Systemic inflammation is associated with inferior disease control and survival in stage III non-small cell lung cancer.

Non-small cell lung cancer (NSCLC) inflammation systemic immune-inflammation index (SII)

Journal

Annals of translational medicine
ISSN: 2305-5839
Titre abrégé: Ann Transl Med
Pays: China
ID NLM: 101617978

Informations de publication

Date de publication:
Feb 2021
Historique:
entrez: 12 3 2021
pubmed: 13 3 2021
medline: 13 3 2021
Statut: ppublish

Résumé

The systemic immune-inflammation index (SII) correlates with patient survival in various types of solid malignancies, including non-small cell lung cancer (NSCLC). However, limited information is available on the prognostic implication and disease-specific survival of SII in patients undergoing definitive chemoradiation therapy (CRT) for stage III NSCLC. We retrospectively reviewed 125 patients who underwent curative intent CRT for stage III NSCLC with sufficient laboratory assessment from 2010-2019. SII was calculated at the time of diagnosis as platelet count × neutrophil count/lymphocyte count. Chi-squared analysis was used to compare categorical variables. A Kaplan-Meier analysis was performed to estimate progression-free survival (PFS), disease specific survival (DSS), and overall survival (OS) rates, with Cox regression used to determine absolute hazards. At a median follow-up of 19.7 months, 5-year OS, DSS, and PFS rates were 22.6%, 30.9%, and 13.4%, respectively. A low SII (<1,266) at diagnosis was independently associated with an improved OS (HR: 0.399, 95%, CI: 0.247-0.644, P<0.001), DSS (HR: 0.383, 95%, CI: 0.228-0.645, P<0.001), and PFS (HR: 0.616, 95%, CI: 0.407-0.932, P=0.022). We did not detect an association between SII and freedom from recurrence (FFR), freedom from locoregional recurrence (FFLRR), or freedom from distant recurrence (FFDR). NSAID (1,483.4 Low SII scores were independently associated with improved OS, DSS, and PFS rates in patients with stage III NSCLC undergoing definitive CRT. NSAIDs and statin usage may be associated with lower SII at diagnosis of NSCLC. This study suggests that SII may be an effective prognostic indicator of patient mortality. Further investigation of the therapeutic potential of these agents in patients with an elevated SII in this setting may be warranted.

Sections du résumé

BACKGROUND BACKGROUND
The systemic immune-inflammation index (SII) correlates with patient survival in various types of solid malignancies, including non-small cell lung cancer (NSCLC). However, limited information is available on the prognostic implication and disease-specific survival of SII in patients undergoing definitive chemoradiation therapy (CRT) for stage III NSCLC.
METHODS METHODS
We retrospectively reviewed 125 patients who underwent curative intent CRT for stage III NSCLC with sufficient laboratory assessment from 2010-2019. SII was calculated at the time of diagnosis as platelet count × neutrophil count/lymphocyte count. Chi-squared analysis was used to compare categorical variables. A Kaplan-Meier analysis was performed to estimate progression-free survival (PFS), disease specific survival (DSS), and overall survival (OS) rates, with Cox regression used to determine absolute hazards.
RESULTS RESULTS
At a median follow-up of 19.7 months, 5-year OS, DSS, and PFS rates were 22.6%, 30.9%, and 13.4%, respectively. A low SII (<1,266) at diagnosis was independently associated with an improved OS (HR: 0.399, 95%, CI: 0.247-0.644, P<0.001), DSS (HR: 0.383, 95%, CI: 0.228-0.645, P<0.001), and PFS (HR: 0.616, 95%, CI: 0.407-0.932, P=0.022). We did not detect an association between SII and freedom from recurrence (FFR), freedom from locoregional recurrence (FFLRR), or freedom from distant recurrence (FFDR). NSAID (1,483.4
CONCLUSIONS CONCLUSIONS
Low SII scores were independently associated with improved OS, DSS, and PFS rates in patients with stage III NSCLC undergoing definitive CRT. NSAIDs and statin usage may be associated with lower SII at diagnosis of NSCLC. This study suggests that SII may be an effective prognostic indicator of patient mortality. Further investigation of the therapeutic potential of these agents in patients with an elevated SII in this setting may be warranted.

Identifiants

pubmed: 33708854
doi: 10.21037/atm-20-6710
pii: atm-09-03-227
pmc: PMC7940875
doi:

Types de publication

Journal Article

Langues

eng

Pagination

227

Informations de copyright

2021 Annals of Translational Medicine. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm-20-6710). The authors have no conflicts of interest to declare.

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Auteurs

Emily Keit (E)

Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, USA.

Brendan Coutu (B)

Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, USA.

Weining Zhen (W)

Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, USA.

Chi Zhang (C)

Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, USA.

Chi Lin (C)

Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, USA.

Nathan Bennion (N)

Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, USA.

Apar Kishor Ganti (AK)

Division of Hematology/Oncology, Department of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Division of Hematology/Oncology, Department of Medicine, VA Nebraska Western Iowa Health Care System, Omaha, NE, USA.

Vinicius Ernani (V)

Division of Hematology/Oncology, Department of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.

Michael Baine (M)

Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, USA.

Classifications MeSH