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Articles

Geriatric Nutritional Risk Index as a Predictor of Prognosis in Metastatic Renal Cell Carcinoma Treated with Nivolumab

ORCID Icon, , , , , , , , , & show all
Pages 670-677 | Received 27 Jun 2022, Accepted 22 Nov 2022, Published online: 30 Nov 2022
 

Abstract

Background

The Geriatric Nutritional Risk Index (GNRI) has been reported as a screening tool to assess the nutrition-related risk with mortality in older patients and those with the various diseases. However, the prognostic value of GNRI in metastatic renal cell carcinoma (mRCC) patients receiving nivolumab therapy remains unclear.

Methods

Fifty-six consecutive patients with mRCC receiving nivolumab between September 2013 and August 2020 at our institution were retrospectively analyzed. The survival outcomes and prognostic factors associated with overall survival (OS) were statistically analyzed.

Results

Thirteen and forty-three patients were classified with low (GNRI < 92) and high (GNRI ≥ 92) GNRI, respectively. Patients with low GNRI demonstrated significantly shorter OS (P = 0.0002) than those with high GNRI. In multivariate analysis, GNRI at the time of nivolumab (P = 0.008) was extracted as the predictor for OS in addition to Karnofsky performance status (KPS) (P = 0.016). Integration of the GNRI into the International Metastatic Renal Cell Cancer Database Consortium (IMDC) risk classification improved the c-index from 0.761 to 0.833 (combination of GNRI with IMDC risk classification) and to 0.778 (substitution of GNRI with KPS in IMDC risk classification).

Conclusions

GNRI was a significant prognostic biomarker in mRCC patients receiving nivolumab.

Author contributions

Conception and design: RF, TY, SY, administrative support: TY, JY, collection and assembly of data: RF, TY, data analysis and interpretation: RF, MF, KT, manuscript writing: RF. All authors final approval of manuscript.

Disclosure statement

T. Yuasa received remuneration for a lecture from Astellas (Tokyo, Japan), Sanofi Japan (Tokyo, Japan), Pfizer Japan (Tokyo, Japan), Novartis Pharma Japan (Tokyo, Japan), Ono Pharma (Osaka, Japan), Bristol-Myers Squibb Japan (Tokyo, Japan), Janssen Pharmaceutical K.K Japan (Tokyo, Japan), MSD Japan (Tokyo, Japan), and Daiichi-Sankyo (Tokyo, Japan). The other authors have declared no conflicts of interest.

Additional information

Funding

This work was partly supported by JSPS KAKENHI under Grant number 16K11035 (T.Y.).

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