Bracarda Sergio, Negrier Sylvie, Casper Jochen, Porta Camillo, Schmidinger Manuela, Larkin James, Gross Goupil Marine, Escudier Bernard
a Ospedale San Donato , USL Toscana Sud-Est , Arezzo , Italy.
b Leon Berard Cancer Center , Lyon , France.
Expert Rev Anticancer Ther. 2017 Mar;17(3):227-233. doi: 10.1080/14737140.2017.1276830. Epub 2017 Jan 3.
Currently, sunitinib is a standard of care in first-line treatment for metastatic renal cell carcinoma (mRCC). However, with the standard 4/2 schedule (sunitinib 50 mg/day; 4 consecutive weeks on treatment; 2 weeks' rest), 50% of patients require dose reductions to mitigate toxicity, highlighting the need to investigate alternative dosing schedules that improve tolerability without compromising efficacy. Areas covered: We present a concise critical review of published studies comparing the efficacy and safety of the 4/2 and 2/1 schedule (2 weeks on treatment; 1 week rest) for sunitinib. While all studies evaluating the 2/1 schedule have a low level of evidence, the results indicate that the 2/1 schedule improves tolerability compared with the 4/2 schedule, including significant reductions in the incidence of specific adverse events. It was not possible to make any definitive conclusions regarding efficacy due to methodologic limitations of these studies. Expert commentary: In the absence of strong evidence supporting the safety and efficacy of the 2/1 schedule, we recommend that patients should be initiated on sunitinib therapy with the standard 4/2 schedule and only be switched to the 2/1 schedule after the development of dose-limiting toxicities from weeks 3-4 (cycle 1) of the 4/2 schedule cycle.
目前,舒尼替尼是转移性肾细胞癌(mRCC)一线治疗的标准用药。然而,按照标准的4/2给药方案(舒尼替尼50毫克/天;连续治疗4周;休息2周),50%的患者需要降低剂量以减轻毒性,这凸显了研究替代给药方案的必要性,这些方案要在不影响疗效的情况下提高耐受性。涵盖领域:我们对已发表的比较舒尼替尼4/2和2/1给药方案(治疗2周;休息1周)疗效和安全性的研究进行了简要的批判性综述。虽然所有评估2/1给药方案的研究证据水平都较低,但结果表明,与4/2给药方案相比,2/1给药方案提高了耐受性,包括特定不良事件发生率的显著降低。由于这些研究的方法学局限性,无法就疗效得出任何明确结论。专家评论:在缺乏有力证据支持2/1给药方案的安全性和疗效的情况下,我们建议患者应按照标准的4/2给药方案开始舒尼替尼治疗,只有在4/2给药方案周期的第3 - 4周(第1周期)出现剂量限制性毒性后,才切换到2/1给药方案。