Study of Electronic Brachytherapy for Cutaneous Basal Cell Carcinoma

Electronic brachytherapy (EBT) offers an isotope-free radiation therapy modality for the treatment of specific skin lesions, especially non-melanoma skin cancers (NMSC). Within the treatment of NMSC, surgical removal of the lesion is currently the treatment of choice for the majority of cases. However in an estimated 10-15% of NMSC patients, surgery might not be the best treatment option. Location of the tumour in cosmetically sensitive areas, patient comorbidities, old age, use of anti-coagulation etc. might all be reasons to select radiotherapy as first choice of treatment. The objective of ths study will be to determine histologically confirmed clinical efficacy, safety, and usability of Electronic Brachytherapy, an innovative treatment for Basal Cell Carcinoma (BCC).

Study Overview

• Status: Completed
• Conditions: Carcinoma, Basal Cell
• Intervention / Treatment: Device: Electronic Brachytherapy (6,1 Gy); Device: Electronic Brachytherapy (7 Gy)

Detailed Description

• Rationale: Electronic brachytherapy (EBT) offers an isotope-free radiation therapy modality for the treatment of specific skin lesions, especially non-melanoma skin cancers (NMSC). Within the treatment of NMSC, surgical removal of the lesion is currently the treatment of choice for the majority of cases. However in an estimated 10-15% of NMSC patients, surgery might not be the best treatment option. Location of the tumour in cosmetically sensitive areas, patient comorbidities, old age, use of anti-coagulation etc. might all be reasons to select radiotherapy as first choice of treatment.
• Objective: To determine histologically confirmed clinical efficacy, safety, and usability of Electronic Brachytherapy, an innovative treatment for Basal Cell Carcinoma (BCC).
• Study design: Prospective, out-patient based, single centre, single treatment modality
• Study population: 40 patients, >18 years old, having at least 1 BCC. Intervention: BCC will be treated with EBT, using low-energy X-rays. Area of the lesion will be evaluated for tumour presence and size before, during and at 2 weeks, 6 weeks and 3 months after treatment. If the patient has more than one BCC, all of them will be treated with Electronic Brachytherapy but only the largest one will be analysed in the study.
• Main study parameters/endpoints: Local control of BCC.
• Secondary parameters: Acute skin toxicity, skin cosmesis, and care giver satisfaction, and patient satisfaction.
• Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients will be exposed to low-energy X-rays. Required site-visits are: 1 pretreatment visits (intake/informed consent and biopsy), 6 treatment visits over the course of 2-3 weeks, 6 control-visits 2 weeks, 6 weeks, 3 months, 6 months, 12 months and 24 months after treatment.
• Patients will also be asked to complete a short questionnaire to evaluate their quality of life.

• Study Type: Interventional
• Enrollment (Actual): 40
• Phase: Not Applicable

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Men or women ≥18 years old.
• Estimated life expectancy of ≥5 years
• Histopathologic diagnosis of early and primary Basal Cell Carcinoma (BCC)
• Clinical stage of BCC: T1 or T2 (by AJCC 2010 criteria, see Table 1)
• Histological subtypes: Superficial BCC or nodular BCC
• Maximum diameter of lesion: 20 mm
• Maximum depth of invasion: 4 mm.
• Ability to provide informed consent
• Punch biopsy of primary tumor to depth of reticular dermis

Exclusion Criteria:

• Men or women <18 years old.
• Estimated life expectancy <5 years.
• BCC that was previously treated (ie, recurrent BCC)
• BCC in region adjacent to or overlapping with region of prior radiotherapy
• BCC on irregular surface (ie, target area not flat)
• BCC adjacent to or overlapping with burn or scar
• BCC in area prone to trauma
• BCC in area with compromised lymphatic drainage or vascular supply
• Inflammatory process in target area
• Pregnancy or lactation
• Collagen vascular disease (lupus, scleroderma, rheumatoid arthritis)
• Diabetes that is poorly controlled (Hg A1c >7%)
• Genetic disorder predisposing patient to skin cancers or radiation sensitivity (basal cell nevus syndrome, xeroderma pigmentosum, ataxia telangiectasia mutans)
• Receipt of treatment with another investigational device or drug
• Receipt of drug that will affect biologic response to radiation (radiosensitizer or radioprotector)
• Receipt or plan to receive chemotherapy within 6 weeks of radiation therapy
• High likelihood of protocol non-compliance (in opinion of investigator)

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Group 1; For the first 20 patients, a total dose of 36.6 Gy is planned over 6 fractions of 6.1 Gy, given 2 days week, 3 weeks or lees at least 2 days apart each fraction.	Device: Electronic Brachytherapy (6,1 Gy); A total dose of 36.6 Gy is planned over 6 fractions of 6.1 Gy, given 2 days/week, during 3 weeks or lees, at least 2 days apart each fraction.
Experimental: Group 2; For the next 20 patients a total dose of 42 Gy is planned over 6 fractions of 7 Gy, given 2 days week 3 weeks or lees at least 2 days apart each fraction.	Device: Electronic Brachytherapy (7 Gy); A total a dose of 42 Gy is planned over 6 fractions of 7 Gy, given 2 days/week during 3 weeks or lees, at least 2 days apart each fraction.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Clinical Response of Electronic Brachytherapy	Response criteria: Complete response (disappearance of tumor), partial response persistence with tumor size reduction), no response (no change in tumor size), tumor progression (increase in tumor size).	2 weeks after treatment
Clinical Response of Electronic Brachytherapy	Response criteria: Complete response (disappearance of tumor), partial response persistence with tumor size reduction), no response (no change in tumor size), tumor progression (increase in tumor size).	6 weeks after treatment
Clinical Response of Electronic Brachytherapy	Response criteria: Complete response (disappearance of tumor), partial response persistence with tumor size reduction), no response (no change in tumor size), tumor progression (increase in tumor size).	3 months after treatment
Clinical Response of Electronic Brachytherapy	Response criteria: Complete response (disappearance of tumor), partial response persistence with tumor size reduction), no response (no change in tumor size), tumor progression (increase in tumor size).	6 months after treatment
Clinical Response of Electronic Brachytherapy	Response criteria: Complete response (disappearance of tumor), partial response persistence with tumor size reduction), no response (no change in tumor size), tumor progression (increase in tumor size).	12 months after treatment
Clinical Response of Electronic Brachytherapy	Response criteria: Complete response (disappearance of tumor), partial response persistence with tumor size reduction), no response (no change in tumor size), tumor progression (increase in tumor size).	24 months after treatment

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Patient quality of life	Patient quality of life before and after treatment with Esteya Electronic brachytherapy will be measured using the validated Skindex 16 questionnaire. Patient quality of life will be measured before treatment and at 3 months post treatment.	Before treatment and at 3 months post treatment.
Rate of grade ≥3-4 adverse events	The study will use the EORTC-RTOG and Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 for assessing toxicity related to brachytherapy. Grade 4 or higher adverse events will be reported, with the exception of grade 4 radiation dermatitis. Grade 5 radiation dermatitis will be reported.	2 weeks, 6 weeks, 3 months, 6 months, 12 months and 24 months after treatment.
Caregiver experience (questionnaire)	User experience with the Esteya electronic brachytherapy device will be measured using the USE Questionnaire (http://hcibib.org/perlman/question.cgi?form=USE). All users of the device will be asked to fill in one questionnaire after their last use of the treatment device. Only one questionnaire will be filled in per user.	3 weeks

Collaborators and Investigators

• Sponsor: Instituto de Investigacion Sanitaria La Fe

Study record dates

Study Major Dates

• Study Start: July 1, 2013
• Primary Completion (Actual): July 1, 2016
• Study Completion (Actual): July 1, 2016

Study Registration Dates

• First Submitted: October 13, 2016
• First Submitted That Met QC Criteria: October 17, 2016
• First Posted (Estimate): October 19, 2016

Study Record Updates

• Last Update Posted (Estimate): October 19, 2016
• Last Update Submitted That Met QC Criteria: October 17, 2016
• Last Verified: October 1, 2016

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Neoplasms, Glandular and Epithelial; Neoplasms, Basal Cell; Carcinoma; Carcinoma, Basal Cell
• Other Study ID Numbers: BCCBrachy

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Undecided