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Comparison between adult comorbidity evaluation-27 and Charlson Comorbidity Index in head and neck oncology
Sierat Ahmad Khan1, Diako Berzenji1, Atilla Gül2
1Department of Otorhinolaryngology and Head and Neck Surgery, Erasmus MC Cancer Institute, Erasmus University Medical Center, Doctor Molewaterplein 40, 3015 GD Rotterdam, The Netherlands.
Objectives:
To determine whether Adult Comorbidity Evaluation-27 (ACE-27) or Charlson Comorbidity Index (CCI) is more accurate in predicting overall survival in head and neck squamous cell cancer (HNSCC) patients.
Methods:
A retrospective study was conducted on all patients with a primary HNSCC diagnosis and treatment between January 1st, 2010, and December 31th, 2013 at ErasmusMC, the Netherlands. Medical records were reviewed for patient data. The following covariables were considered: sex, age, subsite of the index HNSCC, treatment, TNM-stage, tobacco use and alcohol use. Significant covariables were identified with Kaplan-Meier analyses. Two Cox-regression models were made including the covariables and each comorbidity model. The primary endpoint was the c-statistic, with overall survival as the dependent variable and the covariables as the independent variables in the comorbidity models.
Results:
A total of 1,193 patients were included in the study, with an average age of 63.9 years (SD:10.7). In the Kaplan-Meier analysis, all variables, except sex, demonstrated a significant correlation with 5-year-overall survival. According to the Cox regression analysis, there was a HR of 2.462 (95 %CI:1.630-3.718) for a CCI of ≥ 5. The HR at an ACE-27 score of 3 was 1.969 (95 %CI:1.457-2.660). The model that incorporated the CCI score resulted in an average c-statistic of 0.6783 (range:0.6524-0.6935), while the mean c-statistic for the model with the ACE-27 was 0.6790 (range:0.6364-0.6973).
Conclusion:
In individuals diagnosed with HNSCC, both the ACE-27 and CCI serve as independent factors that reflect overall survival. Their predictive capabilities are comparable, allowing for their interchangeable use in both clinical and research contexts.
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