Department of Diagnostic and Molecular Imaging, Radiation Therapy and Interventional Radiology, University Hospital "Tor Vergata", Viale Oxford 81, 00133, Rome, Italy.
Hepatology Unit, University Hospital "Tor Vergata", Rome, Italy.
Radiol Med. 2020 Jan;125(1):98-106. doi: 10.1007/s11547-019-01093-x. Epub 2019 Oct 3.
To evaluate safety and efficacy of degradable starch microspheres (DSMs) TACE in a large clinical cohort of patients with unresectable HCC.
This is a single-center consecutive patients cohort study. The study was approved by local institutional ethics committee. Written informed consent was obtained. From December 2013 to March 2018, 137 cirrhotic patients with unresectable HCC were enrolled. For DSMs-TACE, a mixture of 4 mL of DSMs, 6 mL of non-ionic contrast and doxorubicin at a dose of 50 mg/m were used. Primary end point was long-term outcome, in terms of time to progression (TTP) and overall survival (OS). Secondary endpoints were: safety, liver toxicity, 1-month percentage of tumor necrosis according to the modified RECIST criteria.
Two hundred and sixty-seven DSMs-TACE were performed in 137 HCC patients (33 patients in BCLC stage A, 84 patients in BCLC stage B, and 20 in stage C). Patients had a mean nodule number of 3.5 ± 1.2 (SD). Major complications were observed in 6.8% of cases. Post-embolization syndrome was common (101 patients 73.7%). According to mRecist criteria, a high objective response rate was obtained even after just one treatment (84.3% of patients showed complete response or partial response). The median TTP and OS after DSMs-TACE were 12 months and 36 months, respectively. OS at 6 months, 1 year, 2 and 3 years was 98%, 81.3%, 57.9%, 34.9%, respectively.
DSMs-TACE is a safe and effective therapy for patients with HCC, allowing to obtain a good rate of OS with excellent local tumor control.
评估可降解淀粉微球(DSMs)TACE 在大量不可切除 HCC 患者中的安全性和疗效。
这是一项单中心连续患者队列研究。该研究获得了当地机构伦理委员会的批准。获得了书面知情同意。从 2013 年 12 月至 2018 年 3 月,共纳入 137 例肝硬化不可切除 HCC 患者。对于 DSMs-TACE,使用 4mL DSMs、6mL 非离子型造影剂和 50mg/m 的多柔比星混合液。主要终点是无进展生存期(TTP)和总生存期(OS)的长期结果。次要终点是:安全性、肝毒性、根据改良 RECIST 标准评估的 1 个月肿瘤坏死百分比。
137 例 HCC 患者共进行了 267 次 DSMs-TACE(BCLC 分期 A 33 例,BCLC 分期 B 84 例,C 期 20 例)。患者的平均结节数为 3.5±1.2(SD)。6.8%的病例观察到严重并发症。栓塞后综合征很常见(101 例,73.7%)。根据 mRecist 标准,即使只进行一次治疗,也能获得较高的客观缓解率(84.3%的患者显示完全缓解或部分缓解)。DSMs-TACE 后的中位 TTP 和 OS 分别为 12 个月和 36 个月。DSMs-TACE 后 6 个月、1 年、2 年和 3 年的 OS 分别为 98%、81.3%、57.9%和 34.9%。
DSMs-TACE 是 HCC 患者安全有效的治疗方法,可获得良好的 OS 率和出色的局部肿瘤控制率。