Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Radiat Oncol. 2010 Feb 12;5:12. doi: 10.1186/1748-717X-5-12.
Three-dimensional conformal radiation therapy (3DCRT)/intensity-modulated radiation therapy (IMRT) combined with or without transcatheter arterial chemoembolization (TACE) for locally advanced hepatocellular carcinoma (HCC) has shown favorable outcomes in local control and survival of locally advanced HCC. However, intra-hepatic spreading and metastasis are still the predominant treatment failure patterns. Sorafenib is a multikinase inhibitor with effects against tumor proliferation and angiogenesis. Maintenance Sorafenib would probably prevent or delay the intrahepatic and extrahepatic spread of HCC after radiotherapy, which provides the rationale for the combination of these treatment modalities.
Patients with solitary lesion (bigger than 5 cm in diameter) histologically or cytologically confirmed HCC receive TACE (1-3 cycles) plus 3DCRT/IMRT 4-6 weeks later. Maintenance Sorafenib will be administered only for the patients with non-progression disease 4 to 6 weeks after the completion of radiotherapy. The dose will be 400 mg, p.o., twice a day. Sorafenib will be continuously given for 12 months unless intolerable toxicities and/or tumor progression. If no more than 3 patients discontinue Sorafenib treatment who experience dose-limiting toxicity after necessary dose modification and delay and/or radiation-induced liver disease in the first 15 enrolled patients, the study will recruit second fifteen patients for further evaluating safety and efficacy of treatment. Hypothesis of the current study is that Sorafenib as a maintenance therapy after combined therapy of 3DCRT/IMRT and TACE is safe and superior to radiotherapy combined with TACE alone in terms of time to progression (TTP), progression-free survival (PFS) and overall survival (OS) in comparison to historical data.
A recent meta-analysis showed TACE in combination with radiotherapy, improved the survival and the tumor response of patients, and was thus more therapeutically beneficial. In this study, local therapy for HCC is the combination of TACE and radiotherapy. Radiation exposure as a kind of stress might induce the compensatory activations of multiple intracellular signaling pathway mediators, such as PI3K, MAPK, JNK and NF-kB. Vascular endothelial growth factor (VEGF) was identified as one factor that was increased in a time- and dose-dependent manner after sublethal irradiation of HCC cells in vitro, translating to enhanced intratumor angiogenesis in vivo. Therefore, Sorafenib-mediated blockade of the Raf/MAPK and VEGFR pathways might enhance the efficacy of radiation, when Sorafenib is followed sequentially as a maintenance modality. (ClinicalTrials.gov number, NCT00999843.).
对于局部晚期肝细胞癌(HCC),三维适形放疗(3DCRT)/调强放疗(IMRT)联合或不联合经导管动脉化疗栓塞(TACE)的局部控制和生存结果均显示出良好的效果。然而,肝内播散和转移仍然是主要的治疗失败模式。索拉非尼是一种多激酶抑制剂,对肿瘤增殖和血管生成有作用。放疗后维持索拉非尼可能会预防或延迟 HCC 的肝内和肝外扩散,这为这些治疗方法的联合提供了依据。
对经组织学或细胞学证实的孤立性病变(直径大于 5cm)的 HCC 患者进行 TACE(1-3 个周期),4-6 周后进行 3DCRT/IMRT。仅对放疗后无进展疾病的患者在放疗结束后 4-6 周给予维持索拉非尼治疗。剂量为 400mg,口服,每日两次。除非出现不可耐受的毒性和/或肿瘤进展,否则索拉非尼将持续治疗 12 个月。如果在前 15 名入组患者中,仅有不超过 3 名患者因剂量限制毒性而停止索拉非尼治疗,需要调整剂量和/或出现放射性肝损伤,将进一步招募 15 名患者,以进一步评估治疗的安全性和有效性。目前研究的假设是,与单独放疗联合 TACE 相比,在接受 3DCRT/IMRT 和 TACE 联合治疗后,索拉非尼作为维持治疗是安全的,在进展时间(TTP)、无进展生存期(PFS)和总生存期(OS)方面更具优势。
最近的一项荟萃分析表明,TACE 联合放疗可提高患者的生存率和肿瘤反应,因此更具治疗益处。在这项研究中,HCC 的局部治疗是 TACE 和放疗的联合。辐射暴露作为一种应激源,可能会诱导细胞内信号通路介质的代偿激活,如 PI3K、MAPK、JNK 和 NF-kB。血管内皮生长因子(VEGF)是 HCC 细胞体外亚致死照射后呈时间和剂量依赖性增加的一种因子,可转化为体内肿瘤内血管生成增强。因此,当索拉非尼作为维持治疗的序贯治疗时,索拉非尼介导的 Raf/MAPK 和 VEGFR 通路阻断可能会增强放疗的疗效。(临床试验编号,NCT00999843.)。