Cancer Medicine (Nov 2016)

Role of comorbidity on outcome of head and neck cancer: a population‐based study in Thuringia, Germany

  • Irene Göllnitz,
  • Johanna Inhestern,
  • Thomas G. Wendt,
  • Jens Buentzel,
  • Dirk Esser,
  • Daniel Böger,
  • Andreas H. Mueller,
  • Jörn‐Uwe Piesold,
  • Stefan Schultze‐Mosgau,
  • Ekkehard Eigendorff,
  • Peter Schlattmann,
  • Orlando Guntinas‐Lichius

DOI
https://doi.org/10.1002/cam4.882
Journal volume & issue
Vol. 5, no. 11
pp. 3260 – 3271

Abstract

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Abstract To examine the impact of comorbidity on overall survival (OS) in a population‐based study of patients with head and neck cancer who were treated between 2009 and 2011. Data of 1094 patients with primary head and neck carcinomas without distant metastasis from the Thuringian cancer registries were evaluated concerning the influence of patient's characteristics and comorbidity on OS. Data on comorbidity prior to head and neck cancer diagnosis was adapted to the Charlson Comorbidity (CCI), age‐adjusted CCI (ACCI), head and neck CCI (HNCCI), simplified comorbidity score (SCS), and to the Adult Comorbidity Evaluation–27 (ACE‐27). Most patients were male (80%; median age: 60 years; 50% stage IV tumors). Smoking, alcohol abuse, and anemia were registered for 38%, 33%, and 23% of the patients, respectively. Predominant therapy was surgery + radiochemotherapy (30%), surgery (29%), and surgery + radiotherapy (21%). Mean CCI, ACCI, HNCCI, SCS and ACE‐27 were 1.0 ± 1.5, 2.6 ± 2.1, 0.6 ± 0.8, 4.4 ± 4.2, and 0.9 ± 0.9, respectively. Median follow‐up was 25.7 months. Multivariable analyses showed that higher age, higher UICC stage, no therapy, including surgery or radiotherapy, alcohol abuse, and anemia, higher comorbidity were independent risk factors for worse OS (all P < 0.05). According to the discriminatory power analysis none of the five comorbidity scores was superior to the other scores to prognosticate OS. This population‐based study showed that comorbidity is frequent in German patients with head and neck cancer and is an important risk factor for poor OS. Comorbidity should be routinely assessed and taken into account in prospective clinical trials.

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