Risk factors for aspiration pneumonia during concurrent chemoradiotherapy or bio-radiotherapy for head and neck cancer.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
04 Mar 2020
Historique:
received: 27 06 2019
accepted: 26 02 2020
entrez: 6 3 2020
pubmed: 7 3 2020
medline: 24 10 2020
Statut: epublish

Résumé

Aspiration pneumonia is one of the most important side effects of chemoradiotherapy (CRT) and bio-radiotherapy (BRT) in patients with head and neck cancer (HNC). Aspiration pneumonia can lead to cancer-related mortality in HNC patients. However, the relationship between aspiration pneumonia occurring during CRT or BRT for HNC and treatment outcomes in HNC patients is not well characterized. In this study, we assessed the influence of aspiration pneumonia on treatment outcomes and sought to identify the clinical risk factors for aspiration pneumonia during definitive CRT and BRT in HNC patients. We retrospectively assessed the data pertaining to patients with locally advanced HNC who received definitive CRT or BRT at the Shizuoka Cancer Center between August 2006 and December 2016. Among the 374 HNC patients who received CRT or BRT, 95 (25.4%) developed aspiration pneumonia during treatment. Aspiration pneumonia was significantly associated with therapeutic response to CRT or BRT (multivariate adjusted odds ratio for complete response, 0.52, p = 0.020) and poor overall survival (multivariate adjusted hazard ratio for overall survival, 1.58, p = 0.024). The multivariate analyses identified four independent factors for aspiration pneumonia: poor oral hygiene, high N-classification, hypoalbuminemia before treatment, and inpatient treatment. Aspiration pneumonia occurring during CRT or BRT has a detrimental effect on the therapeutic response and survival of HNC patients. Careful attention should be paid to these risk factors for aspiration pneumonia in HNC patients undergoing CRT or BRT.

Sections du résumé

BACKGROUND BACKGROUND
Aspiration pneumonia is one of the most important side effects of chemoradiotherapy (CRT) and bio-radiotherapy (BRT) in patients with head and neck cancer (HNC). Aspiration pneumonia can lead to cancer-related mortality in HNC patients. However, the relationship between aspiration pneumonia occurring during CRT or BRT for HNC and treatment outcomes in HNC patients is not well characterized. In this study, we assessed the influence of aspiration pneumonia on treatment outcomes and sought to identify the clinical risk factors for aspiration pneumonia during definitive CRT and BRT in HNC patients.
METHODS METHODS
We retrospectively assessed the data pertaining to patients with locally advanced HNC who received definitive CRT or BRT at the Shizuoka Cancer Center between August 2006 and December 2016.
RESULTS RESULTS
Among the 374 HNC patients who received CRT or BRT, 95 (25.4%) developed aspiration pneumonia during treatment. Aspiration pneumonia was significantly associated with therapeutic response to CRT or BRT (multivariate adjusted odds ratio for complete response, 0.52, p = 0.020) and poor overall survival (multivariate adjusted hazard ratio for overall survival, 1.58, p = 0.024). The multivariate analyses identified four independent factors for aspiration pneumonia: poor oral hygiene, high N-classification, hypoalbuminemia before treatment, and inpatient treatment.
CONCLUSIONS CONCLUSIONS
Aspiration pneumonia occurring during CRT or BRT has a detrimental effect on the therapeutic response and survival of HNC patients. Careful attention should be paid to these risk factors for aspiration pneumonia in HNC patients undergoing CRT or BRT.

Identifiants

pubmed: 32131771
doi: 10.1186/s12885-020-6682-1
pii: 10.1186/s12885-020-6682-1
pmc: PMC7057640
doi:

Substances chimiques

Rituximab 4F4X42SYQ6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

182

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Auteurs

Hiromichi Shirasu (H)

Shizuoka Cancer Center, Division of Gastrointestinal Oncology, 1007 Shimonagakubo Nagaizumi-cho Sunto-gun, Shizuoka, 411-8777, Japan.

Tomoya Yokota (T)

Shizuoka Cancer Center, Division of Gastrointestinal Oncology, 1007 Shimonagakubo Nagaizumi-cho Sunto-gun, Shizuoka, 411-8777, Japan. t.yokota@scchr.jp.

Satoshi Hamauchi (S)

Shizuoka Cancer Center, Division of Gastrointestinal Oncology, 1007 Shimonagakubo Nagaizumi-cho Sunto-gun, Shizuoka, 411-8777, Japan.

Yusuke Onozawa (Y)

Shizuoka Cancer Center, Division of Medical Oncology, Sunto-gun, Shizuoka, Japan.

Hirofumi Ogawa (H)

Shizuoka Cancer Center, Division of Radiation Oncology and Proton Therapy, Sunto-gun, Shizuoka, Japan.

Tsuyoshi Onoe (T)

Shizuoka Cancer Center, Division of Radiation Oncology and Proton Therapy, Sunto-gun, Shizuoka, Japan.

Tetsuro Onitsuka (T)

Shizuoka Cancer Center, Division of Head and Neck Surgery, Sunto-gun, Shizuoka, Japan.

Takashi Yurikusa (T)

Shizuoka Cancer Center, Division of Dentistry and Oral Surgery, Sunto-gun, Shizuoka, Japan.

Keita Mori (K)

Shizuoka Cancer Center, Clinical Research Center, Sunto-gun, Shizuoka, Japan.

Hirofumi Yasui (H)

Shizuoka Cancer Center, Division of Gastrointestinal Oncology, 1007 Shimonagakubo Nagaizumi-cho Sunto-gun, Shizuoka, 411-8777, Japan.

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Classifications MeSH