Bloodstream infections in head and neck cancer patients after curative-intent radiotherapy: a population-based study from the Danish Head and Neck Cancer Group database
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Bloodstream infections in head and neck cancer patients after curative-intent radiotherapy : a population-based study from the Danish Head and Neck Cancer Group database. / Jensen, Kristian Hastoft; Vogelius, Ivan; Moser, Claus Ernst; Andersen, Elo; Eriksen, Jesper Grau; Johansen, Jørgen; Farhadi, Mohammad; Andersen, Maria; Overgaard, Jens; Friborg, Jeppe.
In: British Journal of Cancer, Vol. 125, 2021, p. 458-464.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Bloodstream infections in head and neck cancer patients after curative-intent radiotherapy
T2 - a population-based study from the Danish Head and Neck Cancer Group database
AU - Jensen, Kristian Hastoft
AU - Vogelius, Ivan
AU - Moser, Claus Ernst
AU - Andersen, Elo
AU - Eriksen, Jesper Grau
AU - Johansen, Jørgen
AU - Farhadi, Mohammad
AU - Andersen, Maria
AU - Overgaard, Jens
AU - Friborg, Jeppe
N1 - Publisher Copyright: © 2021, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2021
Y1 - 2021
N2 - Background: Patients with head and neck squamous cell carcinoma (HNSCC) undergoing radiotherapy (RT) or chemoradiation (CRT) may become immunocompromised. In this population-based study, we aimed to investigate the risk factors, microbiological aetiologies, prognosis and impact on early non-cancer mortality of bloodstream infections (BSIs) after RT/CRT. Methods: Patients with HNSCC of the pharynx, larynx and oral cavity treated with curative-intent RT/CRT in Denmark between 2010 and 2017 and subsequent BSI episodes occurring within 18 months of RT/CRT initiation were identified in national registries. Results: We included 5674 patients and observed 238 BSIs. Increasing age, stage and performance status were significantly associated with an elevated BSI risk, while sex, smoking and high-grade mucositis were not. Human papillomavirus-positive oropharyngeal cancer patients had a decreased risk. Staphylococcus aureus accounted for 34% of episodes occurring during the first 3 months. The 30-day post-BSI mortality rate was 26% (95% confidence interval: 19–32) and BSIs were involved in 10% of early non-cancer deaths. Conclusion: The risk of BSI development is associated with several patient- and disease-related factors and BSIs contribute considerably to early non-cancer mortality. Empiric antibiotic treatment regimens should prioritise coverage for S. aureus when treating suspected systemic infection in this population.
AB - Background: Patients with head and neck squamous cell carcinoma (HNSCC) undergoing radiotherapy (RT) or chemoradiation (CRT) may become immunocompromised. In this population-based study, we aimed to investigate the risk factors, microbiological aetiologies, prognosis and impact on early non-cancer mortality of bloodstream infections (BSIs) after RT/CRT. Methods: Patients with HNSCC of the pharynx, larynx and oral cavity treated with curative-intent RT/CRT in Denmark between 2010 and 2017 and subsequent BSI episodes occurring within 18 months of RT/CRT initiation were identified in national registries. Results: We included 5674 patients and observed 238 BSIs. Increasing age, stage and performance status were significantly associated with an elevated BSI risk, while sex, smoking and high-grade mucositis were not. Human papillomavirus-positive oropharyngeal cancer patients had a decreased risk. Staphylococcus aureus accounted for 34% of episodes occurring during the first 3 months. The 30-day post-BSI mortality rate was 26% (95% confidence interval: 19–32) and BSIs were involved in 10% of early non-cancer deaths. Conclusion: The risk of BSI development is associated with several patient- and disease-related factors and BSIs contribute considerably to early non-cancer mortality. Empiric antibiotic treatment regimens should prioritise coverage for S. aureus when treating suspected systemic infection in this population.
U2 - 10.1038/s41416-021-01430-w
DO - 10.1038/s41416-021-01430-w
M3 - Journal article
C2 - 34017084
AN - SCOPUS:85105978114
VL - 125
SP - 458
EP - 464
JO - The British journal of cancer. Supplement
JF - The British journal of cancer. Supplement
SN - 0007-0920
ER -
ID: 302050612