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抗血管生成治疗联合放疗治疗肝细胞癌。

Angiogenic blockade and radiotherapy in hepatocellular carcinoma.

机构信息

Department of Radiation Therapy & Oncology, Shin-Kong Memorial Hospital, Taipei, Taiwan.

出版信息

Int J Radiat Oncol Biol Phys. 2010 Sep 1;78(1):188-93. doi: 10.1016/j.ijrobp.2009.07.1725. Epub 2010 Feb 3.

Abstract

PURPOSE

We report our preliminary experience of combining sunitinib and helical tomotherapy in patients with advanced HCC.

METHODS AND MATERIALS

Records of patients with advanced hepatocellular carcinoma (HCC) treated with helical tomotherapy and sunitinib after radiation therapy (RT) from March 2007 to August 2008 were retrospectively reviewed. We report acute toxicities, radiologic response, serial alpha-fetoprotein (AFP) kinetics, and survival.

RESULTS

Of 23 evaluable patients, 60% had >or=2 hepatic lesions, extrahepatic disease was present in 5 (21.7%), and all received 2 tablets (25 mg) of sunitinib at least 1 week before, during, and 2 weeks after RT. Thirteen patients continued maintenance sunitinib after RT until disease progression. Hypofractionated RT with a median target dose of 52.5 Gy/15 fractions was delivered. An objective response was achieved in 74% of patients. The 1-year survival rate was 70%, with median survival of 16 months. Multivariate analysis showed that maintenance sunitinib was the most significant factor for survival. The time to progression was 10 months in the maintenance group compared with 4 months in the control group. Eighteen out of 21 patients with elevated AFP (85.7%) had >or=50% decline of AFP within 2 months after RT. There were three episodes of upper gastrointestinal bleeding and one episode of pancreatitis; 10 patients had >or=Grade 2 elevation of liver enzymes, and 15 had >or=Grade 2 thrombocytopenia.

CONCLUSIONS

These preliminary results suggest that sunitinib and helical tomotherapy yield high Response Evaluation Criteria in Solid Tumors (RECIST) and AFP response rates in advanced HCC with an acceptable safety profile. Maintenance sunitinib after RT potentially prolongs survival. A randomized trial is warranted.

摘要

目的

我们报告了将舒尼替尼与螺旋断层放疗联合用于晚期 HCC 患者的初步经验。

方法与材料

回顾性分析了 2007 年 3 月至 2008 年 8 月接受螺旋断层放疗和舒尼替尼治疗的晚期肝细胞癌(HCC)患者的记录。报告了急性毒性、影像学反应、连续甲胎蛋白(AFP)动力学和生存率。

结果

23 例可评估患者中,60%有≥2 个肝病灶,5 例(21.7%)存在肝外疾病,所有患者在放疗前至少 1 周、放疗期间和放疗后 2 周内至少服用 2 片(25mg)舒尼替尼。13 例患者在放疗后继续维持舒尼替尼治疗,直至疾病进展。采用中靶剂量为 52.5Gy/15 次的分割放疗。74%的患者达到客观缓解。1 年生存率为 70%,中位生存期为 16 个月。多因素分析表明,维持性舒尼替尼是生存的最重要因素。维持组的进展时间为 10 个月,对照组为 4 个月。21 例 AFP 升高的患者中有 18 例(85.7%)在放疗后 2 个月内 AFP 下降≥50%。有 3 例上消化道出血和 1 例胰腺炎;10 例患者肝酶升高≥2 级,15 例患者血小板减少≥2 级。

结论

这些初步结果表明,舒尼替尼与螺旋断层放疗联合用于晚期 HCC 患者,可获得较高的实体瘤反应评估标准(RECIST)和 AFP 反应率,安全性可接受。放疗后维持性舒尼替尼治疗可能延长生存期。需要进行随机试验。

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