Department of Oncology, Asan Medical Centre, University of Ulsan College of Medicine, Seoul 138-736, Korea.
Chemotherapy. 2012;58(6):468-74. doi: 10.1159/000346484. Epub 2013 Mar 20.
This study investigated the efficacy and toxicity of sorafenib and sunitinib as primary treatment for patients with metastatic renal cell carcinoma (mRCC).
We identified 49 and 220 patients treated with sorafenib and sunitinib, respectively, as first-line therapy in the Asan Medical Centre from April 2005 to March 2011.
Disease control rates of 71 and 74% were achieved with sorafenib and sunitinib, respectively (p = 0.687). After a median follow-up of 27.6 months, progression-free survival (PFS) and overall survival (OS) were not significantly different between the sorafenib and the sunitinib group (PFS 8.6 vs. 9.9 months, respectively, p = 0.948, and OS 25.7 vs. 22.6 months, p = 0.774). Patients treated with sorafenib required dose reduction due to toxicities less frequently than those treated with sunitinib (37 vs. 54%, p = 0.034). Haematological toxicity of grade 3 or 4 was more common in the sunitinib group than in the sorafenib group (45 vs. 4%, p < 0.001). Multivariate analysis showed old age, Heng's risk group, and bone and liver metastases, but not the type of vascular endothelial growth factor tyrosine kinase inhibitor, were independent prognostic factors affecting OS.
The results of this study indicate that sorafenib has comparable efficacy to sunitinib in the treatment of mRCC patients and fewer and less severe toxicities, but the number of patients included in the study was small.
本研究旨在评估索拉非尼和舒尼替尼作为转移性肾细胞癌(mRCC)患者一线治疗方案的疗效和毒性。
我们在 2005 年 4 月至 2011 年 3 月期间,在 Asan 医疗中心共鉴定了 49 例和 220 例分别接受索拉非尼和舒尼替尼一线治疗的 mRCC 患者。
索拉非尼和舒尼替尼的疾病控制率分别为 71%和 74%(p=0.687)。中位随访 27.6 个月后,两组的无进展生存期(PFS)和总生存期(OS)均无显著差异(PFS 分别为 8.6 和 9.9 个月,p=0.948,OS 分别为 25.7 和 22.6 个月,p=0.774)。因毒性而减少剂量的患者中,接受索拉非尼治疗的患者少于接受舒尼替尼治疗的患者(37%比 54%,p=0.034)。舒尼替尼组比索拉非尼组更常见 3 级或 4 级血液学毒性(45%比 4%,p<0.001)。多变量分析表明,年龄较大、Heng 的危险分组、骨和肝转移,而不是血管内皮生长因子酪氨酸激酶抑制剂的类型,是影响 OS 的独立预后因素。
本研究结果表明,索拉非尼在治疗 mRCC 患者方面与舒尼替尼疗效相当,且毒性更小、更轻,但研究纳入的患者数量较少。