Genitourinary Oncology Service, Institute of Oncology, Meir Medical Center, Sackler School of Medicine, Tel Aviv University, Kfar Saba, Israel.
Cancer Res Treat. 2016 Jan;48(1):281-7. doi: 10.4143/crt.2014.289. Epub 2015 Mar 5.
Studies suggested the existence of a 'trial effect', in which for a given treatment, participation in a clinical trial is associated with a better outcome. Sunitinib is a standard treatment for metastatic renal cell carcinoma (mRCC). We aimed to study the effect of clinical trial participation on the outcome of mRCC patients treated with sunitinib, which at present, is poorly defined.
The records of mRCC patients treated with sunitinib between 2004-2013 in 7 centers across 2 countries were reviewed. We compared the response rate (RR), progression free survival (PFS), and overall survival (OS), between clinical trial participants (n=49) and a matched cohort of non-participants (n=49) who received standard therapy. Each clinical trial participant was individually matched with a non-participant by clinicopathologic factors. PFS and OS were determined by Cox regression.
The groups were matched by age (median 64), gender (male 67%), Heng risk (favorable 25%, intermediate 59%, poor 16%), prior nephrectomy (92%), RCC histology (clear cell 86%), pre-treatment NLR (>3 in 55%, n=27), sunitinib induced hypertension (45%), and sunitinib dose reduction/treatment interruption (41%). In clinical trial participants versus non-participants, RR was partial response/stable disease 80% (n=39) versus 74% (n=36), and progressive disease 20% (n=10) versus 26% (n=13) (p=0.63, OR 1.2). The median PFS was 10 versus 11 months (HR=0.96, p=0.84), and the median OS 23 versus 24 months (HR=0.97, p=0.89).
In mRCC patients treated with sunitinib, the outcome of clinical trial participants was similar to that of non-participants who received standard therapy.
研究表明存在“试验效应”,即在给予相同治疗的情况下,参与临床试验与更好的治疗结果相关。舒尼替尼是转移性肾细胞癌(mRCC)的标准治疗方法。我们旨在研究临床试验参与对接受舒尼替尼治疗的 mRCC 患者结局的影响,目前对此知之甚少。
回顾了 2004 年至 2013 年间在 2 个国家的 7 个中心接受舒尼替尼治疗的 mRCC 患者的记录。我们比较了临床试验参与者(n=49)和接受标准治疗的非参与者(n=49)的反应率(RR)、无进展生存期(PFS)和总生存期(OS)。对每个临床试验参与者均通过临床病理因素与非参与者进行个体匹配。通过 Cox 回归确定 PFS 和 OS。
两组在年龄(中位数 64 岁)、性别(男性 67%)、Heng 风险(有利 25%、中等 59%、不良 16%)、术前肾切除术(92%)、RCC 组织学(透明细胞 86%)、治疗前 NLR(>3 占 55%,n=27)、舒尼替尼诱导的高血压(45%)和舒尼替尼剂量减少/治疗中断(41%)方面进行了匹配。与非参与者相比,临床试验参与者的 RR 为部分缓解/稳定疾病 80%(n=39)与 74%(n=36),进展性疾病 20%(n=10)与 26%(n=13)(p=0.63,OR 1.2)。中位 PFS 为 10 个月与 11 个月(HR=0.96,p=0.84),中位 OS 为 23 个月与 24 个月(HR=0.97,p=0.89)。
在接受舒尼替尼治疗的 mRCC 患者中,临床试验参与者的结局与接受标准治疗的非参与者相似。