Liu Xiu-Lan, Xue Hui-Ying, Chu Qian, Liu Jin-Yu, Li Juan
Department of Pharmacy.
Department of Oncology, Tongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, P.R. China.
Medicine (Baltimore). 2020 Mar;99(13):e19570. doi: 10.1097/MD.0000000000019570.
To evaluate the safety and efficiency of sunitinib and sorafenib in the treatment of renal cell carcinoma (RCC).Databases were searched up till February 28, 2018. Two reviewers independently assessed trials for eligibility, quality, and extracted relevant data. Results are expressed as risk ratio (RR) or hazard ratio (HR) with 95% confidence intervals (CI). Six studies including 3112 patients were accessed. Sorafenib group exhibited higher median progression-free survival (mPFS) compared to sunitinib group (MD, -1.30; 95% CI, -2.56 to -0.03), especially in the first-line treatment (MD, -1.33; 95% CI, -2.61 to -0.04). However, sunitinib significantly reduced the risk of progression-free survival (PFS) compared to sorafenib (HR, 0.71; 95% CI, 0.6-0.82). Sunitinib also significantly reduced risk of overall survival (OS) compared to sorafenib (HR, 0.79; 95% CI, 0.65-0.92), while median OS was similar in both groups (MD, -0.48; 95% CI, -3.40-2.43). With regards to safety, the risk of rash (RR, 0.31, 95% CI, 0.12-0.79) was greater in sunitinib than sorafenib group, while the risk of decreased appetite (RR 2.10, 95% CI: 1.33-3.30) and dehydration (RR 2.73, 95% CI: 1.14-6.56) was smaller in contrast.Based on risk of PFS and OS, sunitinib was a better treatment option for RCC treatment while patients faced with severe skin reaction. And for those Asian patients classified under MSKCC moderate risk, whether in first or second-line treatment, had difficulty in feeding, sorafenib is a better choice for prolong mPFS.
评估舒尼替尼和索拉非尼治疗肾细胞癌(RCC)的安全性和有效性。检索数据库至2018年2月28日。两名研究者独立评估试验的合格性、质量并提取相关数据。结果以风险比(RR)或风险比(HR)及95%置信区间(CI)表示。纳入6项研究,共3112例患者。与舒尼替尼组相比,索拉非尼组的中位无进展生存期(mPFS)更长(MD,-1.30;95%CI,-2.56至-0.03),尤其是在一线治疗中(MD,-1.33;95%CI,-2.61至-0.04)。然而,与索拉非尼相比,舒尼替尼显著降低了无进展生存期(PFS)风险(HR,0.71;95%CI,0.6 - 0.82)。与索拉非尼相比,舒尼替尼也显著降低了总生存期(OS)风险(HR,0.79;95%CI,0.65 - 0.92),而两组的中位OS相似(MD,-0.48;95%CI,-3.40 - 2.43)。在安全性方面,舒尼替尼组皮疹风险(RR,0.31,95%CI,0.12 - 0.79)高于索拉非尼组,而食欲减退风险(RR 2.10,95%CI:1.33 - 3.30)和脱水风险(RR 2.73,95%CI:1.14 - 6.56)则低于索拉非尼组。基于PFS和OS风险,对于RCC治疗且面临严重皮肤反应的患者,舒尼替尼是更好的治疗选择。而对于那些根据MSKCC中度风险分类的亚洲患者,无论一线还是二线治疗,存在进食困难时,索拉非尼是延长mPFS的更好选择。