Cancers (Aug 2022)

The Association between a Decrease in On-Treatment Neutrophil-to-Eosinophil Ratio (NER) at Week 6 after Ipilimumab Plus Nivolumab Initiation and Improved Clinical Outcomes in Metastatic Renal Cell Carcinoma

  • Yu-Wei Chen,
  • Matthew D. Tucker,
  • Landon C. Brown,
  • Hesham A. Yasin,
  • Kristin K. Ancell,
  • Andrew J. Armstrong,
  • Kathryn E. Beckermann,
  • Nancy B. Davis,
  • Michael R. Harrison,
  • Elizabeth G. Kaiser,
  • Renee K. McAlister,
  • Kerry R. Schaffer,
  • Deborah E. Wallace,
  • Daniel J. George,
  • W. Kimryn Rathmell,
  • Brian I. Rini,
  • Tian Zhang

DOI
https://doi.org/10.3390/cancers14153830
Journal volume & issue
Vol. 14, no. 15
p. 3830

Abstract

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A lower baseline neutrophil-to-eosinophil ratio (NER) has been associated with improved responses to immune checkpoint inhibitors (ICI)-treated metastatic renal cell carcinoma (mRCC). This study investigated the decrease in NER at week 6 after ipilimumab/nivolumab (ipi/nivo) initiation and treatment responses in mRCC. A retrospective study of ipi/nivo-treated mRCC at two US academic cancer centers was conducted. A landmark analysis at week 6 was performed to assess the association between the change in NER and clinical responses (progression-free survival (PFS)/overall survival (OS)). Week 6 NER was modeled as a continuous variable, after log transformation (Ln NER), and a categorical variable by percent change. There were 150 mRCC patients included: 78% had clear cell histology, and 78% were IMDC intermediate/poor risk. In multivariable regression analysis, every decrease of 1 unit of Ln NER at week 6 was associated with improved PFS (adjusted hazard ratio (AHR): 0.78, p-value:0.005) and OS (AHR: 0.67, p-value: 0.002). When NER was modeled by percent change, decreased NER > 50% was associated with improved PFS (AHR: 0.55, p-value: 0.03) and OS (AHR: 0.37, p-value: 0.02). The decrease in week 6 NER was associated with improved PFS/OS in ipi/nivo-treated mRCC. Prospective studies are warranted to validate NER change as a biomarker to predict ICI responses.

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