at 1 month. The number of patients with abnormal aspartate aminotransferase (AST) did not increase at 1 week but elevated at 1 month. After the second cycle of DEB-TACE or cTACE treatment, no difference was observed between cTACE and DEB-TACE in terms of all adverse events (AEs) at all visits, and most of the AEs did not change after the second cycle in both groups. The most common AEs after the first and second treatment cycles were pain, fever, and nausea/vomiting. These results demonstrate that DEB-TACE offers patients with BCLC stage C liver cancer a clinically active short-term treatment that is safe and relatively well tolerated.

摘要

本研究旨在探讨载药微球动脉化疗栓塞术(DEB-TACE)治疗巴塞罗那临床肝癌(BCLC)C 期肝癌患者的疗效和安全性。在 39 例 BCLC C 期肝癌患者中,DEB-TACE 治疗第一周期后,2 例(5.1%)和 24 例(61.5%)患者获得完全缓解(CR)和部分缓解(PR),总客观缓解率(ORR)为 66.7%。对于第二周期的治疗,接受 DEB-TACE 的患者的 ORR 高于接受 cTACE 的患者(57.1%比 11.1%)。DEB-TACE 治疗第一周期后,1 周时白蛋白(ALB)、总蛋白(TP)、总胆红素(TBIL)和丙氨酸氨基转移酶(ALT)异常的百分比恶化,并在 1 个月时恢复正常。1 周时,天冬氨酸氨基转移酶(AST)异常的患者数量没有增加,但在 1 个月时升高。在接受 DEB-TACE 或 cTACE 治疗第二周期后,cTACE 和 DEB-TACE 在所有访视时的所有不良事件(AE)方面均无差异,并且两组中大多数 AE 在第二周期后均未改变。第一和第二治疗周期后最常见的 AE 是疼痛、发热和恶心/呕吐。这些结果表明,DEB-TACE 为 BCLC C 期肝癌患者提供了一种安全且相对耐受良好的短期临床有效治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2100/7848450/e3a7d7cf00a1/OR-27-565-g001.jpg

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