3D Printed Rigid Bolus Versus Silicone Bolus for Treatment of Tumors Involving the Skin: A Comparative Study
Primary Purpose
Skin Neoplasm Malignant, Skin Cancer
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Ingeo Biopolymer (PLA)
Ecoflex 030
Sponsored by
About this trial
This is an interventional other trial for Skin Neoplasm Malignant focused on measuring Radiation Therapy, Radiation Dosimetry, Patient Reported Outcomes, 3D-printed bolus
Eligibility Criteria
Inclusion Criteria:
- Pathologically (histologically or cytologically) proven diagnosis of a primary skin cancer or metastatic cancer with involvement of the skin or underlying soft tissues
- Being treated with radiation therapy that requires the use of bolus to ensure adequate radiotherapy dose to the skin in the affected area
- Planned for palliative or curative intent radiotherapy using megavoltage (MV) photons
- Site of involvement has significant contour change, leading to anticipated challenges using conventional bolus material
- Patient must be competent and able to complete informed consent
- Age ≥ 18
- Women of childbearing potential must be proven to not be pregnant or breast feeding
Exclusion Criteria:
- Patient being treated with a radiotherapy technique that does not require bolus
- Patient being treated with a radiotherapy technique other than MV photons (i.e. electrons, brachytherapy, kilovoltage (kV) photons)
- Patient of childbearing potential who is pregnant, actively trying to become pregnant or breast feeding
- Allergy to silicone or other components of either the 3D printed rigid or flexible bolus.
- Size of the bolus required for treatment exceeds 25cm in maximum diameter
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Alternating 3D boluses
Arm Description
Both rigid and flexible 3D printed boluses made for each patient. Each is used on alternate days during radiation therapy.
Outcomes
Primary Outcome Measures
Air Gap measurement
Measurement of the gap between the bolus and the surface of the patient
Planned versus expected radiation duse
Comparison of the planned radiation dose at skin, and that measured during radiation therapy treatment
Secondary Outcome Measures
Ease of Use
Time required to place bolus in proper location prior to each radiation therapy treatment
Radiation Therapist ease of use
Radiation therapists asked to rate ease of use for each type of bolus
Challenges with Bolus Use
Comparison of the number of times each bolus could not be adequately applied prior to radiation therapy treatment
Patient Reported Outcomes
Patients asked about comfort associated with each bolus, their preference between the two, and any other feedback on the boluses
Fabrication time
Comparison of average fabrication time for each type of bolus
Successful fabrication
Comparison of percentage of cases for which an acceptable bolus could be created for each type of bolus
Full Information
NCT ID
NCT04176900
First Posted
November 22, 2019
Last Updated
September 28, 2023
Sponsor
Nova Scotia Cancer Centre
1. Study Identification
Unique Protocol Identification Number
NCT04176900
Brief Title
3D Printed Rigid Bolus Versus Silicone Bolus for Treatment of Tumors Involving the Skin: A Comparative Study
Official Title
3D Printed Rigid Bolus Versus Silicone Bolus: A Comparative Study
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Closed during Covid Pandemic, and no longer supported locally
Study Start Date
March 2020 (Anticipated)
Primary Completion Date
September 28, 2023 (Actual)
Study Completion Date
September 28, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nova Scotia Cancer Centre
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study compares two types of 3D-printed skin bolus (rigid and flexible) used to optimize the treatment of tumors/cancers involving the skin. Each patient will have both types of bolus made, with each will be used on alternating days. The goal is to determine if one type of bolus provides a better fit and thus radiotherapy plan, the ease of use of each type of bolus, and patient reported feedback.
Detailed Description
Need for Skin Bolus during Radiotherapy for Cancers that Involve the Skin Using standard megavoltage (MV) radiotherapy to treat tumors that involve the skin is technically challenging as without modification, the high-energy radiotherapy machines under-dose the superficial tissue. This is a problem, as this may lead to an inadequate radiation dose being delivered to the skin, thus compromising tumor control. To compensate for this, a flexible polymer material ("bolus") measuring 5-10mm in thickness is placed over the skin during radiotherapy.
There are many types of boluses used internationally from rubber to candle wax slabs. The bolus allows the radiation dose to build up so that a sufficient dose is deposited at the skin. Use of bolus for cancers involving the skin is considered the standard of care when using conventional MV radiotherapy.
Challenges of Using Conventional Bolus Many standard boluses are slightly flexible, but are not able to follow significant changes in the underlying contours. When a bolus is not able to follow an individual's unique 'peaks and valleys' in contour, it can lead to air gaps between the bolus and the skin. An air gap, which is easily seen during imaging, can also vary on a day-to-day basis due to slight changes in positioning of the bolus prior to radiotherapy treatment. The varying air gaps can affect how much radiation dose is getting to the skin, and can potentially lead to under-dosing of the cancer cells in the skin. Even small air gaps (i.e. 5mm in thickness), can cause a 5% error in dose, which exceeds the safe tolerance for treatment.
Areas where this can be a problem are where the patient's anatomy undergoes significant topographical changes in a small area. Examples of this include the ear, nose, top of head. Patients with metastatic cancer can also have large lymph nodes or masses that are growing towards the skin that can be difficult to accommodate with standard bolus materials.
3D-Printed Bolus One method to overcome challenging anatomy for cases that require skin bolus for radiotherapy is the use of 3D-printed bolus. This technology uses data acquired from a CT scan of the affected area. The patients contour can then be used to create an individualized bolus that matches the patient contour for the treatment field. This technology has been demonstrated to improve fit (less air gaps) and decreased radiotherapy treatment time. The bolus used in this study was rigid.
Trial design and Rationale Other than the chestwall study, the literature on 3D-printed bolus for radiotherapy has focused on the dosimetry and feasibility of using this technology. However, it is used in an ad hoc method in many centers, using various workflows. There are no studies examining which type of bolus provides the best radiotherapy plan, is the easiest to use at the radiation therapy machines or which is preferred by patients.
To fill this gap, this study will aim to answer a few questions. It will compare the use of rigid 3D-printed bolus (most commonly used and reported in the literature) versus a flexible silicone 3D-printed bolus. Both types of bolus will be used to treat patients with cancers involving the skin. This will allow comparison of radiotherapy plans for each patient between the two types of bolus where each subject is his/her own control. The study will also collect data about real-time set-up using each bolus and feedback from radiation therapists (deliver radiation treatments) about the ease of use of each. Lastly, patients will complete a short survey to provide feedback about comfort with use of each type of bolus and to determine if one type of bolus is favored over the other.
This data will be instrumental is determining the standard of care of the use of 3D-printed bolus as it will assess two types of bolus in three domains: ability to help generate an adequate radiotherapy plan, ease of use by the specialists that deliver the radiotherapy (radiation therapists) and patient reported feedback.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Skin Neoplasm Malignant, Skin Cancer
Keywords
Radiation Therapy, Radiation Dosimetry, Patient Reported Outcomes, 3D-printed bolus
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All patients will have both the rigid and flexible 3D printed boluses made. Each will be used on alternate days during radiation therapy treatments.
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Alternating 3D boluses
Arm Type
Experimental
Arm Description
Both rigid and flexible 3D printed boluses made for each patient. Each is used on alternate days during radiation therapy.
Intervention Type
Other
Intervention Name(s)
Ingeo Biopolymer (PLA)
Other Intervention Name(s)
3D-Fuel PLA
Intervention Description
Biopolymer used for 3D-printing of rigid bolus
Intervention Type
Other
Intervention Name(s)
Ecoflex 030
Other Intervention Name(s)
Body Double & Body Double SILK, Dragon Skin Series & F/X Pro, Encapso K, Equinox Series, EZ Brush Silicone, EZ-Spray Silicone Series, Mold Max Series, Mold Star Series, OOMOO Series, PoYo Putty 40, Psycho Paint, Rebound Series, Rubber Glass, Silicone 1515, 1603, 3030, 1708, Skin Tite, Smooth-Sil Series, Solaris, SomaFoama Series, SORTA-Clear Series
Intervention Description
Polymer used for the 3D-printed flexible bolus
Primary Outcome Measure Information:
Title
Air Gap measurement
Description
Measurement of the gap between the bolus and the surface of the patient
Time Frame
6 weeks
Title
Planned versus expected radiation duse
Description
Comparison of the planned radiation dose at skin, and that measured during radiation therapy treatment
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Ease of Use
Description
Time required to place bolus in proper location prior to each radiation therapy treatment
Time Frame
6 weeks
Title
Radiation Therapist ease of use
Description
Radiation therapists asked to rate ease of use for each type of bolus
Time Frame
6 weeks
Title
Challenges with Bolus Use
Description
Comparison of the number of times each bolus could not be adequately applied prior to radiation therapy treatment
Time Frame
6 weeks
Title
Patient Reported Outcomes
Description
Patients asked about comfort associated with each bolus, their preference between the two, and any other feedback on the boluses
Time Frame
6 weeks
Title
Fabrication time
Description
Comparison of average fabrication time for each type of bolus
Time Frame
2 weeks
Title
Successful fabrication
Description
Comparison of percentage of cases for which an acceptable bolus could be created for each type of bolus
Time Frame
2 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Pathologically (histologically or cytologically) proven diagnosis of a primary skin cancer or metastatic cancer with involvement of the skin or underlying soft tissues
Being treated with radiation therapy that requires the use of bolus to ensure adequate radiotherapy dose to the skin in the affected area
Planned for palliative or curative intent radiotherapy using megavoltage (MV) photons
Site of involvement has significant contour change, leading to anticipated challenges using conventional bolus material
Patient must be competent and able to complete informed consent
Age ≥ 18
Women of childbearing potential must be proven to not be pregnant or breast feeding
Exclusion Criteria:
Patient being treated with a radiotherapy technique that does not require bolus
Patient being treated with a radiotherapy technique other than MV photons (i.e. electrons, brachytherapy, kilovoltage (kV) photons)
Patient of childbearing potential who is pregnant, actively trying to become pregnant or breast feeding
Allergy to silicone or other components of either the 3D printed rigid or flexible bolus.
Size of the bolus required for treatment exceeds 25cm in maximum diameter
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lara R Best, MD, FRCPC
Organizational Affiliation
Nova Scotia Cancer Centre
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
27475278
Citation
Canters RA, Lips IM, Wendling M, Kusters M, van Zeeland M, Gerritsen RM, Poortmans P, Verhoef CG. Clinical implementation of 3D printing in the construction of patient specific bolus for electron beam radiotherapy for non-melanoma skin cancer. Radiother Oncol. 2016 Oct;121(1):148-153. doi: 10.1016/j.radonc.2016.07.011. Epub 2016 Jul 27.
Results Reference
background
PubMed Identifier
30340612
Citation
Dipasquale G, Poirier A, Sprunger Y, Uiterwijk JWE, Miralbell R. Improving 3D-printing of megavoltage X-rays radiotherapy bolus with surface-scanner. Radiat Oncol. 2018 Oct 19;13(1):203. doi: 10.1186/s13014-018-1148-1.
Results Reference
background
PubMed Identifier
30402935
Citation
Kong Y, Yan T, Sun Y, Qian J, Zhou G, Cai S, Tian Y. A dosimetric study on the use of 3D-printed customized boluses in photon therapy: A hydrogel and silica gel study. J Appl Clin Med Phys. 2019 Jan;20(1):348-355. doi: 10.1002/acm2.12489. Epub 2018 Nov 7.
Results Reference
background
PubMed Identifier
29452866
Citation
Robar JL, Moran K, Allan J, Clancey J, Joseph T, Chytyk-Praznik K, MacDonald RL, Lincoln J, Sadeghi P, Rutledge R. Intrapatient study comparing 3D printed bolus versus standard vinyl gel sheet bolus for postmastectomy chest wall radiation therapy. Pract Radiat Oncol. 2018 Jul-Aug;8(4):221-229. doi: 10.1016/j.prro.2017.12.008. Epub 2017 Dec 24.
Results Reference
background
Links:
URL
https://www.canada.ca/en/public-health/services/chronic-diseases/cancer/non-melanoma-skin-cancer.html
Description
Government of Canada. Non Melanoma Skin Cancer. 2014.
URL
https://www.nccn.org/professionals/physician_gls/pdf/squamous.pdf
Description
National Comprehensive Cancer Network (NCCN). Squamous Cell Skin Cancer. NCCN Clinical Practice Guidelines in Oncology. Version 1.2020.
Learn more about this trial
3D Printed Rigid Bolus Versus Silicone Bolus for Treatment of Tumors Involving the Skin: A Comparative Study
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