Adjuvant Atezolizumab in Patients with Sarcomatoid Renal Cell Carcinoma: A Prespecified Subgroup Analysis of IMmotion010.

IF 8.3 1区 医学 Q1 ONCOLOGY European urology oncology Pub Date : 2024-07-01 DOI:10.1016/j.euo.2024.06.006
Jose Antonio Karam, Robert Uzzo, Axel Bex, William Leung, Connie Tat, Alan Nicholas, Alexander Andreev-Drakhlin, Mahrukh Huseni, Sumanta Kumar Pal, Viraj A Master
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Abstract

Patients with sarcomatoid renal cell carcinoma (sRCC) have a poor prognosis. In the randomised, double-blind phase 3 IMmotion010 trial (NCT03024996), adjuvant atezolizumab did not demonstrate a disease-free survival (DFS) benefit versus placebo in the overall population of patients with locoregional renal cell carcinoma with an increased risk of recurrence following surgery. This prespecified subgroup analysis of efficacy and safety was completed in 104 patients with sRCC. Baseline characteristics were similar between treatment arms. At a median follow-up of 45 mo, the median DFS was not evaluable (NE; 95% confidence interval [CI], 12 mo-NE) in the atezolizumab arm (n = 37) and 23 mo (95% CI, 11-NE) in the placebo arm (n = 66; hazard ratio 0.77 [95% CI, 0.44-1.4]). In the sRCC subgroup, grade 3/4 treatment-related adverse events (TRAEs) occurred in one patient (2.7%) in the atezolizumab arm and two patients (3.0%) in the placebo arm. By comparison, 54 of 353 patients (15%) and 16 of 317 patients (5.0%) with non-sarcomatoid histology reported grade 3/4 TRAEs in the respective arms. In conclusion, the difference in DFS was not statistically significant between adjuvant atezolizumab and placebo in patients with sRCC. The safety profile was similar between patients with sRCC and non-sRCC. PATIENT SUMMARY: Patients with a specific type of locoregional kidney cancer (tumours with sarcomatoid features) were treated with atezolizumab or placebo after surgery. Slightly more patients treated with atezolizumab lived longer without the disease getting worse than those treated with placebo, although this finding was not statistically significant. The side effects were similar to those seen in patients with other types of kidney cancer treated with atezolizumab in the same study (IMmotion010). In patients with sarcomatoid kidney cancer, atezolizumab was tolerable and may be more effective than placebo, but this requires further study.

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肉瘤型肾细胞癌患者的阿特珠单抗辅助治疗:IMMOTION010 的预设亚组分析。
肉瘤型肾细胞癌(sRCC)患者预后较差。在随机双盲3期IMmotion010试验(NCT03024996)中,在手术后复发风险增加的局部肾细胞癌患者总体中,阿特珠单抗辅助治疗与安慰剂相比未显示出无病生存期(DFS)优势。这项预设的疗效和安全性亚组分析是在104例sRCC患者中完成的。各治疗组的基线特征相似。在中位随访45个月时,atezolizumab治疗组(n = 37)和安慰剂治疗组(n = 66)的中位DFS分别为不可评估(NE;95% 置信区间 [CI],12 mo-NE)和23个月(95% CI,11-NE);危险比为0.77 [95% CI,0.44-1.4]。在sRCC亚组中,atezolizumab治疗组有一名患者(2.7%)发生了3/4级治疗相关不良事件(TRAE),安慰剂治疗组有两名患者(3.0%)发生了此类不良事件。相比之下,353例患者中有54例(15%)和317例非肉瘤组织学患者中有16例(5.0%)报告了3/4级TRAE。总之,在sRCC患者中,辅助阿特珠单抗与安慰剂在DFS方面的差异没有统计学意义。sRCC患者和非sRCC患者的安全性相似。患者总结:特定类型的局部肾癌(具有肉瘤特征的肿瘤)患者在术后接受阿特珠单抗或安慰剂治疗。与接受安慰剂治疗的患者相比,接受atezolizumab治疗的患者在病情没有恶化的情况下存活时间略长,但这一结果并不具有统计学意义。副作用与同一项研究(IMmotion010)中接受阿特珠单抗治疗的其他类型肾癌患者的副作用相似。在肉瘤型肾癌患者中,atezolizumab的耐受性良好,而且可能比安慰剂更有效,但这还需要进一步研究。
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来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
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