整合帕唑帕尼或卡博扎替尼治疗的转移性肾癌患者的红细胞特征和血红蛋白水平:一种易于利用的预后评分。

Giulia Mazzaschi, Alessandro Lazzarin, Matteo Santoni, Francesca Trentini, Ugo De Giorgi, Nicole Brighi, Chiara Tommasi, Silvia Puglisi, Orazio Caffo, Stefania Kinspergher, Alessia Mennitto, Carlo Cattrini, Elena Verzoni, Alessandro Rametta, Marco Stellato, Andrea Malgeri, Giandomenico Roviello, Enrico Maria Silini, Pasquale Rescigno, Sara Elena Rebuzzi, Giuseppe Fornarini, Federico Quaini, Giulia Claire Giudice, Giuseppe Luigi Banna, Sebastiano Buti
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引用次数: 0

摘要

背景:免疫检查点抑制剂(ICIs)的出现彻底改变了转移性肾细胞癌(mRCC)的治疗前景。尽管如此,靶向血管内皮生长因子(VEGF)轴的酪氨酸激酶抑制剂(TKIs)仍然发挥着关键作用。本研究的目的是探讨在接受抗VEGF TKIs治疗的mRCC患者中,基于血红蛋白(Hb)浓度、平均红细胞体积(MCV)和红细胞分布宽度(RDW)的综合血液评分的预后表现。主要终点是将Hb、MCV和RDW与无进展生存期(PFS)和总生存期(OS)相关联。材料和方法:我们的多中心回顾性观察性研究涉及2012年1月至2020年12月在九个意大利中心接受帕唑帕尼或卡博扎替尼治疗的mRCC患者。在基线时收集临床记录和实验室数据,包括Hb水平、MCV和RDW。进行描述性统计和单变量和多变量分析。结果:我们纳入了301例mRCC患者,其中179例(59%)接受了帕唑帕尼治疗,122例(41%)接受了卡博扎替尼治疗。我们认为基线Hb≥12 g/dL、MCV>87 fL和RDW≤16%是良好的预后因素;因此,开发了能够描绘4个不同类别的多参数评分。良好预后因素的数量与显著延长的PFS和OS相关(两者均为0.001)。因此,我们通过将病例分为两组(2-3对0-1,好因素),制定了基于红细胞的评分。对PFS和OS的影响更为显著(中位PFS(mPFS):16.3个月对7.9个月;中位OS(mOS):33.7 vs 14.1个月)。当单变量和多变量分析挑战时,血液评分在OS方面保持其较高的预后意义(OS的多变量分析HR:0.53,95%CI 0.39-0.75;p<0.001),而对PFS的影响导致临界意义。结论:我们的分析证明了基于易于利用的血液参数(如Hb浓度、MCV和RDW)的多参数评分的预后作用。基于红细胞的评分可能是HIF-1α通路和VEGF轴上调的基础,从而确定可能受益于TKI治疗的选定人群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrating Red Blood Cell Features and Hemoglobin Levels in Metastatic Renal Cell Carcinoma Patients Treated with Pazopanib or Cabozantinib: An Easily Exploitable Prognostic Score.

Background: The advent of immune checkpoint inhibitors (ICIs) has revolutionized the metastatic renal cell carcinoma (mRCC) therapeutic landscape. Nevertheless, tyrosine-kinase inhibitors (TKIs) targeting the vascular endothelial growth factor (VEGF) axis still play a key role. The aim of the present study was to explore the prognostic performance of an integrated blood score, based on hemoglobin (Hb) concentration, mean corpuscular volume (MCV), and red cell distribution width (RDW), in mRCC patients treated with anti-VEGF TKIs. The primary endpoint was to correlate Hb, MCV, and RDW with progression-free survival (PFS) and overall survival (OS).

Materials and methods: Our multicenter retrospective observational study involved mRCC patients treated with pazopanib or cabozantinib from January 2012 to December 2020 in nine Italian centers. Clinical records and laboratory data, including Hb levels, MCV, and RDW, were collected at baseline. Descriptive statistics and univariate and multivariate analyses were performed.

Results: We enrolled 301 mRCC patients of which 179 (59%) underwent pazopanib, and 122 (41%) cabozantinib. We considered baseline Hb ≥12 g/dL, MCV >87 fL, and RDW ≤16% as good prognostic factors; hence, developing a multiparametric score capable of delineating 4 different categories. The number of good prognostic factors was associated with significantly longer PFS and OS (p < 0.001 for both). Therefore, we developed a red blood cell-based score by stratifying cases into two groups (2-3 versus 0-1, good factors). The impact on PFS and OS was even more striking (median PFS (mPFS): 16.3 vs 7.9 months; median OS (mOS): 33.7 vs 14.1 months)), regardless of the TKI agent. When challenged with univariate and multivariate analysis, the blood score maintained its high prognostic significance in terms of OS (multivariate analysis HR for OS: 0.53, 95% CI 0.39-0.75; p < 0.001, respectively), while the impact on PFS resulted in borderline significance.

Conclusions: Our analyses demonstrate the prognostic role of a multiparametric score based on easily exploitable blood parameters, such as Hb concentration, MCV, and RDW. The red blood cell-based score may underlie the upregulation of the HIF-1α pathway and VEGF axis, thereby identifying a selected population who is likely to benefit from TKI therapy.

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