Efficacy of Prophylactic Treatment With Antibiotics During Concomitant Chemoradiotherapy in Patients With Head and Neck Cancer to Prevent Aspiration Pneumonia
- Conditions
- Head and Neck Cancer
- Interventions
- Drug: amoxicillin/clavulanic acid suspension
- Registration Number
- NCT01598402
- Lead Sponsor
- Radboud University Medical Center
- Brief Summary
Patients with locally advanced head and neck cancer treated with chemo-radiotherapy have (during and shortly after this treatment) a high risk of developing pneumonia by aspiration. This pneumonia is often associated with a hospital admission and affects the quality of life.
The purpose of the study, is to determine whether prophylactic antibiotics may decrease the development of pneumonia. Prophylactic antibiotics means that there are no signs of pneumonia are already
- Detailed Description
Concomitant chemoradiotherapy (CRT) is used in locally advanced head and neck cancer (LAHNC). It will be administered to patients for unresectable disease or for organ preservation as primary treatment. Furthermore, it can be used as postoperative treatment in case high risk recurrent disease is present. This treatment induces a high rate of acute toxicity, such as mucositis, dermatitis, dysphagia, anorexia, and pain. Swallowing dysfunction and aspiration are seen in a high proportion (30%-100%) of patients and with an immense impact on Quality of life (QoL).
Around half of the patients will develop an aspiration pneumonia during or shortly after the treatment.
Patients, who develop fever during concomitant chemoradiotherapy, are most of the time admitted in the hospital. In the differential diagnosis pneumonia is on the first place in all those patients. The standard diagnostic procedures consist of a chest X-ray and culture of the sputum and blood. Pneumonia can lead to mortality in this frail patient group.
The treatment of patients treated with chemoradiotherapy who develop fever and have a definite or suspected pneumonia, is administration of antibiotics, most frequently intravenous amoxicillin/clavulanic acid.
LAHNC patients who are smoking and/or with malnutrition are at the highest risk of getting a pneumonia during or after radiotherapy. Because smoking is one of the risk factors of developing head and neck cancer chronic obstructive pulmonary disease (COPD) is frequently present in this group. Also, COPD is a known risk factor for developing pneumonias.
Aspiration is seen in all primary sites of head and neck cancer, sometimes it is seen more frequently in patients with cancer of the larynx and hypopharynx. No data of prophylactic administration of antibiotics are available in LAHNC patients. However, a Cochrane review was published to assess the effects of prophylactic antibiotic regimens for the prevention of respiratory tract infections(RTIs) and overall mortality in adults receiving intensive care.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 106
- Patients with LAHNC which will be treated with CRT as discussed by a multidisciplinary team (i.e. a head and neck surgeon, a medical oncologist, and a radiation oncologist). This can be CRT as primary treatment or postoperative CRT.
- Written informed consent
- Expected adequacy of follow-up
- Patients with pneumonia within the last 14 days before start of CRT
- Patients with other infections within the last 14 days within the last 14 days before start of CRT
- Patients with use of maintenance antibiotics
- Patients with antibiotic treatment within the last 14 days before start of CRT
- Patients with an allergy on amoxicillin
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description prophylactic treatment amoxicillin/clavulanic acid suspension Administration of prophylactic amoxicillin/clavulanic acid suspension, 625 mg tid, start day 29 after the start of CRT until 14 days after the end of CRT. If a lower airway infection is suspected cultures will be taken and a chest radiography will be made; after that the standard care will be given (in most patients admission to hospital and start of intravenous antibiotics)
- Primary Outcome Measures
Name Time Method the number of definite pneumonia and/ or suspected pneumonia from day 1 of 1 CRT until 3,5 mnd after the last CRT Definite pneumonia:
Evidence of pneumonia on chest radiography or 3 or more of the following:
Sustained fever (temperature\> 100 f \[38°C\]), Rales or rhonchi on chest auscultation Sputum Gram stain showing substantial leukocytes Sputum culture showing a respiratory pathogen
Suspected pneumonia:
At least 2 of the 4 following features are present, without evidence of pneumonia on chest radiography:
Sustained fever (temperature\> 100 f \[38°C\]) Rales or rhonchi on chest auscultation Sputum Gram stain showing substantial leukocytes Sputum culture showing a respiratory pathogen
- Secondary Outcome Measures
Name Time Method effects on Quality of Life Baseline, Day 28 last day of CRT, 3,5 months after CRT to investigate the effects on QoL after prophylactic treatment with antibiotics
Patients fill in the following questionnaires:
QLQ-C30, EORTC H\&N35, PSHHN, EQ-5D and the VAS, SF-36Number and kind of positive blood cultures from day 1 of 1 CRT until 3,5 mnd after the last CRT number of admissions to hospital from day 1 of 1 CRT until 3,5 mnd after the last CRT Number of days of admission from day 1 of 1 CRT until 3,5 mnd after the last CRT Effects on mortality from day 1 of 1 CRT until 3,5 mnd after the last CRT Mortality due to definite and/or suspected pneumonia
effects on mucositis: grade and duration from day 1 of 1 CRT until 3,5 mnd after the last CRT Mucositis grade according to CTCAE v.4.0 and duration
side effects of amoxicillin/clavulanic acid from day 1 of 1 CRT until 3,5 mnd after the last CRT side effects of amoxicillin/clavulanic acid
Effects on numbers and causative agents of infections at other sites during follow up numbers and causative agents of infections at other sites during follow up (3.5 months after the end of CRT)
Trial Locations
- Locations (6)
University Medical Center Nijmegen st Radboud
🇳🇱Nijmegen, Gelderland, Netherlands
Medisch centrum Leeuwarden
🇳🇱Leeuwarden, Netherlands
University Medical Centre Groningen
🇳🇱Groningen, Netherlands
Medisch Centrum Alkmaar
🇳🇱Alkmaar, Netherlands
Academical Hospital Maastricht (AZM)
🇳🇱Maastricht, Netherlands
Ziekenhuis Rijnstate
🇳🇱Arnhem, Gelderland, Netherlands