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Efficacy of Prophylactic Treatment With Antibiotics During Concomitant Chemoradiotherapy in Patients With Head and Neck Cancer to Prevent Aspiration Pneumonia (PANTAP)

Primary Purpose

Head and Neck Cancer

Status
Unknown status
Phase
Phase 2
Locations
Netherlands
Study Type
Interventional
Intervention
amoxicillin/clavulanic acid suspension
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Head and Neck Cancer focused on measuring LAHNC, Locally Advanced Head and Neck Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

Sites / Locations

  • Ziekenhuis RijnstateRecruiting
  • University Medical Center Nijmegen st RadboudRecruiting
  • Medisch Centrum Alkmaar
  • University Medical Centre GroningenRecruiting
  • Medisch centrum Leeuwarden
  • Academical Hospital Maastricht (AZM)

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

No prophylactic treatment

prophylactic treatment

Arm Description

When 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).

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)

Outcomes

Primary Outcome Measures

the number of definite pneumonia and/ or suspected pneumonia
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

effects on Quality of Life
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-36
Number and kind of positive blood cultures
number of admissions to hospital
Number of days of admission
Effects on mortality
Mortality due to definite and/or suspected pneumonia
effects on mucositis: grade and duration
Mucositis grade according to CTCAE v.4.0 and duration
side effects of amoxicillin/clavulanic acid
side effects of amoxicillin/clavulanic acid
Effects on numbers and causative agents of infections at other sites
numbers and causative agents of infections at other sites during follow up (3.5 months after the end of CRT)

Full Information

First Posted
February 2, 2012
Last Updated
July 12, 2013
Sponsor
Radboud University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01598402
Brief Title
Efficacy of Prophylactic Treatment With Antibiotics During Concomitant Chemoradiotherapy in Patients With Head and Neck Cancer to Prevent Aspiration Pneumonia
Acronym
PANTAP
Official Title
Efficacy and Cost Efficacy of Prophylactic Treatment With Antibiotics During Concomitant Chemoradiotherapy in Patients With Locally Advanced Head and Neck Cancer to Prevent Aspiration Pneumonia. A Randomized Phase II-III Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2013
Overall Recruitment Status
Unknown status
Study Start Date
December 2011 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
December 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Cancer
Keywords
LAHNC, Locally Advanced Head and Neck Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
106 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
No prophylactic treatment
Arm Type
No Intervention
Arm Description
When 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).
Arm Title
prophylactic treatment
Arm Type
Experimental
Arm Description
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)
Intervention Type
Drug
Intervention Name(s)
amoxicillin/clavulanic acid suspension
Other Intervention Name(s)
The total duration of the use of amoxicillin /clavulanic acid suspension will be between 20 and 27 days.
Intervention Description
625 mg tid, start day 29 after the start of CRT until 14 days after the end of CRT
Primary Outcome Measure Information:
Title
the number of definite pneumonia and/ or suspected pneumonia
Description
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
Time Frame
from day 1 of 1 CRT until 3,5 mnd after the last CRT
Secondary Outcome Measure Information:
Title
effects on Quality of Life
Description
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-36
Time Frame
Baseline, Day 28 last day of CRT, 3,5 months after CRT
Title
Number and kind of positive blood cultures
Time Frame
from day 1 of 1 CRT until 3,5 mnd after the last CRT
Title
number of admissions to hospital
Time Frame
from day 1 of 1 CRT until 3,5 mnd after the last CRT
Title
Number of days of admission
Time Frame
from day 1 of 1 CRT until 3,5 mnd after the last CRT
Title
Effects on mortality
Description
Mortality due to definite and/or suspected pneumonia
Time Frame
from day 1 of 1 CRT until 3,5 mnd after the last CRT
Title
effects on mucositis: grade and duration
Description
Mucositis grade according to CTCAE v.4.0 and duration
Time Frame
from day 1 of 1 CRT until 3,5 mnd after the last CRT
Title
side effects of amoxicillin/clavulanic acid
Description
side effects of amoxicillin/clavulanic acid
Time Frame
from day 1 of 1 CRT until 3,5 mnd after the last CRT
Title
Effects on numbers and causative agents of infections at other sites
Description
numbers and causative agents of infections at other sites during follow up (3.5 months after the end of CRT)
Time Frame
during follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
C. van Herpen, Md
Phone
+31 24 361 03 53
Email
c.vanherpen@onco.umcn.nl
First Name & Middle Initial & Last Name or Official Title & Degree
C. Driessen, drs
Phone
+31 24 361 11 11
Ext
*pager: 3438
Email
c.driessen@onco.umcn.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
C. van Herpen, MD
Organizational Affiliation
University Medical Centre Nijmegen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ziekenhuis Rijnstate
City
Arnhem
State/Province
Gelderland
ZIP/Postal Code
6800 TA
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
J. Blaisse, Md
Phone
+31 26-3788888
Email
jblaiss@alysis.nl
First Name & Middle Initial & Last Name & Degree
S. Brouwer
Phone
+31 26-3788888
Email
sbrouwer@rijnstate.nl
First Name & Middle Initial & Last Name & Degree
J. Blaisse, Md
Facility Name
University Medical Center Nijmegen st Radboud
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6525 GH
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
C. van Herpen, Md
Phone
+31 24 361 03 53
Email
c.vanherpen@onco.umcn.nl
First Name & Middle Initial & Last Name & Degree
C. Driessen, drs
Phone
+31 24 361 11 11
Ext
pager 3438
Email
c.driessen@onco.umcn.nl
First Name & Middle Initial & Last Name & Degree
C.M.L van Herpen, Md, Phd
First Name & Middle Initial & Last Name & Degree
C. Driessen, drs
Facility Name
Medisch Centrum Alkmaar
City
Alkmaar
ZIP/Postal Code
1815 JD
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
C. Smorenburg, Md
Phone
+31 72-5484444
Email
c.h.smorenburg@mca.nl
First Name & Middle Initial & Last Name & Degree
M. Komen
Phone
+31 72-5484444
Email
manon.komen@mca.nl
First Name & Middle Initial & Last Name & Degree
C. Smorenburg, Md
Facility Name
University Medical Centre Groningen
City
Groningen
ZIP/Postal Code
9700 RB
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
J. Gietema, Md
Phone
+31 50 361 61 61
Email
j.a.gietema@med.umcg.nl
First Name & Middle Initial & Last Name & Degree
G. Sieling
Phone
+31 50 361 61 61
Email
g.c.m.sieling@umcg.nl
First Name & Middle Initial & Last Name & Degree
J. Gietema, Md
Facility Name
Medisch centrum Leeuwarden
City
Leeuwarden
ZIP/Postal Code
8934 AD
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
E. Fiets, Md
Phone
+31 58-2866666
Email
edward.fiets@znb.nl
First Name & Middle Initial & Last Name & Degree
T. Rienks
Phone
+31 58-2866666
Email
tineke.rienks@znb.nl
First Name & Middle Initial & Last Name & Degree
E. Fiets, Md
Facility Name
Academical Hospital Maastricht (AZM)
City
Maastricht
Country
Netherlands
Individual Site Status
Not yet recruiting
Facility Contact:
Email
ann.hoeben@mumc.nl
First Name & Middle Initial & Last Name & Degree
A. Hoeben, PhD

12. IPD Sharing Statement

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Efficacy of Prophylactic Treatment With Antibiotics During Concomitant Chemoradiotherapy in Patients With Head and Neck Cancer to Prevent Aspiration Pneumonia

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