The relationship between pan-immune-inflammation value and survival outcomes in patients with metastatic renal cell carcinoma treated with nivolumab in the second line and beyond: A Turkish oncology group kidney cancer consortium (TKCC) study

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Date
2022Author
Tural, DenizYekeduz, Emre
Erturk, Ismail
Karakaya, Serdar
Erol, Cihan
Ercelep, Ozlem
Arslan, Cagatay
Sever, Ozlem Nuray
Senturk Oztas, Nihan
Kucukarda, Ahmet
Can, Orcun
Oksuzoglu, Berna
Sendur, Mehmet Ali
Karadurmus, Nuri
Urun, Yuksel
Kilickap, Saadettin
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Yekedüz E, Tural D, Ertürk İ, Karakaya S, Erol C, Ercelep Ö, Arslan Ç, Sever ÖN, Kılıçkap S, Şentürk Öztaş N, Küçükarda A, Can O, Öksüzoğlu B, Şendur MA, Karadurmuş N, Ürün Y. The relationship between pan-immune-inflammation value and survival outcomes in patients with metastatic renal cell carcinoma treated with nivolumab in the second line and beyond: a Turkish oncology group kidney cancer consortium (TKCC) study. J Cancer Res Clin Oncol. 2022 May 26. doi: 10.1007/s00432-022-04055-5. Epub ahead of print. PMID: 35616728.Abstract
Background Pan-immune-infammation value (PIV) is an easily accessible immune marker based on peripheral blood to
estimate prognosis in patients with cancer. This study evaluates the prognostic value of PIV in patients with metastatic renal
cell carcinoma (mRCC) treated with nivolumab.
Methods In this retrospective cohort study, patients with mRCC treated with nivolumab in the second line and beyond were
selected from the Turkish Oncology Group Kidney Cancer Consortium (TKCC) database. PIV was calculated using the
following formula: neutrophil (103
/mm3
) x monocyte (103
/mm3
) x platelet (103
/mm3
)/lymphocyte (103
/mm3
).
Results A total of 152 patients with mRCC were included in this study. According to cut-of value for PIV, 77 (50.7%) and
75 (49.3%) patients fell into PIV-low (≤ 372) and PIV-high (>372) groups, respectively. In multivariate analysis, PIV-high
(HR: 1.64, 95% CI 1.04–2.58, p=0.033 for overall survival (OS); HR: 1.55, 95% CI 1.02–2.38, p=0.042 for progression-free
survival (PFS)) was independent risk factor for OS and PFS after adjusting for confounding variables, such as performance
score, the International mRCC Database Consortium (IMDC) risk score, and liver metastasis.
Conclusion This study established that pre-treatment PIV might be a prognostic biomarker in patients with mRCC treated
with nivolumab in the second line and beyond.