Sorafenib and locoregional deep electro-hyperthermia in advanced hepatocellular carcinoma: A phase II study

被引:31
|
作者
Gadaleta-Caldarola, Gennaro [1 ]
Infusino, Stefania [2 ]
Galise, Ida [3 ]
Ranieri, Girolamo [1 ]
Vinciarelli, Gianluca [1 ]
Fazio, Vito [1 ]
Divella, Rosa [4 ]
Daniele, Antonella [4 ]
Filippelli, Gianfranco [2 ]
Gadaleta, Cosmo Damiano [1 ]
机构
[1] Natl Canc Inst Giovanni Paolo II, Natl Canc Res Ctr, Intervent Radiol & Med Oncol Unit, I-70124 Bari, Italy
[2] S Francesco di Paola Hosp, Med Oncol Unit, I-87027 Paola, Italy
[3] Natl Canc Inst Giovanni Paolo II, Natl Canc Res Ctr, Apulia Canc Registry, Stat & Epidemiol Unit, I-70124 Bari, Italy
[4] Natl Canc Inst Giovanni Paolo II, Natl Canc Res Ctr, Clin Pathol Lab, I-70124 Bari, Italy
关键词
carcinoma; electro-hyperthermia; hepatocellular; sorafenib; EPITHELIAL-MESENCHYMAL TRANSITION; ANGIOGENESIS; THERAPY;
D O I
10.3892/ol.2014.2376
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The standard treatment for advanced hepatocellular carcinoma (HCC) is sorafenib, a multikinase inhibitor of tumor cell proliferation and angiogenesis. Hyperthermia inhibits angiogenesis and promotes apoptosis. Potential synergic anti-angiogenic and proapoptotic effects represent the rationale for combining sorafenib with electro-hyperthermia (EHY) in HCC. A total of 21 patients (median age, 64 years; range, 55-73 years) with advanced HCC were enrolled in the current study between February 2009 and September 2010. EHY was achieved by arranging capacitive electrodes with a deep hypothermia radio-frequency field of 13.56 Mhz at 80 W for 60 min, three times per week for six weeks, followed by two weeks without treatment, in combination with sorafenib at a dose of 800 mg every other day. According to the modified Response Evaluation Criteria in Solid Tumors criteria, 50% achieved stable disease, 5% achieved partial response and 45% achieved progressive disease. No complete response was observed. The progression-free survival (PFS) rate at six months was 38%, while the median PFS and overall survival times were 5.2 [95% confidence interval (CI), 4.2-6.2) and 10.4 (95% CI, 10-11) months, respectively. The overall incidence of treatment-related adverse events was 80%, predominantly of grade 1 or 2. Grade 3 toxicity included fatigue, diarrhea, hand-foot skin reaction and hypertension. In the present study, the sorafenib plus EHY combination was feasible and well tolerated, and no major complications were observed. The initial findings indicated that this combination offers a promising option for advanced HCC.
引用
收藏
页码:1783 / 1787
页数:5
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