Aim: A link has been established between malnutrition, immunological status, and hepatocellular carcinoma (HCC). The prognostic nutritional index (PNI) has been recognized as a prognostic indicator in early-stage HCC and in patients treated with first-line therapy. However, to date, the role of the PNI in HCC patients treated with regorafenib has not been reported. Methods: We undertook a multicentric analysis on a cohort of 284 patients affected by advanced HCC treated with regorafenib. The PNI was calculated as follows: 10 × serum albumin concentration (g/dl) + 0.005 × peripheral lymphocyte count (number/mm3). Univariate and multivariate analyses were used to investigate the association between PNI and survival outcomes. Results: A PNI cut-off value of 44.45 was calculated by a receiver operating characteristic analysis. The median overall survival was 12.8 and 7.8 months for patients with high (>44.45) and low (≤44.45) PNI, respectively (hazard ratio, 0.58; 95% confidence interval, 0.43–0.77; p = 0.0002). In the univariate and multivariate analyses, low PNI value and increased serum bilirubin level emerged as independent prognostic factors for overall survival. No differences were found between high and low PNI in terms of progression-free survival (p = 0.14). Conclusion: If validated, the PNI could represent an easy-to-use prognostic tool able to guide the clinical decision-making process in HCC patients treated with regorafenib.

Role of the prognostic nutritional index in predicting survival in advanced hepatocellular carcinoma treated with regorafenib / Rimini M.; Yoo C.; Lonardi S.; Masi G.; Piscaglia F.; Kim H.-D.; Rizzato M.D.; Salani F.; Ielasi L.; Forgione A.; Bang Y.; Solda C.; Catanese S.; Sansone V.; Ryu M.-H.; Ryoo B.-Y.; Burgio V.; Cucchetti A.; Cascinu S.; Casadei-Gardini A.. - In: HEPATOLOGY RESEARCH. - ISSN 1386-6346. - ELETTRONICO. - 51:7(2021), pp. 796-802. [10.1111/hepr.13669]

Role of the prognostic nutritional index in predicting survival in advanced hepatocellular carcinoma treated with regorafenib

Piscaglia F.;Ielasi L.;Forgione A.;Sansone V.;Cucchetti A.;
2021

Abstract

Aim: A link has been established between malnutrition, immunological status, and hepatocellular carcinoma (HCC). The prognostic nutritional index (PNI) has been recognized as a prognostic indicator in early-stage HCC and in patients treated with first-line therapy. However, to date, the role of the PNI in HCC patients treated with regorafenib has not been reported. Methods: We undertook a multicentric analysis on a cohort of 284 patients affected by advanced HCC treated with regorafenib. The PNI was calculated as follows: 10 × serum albumin concentration (g/dl) + 0.005 × peripheral lymphocyte count (number/mm3). Univariate and multivariate analyses were used to investigate the association between PNI and survival outcomes. Results: A PNI cut-off value of 44.45 was calculated by a receiver operating characteristic analysis. The median overall survival was 12.8 and 7.8 months for patients with high (>44.45) and low (≤44.45) PNI, respectively (hazard ratio, 0.58; 95% confidence interval, 0.43–0.77; p = 0.0002). In the univariate and multivariate analyses, low PNI value and increased serum bilirubin level emerged as independent prognostic factors for overall survival. No differences were found between high and low PNI in terms of progression-free survival (p = 0.14). Conclusion: If validated, the PNI could represent an easy-to-use prognostic tool able to guide the clinical decision-making process in HCC patients treated with regorafenib.
2021
Role of the prognostic nutritional index in predicting survival in advanced hepatocellular carcinoma treated with regorafenib / Rimini M.; Yoo C.; Lonardi S.; Masi G.; Piscaglia F.; Kim H.-D.; Rizzato M.D.; Salani F.; Ielasi L.; Forgione A.; Bang Y.; Solda C.; Catanese S.; Sansone V.; Ryu M.-H.; Ryoo B.-Y.; Burgio V.; Cucchetti A.; Cascinu S.; Casadei-Gardini A.. - In: HEPATOLOGY RESEARCH. - ISSN 1386-6346. - ELETTRONICO. - 51:7(2021), pp. 796-802. [10.1111/hepr.13669]
Rimini M.; Yoo C.; Lonardi S.; Masi G.; Piscaglia F.; Kim H.-D.; Rizzato M.D.; Salani F.; Ielasi L.; Forgione A.; Bang Y.; Solda C.; Catanese S.; Sansone V.; Ryu M.-H.; Ryoo B.-Y.; Burgio V.; Cucchetti A.; Cascinu S.; Casadei-Gardini A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/851743
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