Tom Baker Cancer Centre, University of Calgary, Calgary, AB, Canada.
CancerCare Manitoba, Winnipeg, MB, Canada.
Eur Urol. 2019 Dec;76(6):861-867. doi: 10.1016/j.eururo.2019.07.048. Epub 2019 Aug 22.
In metastatic renal-cell carcinoma (mRCC), recent data have shown efficacy of first-line ipilimumab and nivolumab (ipi-nivo) as well as immuno-oncology (IO)/vascular endothelial growth factor (VEGF) inhibitor combinations. Comparative data between these strategies are limited.
To compare the efficacy of ipi-nivo versus IO-VEGF (IOVE) combinations in mRCC, and describe practice patterns and effectiveness of second-line therapies.
DESIGN, SETTING, AND PARTICIPANTS: Using the International Metastatic Renal-cell Carcinoma Database Consortium (IMDC) dataset, patients treated with any first-line IOVE combination were compared with those treated with ipi-nivo.
All patients received first-line IO combination therapies.
First- and second-line response rates, time to treatment failure (TTF), time to next treatment (TNT), and overall survival (OS) were analysed. Hazard ratios were adjusted for IMDC risk factors.
In total, 113 patients received IOVE combinations and 75 received ipi-nivo. For IOVE combinations versus ipi-nivo, first-line response rates were 33% versus 40% (between-group difference 7%, 95% confidence interval [CI] -8% to 22%, p = 0.4), TTF was 14.3 versus 10.2 mo (p = 0.2), TNT was 19.7 versus 17.9 mo (p = 0.4), and median OS was immature but not statistically different (p = 0.17). Adjusted hazard ratios for TTF, TNT, and OS were 0.71 (95% CI 0.46-1.12, p = 0.14), 0.65 (95% CI 0.38-1.11, p = 0.11), and 1.74 (95% CI 0.82-3.68, p = 0.14), respectively. Sixty-four (34%) patients received second-line treatment. In patients receiving subsequent VEGF-based therapy, second-line response rates were lower in the IOVE cohort than in the ipi-nivo cohort (15% vs 45%; between-group difference 30%, 95% CI 3-57%, p = 0.04; n = 40), though second-line TTF was not significantly different (3.7 vs 5.4 mo; p = 0.4; n = 55). Limitations include the study's retrospective design and sample size.
There were no significant differences in first-line outcomes between IOVE combinations and ipi-nivo. Most patients received VEGF-based therapy in the second line. In this group, second-line response rate was greater in patients who received ipi-nivo initially.
There were no significant differences in key first-line outcomes for patients with metastatic renal-cell carcinoma receiving immuno-oncology/vascular endothelial growth factor inhibitor combinations versus ipilimumab and nivolumab.
在转移性肾细胞癌(mRCC)中,最近的数据显示一线伊匹单抗和纳武单抗(ipi-nivo)以及免疫肿瘤学(IO)/血管内皮生长因子(VEGF)抑制剂联合治疗的疗效。这些策略之间的比较数据有限。
比较 mRCC 中 ipi-nivo 与 IO-VEGF(IOVE)联合治疗的疗效,并描述二线治疗的实践模式和有效性。
设计、地点和参与者:使用国际转移性肾细胞癌数据库联盟(IMDC)数据集,比较接受任何一线 IOVE 联合治疗的患者与接受 ipi-nivo 治疗的患者。
所有患者均接受一线 IO 联合治疗。
分析一线和二线反应率、治疗失败时间(TTF)、下一治疗时间(TNT)和总生存期(OS)。风险比根据 IMDC 风险因素进行调整。
共有 113 名患者接受了 IOVE 联合治疗,75 名患者接受了 ipi-nivo 治疗。对于 IOVE 联合治疗与 ipi-nivo,一线反应率分别为 33%与 40%(组间差异 7%,95%置信区间[CI]为-8%至 22%,p=0.4),TTF 分别为 14.3 与 10.2 个月(p=0.2),TNT 分别为 19.7 与 17.9 个月(p=0.4),中位 OS 尚未成熟但无统计学差异(p=0.17)。TTF、TNT 和 OS 的调整后风险比分别为 0.71(95%CI 0.46-1.12,p=0.14)、0.65(95%CI 0.38-1.11,p=0.11)和 1.74(95%CI 0.82-3.68,p=0.14)。64 名(34%)患者接受了二线治疗。在接受后续 VEGF 治疗的患者中,IOVE 队列的二线反应率低于 ipi-nivo 队列(15% vs 45%;组间差异 30%,95%CI 3%-57%,p=0.04;n=40),尽管二线 TTF 无显著差异(3.7 与 5.4 个月;p=0.4;n=55)。局限性包括研究的回顾性设计和样本量。
IOVE 联合治疗与 ipi-nivo 一线治疗结果无显著差异。大多数患者在二线接受了基于 VEGF 的治疗。在此组中,最初接受 ipi-nivo 治疗的患者二线反应率更高。
接受免疫肿瘤学/血管内皮生长因子抑制剂联合治疗与伊匹单抗和纳武单抗治疗转移性肾细胞癌的患者,其关键一线结局无显著差异。