Survival Prediction by Baseline Systemic Immune-inflammation Index (SII) and its Changes During First-line Platinum-based Treatment in a Caucasian Population of Patients With Metastatic Urothelial Carcinoma (MUC).


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 20 09 2021
revised: 10 10 2021
accepted: 12 10 2021
entrez: 4 11 2021
pubmed: 5 11 2021
medline: 16 11 2021
Statut: ppublish

Résumé

Systemic immune-inflammation index (SII) predicts survival of patients with various malignancies. This study explored the prognostic value of SII in metastatic urothelial carcinoma (MUC) subjects. We evaluated 181 consecutive MUC patients treated with first-line platinum-based therapy. Karnofsky performance status <80% and visceral metastasis were present in 18.2% and 46.4% of patients, respectively. SII was based on platelet × neutrophil/lymphocyte counts. Study population was dichotomized by median into high and low SII groups before the initiation of chemotherapy and at week 6. Progression-free survival (PFS) and overall survival (OS) were estimated by the Kaplan-Meier method and compared with the log-rank test. At median follow-up of 9.6 months, 174 patients experienced disease progression and 173 died. Patients with low SII at baseline and at week 6 had significantly better PFS (HR=0.58; p=0.0002 and HR=0.55; p<0.0001) and OS (HR=0.54; p<0.0001 and HR=0.54; p<0.0001) compared to patients with high SII. Independent prognostic value of SII was confirmed in a multivariate analysis. High SII before chemotherapy that persists at week 6 negatively affects survival. SII at baseline can be used in the stratification of patients within clinical trials and in clinical practice.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Systemic immune-inflammation index (SII) predicts survival of patients with various malignancies. This study explored the prognostic value of SII in metastatic urothelial carcinoma (MUC) subjects.
PATIENTS AND METHODS METHODS
We evaluated 181 consecutive MUC patients treated with first-line platinum-based therapy. Karnofsky performance status <80% and visceral metastasis were present in 18.2% and 46.4% of patients, respectively. SII was based on platelet × neutrophil/lymphocyte counts. Study population was dichotomized by median into high and low SII groups before the initiation of chemotherapy and at week 6. Progression-free survival (PFS) and overall survival (OS) were estimated by the Kaplan-Meier method and compared with the log-rank test.
RESULTS RESULTS
At median follow-up of 9.6 months, 174 patients experienced disease progression and 173 died. Patients with low SII at baseline and at week 6 had significantly better PFS (HR=0.58; p=0.0002 and HR=0.55; p<0.0001) and OS (HR=0.54; p<0.0001 and HR=0.54; p<0.0001) compared to patients with high SII. Independent prognostic value of SII was confirmed in a multivariate analysis.
CONCLUSION CONCLUSIONS
High SII before chemotherapy that persists at week 6 negatively affects survival. SII at baseline can be used in the stratification of patients within clinical trials and in clinical practice.

Identifiants

pubmed: 34732448
pii: 41/11/5749
doi: 10.21873/anticanres.15391
doi:

Substances chimiques

Carboplatin BG3F62OND5
Cisplatin Q20Q21Q62J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5749-5759

Informations de copyright

Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Patrik Palacka (P)

2 Department of Oncology, Comenius University, Faculty of Medicine in Bratislava, Bratislava, Slovak Republic; pal_patrick@yahoo.co.uk.
National Cancer Institute, Bratislava, Slovak Republic.

Jan Slopovsky (J)

2 Department of Oncology, Comenius University, Faculty of Medicine in Bratislava, Bratislava, Slovak Republic.
National Cancer Institute, Bratislava, Slovak Republic.

Jana Obertova (J)

2 Department of Oncology, Comenius University, Faculty of Medicine in Bratislava, Bratislava, Slovak Republic.
National Cancer Institute, Bratislava, Slovak Republic.

Michal Chovanec (M)

2 Department of Oncology, Comenius University, Faculty of Medicine in Bratislava, Bratislava, Slovak Republic.
National Cancer Institute, Bratislava, Slovak Republic.

Katarina Rejlekova (K)

2 Department of Oncology, Comenius University, Faculty of Medicine in Bratislava, Bratislava, Slovak Republic.
National Cancer Institute, Bratislava, Slovak Republic.

Zuzana Sycova-Mila (Z)

National Cancer Institute, Bratislava, Slovak Republic.

Boris Kollarik (B)

Department of Urology, University Hospital in Bratislava, Bratislava, Slovak Republic.

Jozef Mardiak (J)

2 Department of Oncology, Comenius University, Faculty of Medicine in Bratislava, Bratislava, Slovak Republic.
National Cancer Institute, Bratislava, Slovak Republic.

Michal Mego (M)

2 Department of Oncology, Comenius University, Faculty of Medicine in Bratislava, Bratislava, Slovak Republic.
National Cancer Institute, Bratislava, Slovak Republic.

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Classifications MeSH