Targeted Therapy and Immunotherapy: Effect of Body Mass Index on Clinical Outcomes in Patients Diagnosed with Metastatic Renal Cell Carcinoma

IF 1.1 Q4 ONCOLOGY
Kidney Cancer Pub Date : 2019-01-01 DOI:10.3233/KCA-180047
P. Bergerot, C. Bergerot, E. Philip, L. Meza, N. Dizman, J. Hsu, S. Pal
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引用次数: 15

Abstract

Background: Previous research has identified an association between high body mass index (BMI) and better overall survival (OS) in metastatic renal cell carcinoma (mRCC) patients treated with vascular endothelial growth factor-tyrosine kinase inhibitors (VEGF-TKIs). Objective: The current study sought to determine whether the effect of BMI on OS extends beyond VEGF-TKIs to mTOR inhibitors or immunotherapy (IO). Design, Setting and Participants: A retrospective study was conducted among patients diagnosed with mRCC treated at a single institution from 2009 to 2017. Demographic and clinical variables were collected. BMI was characterized as high (≥25 kg/m2) versus low (<25 kg/m2). Outcomes Measurement and Statistical Analysis: The Kaplan-Meier method was used to estimate the difference in OS, with comparisons based on BMI and by treatment type. Results and Limitations: Among 353 patients (M = 64 years old, 73% male) 66% were overweight or obese (BMI ≥ 25 kg/m2). Patients were treated with VEGF-TKI (65%), mTOR (23%), or IO (12%). Among patients treated with VEGF-TKI with low BMI, median OS was 24.0 months (95% CI, 20.7–27.2) versus 36.0 months (95% CI, 18.6–53.3) among patients with high BMI (P = 0.02). The median OS for patients with low BMI treated with mTOR was 18.0 months (95% CI, 2.8–33.1), versus 25.0 months (95% CI, 16.6–33.4) among patients with high BMI (P = 0.04). In contrast, patients with low BMI treated with IO had a median OS of 23.6 months (95% CI, 17.5–29.7) versus 19.9 months (95% CI, 10.6–29.2) among patients with high BMI (P = 0.26). The retrospective nature and the small sample size are the main limitations of this study. Conclusions: High-BMI was associated with improved OS in patients with mRCC treated with VEGF-TKI and mTOR, but the inverse trend was observed among patients receiving IO. Our data highlight the need to reassess this phenomenon in the context of IO-based regimens.
靶向治疗和免疫治疗:体重指数对转移性肾癌患者临床预后的影响
背景:先前的研究已经发现,在接受血管内皮生长因子-酪氨酸激酶抑制剂(VEGF-TKIs)治疗的转移性肾癌(mRCC)患者中,高体重指数(BMI)与更好的总生存率(OS)之间存在关联。目的:目前的研究旨在确定BMI对OS的影响是否从VEGF-TKIs延伸到mTOR抑制剂或免疫治疗(IO)。设计、环境和参与者:对2009年至2017年在单一机构接受治疗的mRCC患者进行了回顾性研究。收集人口学和临床变量。BMI分为高(≥25 kg/m2)和低(<25 kg/m2)。结果测量与统计分析:采用Kaplan-Meier法估计OS的差异,并根据BMI和治疗类型进行比较。结果与局限性:353例患者(M = 64岁,73%为男性)中,66%超重或肥胖(BMI≥25 kg/m2)。患者接受VEGF-TKI(65%)、mTOR(23%)或IO(12%)治疗。在接受VEGF-TKI治疗的低BMI患者中,中位OS为24.0个月(95% CI, 20.7-27.2),而在高BMI患者中,中位OS为36.0个月(95% CI, 18.6-53.3) (P = 0.02)。接受mTOR治疗的低BMI患者的中位OS为18.0个月(95% CI, 2.8-33.1),而高BMI患者的中位OS为25.0个月(95% CI, 16.6-33.4) (P = 0.04)。相比之下,接受IO治疗的低BMI患者的中位OS为23.6个月(95% CI, 17.5-29.7),而高BMI患者的中位OS为19.9个月(95% CI, 10.6-29.2) (P = 0.26)。回顾性和小样本量是本研究的主要局限性。结论:在接受VEGF-TKI和mTOR治疗的mRCC患者中,高bmi与OS改善相关,但在接受IO治疗的患者中观察到相反的趋势。我们的数据强调需要在基于io的方案背景下重新评估这一现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Kidney Cancer
Kidney Cancer Multiple-
CiteScore
0.90
自引率
8.30%
发文量
23
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