Stereotactic Radiotherapy of Hepatocellular Carcinoma: Preliminary Results

被引:88
|
作者
Louis, C. [1 ,2 ]
Dewas, S. [1 ]
Mirabel, X. [1 ,3 ]
Lacornerie, T. [1 ]
Adenis, A. [3 ]
Bonodeau, F. [4 ]
Lartigau, E. [1 ]
机构
[1] Ctr Oscar Lambret, Acad Radiat Oncol Dept, F-59020 Lille, France
[2] Domaine Univ Sart Tilman, Dept Radiat Therapy, Univ Hosp, B-4000 Liege, Belgium
[3] Ctr Oscar Lambret, Gastrointestinal Oncol Dept, F-59020 Lille, France
[4] Ctr Oscar Lambret, Med Imaging Dept, Serv Radiotherapie, F-59020 Lille, France
关键词
Stereotactic radiation therapy; Hepatocellular carcinoma; SQUAMOUS-CELL CARCINOMA; BODY RADIATION-THERAPY; PHASE-II TRIAL; CURRENT MANAGEMENT; LIVER-TUMORS; LUNG-CANCER; CIRRHOSIS; BEVACIZUMAB; SORAFENIB; ERLOTINIB;
D O I
10.1177/153303461000900506
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Stereotactic radiotherapy (SRT) offers a treatment option for hepatocellular carcinoma (HCC) patients that are not eligible for surgery, embolization, chemotherapy, or radiofrequency ablation. We have evaluated the feasibility, tolerance and toxicity of SRT for 25 HCC patients who were not eligible for these other modalities. The patients (6 women and 19 men) were treated with CyberKnife stereotactic radiotherapy using respiratory motion tracking. All patients had liver cirrhosis with an Eastern Cooperative Oncology Group (ECOG) performance score of less than 2 and pre-treatment Child scores ranging from A5 to B9. A total dose of 45 Gy in three fractions of 15 Gy each was prescribed to the 80% isodose line (95% of the PTV received 45 Gy) and delivered to the target volume over 10 to 12 days. Overall the treatment was well tolerated with two Grade 3 acute toxicities and no acute Grade 4 toxicities. Late toxicity was minimal with all observed late toxicities occurring within the first six months of follow-up. Three hepatic recurrences at a distance from the target and one metastasis were observed. The actuarial 1- and 2-year local control rate was 95% (95% CI: 69-95%). At a median overall follow-up of 12,7 months (range, 1-24 months), six of the twenty-five (24%) patients have died. Overall actuarial survival at 1- and 2-years was 79% (95% CI: 52-92%) and 52% (95% CI: 19-78%), respectively. Our results suggest promising therapeutic efficacy and good clinical tolerance to CyberKnife SRT treatment for HCC patients not eligible for other treatment modalities.
引用
收藏
页码:479 / 487
页数:9
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