Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Jan 23:2021:6688138.
doi: 10.1155/2021/6688138. eCollection 2021.

Prechemoradiotherapy Systemic Inflammation Response Index Stratifies Stage IIIB/C Non-Small-Cell Lung Cancer Patients into Three Prognostic Groups: A Propensity Score-Matching Analysis

Affiliations

Prechemoradiotherapy Systemic Inflammation Response Index Stratifies Stage IIIB/C Non-Small-Cell Lung Cancer Patients into Three Prognostic Groups: A Propensity Score-Matching Analysis

Erkan Topkan et al. J Oncol. .

Abstract

Purpose: We explored the prognostic influence of the systemic inflammation response index (SIRI) on the survival outcomes of stage IIIB/C non-small-cell lung cancer (NSCLC) patients who underwent concurrent chemoradiotherapy.

Methods: Present propensity score-matching (PSM) analysis comprised 876 stage IIIB/C NSCLC patients who received 1-3 cycles of platinum-based doublets concurrent with thoracic radiotherapy from 2007 to 2017. The primary and secondary objectives were the relationships between the SIRI values and overall (OS) and progression-free survival, respectively. Propensity scores were calculated for SIRI groups to adjust for confounders and to facilitate well-balanced comparability between the SIRI groups by creating 1 : 1 matched study groups.

Results: The receiver operating characteristic curve analysis identified an optimal SIRI cutoff at 1.9 for OS (AUC: 78.8%; sensitivity: 73.7%; specificity: 70.7%) and PFS (AUC: 80.5%; sensitivity: 75.8%; specificity: 72.9%) and we grouped the patients into two PSM cohorts: SIRI < 1.9 (N = 304) and SIRI ≥ 1.9 (N = 304), respectively. The SIRI ≥ 1.9 cohort had significantly worse median OS (P < 0.001) and PFS (P < 0.001) than their SIRI < 1.9 companions. The further combination of SIRI with disease stage exhibited that the SIRI-1 (IIIB and SIRI < 1.9) and SIRI-3 (IIIC and SIRI ≥ 1.9) cohorts had the best and worst outcomes, respectively, with SIRI-2 cohort (IIIB and SIRI ≥ 1.9 or IIIC and SIRI < 1.9) being remained in between (P < 0.001 for OS and PFS, separately). In multivariate analysis, the two- and three-laddered stratifications per the 1.9 cutoffs and SIRI groups retained their independent significance, individually.

Conclusions: The SIRI ≥ 1.9 independently prognosticated significantly worse OS and PFS results and plated the stage IIIB/C patients into three fundamentally distinct prognostic groups.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
Results of receiver operating characteristic curve analyses: (a) progression-free survival; (b) overall survival.
Figure 2
Figure 2
Comparative survival outcomes according to pretreatment SIRI groups (red line: SIRI < 1.9 and dark blue line: SIRI ≥ 1.9): (a) progression-free survival; (b) overall survival.
Figure 3
Figure 3
Comparative survival outcomes according to grouping composite disease stage and pretreatment SIRI groups (red line: Group 1, IIIB and SIRI < 1.9; dark blue line: Group 2, IIIB and SIRI ≥ 1.9; green line: Group 3, IIIC and SIRI < 1.9; and orange line: Group 4, IIIC and SIRI ≥ 1.9): (a) progression-free survival; (b) overall survival.
Figure 4
Figure 4
Comparative survival outcomes according to three-laddered pretreatment SIRI groups (red line: SIRI-1, IIIB and SIRI < 1.9; dark blue line: SIRI-2, IIIB and SIRI ≥ 1.9 or IIIC and SIRI < 1.9; and green line: SIRI-3, IIIC and SIRI ≥ 1.9): (a) progression-free survival; (b) overall survival.

References

    1. Furuse K., Fukuoka M., Kawahara M., et al. Phase III study of concurrent versus sequential thoracic radiotherapy in combination with mitomycin, vindesine, and cisplatin in unresectable stage III non-small-cell lung cancer. Journal of Clinical Oncology. 1999;17(9):p. 2692. doi: 10.1200/jco.1999.17.9.2692. - DOI - PubMed
    1. Curran W. J., Jr., Paulus R., Langer C. J., et al. Sequential vs concurrent chemoradiation for stage III non-small cell lung cancer: randomized phase III trial RTOG 9410. JNCI Journal of the National Cancer Institute. 2011;103(19):1452–1460. doi: 10.1093/jnci/djr325. - DOI - PMC - PubMed
    1. Wrona A. Role of immunotherapy in stage III nonsmall cell lung cancer. Current Opinion in Oncology. 2019;31(1):18–23. doi: 10.1097/cco.0000000000000493. - DOI - PubMed
    1. Bradley J. D., Paulus R., Komaki R., et al. Standard-dose versus high-dose conformal radiotherapy with concurrent and consolidation carboplatin plus paclitaxel with or without cetuximab for patients with stage IIIA or IIIB non-small-cell lung cancer (RTOG 0617): a randomised, two-by-two factorial phase 3 study. The Lancet Oncology. 2015;16(2):187–199. doi: 10.1016/s1470-2045(14)71207-0. - DOI - PMC - PubMed
    1. Crohns M., Saarelainen S., Laine S., Poussa T., Alho H., Kellokumpu-Lehtinen P. Cytokines in bronchoalveolar lavage fluid and serum of lung cancer patients during radiotherapy-association of interleukin-8 and VEGF with survival. Cytokine. 2010;50(1):30–36. doi: 10.1016/j.cyto.2009.11.017. - DOI - PubMed

LinkOut - more resources