Inha University College of Medicine, Incheon, Korea.
Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Investig Clin Urol. 2024 Sep;65(5):423-434. doi: 10.4111/icu.20240052.
This study aimed to assess the prognostic role of body mass index (BMI) in patients with metastatic renal cell carcinoma (mRCC) treated with first-line immune checkpoint inhibitor (ICI)-based therapy. We searched for relevant studies in the MEDLINE, Embase, and Cochrane Library databases. The initial search yielded 599 records, of which seven articles (2,517 patients) were selected for analysis. Patients with a high BMI had a favorable overall survival (OS) based on hazard ratio (HR) (crude HR 0.69, 95% confidence interval [CI] 0.57-0.83, p<0.0001; adjusted (a)HR 0.75, 95% CI 0.59-0.95, p=0.02), but not relative risk (RR 0.88, 95% CI 0.67-1.16, p=0.37). In the subgroup analysis, patients with a high BMI had better OS in the ICI with tyrosine kinase inhibitor (TKI) subgroup (aHR 0.71, 95% CI 0.55-0.92, p=0.01), while no significant difference was found in the ICI-only subgroup (aHR 1.02, 95% CI 0.56-1.87, p=0.95). Adjusted statistics for progression-free survival (PFS) were assessable in predominantly ICI-only studies and demonstrated a favorable outcome for patients with a low BMI (aHR 1.67, 95% CI 1.14-2.45, p=0.01). In conclusion, the impact of high BMI varies depending on the treatment type, exhibiting a favorable correlation with OS within ICI with TKI subgroup, but indicating an adverse association with PFS in the ICI-only subgroup. Further research is needed to clarify the influence of BMI by stratifying patients into ICI-only and ICI with TKI treatment to provide more insights.
这项研究旨在评估体质量指数(BMI)在接受一线免疫检查点抑制剂(ICI)为基础治疗的转移性肾细胞癌(mRCC)患者中的预后作用。我们在 MEDLINE、Embase 和 Cochrane 图书馆数据库中搜索了相关研究。初步搜索产生了 599 条记录,其中 7 篇文章(2517 名患者)被选中进行分析。根据风险比(HR)(粗 HR 0.69,95%置信区间 [CI] 0.57-0.83,p<0.0001;调整后(a)HR 0.75,95%CI 0.59-0.95,p=0.02),BMI 较高的患者具有较好的总生存期(OS),但相对风险(RR)无差异(0.88,95%CI 0.67-1.16,p=0.37)。在亚组分析中,BMI 较高的患者在 ICI 联合酪氨酸激酶抑制剂(TKI)亚组中具有更好的 OS(aHR 0.71,95%CI 0.55-0.92,p=0.01),而在 ICI 单药亚组中无显著差异(aHR 1.02,95%CI 0.56-1.87,p=0.95)。在主要为 ICI 单药研究中,可评估无进展生存期(PFS)的调整统计学数据,表明 BMI 较低的患者有较好的结果(aHR 1.67,95%CI 1.14-2.45,p=0.01)。总之,BMI 的影响取决于治疗类型,在 ICI 联合 TKI 亚组中与 OS 呈正相关,但在 ICI 单药亚组中与 PFS 呈负相关。需要进一步研究来明确 BMI 的影响,通过将患者分层为 ICI 单药和 ICI 联合 TKI 治疗来提供更多的见解。