Head and Neck Squamous Cell Carcinoma
Conditions
Keywords
head and neck squamous cell carcinoma, nasopharyngeal carcinoma, oral mucositis, Streptococcus salivarius K12
Brief summary
To evaluate the efficacy and safety of Streptococcus salivarius K12 for prevention and treatment of oral mucositis in patients undergoing radiotherapy for malignant head and neck tumors.
Detailed description
The goal of this clinical trial is to evaluate the efficacy and safety of Streptococcus salivarius K12 in reducing the incidence, duration, and severity of severe oral mucositis (SOM). The main questions it aims to answer are whether Streptococcus salivarius K12 can effectively prevent and treat radiation-induced oral mucositis and whether it will cause adverse events in patients undergoing radiotherapy. Participants will be instructed to suck a Streptococcus salivarius K12 or placebo lozenge three times daily from the beginning to the end of RT. After using the lozenges, the patients should avoid eating, drinking and conducting any oral hygiene activities for at least 1 hour. Researchers will compare Streptococcus salivarius K12 group and placebo group to see if oral probiotic are beneficial in preventing and treating oral mucositis in patients undergoing radiotherapy.
Interventions
DRUGStreptococcus salivarius K12
The patients in intervention group were treated with Streptococcus salivarius K12 lozenges three times a day after gargling from the first day of radiotherapy up to 1 week after the end of treatment. Streptococcus salivarius K12 is dissolved in the mouth and then swallowed.
DRUGStreptococcus salivarius K12 simulants
Patients in control group were treated with Streptococcus salivarius K12 simulants, and its use method and use time are the same as intervention group.
Sponsors
West China Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Patients with non-metastatic head and neck malignant tumor diagnosed by histopathology; * Aged 18 to 80 years; * Systemic functional status Eastern Cooperative Oncology Group (ECOG) (Appendix 1) rating ≤2; * Receiving definitive RT or postoperative adjuvant RT at a dose of 60-72Gy with/without concurrent chemotherapy; * Sign the informed consent
Exclusion criteria
* Patients with known allergy to probiotic or severe allergic constitution; * Using antibiotics/antifungal drugs within 1 month or using antimicrobial mouthwash within 1 week before the study; * Poor oral hygiene and/or severe periodontal diseases; * Any previous RT to the head and neck region; * Deemed unsuitable for the study by the investigators (concomitant with any other severe diseases).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The incidence of Severe Oral mucositis (WHO grade ≥3) | From the start of radiotherapy to 8 weeks after completion of radiotherapy | Oral mucositis is assessed by trained physicians according to World Health Organization (WHO) oral toxicity Scale. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Xerostomia | 1 week before radiotherapy ; at the middle of radiotherapy (3 weeks after the start of radiotherapy) ; at the end of radiotherapy (the last radiation dose received, usually 6 or 6.5 weeks); and 1, 3, 6, 9 and 12 months after the end of radiotherapy | Patients self-rated xerostomia according to summated xerostomia inventory (SXI), and researchers measured saliva flow rates. |
| functional assessment of cancer therapy-head and neck (FACT- H&N) quality of life questionnaire. | 1 week before radiotherapy; at the end of radiotherapy(the last radiation dose received, usually 6 or 6.5 weeks); ; and 1, 3, 6, 9 and 12 months after the end of radiotherapy | FACT- H&N quality of life questionnaire. |
| Adverse events | From the first day of radiotherapy to the day of the last radiation dose received, usually 6 or 6.5 weeks | Common Terminology Criteria for Adverse Events (CTCAE) 5.0 version |
| The duration of Severe Oral mucositis (WHO grade ≥3) | From the start of radiotherapy to 8 weeks after completion of radiotherapy | The first determination of SOM to the first instance of non-severe OM (WHO grade \<3), without a subsequent instance of SOM. Patients without observed SOM were assigned a duration of 0 days. |
| Taste function | 1 week before radiotherapy ; at the middle of radiotherapy (3 weeks after the start of radiotherapy) ; at the end of radiotherapy (the last radiation dose received, usually 6 or 6.5 weeks); and 1, 3, 6, 9 and 12 months after the end of radiotherapy | Electrogustometer test and taste strips test. |
| The number of patients who missed five or more consecutive radiation fractions. | The time period is the period from the start of radiotherapy to the completion of radiotherapy | The number of patients who missed five or more consecutive radiations and the reasons for this are recorded during radiotherapy. |
| Mouth and throat soreness (MTS) scores | The time period is the period from the start of radiotherapy to the completion of radiotherapy.The evaluation period is approximately 6 weeks and 6 1/2 weeks | Patients report mouth and throat soreness (MTS) scores (Likert scale 1 to 5) via the oral mucositis weekly questionnaire （OMWQ）. Higher score indicates more severe symptoms. |
| Oral activities scores | The time period is the period from the start of radiotherapy to the completion of radiotherapy. The evaluation period is approximately 6 weeks and 6 1/2 weeks | Patients report the degree to the impact of MTS on oral activities (including swallowing, drinking, eating, talking, sleeping) (Likert scale 1 to 5) via the oral mucositis weekly questionnaire （OMWQ）. Higher score indicates more severe symptoms. |
| The time to onset of Severe Oral mucositis (WHO grade ≥3) | From the start of radiotherapy to 8 weeks after completion of radiotherapy | Time from the first day of radiotherapy to the first determination of SOM. Patients without observed SOM were assigned onset days of 6 or 6.5 weeks. |
Countries
China
Outcome results
None listed