Association between decline of neutrophil-to-eosinophil ratio (NER) at week 6 after ipilimumab plus nivolumab initiation and improved clinical outcomes in metastatic renal cell carcinoma (mRCC).

Authors

Yu-Wei Chen

Yu-Wei Chen

Vanderbilt Ingram Cancer Center, Nashville, TN

Yu-Wei Chen , Matthew D Tucker , Landon Carter Brown , Hesham Abdallah Yasin , Kristin Kathleen Ancell , Andrew J. Armstrong , Katy Beckermann , Nancy B. Davis , Michael Roger Harrison , Elizabeth Kaiser , Renee McAlister , Kerry Schaffer , Deborah Wallace , Daniel J. George , Wendy Kimryn Rathmell , Brian I. Rini , Tian Zhang

Organizations

Vanderbilt Ingram Cancer Center, Nashville, TN, Levine Cancer Institute Morehead, Charlotte, NC, Vanderbilt-Ingram Cancer Center, Nashville, TN, Duke Cancer Institute Center for Prostate and Urologic Cancers, Duke University School of Medicine, Durham, NC, Duke Cancer Institute Center for Prostate and Urologic Cancers, Duke University, Durham, NC, Vanderbilt University Medical Center, Nashville, TN, Duke Cancer Institute, Durham, NC, UT Southwestern Medical Center, Dallas, TX

Research Funding

U.S. National Institutes of Health

Background: Low baseline NER has been associated with improved response to immunotherapy in mRCC (PMID:34732251). The current study aimed to investigate the early decline of NER at week 6 after ipilimumab/nivolumab (ipi/nivo) initiation and treatment responses in mRCC. Methods: Retrospective chart review of ipi/nivo-treated mRCC patients at Vanderbilt-Ingram Cancer Center and Duke Cancer Institute was conducted. Landmark analysis at week 6 after ipi/nivo initiation was performed to assess the association between change in NER and clinical responses [progression-free survival (PFS)/overall survival (OS)]. Results: There were 150 mRCC patients included in the analysis: 78% had clear cell histology, 78% were IMDC intermediate/poor risk, and 74% were male. The median follow-up time was 11.9 months. After ipi/nivo initiation, the median NER decreased from 23.8 (interquartile range: 15.0-57.1) at baseline to 19.8 (10.6-40.8) at week 6; 102 (68%) patients had decreased NER. The NER at week 6 was grouped by percent change (≥ 50% decrease vs <50% decrease vs increase). In multivariable regression analysis after adjustment for age, sex, race, IMDC risk group, baseline NER, histology, prior systemic therapy, and prior nephrectomy (Table), decreased NER ≥ 50% was associated with improved PFS [adjusted hazard ratio (AHR): 0.55, p-value: 0.03] and OS (AHR: 0.38, p-value: 0.02) (Table). Stratified analysis was conducted by baseline NER [≥vs < baseline median NER (23.8)]: decreased NER ≥ 50% was associated with improved PFS (AHR: 0.46, p-value: 0.048) and OS (AHR: 0.29, p-value: 0.01) in the subgroup with high baseline NER. These associations were not observed in the subgroup with low baseline NER (p-value for PFS: 0.25; p-value for OS: 0.61). Conclusions: The decline of NER ≥50% at week 6 after ipi/nivo initiation was associated with improved PFS/OS in mRCC patients with high baseline NER. Prospective studies are warranted to validate NER change as a biomarker to predict response to ICIs in mRCC.

Association between change in NER at week 6 and clinical responses.

ORR
PFS
OS

%
Median (95%), monthsAHR (95%)
Median (95%), monthsAHR (95%)
All patients (N=150)





 Decreased NER ≥ 50% (N=44)
43%
7.5 (3.7-10.1)
0.55 (0.31-0.95)
NR (15.3-NR)
0.38 (0.17-0.85)
 Decreased NER < 50% (N=58)
36%
6.6 (2.5-13)
0.63 (0.38-1.05)
NR (22.5-NR)
0.52 (0.24-1.13)
 Increased NER (N=48)
25%
2.5 (1.4-4.2)
Ref
19.5 (7.6-NR)
Ref
Subgroup with high baseline NER (N=75)





 Decreased NER ≥ 50% (N=32)
41%
7.2 (1.8-10.0)
0.46 (0.22-1.00)
25.9 (12-NR)
0.29 (0.11-0.76)
 Decreased NER < 50% (N=23)
26%
2.2 (1.2-9.1)
0.59 (0.26-1.31)
28.2 (7.6-NR)
0.48 (0.17-1.41)
 Increased NER (N=20)
20%
1.7 (0.4-2.5)
Ref
7.0 (2.6-14.1)
Ref

PFS and OS were estimated by landmark analysis calculating from week 6 after ipi/nivo initiation.NR: not-reached.

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Abstract Details

Meeting

2022 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Genitourinary Cancer—Kidney and Bladder

Track

Genitourinary Cancer—Kidney and Bladder

Sub Track

Kidney Cancer

Citation

J Clin Oncol 40, 2022 (suppl 16; abstr 4527)

DOI

10.1200/JCO.2022.40.16_suppl.4527

Abstract #

4527

Poster Bd #

18

Abstract Disclosures