Predictive impact of C-reactive protein to albumin ratio for recurrent or metastatic head and neck squamous cell carcinoma receiving nivolumab
Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer, including recurrent or metastatic head and neck cancer (R/M HNSCC) treated with nivolumab, the usefulness of the pretreatment C-reactive protein/albumin ratio...
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Published in | Scientific reports Vol. 11; no. 1; p. 2741 |
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02.02.2021
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Abstract | Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer, including recurrent or metastatic head and neck cancer (R/M HNSCC) treated with nivolumab, the usefulness of the pretreatment C-reactive protein/albumin ratio (CAR) as a prognostic marker remains to be clarified. This study aimed to analyze the clinical usability of the CAR in comparison with that of the NLR. 46 R/M HNSCC patients treated with nivolumab were retrospectively analyzed. The optimal cutoff value for the CAR was calculated using receiver operating characteristic curve analysis. The optimal cutoff value for the CAR was set to 0.30. On multivariate analyses, a high CAR was significantly associated with poor overall survival (adjusted HR, 2.19; 95% CI, 1.42–3.47;
p
< 0.01) and progression-free survival (adjusted HR, 1.98; 95% CI, 1.38–2.80;
p
< 0.01). The overall response rate and disease control rate for the high CAR patients were lower than for the low CAR patients. The CAR had significantly higher area under the curve values than the NLR at 2 and 4 months. The pretreatment CAR might be an independent marker for prognosis and efficacy in R/M HNSCC patients treated with nivolumab. |
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AbstractList | Abstract
Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer, including recurrent or metastatic head and neck cancer (R/M HNSCC) treated with nivolumab, the usefulness of the pretreatment C-reactive protein/albumin ratio (CAR) as a prognostic marker remains to be clarified. This study aimed to analyze the clinical usability of the CAR in comparison with that of the NLR. 46 R/M HNSCC patients treated with nivolumab were retrospectively analyzed. The optimal cutoff value for the CAR was calculated using receiver operating characteristic curve analysis. The optimal cutoff value for the CAR was set to 0.30. On multivariate analyses, a high CAR was significantly associated with poor overall survival (adjusted HR, 2.19; 95% CI, 1.42–3.47;
p
< 0.01) and progression-free survival (adjusted HR, 1.98; 95% CI, 1.38–2.80;
p
< 0.01). The overall response rate and disease control rate for the high CAR patients were lower than for the low CAR patients. The CAR had significantly higher area under the curve values than the NLR at 2 and 4 months. The pretreatment CAR might be an independent marker for prognosis and efficacy in R/M HNSCC patients treated with nivolumab. Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer, including recurrent or metastatic head and neck cancer (R/M HNSCC) treated with nivolumab, the usefulness of the pretreatment C-reactive protein/albumin ratio (CAR) as a prognostic marker remains to be clarified. This study aimed to analyze the clinical usability of the CAR in comparison with that of the NLR. 46 R/M HNSCC patients treated with nivolumab were retrospectively analyzed. The optimal cutoff value for the CAR was calculated using receiver operating characteristic curve analysis. The optimal cutoff value for the CAR was set to 0.30. On multivariate analyses, a high CAR was significantly associated with poor overall survival (adjusted HR, 2.19; 95% CI, 1.42–3.47; p < 0.01) and progression-free survival (adjusted HR, 1.98; 95% CI, 1.38–2.80; p < 0.01). The overall response rate and disease control rate for the high CAR patients were lower than for the low CAR patients. The CAR had significantly higher area under the curve values than the NLR at 2 and 4 months. The pretreatment CAR might be an independent marker for prognosis and efficacy in R/M HNSCC patients treated with nivolumab. Abstract Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer, including recurrent or metastatic head and neck cancer (R/M HNSCC) treated with nivolumab, the usefulness of the pretreatment C-reactive protein/albumin ratio (CAR) as a prognostic marker remains to be clarified. This study aimed to analyze the clinical usability of the CAR in comparison with that of the NLR. 46 R/M HNSCC patients treated with nivolumab were retrospectively analyzed. The optimal cutoff value for the CAR was calculated using receiver operating characteristic curve analysis. The optimal cutoff value for the CAR was set to 0.30. On multivariate analyses, a high CAR was significantly associated with poor overall survival (adjusted HR, 2.19; 95% CI, 1.42–3.47; p < 0.01) and progression-free survival (adjusted HR, 1.98; 95% CI, 1.38–2.80; p < 0.01). The overall response rate and disease control rate for the high CAR patients were lower than for the low CAR patients. The CAR had significantly higher area under the curve values than the NLR at 2 and 4 months. The pretreatment CAR might be an independent marker for prognosis and efficacy in R/M HNSCC patients treated with nivolumab. Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer, including recurrent or metastatic head and neck cancer (R/M HNSCC) treated with nivolumab, the usefulness of the pretreatment C-reactive protein/albumin ratio (CAR) as a prognostic marker remains to be clarified. This study aimed to analyze the clinical usability of the CAR in comparison with that of the NLR. 46 R/M HNSCC patients treated with nivolumab were retrospectively analyzed. The optimal cutoff value for the CAR was calculated using receiver operating characteristic curve analysis. The optimal cutoff value for the CAR was set to 0.30. On multivariate analyses, a high CAR was significantly associated with poor overall survival (adjusted HR, 2.19; 95% CI, 1.42–3.47; p < 0.01) and progression-free survival (adjusted HR, 1.98; 95% CI, 1.38–2.80; p < 0.01). The overall response rate and disease control rate for the high CAR patients were lower than for the low CAR patients. The CAR had significantly higher area under the curve values than the NLR at 2 and 4 months. The pretreatment CAR might be an independent marker for prognosis and efficacy in R/M HNSCC patients treated with nivolumab. Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer, including recurrent or metastatic head and neck cancer (R/M HNSCC) treated with nivolumab, the usefulness of the pretreatment C-reactive protein/albumin ratio (CAR) as a prognostic marker remains to be clarified. This study aimed to analyze the clinical usability of the CAR in comparison with that of the NLR. 46 R/M HNSCC patients treated with nivolumab were retrospectively analyzed. The optimal cutoff value for the CAR was calculated using receiver operating characteristic curve analysis. The optimal cutoff value for the CAR was set to 0.30. On multivariate analyses, a high CAR was significantly associated with poor overall survival (adjusted HR, 2.19; 95% CI, 1.42-3.47; p < 0.01) and progression-free survival (adjusted HR, 1.98; 95% CI, 1.38-2.80; p < 0.01). The overall response rate and disease control rate for the high CAR patients were lower than for the low CAR patients. The CAR had significantly higher area under the curve values than the NLR at 2 and 4 months. The pretreatment CAR might be an independent marker for prognosis and efficacy in R/M HNSCC patients treated with nivolumab. |
ArticleNumber | 2741 |
Author | Mitsugi, Kenji Otsuka, Taiga Tamura, Shingo Ito, Mamoru Shirakawa, Tsuyoshi Baba, Eishi Tanaka, Risa Tsuchihashi, Kenji Koreishi, Sakuya Isobe, Taichi Shimokawa, Hozumi Ohmura, Hirofumi Kusaba, Hitoshi Shinohara, Yudai Ariyama, Hiroshi Tanoue, Kenro Akashi, Koichi Matsushita, Yuzo |
Author_xml | – sequence: 1 givenname: Kenro surname: Tanoue fullname: Tanoue, Kenro organization: Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University – sequence: 2 givenname: Shingo surname: Tamura fullname: Tamura, Shingo organization: Department of Medical Oncology, Clinical Research Institute, National Hospital Organization Kyushu Medical Center – sequence: 3 givenname: Hitoshi surname: Kusaba fullname: Kusaba, Hitoshi organization: Department of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital – sequence: 4 givenname: Yudai surname: Shinohara fullname: Shinohara, Yudai organization: Department of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital – sequence: 5 givenname: Mamoru surname: Ito fullname: Ito, Mamoru organization: Department of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital – sequence: 6 givenname: Kenji surname: Tsuchihashi fullname: Tsuchihashi, Kenji organization: Department of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital – sequence: 7 givenname: Tsuyoshi surname: Shirakawa fullname: Shirakawa, Tsuyoshi organization: Karatsu Higashi-Matsuura Medical Association Center – sequence: 8 givenname: Taiga surname: Otsuka fullname: Otsuka, Taiga organization: Department of Internal Medicine, Minato Medical Clinic – sequence: 9 givenname: Hirofumi surname: Ohmura fullname: Ohmura, Hirofumi organization: Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University – sequence: 10 givenname: Taichi surname: Isobe fullname: Isobe, Taichi organization: Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University – sequence: 11 givenname: Hiroshi surname: Ariyama fullname: Ariyama, Hiroshi organization: Department of Hematology, Oncology and Cardiovascular Medicine, Kyushu University Hospital – sequence: 12 givenname: Sakuya surname: Koreishi fullname: Koreishi, Sakuya organization: Department of Medical Oncology, Clinical Research Institute, National Hospital Organization Kyushu Medical Center – sequence: 13 givenname: Yuzo surname: Matsushita fullname: Matsushita, Yuzo organization: Department of Medical Oncology, Clinical Research Institute, National Hospital Organization Kyushu Medical Center – sequence: 14 givenname: Hozumi surname: Shimokawa fullname: Shimokawa, Hozumi organization: Department of Medical Oncology, Clinical Research Institute, National Hospital Organization Kyushu Medical Center – sequence: 15 givenname: Risa surname: Tanaka fullname: Tanaka, Risa organization: Department of Medical Oncology, Hamanomachi Hospital – sequence: 16 givenname: Kenji surname: Mitsugi fullname: Mitsugi, Kenji organization: Department of Medical Oncology, Hamanomachi Hospital – sequence: 17 givenname: Koichi surname: Akashi fullname: Akashi, Koichi organization: Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences, Kyushu University – sequence: 18 givenname: Eishi surname: Baba fullname: Baba, Eishi email: e-baba@intmed1.med.kyushu-u.ac.jp organization: Department of Oncology and Social Medicine, Graduate School of Medical Sciences, Kyushu University |
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Snippet | Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer, including... Abstract Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer,... Abstract Although the neutrophil to lymphocyte ratio (NLR) was reported to be a predictive biomarker for clinical outcomes in various types of cancer,... |
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SubjectTerms | 631/67/1536 631/67/1857 631/67/580 Albumin C-reactive protein Disease control Head & neck cancer Humanities and Social Sciences Immunotherapy Leukocytes (neutrophilic) Lymphocytes Medical prognosis Metastases Metastasis Monoclonal antibodies multidisciplinary Science Science (multidisciplinary) Squamous cell carcinoma Targeted cancer therapy |
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Title | Predictive impact of C-reactive protein to albumin ratio for recurrent or metastatic head and neck squamous cell carcinoma receiving nivolumab |
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