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Low-level Laser Therapy to Prevent Oral Mucositis in Head and Neck Patients

Primary Purpose

Squamous Cell Carcinoma of Nasopharynx, Squamous Cell Carcinoma of Oropharynx, Squamous Cell Carcinoma of Hypopharynx

Status
Completed
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Low Level Laser Therapy- (DMC, São Paulo, Brazil)
Placebo (DMC, São Paulo, Brazil)
Sponsored by
Instituto Nacional de Cancer, Brazil
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Squamous Cell Carcinoma of Nasopharynx focused on measuring Oral mucositis, Low Level Laser Therapy, Head and neck cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years
  • Histological diagnosis of squamous cell carcinoma (nasopharynx, oropharynx and hypopharynx)
  • Candidates for surgery or treatment for organ preservation
  • Performance status (PS) of 0 or 1 according to the Eastern Cooperative Oncology Group (ECOG)
  • Indication for radiotherapy and concurrent platinum-based chemotherapy
  • Oral mucosa intact
  • Agree to follow the protocol of oral hygiene
  • Informed consent.

Exclusion Criteria:

  • Patients using medication for treatment and or prevention of mucositis
  • Patients incapable of treatment compliance or of performing the protocol of oral hygiene

Sites / Locations

  • Instituto Nacional de Cancer

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Low Level Laser Therapy

Arm Description

Patients in the placebo group received the same treatment during the same time, but in this case the laser tip produced no light.

The investigators used a Low Level Laser Therapy, diode laser (DMC, São Paulo, Brazil) InGaAlP (indium phosphide, gallium and aluminum), with 100mW, 4J/cm ², with an area of 0.24 cm ². The laser was daily applied by a dentist and touched the mucosa of the lips, right and left buccal mucosa, left and right lateral tongue border, buccal floor and ventral tongue, totaling nine points per region.

Outcomes

Primary Outcome Measures

Incidence and / or Severity of Oral Mucositis
The oral cavities of all patients were evaluated daily, from the first day until the last day of treatment. We used the scales of mucositis of the World Health Organization (WHO) and the Oral Mucositis Assessment Scale (OMAS) and a visual analogue scale (VAS) for pain assessment.

Secondary Outcome Measures

Oral Mucositis Survival Free, Pain, Opioid Treatment, Hospitalization, Treatment Interruption, Treatment Delay, Patient Weight Loss, Nasogastric Tube or of a Gastrostomy.
Oral mucositis survival free, pain, opioid treatment, hospitalization, treatment interruption, treatment delay, patient weight loss, nasogastric tube or of a gastrostomy.The oral cavities of all patients were evaluated, from the first day to the last day of treatment.

Full Information

First Posted
September 20, 2011
Last Updated
March 7, 2014
Sponsor
Instituto Nacional de Cancer, Brazil
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1. Study Identification

Unique Protocol Identification Number
NCT01439724
Brief Title
Low-level Laser Therapy to Prevent Oral Mucositis in Head and Neck Patients
Official Title
Phase III Trial of Low-level Laser Therapy to Prevent Induced Oral Mucositis in Head and Neck Cancer Patients Submitted to Concurrent Chemoradiation
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
June 2008 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto Nacional de Cancer, Brazil

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Oral mucositis remains a limiting factor in in head and neck squamous cell carcinomas patients treated with chemoradiation leading to pain, dysphagia, and weight loss. Low-level laser therapy emerges as a promising, preventive therapy of chemoradiation-induced OM. This study was designed to assess the efficacy of Low Level Laser Therapy (LLLT) in reducing the incidence and/or severity of oral mucositis.
Detailed Description
Assuming oral mucositis grade 3 for placebo 0.4 (P0); laser group 0.15 (P1) ; β=0.2; α=0.05, sample size was 94 pts. From Jun 2007 to Dec 2010, 47 laser group and 47 placebo patients bearer of head and neck squamous cell carcinomas of nasopharynx, oropharynx and hypopharynx entered a prospective, randomized, double blind, placebo-controlled, phase III trial. chemoradiotherapy consisted of conventional radiotherapy 70.2 Gray (Gy) (1.8Gy/d, 5 times/wk) + concurrent cisplatin 100 mg/m2 every 3 weeks. The primary end point was the incidence of grade 3-4 oral mucositis. The Low-level laser therapy used daily, was a diode indium phosphide, gallium and aluminum (InGaAlP), 660nm-100 milliwatts (mW)-4 Joules (J)/cm²(DMC, São Carlos, São Paulo, Brazil). Oral mucositis evaluation was done by WHO and Oral Mucositis Assessment Scale (OMAS) scale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Squamous Cell Carcinoma of Nasopharynx, Squamous Cell Carcinoma of Oropharynx, Squamous Cell Carcinoma of Hypopharynx
Keywords
Oral mucositis, Low Level Laser Therapy, Head and neck cancer

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
94 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Patients in the placebo group received the same treatment during the same time, but in this case the laser tip produced no light.
Arm Title
Low Level Laser Therapy
Arm Type
Experimental
Arm Description
The investigators used a Low Level Laser Therapy, diode laser (DMC, São Paulo, Brazil) InGaAlP (indium phosphide, gallium and aluminum), with 100mW, 4J/cm ², with an area of 0.24 cm ². The laser was daily applied by a dentist and touched the mucosa of the lips, right and left buccal mucosa, left and right lateral tongue border, buccal floor and ventral tongue, totaling nine points per region.
Intervention Type
Device
Intervention Name(s)
Low Level Laser Therapy- (DMC, São Paulo, Brazil)
Other Intervention Name(s)
Low Power Laser Therapy, Low Energy Laser Therapy
Intervention Description
Diode laser (DMC,São Paulo, Brazil) InGaAlP (indium phosphide, gallium and aluminum), with 100 mW, 4J/cm ², with an area of 0.24 cm ². The laser was daily applied by a dentist and touched the mucosa of the lips, right and left buccal mucosa, left and right lateral tongue border, buccal floor and ventral tongue, totaling nine points per region.
Intervention Type
Device
Intervention Name(s)
Placebo (DMC, São Paulo, Brazil)
Other Intervention Name(s)
Low power laser therapy, Low energy laser therapy
Intervention Description
The placebo (DMC, São Paulo, Brazil) was daily applied by a dentist and touched the mucosa of the lips, right and left buccal mucosa, left and right lateral tongue border, buccal floor and ventral tongue, totaling nine points per region.Patients in the placebo group received the same treatment during the same time, but in this case the laser tip produced no light.
Primary Outcome Measure Information:
Title
Incidence and / or Severity of Oral Mucositis
Description
The oral cavities of all patients were evaluated daily, from the first day until the last day of treatment. We used the scales of mucositis of the World Health Organization (WHO) and the Oral Mucositis Assessment Scale (OMAS) and a visual analogue scale (VAS) for pain assessment.
Time Frame
7 weeks
Secondary Outcome Measure Information:
Title
Oral Mucositis Survival Free, Pain, Opioid Treatment, Hospitalization, Treatment Interruption, Treatment Delay, Patient Weight Loss, Nasogastric Tube or of a Gastrostomy.
Description
Oral mucositis survival free, pain, opioid treatment, hospitalization, treatment interruption, treatment delay, patient weight loss, nasogastric tube or of a gastrostomy.The oral cavities of all patients were evaluated, from the first day to the last day of treatment.
Time Frame
7 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years Histological diagnosis of squamous cell carcinoma (nasopharynx, oropharynx and hypopharynx) Candidates for surgery or treatment for organ preservation Performance status (PS) of 0 or 1 according to the Eastern Cooperative Oncology Group (ECOG) Indication for radiotherapy and concurrent platinum-based chemotherapy Oral mucosa intact Agree to follow the protocol of oral hygiene Informed consent. Exclusion Criteria: Patients using medication for treatment and or prevention of mucositis Patients incapable of treatment compliance or of performing the protocol of oral hygiene
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heliton S Antunes, DDS, PhD
Organizational Affiliation
Instituto Nacional de Cancer, Brazil
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Carlos G Ferreira, MD, PhD
Organizational Affiliation
Instituto Nacional de Cancer, Brazil
Official's Role
Study Director
Facility Information:
Facility Name
Instituto Nacional de Cancer
City
Rio de Janeiro
ZIP/Postal Code
20231-050
Country
Brazil

12. IPD Sharing Statement

Citations:
PubMed Identifier
26559740
Citation
Antunes HS, Schluckebier LF, Herchenhorn D, Small IA, Araujo CM, Viegas CM, Rampini MP, Ferreira EM, Dias FL, Teich V, Teich N, Ferreira CG. Cost-effectiveness of low-level laser therapy (LLLT) in head and neck cancer patients receiving concurrent chemoradiation. Oral Oncol. 2016 Jan;52:85-90. doi: 10.1016/j.oraloncology.2015.10.022. Epub 2015 Nov 11.
Results Reference
derived
Links:
URL
http://www.inca.gov.br
Description
Click here for more information about Instituto Nacional de Cancer- Brazil

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Low-level Laser Therapy to Prevent Oral Mucositis in Head and Neck Patients

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