Predicting the treatment outcome of nivolumab in recurrent or metastatic head and neck squamous cell carcinoma: prognostic value of combined performance status and modified Glasgow prognostic score

Purpose The importance of nivolumab for recurrent or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) is rapidly increasing. However, prognostic factors have not been determined for predicting treatment outcome. We aimed to investigate the prognostic factors in R/M HNSCC patients treat...

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Veröffentlicht in:European archives of oto-rhino-laryngology 2020-08, Vol.277 (8), p.2341-2347
Hauptverfasser: Ueki, Yushi, Takahashi, Takeshi, Ota, Hisayuki, Shodo, Ryusuke, Yamazaki, Keisuke, Horii, Arata
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container_issue 8
container_start_page 2341
container_title European archives of oto-rhino-laryngology
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creator Ueki, Yushi
Takahashi, Takeshi
Ota, Hisayuki
Shodo, Ryusuke
Yamazaki, Keisuke
Horii, Arata
description Purpose The importance of nivolumab for recurrent or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) is rapidly increasing. However, prognostic factors have not been determined for predicting treatment outcome. We aimed to investigate the prognostic factors in R/M HNSCC patients treated with nivolumab. Methods This retrospective study included 42 patients with R/M HNSCC who received nivolumab therapy. Correlations of overall survival (OS) with various patient characteristics including age, recurrent/metastatic site, performance status (PS), programmed death-ligand 1 positivity, body mass index, neutrophil-to-lymphocyte ratio, modified Glasgow prognostic score (mGPS), previous cetuximab administration, and immune-related adverse events were investigated. Results The overall response rate and disease control rate were 16.7% and 45.2%, respectively. Estimated 1-year OS and progression-free survival (PFS) were 56.4% and 24.5%, respectively. Multivariate analysis revealed that PS = 2 (hazard ratio 0.147; 95% CI 0.041–0.527; p  = 0.003) and mGPS = 2 (hazard ratio 0.188; 95% CI, 0.057–0.620; p  = 0.006) were independent predictors of poor OS. Given that the PS and mGPS were independent prognostic factors, we classified patients into three groups according to PS and mGPS: Group 1, both PS and mGPS were 0 or 1 ( n  = 30); Group 2, either PS or mGPS was 2 ( n  = 9); Group 3, both PS and mGPS were 2 ( n  = 3). The OS curves were significantly stratified among the three groups. Conclusion The combination of PS and mGPS accurately predicted OS after nivolumab therapy. Preventive intervention to maintain general condition without simultaneously exceeding level 2 of PS and mGPS might be important for improving treatment outcomes of nivolumab.
doi_str_mv 10.1007/s00405-020-05945-5
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However, prognostic factors have not been determined for predicting treatment outcome. We aimed to investigate the prognostic factors in R/M HNSCC patients treated with nivolumab. Methods This retrospective study included 42 patients with R/M HNSCC who received nivolumab therapy. Correlations of overall survival (OS) with various patient characteristics including age, recurrent/metastatic site, performance status (PS), programmed death-ligand 1 positivity, body mass index, neutrophil-to-lymphocyte ratio, modified Glasgow prognostic score (mGPS), previous cetuximab administration, and immune-related adverse events were investigated. Results The overall response rate and disease control rate were 16.7% and 45.2%, respectively. Estimated 1-year OS and progression-free survival (PFS) were 56.4% and 24.5%, respectively. Multivariate analysis revealed that PS = 2 (hazard ratio 0.147; 95% CI 0.041–0.527; p  = 0.003) and mGPS = 2 (hazard ratio 0.188; 95% CI, 0.057–0.620; p  = 0.006) were independent predictors of poor OS. Given that the PS and mGPS were independent prognostic factors, we classified patients into three groups according to PS and mGPS: Group 1, both PS and mGPS were 0 or 1 ( n  = 30); Group 2, either PS or mGPS was 2 ( n  = 9); Group 3, both PS and mGPS were 2 ( n  = 3). The OS curves were significantly stratified among the three groups. Conclusion The combination of PS and mGPS accurately predicted OS after nivolumab therapy. 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However, prognostic factors have not been determined for predicting treatment outcome. We aimed to investigate the prognostic factors in R/M HNSCC patients treated with nivolumab. Methods This retrospective study included 42 patients with R/M HNSCC who received nivolumab therapy. Correlations of overall survival (OS) with various patient characteristics including age, recurrent/metastatic site, performance status (PS), programmed death-ligand 1 positivity, body mass index, neutrophil-to-lymphocyte ratio, modified Glasgow prognostic score (mGPS), previous cetuximab administration, and immune-related adverse events were investigated. Results The overall response rate and disease control rate were 16.7% and 45.2%, respectively. Estimated 1-year OS and progression-free survival (PFS) were 56.4% and 24.5%, respectively. Multivariate analysis revealed that PS = 2 (hazard ratio 0.147; 95% CI 0.041–0.527; p  = 0.003) and mGPS = 2 (hazard ratio 0.188; 95% CI, 0.057–0.620; p  = 0.006) were independent predictors of poor OS. Given that the PS and mGPS were independent prognostic factors, we classified patients into three groups according to PS and mGPS: Group 1, both PS and mGPS were 0 or 1 ( n  = 30); Group 2, either PS or mGPS was 2 ( n  = 9); Group 3, both PS and mGPS were 2 ( n  = 3). The OS curves were significantly stratified among the three groups. Conclusion The combination of PS and mGPS accurately predicted OS after nivolumab therapy. 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However, prognostic factors have not been determined for predicting treatment outcome. We aimed to investigate the prognostic factors in R/M HNSCC patients treated with nivolumab. Methods This retrospective study included 42 patients with R/M HNSCC who received nivolumab therapy. Correlations of overall survival (OS) with various patient characteristics including age, recurrent/metastatic site, performance status (PS), programmed death-ligand 1 positivity, body mass index, neutrophil-to-lymphocyte ratio, modified Glasgow prognostic score (mGPS), previous cetuximab administration, and immune-related adverse events were investigated. Results The overall response rate and disease control rate were 16.7% and 45.2%, respectively. Estimated 1-year OS and progression-free survival (PFS) were 56.4% and 24.5%, respectively. Multivariate analysis revealed that PS = 2 (hazard ratio 0.147; 95% CI 0.041–0.527; p  = 0.003) and mGPS = 2 (hazard ratio 0.188; 95% CI, 0.057–0.620; p  = 0.006) were independent predictors of poor OS. Given that the PS and mGPS were independent prognostic factors, we classified patients into three groups according to PS and mGPS: Group 1, both PS and mGPS were 0 or 1 ( n  = 30); Group 2, either PS or mGPS was 2 ( n  = 9); Group 3, both PS and mGPS were 2 ( n  = 3). The OS curves were significantly stratified among the three groups. Conclusion The combination of PS and mGPS accurately predicted OS after nivolumab therapy. Preventive intervention to maintain general condition without simultaneously exceeding level 2 of PS and mGPS might be important for improving treatment outcomes of nivolumab.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32239313</pmid><doi>10.1007/s00405-020-05945-5</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-1699-7891</orcidid></addata></record>
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subjects Head and Neck
Head and Neck Neoplasms - drug therapy
Head and Neck Surgery
Humans
Medicine
Medicine & Public Health
Neurosurgery
Nivolumab
Otorhinolaryngology
Prognosis
Retrospective Studies
Squamous Cell Carcinoma of Head and Neck - drug therapy
Treatment Outcome
title Predicting the treatment outcome of nivolumab in recurrent or metastatic head and neck squamous cell carcinoma: prognostic value of combined performance status and modified Glasgow prognostic score
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