The Elekta Esteya® electronic brachytherapy system in non-melanoma skin cancers: A post-market observational study
- PMID: 39943976
- PMCID: PMC11812133
- DOI: 10.5114/jcb.2024.146795
The Elekta Esteya® electronic brachytherapy system in non-melanoma skin cancers: A post-market observational study
Abstract
Purpose: The study was conducted to provide support for the delivery of electronic brachytherapy (EBx) in patients with low-risk non-melanoma skin cancer (NMSC) lesions who prefer and benefit a non-surgical treatment.
Material and methods: This study included 205 patients with a total of 236 lesions. Six centers participated in this study using high-dose-rate EBx in NMSC. Eligible patients had pathologically confirmed basal cell or squamous cell carcinoma of clinical stage Tis, T1, or T2, with two or fewer high-risk clinical or pathologic features. Treatment doses were chosen from a set of fractionation schemes delivering 69-72 Gy (BED). Maximum follow-up was 5 years.
Results: The median age was 74 (range, 56-96) years, and 62% of the subjects were males and 38% females. The median follow-up was 24.2 months, with a maximum of 73.5 months. Healthcare professional (HCP) and patient-rated cosmesis were rated excellent/good (E/G) by both groups at 90-100% rates, except for HCP ratings of 1-3 months post-EBx, where cosmesis was rated 83-87% E/G. Erythema was the most common acute adverse event (34.1% at 1 month), rebounding back to zero by 6 months. There was a single lesion recurrence.
Conclusions: This report provides additional phase IV clinical data on NMSC treated with electronic brachytherapy. With 2-year median follow-up, there was one recurrence (0.42%). Patients tolerated the treatments well, as evidenced by strong and longitudinal scores on the skin cancer index as well as cosmetic evaluations performed by both patients and healthcare providers. Adverse rates were low, except for expected acute erythema, chronic hypopigmentation, and telangiectasia. The study provides additional information on EBx delivery for low-risk NMSC lesions in patents who prefer non-surgical treatment, especially those at risk for surgical complications, surgical cosmesis issues, keloid formation, wound care issues, and use of anticoagulant therapy.
Keywords: brachytherapy; electronic brachytherapy; non-melanoma skin cancer treatment; radiation therapy; radiotherapy.
Copyright © 2024 Termedia.
Conflict of interest statement
The authors declare no conflict of interest.
Figures
Similar articles
-
Long-term clinical outcomes of non-melanoma skin cancer patients treated with electronic brachytherapy.J Contemp Brachytherapy. 2023 Feb;15(1):9-14. doi: 10.5114/jcb.2023.125580. Epub 2023 Feb 28. J Contemp Brachytherapy. 2023. PMID: 36970438 Free PMC article.
-
The initial experience of electronic brachytherapy for the treatment of non-melanoma skin cancer.Radiat Oncol. 2010 Sep 28;5:87. doi: 10.1186/1748-717X-5-87. Radiat Oncol. 2010. PMID: 20875139 Free PMC article.
-
Custom mold applicator high-dose-rate brachytherapy for nonmelanoma skin cancer-An analysis of 273 lesions.Brachytherapy. 2018 May-Jun;17(3):601-608. doi: 10.1016/j.brachy.2018.01.002. Epub 2018 Feb 15. Brachytherapy. 2018. PMID: 29398593
-
Non-melanoma skin cancer treated with high-dose-rate brachytherapy: a review of literature.J Contemp Brachytherapy. 2016 Dec;8(6):533-540. doi: 10.5114/jcb.2016.64112. Epub 2016 Dec 2. J Contemp Brachytherapy. 2016. PMID: 28115960 Free PMC article. Review.
-
Review: the reemergence of brachytherapy as treatment for non-melanoma skin cancer.J Dermatolog Treat. 2018 Mar;29(2):170-175. doi: 10.1080/09546634.2017.1341617. Epub 2017 Jun 30. J Dermatolog Treat. 2018. PMID: 28604229 Review.
References
-
- Rogers AW, Weinstock MA, Feldman SRet al. . Incidence estimate of nonmelanoma skin cancer (keratinocyte carcinomas) in the U.S. population, 2012. JAMA Dermatol 2015; 151: 1081-1086. - PubMed
-
- Donaldson MR, Coldiron BM. No end in sight: the skin cancer epidemic continues. Semin Cutan Med Surg 2011; 30: 3-5. - PubMed
-
- Martinez JC, Otley CC. The management of melanoma and nonmelanoma skin cancer: a review for the primary care physician. Mayo Clin Proc 2001; 76: 1253-1265. - PubMed
-
- Sun Protection. Cancer Trends Progress Report-2009/2010 Update. National Cancer Institute.
-
- Richmond-Sinclair NM, Pandeya N, Ware RSet al. . Incidence of basal cell carcinoma multiplicity and detailed anatomic distribution: longitudinal study of an Australian population. J Invest Dermatol 2009; 129: 323-328. - PubMed
Publication types
LinkOut - more resources
Full Text Sources
Miscellaneous