Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Cancer Chemother Pharmacol. 2013 Jan;71(1):165-73. doi: 10.1007/s00280-012-1993-9. Epub 2012 Oct 19.
Although sorafenib has been approved for treating advanced hepatocellular carcinoma (HCC), its high cost, frequent adverse events, and unsatisfactory efficacy remain unresolved. We evaluated the efficacy and safety of the combination treatment of localized concurrent chemoradiation therapy (CCRT) for locally advanced HCC with portal vein thrombosis (PVT) and transarterial chemoembolization (TACE) for intrahepatic metastasis.
Between January 2006 and June 2011, 30 patients with HCC with portal vein invasion and intrahepatic metastasis were enrolled. After TACE for intrahepatic metastasis, localized CCRT (45 Gy over 5 weeks with conventional fractionation and hepatic artery infusional chemotherapy using 5-fluorouracil as a radiosensitizer, administered during the first and fifth weeks of radiotherapy) was used to treat main HCC with PVT. The modified response evaluation criteria in solid tumors (mRECIST) were used to evaluate tumor response.
The median age of the patients (26 men, 4 women) was 51 years. Objective response rates were 30.0% (9/30) and 32.1% (9/28) in the intention-to-treat and per protocol analyses, respectively. The median progression-free survival (PFS) and overall survival (OS) were 4.5 and 9.8 months, respectively. Baseline α-fetoprotein (AFP) correlated significantly with PFS (P = 0.008), whereas baseline AFP, completion of the protocol, and overall radiological response influenced OS significantly (all P < 0.05). All adverse events were predictable and manageable with conservative care.
Combination treatment of localized CCRT and TACE was effective and tolerable in patients with locally advanced HCC with PVT and intrahepatic metastasis. This protocol may be an alternative option when sorafenib cannot be prescribed.
虽然索拉非尼已被批准用于治疗晚期肝细胞癌(HCC),但其高成本、频繁的不良反应和不理想的疗效仍未得到解决。我们评估了局部同步放化疗(CCRT)联合经动脉化疗栓塞术(TACE)治疗合并门静脉癌栓(PVT)和肝内转移的局部晚期 HCC 的疗效和安全性。
2006 年 1 月至 2011 年 6 月,我们共纳入 30 例 HCC 合并门静脉侵犯和肝内转移的患者。在 TACE 治疗肝内转移后,采用局部 CCRT(5 周内 45 Gy,常规分割,肝动脉灌注化疗,5-氟尿嘧啶作为增敏剂,在放疗的第一和第五周进行)治疗合并 PVT 的主 HCC。采用改良实体瘤反应评价标准(mRECIST)评价肿瘤反应。
患者的中位年龄为 51 岁(26 名男性,4 名女性)。意向治疗和方案分析的客观缓解率分别为 30.0%(9/30)和 32.1%(9/28)。中位无进展生存期(PFS)和总生存期(OS)分别为 4.5 和 9.8 个月。基线α-胎蛋白(AFP)与 PFS 显著相关(P = 0.008),而基线 AFP、方案完成情况和整体影像学反应显著影响 OS(均 P < 0.05)。所有不良事件均可以通过保守治疗进行预测和管理。
局部 CCRT 联合 TACE 治疗合并 PVT 和肝内转移的局部晚期 HCC 有效且可耐受。当不能使用索拉非尼时,该方案可能是一种替代选择。