Preemptive Treatment With XONRID to Reduce Radiation Induced Dermatitis in Head and Neck Cancer Patients

Head and Neck Cancer Clinical Trial

Official title:

Preemptive Treatment With XONRID a Medical Device to Reduce Radiation Induced Dermatitis in Head and Neck Cancer Patients Receiving Curative Treatment

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02261181
• Other study ID #: INT 52/14
• Status: Completed
• Phase: N/A
• Start date: January 2015
• Est. completion date: January 2019

Study information

• Verified date: September 2021
• Source: Fondazione IRCCS Istituto Nazionale dei Tumori, Milano
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There is a strong need to study products with a preemptive role in radiation dermatitis development, with a trial design taking in account patient subjective evaluation and compliance. XONRID is a promising device for radiation high grade dermatitis prevention; it is a topical gel that prevents and treats skin symptoms such as erythema, itching, burning sensation and pruritus, induced by radiotherapy or other causes.

Description:

The patients will be treated with XONRID + standard of care (SOC) preemptive treatment adopted during radiation treatment for head and neck cancer patients in the Institution. Patients will be planned to receive Intensity-Modulated Radiotherapy Techniques (IMRT or volumetric modulated radiotherapy, VMAT) with conventional fractionation at total dose of 50-66 GY in postoperative setting and 66-70 Gy in radical setting. Radiotherapy will be planned with simultaneous boost (SIB) approaches, using conventional fractionation (1.8-2.12 Gy/die). According to histology, stage and pathology reports, patients could receive concomitant platinum based chemotherapy. The patients will be evaluated at baseline, at weekly intervals during RT and six months after treatment completion by 2 different treating physicians for each visit. The evaluation will consist of a physician-assessed toxicity assessment using the Radiation Therapy Oncology Group (RTOG), and patient-reported outcome measured using the Skindex-16 questionnaire. In addition objective in vivo measurements of skin erythema and pigmentation based on reflectance spectrometry (RS) will be performed. Measurements will be performed before RT, every 5 RT fractions (once a week) up to the end of RT and 6 months after RT completion (same timing as clinical evaluation). Instrumental RS measurement will be performed at five different fixed regions within the area treated with RT, in any cases only on flat skin regions of the neck in an area corresponding to the second node level and in absence of hair or nevus.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: January 2019
• Est. primary completion date: July 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• > 18 years
• Performance status < 2
• Epithelial carcinoma of oropharynx, nasopharynx, larynx, hypopharynx, paranasal sinus and salivary glands
• Planned to receive at least 50 Gy on one side of the neck with at least the 2nd level of neck nodes irradiated
• Postoperative or curative radiation treatment
• Concurrent platinum based chemotherapy is accepted, but not mandatory
• Conventional fractionation (1.8-2.12 GY per fraction, one daily fraction, 5 fractions a week )

Exclusion Criteria:

• Pregnant or lactating women
• Planned to receive concurrent cetuximab
• Previous radiation therapy on the head and neck area
• Cutaneous and connettive diseases (i.e. lupus erythematosus or scleroderma)
• Systemic diseases known to delay the skin healing process such as diabetes mellitus or severe renal failure.
• Use of a tissue-equivalent bolus
• Use of over-the-counter topical medications containing steroids
• Presence of rashes or unhealed wounds in the radiation field
• Recent sun exposure
• Mental conditions that could adversely affect patients' adherence to the study

Related Conditions & MeSH terms

• Dermatitis
• Head and Neck Cancer
• Head and Neck Neoplasms
• Radiodermatitis

Intervention

Device:
• XONRID
The patients will be treated with XONRID + standard of care (SOC) preemptive treatment adopted during radiation treatment for head and neck cancer patients. Patients will be instructed to apply the study cream (XONRID) on the irradiated area two times daily, the first application 1-2 h after the morning radiotherapy session, the second in the evening, starting on the first day of irradiation and continuing until 2 weeks after the completion of the radiation treatments or the development of Grade 3 or 4 skin toxicity. When G3 toxicity will occur the patient will be discontinued from the study medication and the skin toxicity will be managed according to internal guidelines.

Locations

Country	Name	City	State
Italy	Fondazione IRCCS Istituto Nazionale Tumori	Milan

Sponsors (1)

Lead Sponsor	Collaborator
Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Worst skin toxicity	Worst skin toxicity during treatment and until 2 weeks after according to CTCAE , as assessed independently by 2 physicians	14 months
Secondary	MeanPatient Reported Outcome (PRO)	Mean and worst score (measured on a numeric 0-6 scale, where 0= absence of symptom and 6= worst intensity of symptom) of Patient Reported Outcome (PRO) with Skindex 16 questionnaire performed weekly until reaching a total dose of 50 Gy on neck	14 months
Secondary	Median time to G2 radiation dermatitis development	Median time to G2 radiation dermatitis development according to CTCAE	14 months
Secondary	Compliance	Compliance to experimental treatment assumption considering a complete cpmpliance from 0 to 2 applications skipped, a partial compiance from 3 to 10 applications skipped and an absent compliance from 11 to 14 applications skipped.	14 months
Secondary	Grade of late toxicity	Grade of late toxicity (skin fibrosis according to CTCAE) at 6 month follow up visit after treatment ending	14 months