Adjuvant immunotherapy in renal cell carcinoma: a systematic review and meta-analysis

被引:10
作者
Riveros, Carlos [1 ]
Huang, Emily [1 ]
Ranganathan, Sanjana [1 ]
Klaassen, Zachary [2 ]
Rini, Brian [3 ]
Wallis, Christopher J. D. [4 ,5 ,6 ]
Satkunasivam, Raj [1 ,7 ]
机构
[1] Houston Methodist Hosp, Dept Urol, Houston, TX USA
[2] Augusta Univ, Med Coll Georgia, Div Urol, Augusta, GA USA
[3] Vanderbilt Univ, Med Ctr, Div Hematol & Oncol, Nashville, TN USA
[4] Univ Toronto, Univ Hlth Network, Princess Margaret Canc Ctr, Dept Surg,Div Urol & Surg Oncol, Toronto, ON, Canada
[5] Univ Toronto, Div Urol, Toronto, ON, Canada
[6] Mt Sinai Hosp, Div Urol, Toronto, ON, Canada
[7] Houston Methodist Hosp, Dept Urol, 6560 Fannin St,Suite 2100, Houston, TX 77030 USA
关键词
renal cell carcinoma; immunotherapy; adjuvant; disease-free survival; safety; #kcsm; #KidneyCancer; #uroonc; FREE DNA; RISK; PEMBROLIZUMAB; NEPHRECTOMY; RECURRENCE; SUNITINIB; SURVIVAL;
D O I
10.1111/bju.15981
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
ObjectivesTo synthesise available data regarding the disease-free survival (DFS) benefit of adjuvant immune checkpoint inhibitors (ICIs) for patients with renal cell carcinoma (RCC) and evaluate the overall safety profile of ICIs in this setting. Materials and MethodsWe utilised PubMed, Embase, and relevant conference proceedings to identify phase III randomised controlled trials comparing adjuvant ICIs vs placebo/observation for RCC. The primary outcome of interest was DFS. Variables for subgroup analyses were programmed death-ligand 1 (PD-L1) expression, sarcomatoid features, nephrectomy type, and disease-risk category. Secondary outcomes included Grade >= 3 adverse events (AEs), immune-related AEs, and treatment discontinuation due to AEs. All outcomes were analysed using random-effects models owing to inter-study heterogeneity. ResultsAmong the four included studies, one demonstrated a significant DFS benefit. There was considerable clinical and statistical heterogeneity (I-2 = 64%) due to differences in inclusion criteria and interventions. While pooled results across the four studies did not demonstrate a significant benefit in DFS overall (hazard ratio [HR] 0.85, 95% confidence interval [CI] 0.69-1.04) there was significant benefit among patients with positive PD-L1 expression (HR 0.72, 95% CI 0.55-0.94) and sarcomatoid features (HR 0.59, 95% CI 0.38-0.91). ConclusionThe evidence base to date regarding ICIs as adjuvant therapy in RCC is mixed - conclusions are limited by considerable heterogeneity between studies. However, pooled analyses suggest that patients with positive PD-L1 expression or sarcomatoid features are most likely to benefit from adjuvant immunotherapy.
引用
收藏
页码:553 / 561
页数:9
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