Systemic immune-inflammation index changes predict outcome in stage III non-small-cell lung cancer patients treated with concurrent chemoradiotherapy

Although the systemic immune-inflammation index (SII) has been used to predict recurrence and survival in non-small-cell lung cancer (NSCLC) patients, the prognostic significance of change in SII (ΔSII) is unclear for stage III NSCLC patients treated with concurrent chemoradiotherapy (CCRT). In the...

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Veröffentlicht in:Future oncology (London, England) England), 2021-06, Vol.17 (17), p.2141-2149
Hauptverfasser: Huang, Taosheng, Zhang, Huanqian, Zhao, Yunzheng, Li, Yanping, Wang, Guofeng, Zhang, Yunbo, Guo, Dong, Ji, Shengjun, Sun, Zhenyou
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container_issue 17
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container_title Future oncology (London, England)
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creator Huang, Taosheng
Zhang, Huanqian
Zhao, Yunzheng
Li, Yanping
Wang, Guofeng
Zhang, Yunbo
Guo, Dong
Ji, Shengjun
Sun, Zhenyou
description Although the systemic immune-inflammation index (SII) has been used to predict recurrence and survival in non-small-cell lung cancer (NSCLC) patients, the prognostic significance of change in SII (ΔSII) is unclear for stage III NSCLC patients treated with concurrent chemoradiotherapy (CCRT). In the present study we aimed to explore the association between ΔSII and the clinical outcomes of 142 patients with stage III NSCLC treated with CCRT. A total of 142 patients were included in this retrospective study. The SII values were calculated based on laboratory data regarding platelet, neutrophil and lymphocyte counts, and ΔSII was calculated using data acquired before and approximately 2 weeks after CCRT. The receiver operating characteristic curve was used to determine the optimal cut-off value for the peripheral blood inflammation index. Kaplan–Meier analysis and Cox proportional regression were used to analyze the prognostic value of ΔSII for overall survival (OS) and progression-free survival (PFS). The area under the receiver operating characteristic curve for ΔSII (0.708) was larger than those for pre-CCRT SII (0.578) and post-CCRT SII (0.610). The optimal cut-off point for ΔSII was defined as 43. OS and PFS were better in patients with low ΔSII and in multivariate analysis, the ΔSII was an independent predictor of OS and PFS (p = 0.006 and p = 0.017, respectively). ΔSII is related to progression and death in patients with stage III NSCLC. The ΔSII can provide a detailed prognostic prediction for stage III NSCLC. Non-small-cell lung cancer (NSCLC) remains the leading cause of cancer-related death worldwide. For NSCLC patients, due to the occult onset and lack of obvious local symptoms, many patients are diagnosed with stage III disease. Despite carefully implemented treatment with concurrent chemoradiotherapy (CCRT), patients still have poor survival. It is necessary to explore whether biomarkers that predict risk stratification for patients could be used to guide individualized therapy. The systemic immune-inflammation index (SII) serves as a more objective marker in predicting the prognosis of patients with a variety of tumors. The difference in SII before and after treatment (ΔSII) represents the balance between inflammatory and immune status after the antitumor treatment, which may affect the prognosis. This article evaluates the prognostic significance of ΔSII in stage III NSCLC patients receiving chemoradiotherapy and discusses prospects for the fu
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In the present study we aimed to explore the association between ΔSII and the clinical outcomes of 142 patients with stage III NSCLC treated with CCRT. A total of 142 patients were included in this retrospective study. The SII values were calculated based on laboratory data regarding platelet, neutrophil and lymphocyte counts, and ΔSII was calculated using data acquired before and approximately 2 weeks after CCRT. The receiver operating characteristic curve was used to determine the optimal cut-off value for the peripheral blood inflammation index. Kaplan–Meier analysis and Cox proportional regression were used to analyze the prognostic value of ΔSII for overall survival (OS) and progression-free survival (PFS). The area under the receiver operating characteristic curve for ΔSII (0.708) was larger than those for pre-CCRT SII (0.578) and post-CCRT SII (0.610). The optimal cut-off point for ΔSII was defined as 43. OS and PFS were better in patients with low ΔSII and in multivariate analysis, the ΔSII was an independent predictor of OS and PFS (p = 0.006 and p = 0.017, respectively). ΔSII is related to progression and death in patients with stage III NSCLC. The ΔSII can provide a detailed prognostic prediction for stage III NSCLC. Non-small-cell lung cancer (NSCLC) remains the leading cause of cancer-related death worldwide. For NSCLC patients, due to the occult onset and lack of obvious local symptoms, many patients are diagnosed with stage III disease. Despite carefully implemented treatment with concurrent chemoradiotherapy (CCRT), patients still have poor survival. It is necessary to explore whether biomarkers that predict risk stratification for patients could be used to guide individualized therapy. The systemic immune-inflammation index (SII) serves as a more objective marker in predicting the prognosis of patients with a variety of tumors. The difference in SII before and after treatment (ΔSII) represents the balance between inflammatory and immune status after the antitumor treatment, which may affect the prognosis. 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In the present study we aimed to explore the association between ΔSII and the clinical outcomes of 142 patients with stage III NSCLC treated with CCRT. A total of 142 patients were included in this retrospective study. The SII values were calculated based on laboratory data regarding platelet, neutrophil and lymphocyte counts, and ΔSII was calculated using data acquired before and approximately 2 weeks after CCRT. The receiver operating characteristic curve was used to determine the optimal cut-off value for the peripheral blood inflammation index. Kaplan–Meier analysis and Cox proportional regression were used to analyze the prognostic value of ΔSII for overall survival (OS) and progression-free survival (PFS). The area under the receiver operating characteristic curve for ΔSII (0.708) was larger than those for pre-CCRT SII (0.578) and post-CCRT SII (0.610). The optimal cut-off point for ΔSII was defined as 43. OS and PFS were better in patients with low ΔSII and in multivariate analysis, the ΔSII was an independent predictor of OS and PFS (p = 0.006 and p = 0.017, respectively). ΔSII is related to progression and death in patients with stage III NSCLC. The ΔSII can provide a detailed prognostic prediction for stage III NSCLC. Non-small-cell lung cancer (NSCLC) remains the leading cause of cancer-related death worldwide. For NSCLC patients, due to the occult onset and lack of obvious local symptoms, many patients are diagnosed with stage III disease. Despite carefully implemented treatment with concurrent chemoradiotherapy (CCRT), patients still have poor survival. It is necessary to explore whether biomarkers that predict risk stratification for patients could be used to guide individualized therapy. The systemic immune-inflammation index (SII) serves as a more objective marker in predicting the prognosis of patients with a variety of tumors. The difference in SII before and after treatment (ΔSII) represents the balance between inflammatory and immune status after the antitumor treatment, which may affect the prognosis. 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In the present study we aimed to explore the association between ΔSII and the clinical outcomes of 142 patients with stage III NSCLC treated with CCRT. A total of 142 patients were included in this retrospective study. The SII values were calculated based on laboratory data regarding platelet, neutrophil and lymphocyte counts, and ΔSII was calculated using data acquired before and approximately 2 weeks after CCRT. The receiver operating characteristic curve was used to determine the optimal cut-off value for the peripheral blood inflammation index. Kaplan–Meier analysis and Cox proportional regression were used to analyze the prognostic value of ΔSII for overall survival (OS) and progression-free survival (PFS). The area under the receiver operating characteristic curve for ΔSII (0.708) was larger than those for pre-CCRT SII (0.578) and post-CCRT SII (0.610). The optimal cut-off point for ΔSII was defined as 43. OS and PFS were better in patients with low ΔSII and in multivariate analysis, the ΔSII was an independent predictor of OS and PFS (p = 0.006 and p = 0.017, respectively). ΔSII is related to progression and death in patients with stage III NSCLC. The ΔSII can provide a detailed prognostic prediction for stage III NSCLC. Non-small-cell lung cancer (NSCLC) remains the leading cause of cancer-related death worldwide. For NSCLC patients, due to the occult onset and lack of obvious local symptoms, many patients are diagnosed with stage III disease. Despite carefully implemented treatment with concurrent chemoradiotherapy (CCRT), patients still have poor survival. It is necessary to explore whether biomarkers that predict risk stratification for patients could be used to guide individualized therapy. The systemic immune-inflammation index (SII) serves as a more objective marker in predicting the prognosis of patients with a variety of tumors. The difference in SII before and after treatment (ΔSII) represents the balance between inflammatory and immune status after the antitumor treatment, which may affect the prognosis. This article evaluates the prognostic significance of ΔSII in stage III NSCLC patients receiving chemoradiotherapy and discusses prospects for the future.</abstract><cop>England</cop><pub>Future Medicine Ltd</pub><pmid>33635094</pmid><doi>10.2217/fon-2020-1272</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8067-5531</orcidid></addata></record>
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systemic immune-inflammation index
title Systemic immune-inflammation index changes predict outcome in stage III non-small-cell lung cancer patients treated with concurrent chemoradiotherapy
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