eISSN: 2081-2841
ISSN: 1689-832X
Journal of Contemporary Brachytherapy
Current Issue Archive Supplements Articles in Press Journal Information Aims and Scope Editorial Office Editorial Board Register as Author Register as Reviewer Instructions for Authors Abstracting and indexing Subscription Advertising Information Links
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank

1/2023
vol. 15
 
Share:
Share:
Original paper

Long-term clinical outcomes of non-melanoma skin cancer patients treated with electronic brachytherapy

Stephen W. Doggett
1
,
Mark Willoughby
2
,
Kenneth A. Miller
3
,
Erick Mafong
2

1.
Aegis Oncology, Newport Beach, CA, USA
2.
Dermatology and Laser Center of San Diego, San Diego, CA, USA
3.
Kenneth Miller Dermatology, Los Gatos, CA, USA
J Contemp Brachytherapy 2023; 15, 1: 9–14
Online publish date: 2023/02/28
Article file
- Long-term clinical.pdf  [0.20 MB]
Get citation
 
 

Purpose

It is estimated that 5.4 million cases of basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) are diagnosed annually in the United States [1]. About 80% of non-melanoma skin cancers (NMSC) are basal cell carcinoma [2]. Treatment options for patients with NMSC include Mohs micrographic surgery (MMS), curettage with electro-desiccation, surgical excision, 5-fluorouracil (topical, intralesional, intravenous), cryotherapy, toll-like receptor 7 activator (imiquimod), Hedgehog (Hh) pathway inhibitors (vismodegib, sonidegib), PD-1 blockers (pembrolizumab, nivolumab, cemiplimab), photodynamic therapy, and radiation therapy [3-11].

A Cochrane database review concluded that surgical interventions have the lowest recurrence rates among all reviewed therapies, and that non-surgical treatments may be less effective than surgical therapies, but have superior cosmetic outcomes and acceptable recurrence rates [7]. European consensus-based interdisciplinary guidelines note that radiotherapy represents a valid alternative to surgery for facial BCC, especially in elderly patients [8].

European consensus-based interdisciplinary guidelines also notes that radiation therapy represents an alternative to surgery in the treatment of small SCCs in low-risk areas [9]. Lesion recurrence rate for patients at five years after MMS varies depending on primary vs. recurrent lesion, lesion location (high-risk ‘mask’ areas), treatment modality, size, depth, histologic differentiation, perineural involvement, and immune status [3-6, 10-12]. Five-year recurrence rates reported by Rowe et al. and Kauvar et al. were both of 1% [3, 5]. Network meta-analysis by Drucker et al. showed recurrence rate of 3.8% in those treated with MMS [14]. Recurrence rates for primary SCCs reported were 3.1% to 5.3% [4, 6, 15].

A non-surgical treatment option for patients with NMSC, studied previously in a matched-pair cohort study and compared to MMS, is electronic brachytherapy (eBx). The mean follow-up for the eBx arm was 3.3 years with a local control rate of 99.5%, and the MMS arm had a local control rate of 100% [16].

This real-world, multi-center, non-randomized study assessed long-term clinical outcomes of non-melanoma skin cancer (NMSC) patients treated with Axxent® electronic brachytherapy (eBx) system (Xoft, Inc. – a subsidiary of iCAD, Inc., San Jose, CA, USA). Prior to retrospective data collection and prospective follow-up visits, patients who were identified to have completed eBx treatment a minimum of five years ago, and who were available for a prospective long-term follow-up visit, were included in the present study. At the prospective follow-up visit assessment of local control and long-term skin toxicities at the treatment site were collected to determine the durability and long-term safety of eBx for the treatment of NMSC.

Material and methods

The NMSC long-term follow-up study was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki, in accordance with local regulatory requirements, and was approved by an independent central institutional review board Advarra IRB, number: Pro00060222 (Columbia, MD, USA). This study included both a retrospective chart review, and a prospective collection and analysis of follow-up data. Chart reviews were conducted at the sites to determine potential participants who could be contacted for participation in the prospective visits by confirming that the last treatment date was a minimum of five years ago. Once this was confirmed, data was not collected until the patients who were willing to participate returned for their follow-up visit. Follow-up visits were scheduled, and patients had the option of returning to the site for an in-person visit, or attend a video conference for remote participation, a common method for conducting visits by dermatology offices in the USA [13].

For this study, a participant was required to provide verbal consent on video, and this was documented in the informed consent form. If a treated area was in question based on appearance, the study participant was required to undergo a biopsy. For in-person visits, participants provided written informed consent. Once the prospective follow-up visit was completed, retrospective data were collected from electronic medical record. Retrospective data collection included eligibility criteria, demographics and history, verification of the treatment regimen, lesion information, including stage, histology, location, and local control at the treated area. Prospective visits consisted of examination of the previously treated skin lesion for local control at the treatment site. Skin toxicities were assessed according to the Common Terminology Criteria Adverse Events (CTCAE version 5.0) [17].

Patient selection

Patients treated with eBx five or more years ago, who met eligibility criteria, and were willing to undergo a follow-up visit, were selected for this study at four West Coast centers in the United States. The majority of subjects in the study were included in the eBx arm of a prior study conducted by Xoft, Inc. [16].

Inclusion criteria were previously completed treatment for non-melanoma skin cancer using Xoft Axxent electronic brachytherapy system according to standard of care, a minimum of five years prior to the follow-up visit in this study; patient provided informed consent; greater than 40 years of age; pathological diagnosis confirmed as squamous cell carcinoma, squamous cell carcinoma in situ, or basal cell carcinoma prior to treatment; and staging. Patients were excluded if the target area was adjacent to a burn scar, if there was any prior definitive surgical resection of the cancer, such as MMS, known perineural invasion, diagnosis of actinic keratosis, known spread to regional lymph nodes, and known metastatic disease. Lesions were staged as Tis, T1, or T2.

Treatment methods

Surface applicators sizes were 10 mm, 20 mm, 35 mm, and 50 mm in diameter. Surface applicator size was selected based on lesion diameter, which allowed for a 2 mm to 5 mm margin. Prescription dose was 40.0 Gy administered over 8 fractions (5.0 Gy twice weekly), delivered to the skin surface, as previously reported [16, 21, 25].

Study endpoints

The primary effectiveness endpoint was the local control at a minimum of five years from the last eBx treatment, while the primary safety endpoint was long-term skin toxicities at the target treatment site at the time of the follow-up visit. Most common long-term primary toxicities reported are hypopigmentation and telangiectasias [16]. Data for the primary effectiveness endpoint were collected retrospectively once it was determined that the subject could be available for a long-term follow-up visit in this study, and the follow-up visit would be five years or more since the last treatment. Follow-up visits occurred prospectively. Data for the secondary safety endpoint were collected prospectively at the time of the follow-up visit in this study, to identify long-term toxicities.

Statistical analysis

The objective of this study was to report the number and percentage of subjects who had local recurrence, and the number and percentage of subjects who showed a long-term skin toxicity at the follow-up visit. Data were analyzed and reported as descriptive statistics, both categorical and continuous variables, as appropriate.

Results

Patient demographics and lesions characteristics

In total, 183 subjects with 185 lesions were enrolled in this long-term follow-up study from March 9, 2022 to July 18, 2022, at four study centers in Northern and Southern California, out of 307 potential participants who were called. There were three subjects who had less than five years between the last treatment and the follow-up visit. Of the remaining 180 subjects with 182 lesions, all patients met all inclusion criteria and none of the exclusion criteria. The mean age was 82.3 years, with a range of 63 to 96 years; 61.7% were male and 98.9% were white non-Hispanic subjects (Table 1). All lesions were 4 cm in diameter or smaller. The results of 180 and 183 subjects are presented in Tables 1-4. The mean follow-up in this study was 7.5 years (median, 7.6 years; range, 5-9.5 years). All lesions were stage 0, 1, or 2. The majority of the lesions (n = 131, 70.8%) were above the clavicles. If the results include the three subjects who were excluded due to less than 5-year follow-up, the male to female ratio was the same, race and ethnicity was the same, and the three subjects excluded were diagnosed with BCC stage 2. Tables 1-5 demonstrate all the results for both the groups.

Table 1

History and demographic data

Demographic datan = 180 subjects n (%) ≥ 5.0 years of follow-upn = 183 subjects n (%) ≥ 4.4 years of follow-up
Gender
Male111 (61.7)113 (61.7)
Female69 (38.3)70 (38.3)
Race
White179 (99.4)182 (99.5)
Asian1 (0.6)1 (0.5)
Ethnicity
Hispanic4 (2.2)4 (2.2)
Non-Hispanic176 (97.8)179 (97.8)
Diagnosis
BCC91 (50.6)94 (51.4)
SCC89 (49.4)89 (48.6)
Cancer stage
Stage 09 (5.0)9 (4.9)
Stage 1166 (92.2)169 (92.3)
Stage 25 (2.8)5 (2.7)
Age (years)
Mean ±SD82.3 ±6.582.3 ±6.5
Minimum-maximum63-9663-96
Median (IQR)83.0 (77.0-86.5)83.0 (77.0-87.0)
Table 2

Lesion locations

Lesion locationn = 182 lesions n (%)n = 185 lesions n (%)
Scalp17 (9.3)17 (9.2)
Temple6 (3.3)6 (3.2)
Forehead11 (6.0)11 (5.9)
Cheek21 (11.5)22 (11.9)
Chin2 (1.1)2 (1.1)
Neck4 (2.2)4 (2.2)
Pre-auricular2 (1.1)2 (1.1)
Eyelid3 (1.6)3 (1.6)
Lip1 (0.5)1 (0.5)
Nasal dorsum2 (1.1)3 (1.6)
Nasal sidewall21 (11.5)21 (11.4)
Nasal ala11 (6.0)11 (5.9)
Nasal tip17 (9.3)17 (9.2)
Back3 (1.6)3 (1.6)
Chest2 (1.1)2 (1.1)
Upper arm3 (1.6)3 (1.6)
Forearm3 (1.6)3 (1.6)
Hand17 (9.3)18 (9.7)
Helix1 (0.5)1 (0.5)
Antihelix1 (0.5)1 (0.5)
Earlobe8 (4.4)8 (4.3)
Tragus1 (0.5)1 (0.5)
Lower leg22 (12.1)22 (11.9)
Foot3 (1.6)3 (1.6)
Summary of adverse events by locationn = 182 lesions
n (%)
n = 185 lesions
n (%)
Head, neck, above the clavicles129 (70.9)131 (70.8)
Torso (front and back)5 (2.7)5 (2.7)
Upper extremity and hand23 (12.5)24 (12.9)
Lower extremity and foot25 (13.7)25 (13.7)
Table 3

Recurrences

Recurrence by subjectn = 180 subjects n (%) ≥ 5.0 years of follow-upn = 183 subjects n (%) ≥ 4.4 years of follow-up
All2 (1.1)2 (1.1)
Nasal tip1 (0.6)1 (0.5)
Nasal sidewall1 (0.6)1 (0.5)
Recurrence by lesionn = 182 lesions n (%)n = 185 lesions n (%)
All2 (1.1)2 (1.1)
Table 4

Visit types and skin toxicities according to CTCAE [8]

Follow-up visit type by subjectn = 180 subjects n (%) ≥ 5.0 years of follow-upn = 183 subjects n (%) ≥ 4.4 years of follow-up
In person visit117 (65.0)119 (65.0)
Remote telemedicine visit63 (35.0)64 (35.0)
Safety endpoint: skin toxicities by subjectn = 180 subjects n (%) ≥ 5.0 years of follow-upn = 183 subjects n (%) ≥ 4.4 years of follow-up
Yes128 (71.7)130 (71.0)
No52 (28.9)53 (29.0)
Safety endpoint: skin toxicities by lesionOccurrence n = 182, n (%)Occurrence n = 185, n (%)
Hypopigmentation grade 1120 (65.9)122 (65.9)
Telangiectasia grade 141 (22.5)41 (22.2)
Scar grade 12 (1.1)2 (1.1)
Hyperpigmentation grade 12 (1.1)2 (1.1)
Induration grade 21 (0.5)1 (0.5)
Table 5

Follow-up

Follow-up in yearsn = 180 subjects n (%) ≥ 5.0 years of follow-upn = 183 subjects n (%) ≥ 4.4 years of follow-up
Mean (±SD)7.4 ±1.47.4 ±1.4
Median (range)7.7 (5.0-9.5)7.6 (4.4-9.5)
Q1 (25th percentile), Q3 (75th percentile)6.8, 8.66.2, 8.6

NMSC recurrence

The retrospective data analysis revealed the recurrence rate of the 180 subjects with a mean of 7.5 year follow-up (1.1%) (Table 3). Two subjects diagnosed with BCC had one lesion with a recurrence, one subject’s lesion was located on the nasal sidewall, and the recurrence was diagnosed at 2.7 years after treatment. The other subject’s lesion was located on the nasal tip, and the recurrence was diagnosed at 6.5 years after treatment. Both recurrences were treated with MMS. For all 183 subjects, including those who did not meet the minimum of 5 years from last treatment to the follow-up visit in this study, the recurrence rate was 1.1%. There were no recurrences in the 183 subjects newly discovered at the time of the prospective follow-up.

Safety and skin toxicities

Skin toxicities (Table 4) were reported in 71.1% of the subjects. Hypopigmentation grade 1 was the most common skin toxicity, observed in 65.9% of the patients. Telangiectasia grade 1 was observed in 22.5% of the subjects. Other toxicities noted included scarring grade 1 in two subjects (1.1%), hyperpigmentation grade 1 in two subjects (1.1%), and induration grade 2 in one subject (0.5%). In this case, the indurated site was located on the upper back, and did not limit instrumental activities of daily living (ADL). In the overall population, the toxicity rate was 70.1% in the group with 180 subjects, and it was similar (70.0%) in the group with 183 subjects. The types of skin toxicities and severity were equal across both the groups.

Discussion

W.C. Roentgen reported the discovery of X-rays in December, 1895, and within four years, X-rays were being used successfully for the treatment of skin cancers [22]. High energy linear accelerators and high-dose-rate afterloading iridium-192 (192Ir) replaced the low penetrating X-rays of the Roentgen era. These devices required heavy room shielding and protracted courses of treatment. Radiation therapy has been reported to result in low recurrence rates for both primary BCC (7.4%) and recurrent BCC (9.5%) [20-23].

More recently, use of hypofractionation of radiations has been shown to have comparable cosmesis over standard, lengthy treatment schedules. In a meta-analysis of 344 articles utilizing external beam radiation therapy or brachytherapy for BCC/SCC, fewer than 8% of patients experienced poor cosmesis, independent of dose or fractionation regimen [24].

Previous eBx studies showed excellent durable local control and minimal long-term toxicity. These studies utilized low penetrating X-rays of 50 KeV, as opposed to 6 million eV of linear accelerators and 330 KeV of Ir192 brachytherapy. Doggett et al. reported a study of 524 lesions treated with eBx showing a 0.8% failure at 1.04 years follow-up [25]. Bhatnagar reported outcomes for 297 lesions with up to 63 months follow-up (mean, 16.5 months; range, 1-63 months) [21], with one recurrence and excellent cosmesis in 100% of patients at years 4-5. No acute toxicities were reported, and late toxicities occurred in 2% of patients. Paravati et al. retrospectively analyzed 157 NMSC lesions treated with eBx with 3.4 to 34.8 months of follow-up, and two recurrences were noted (at 6.3 and 7.3 months) [26]. Excellent cosmesis was rated in 94.2% of the cases. A matched-pair cohort study with 188 patients in the eBx arm demonstrated that 99.5% were free of recurrence at a mean of 3.4 years post-treatment. Physicians rated cosmesis as “excellent” or “good” in 97.6% of EBT-treated lesions, and 95.7% of MMS-treated lesions [16].

A review of 21 tele-dermatology studies indicated that some studies show a high accuracy of tele-dermatologic diagnoses [13]. Appropriate used criteria previously published by Miller et al. described how the application of eBx can be incorporated into an outpatient dermatology clinic [28].

Our study provides further evidence of the similarity of eBx to Mohs micrographic surgery in terms of local control and mild long-term toxicities. The mean follow-up in this study is now the longest of all previously published eBx studies for the treatment of NMSC [5, 17-19].

Study limitations

This study was designed to address the insufficient long-term efficacy and safety data for the treatment of NMSC with electronic brachytherapy. Although mean follow-up in our study was 7.5 years, which is the longest reported eBx result to date, this was not a randomized controlled trial designed to compare eBx with MMS in subjects with long-term follow-up. 59.6% of the 307 potential participants contacted did participate in the study. The remainder of the potential participants could not be contacted. No contacted potential participant declined to participate in the study.

Comparative studies of surgery vs. radiation therapy report short follow-ups. The Cochrane comprehensive analysis of skin cancer therapies subset comparing radiotherapy against surgical excision (with or without frozen section margin control) extended out only to 4-years [7].

The 7.5 years of follow-up in the current study may be insufficient to identify the true local failure rate for eBx, as a 7.3% of 15-year recurrence rate for primary BCCs treated surgically with whole specimen intra-operative frozen section analysis has been reported [31]. In our study, 51.4% of the lesions were BCC in comparison with the 80% rate of BCC occurrence in the general population, as showed by the American Society of Clinical Oncology [2]. The skewing of lesion numbers toward SCC in this study may mask a higher local control due to the higher failure rate of treated SCC compared with treated BCCs [3-6, 11, 14, 15].

Pathology in this study was not always reported as to the various sub-types of BCC, which may confound reporting of long-term results. BCC is divided into multiple sub-types, such as superficial, nodular, pigmented (low-risk of recurrence) and sclerosing, morphoeic, infiltrating, and basosquamous (high-risk of recurrence). More than one histological sub-type can be detected within a single BCC [30].

Thirty-five per cent of the follow-up visits were performed by tele-dermatology rather than in person due to patients’ fears regarding in-office COVID-19 exposure. While concern might be raised regarding the accuracy of diagnosis based on telemedicine images, a review of 21 tele-dermatology studies indicates that some studies show a high accuracy of diagnosis [13].

Conclusions

This study was designed to address the insufficient long-term efficacy and safety data for the treatment of NMSC with electronic brachytherapy. Electronic brachytherapy for the treatment of non-melanoma skin cancer is safe and effective, showing excellent long-term 98.9% of local control, with a median follow-up of 7.6 years (n = 183) and minimal long-term toxicities. These results of a non-surgical treatment for NMSC provide further support for the use of eBx for the treatment of NMSC.

Acknowledgments

The authors wish to thank Eminence Clinical Research, Inc. (Colorado Springs, CO, USA) for study support and data management, and the site investigators and staff for the conduct of this study.

Disclosure

The authors report no conflict of interest.

References

1 

https://www.cancer.org (accessed August 20, 2022).

3 

Rowe DE, Carroll RJ, Day CL Jr. Long-term recurrence rates in previously untreated (primary) basal cell carcinoma: implications for patient follow-up. J Am Acad Dermatol 1989; 15 (3): 315-328.

4 

Rowe DE, Carroll RJ, Day CL Jr. Prognostic factors for local recurrence, metastasis, and survival rates in squamous cell carcinoma of the skin, ear, and lip. Implications for treatment modality selection. J Am Acad Dermatol 1992; 26 (4): 976-990.

5 

Kauvar ANB, Cronin T Jr, Roenigk R et al. Consensus for non-melanoma skin cancer treatment: basal cell carcinoma, including a cost analysis of treatment methods. Dermatol Surg 2015; 41: 550-571.

6 

Kauvar ANB, Arpey CJ, Hruza G et al. Consensus for nonmelanoma skin cancer treatment, part II: squamous cell carcinoma, including a cost analysis of treatment methods. Dermatol Surg 2015; 41: 1214-1240.

7 

Thomson J, Hogan S, Leonardi-Bee J et al. Interventions for basal cell carcinoma of the skin. Cochrane Database Syst Rev 2020; 11.

8 

Peris K, Fargnoli MC, Garbe C et al. Diagnosis and treatment of basal cell carcinoma: European consensus-based interdisciplinary guidelines. Eur J Cancer 2019; 118: 10-34.

9 

Stratigos A, Garbe C, Lebbe C et al. Diagnosis and treatment of invasive squamous cell carcinoma of the skin: European consensus-based interdisciplinary guideline. Eur J Cancer 2015; 51: 1989-2007.

10 

Gniadecki R, Glud M, Mortensen K et al. Favorable results of Mohs micrographic surgery for basal cell carcinoma. Dan Med J 2015; 62: A5171.

11 

Burns CA, Brown MD. Imiquimod for the treatment of skin cancer. Dermatol Clin 2005; 23: 151-164.

12 

Dika E, Scarfi F, Ferracin M et al. Basal cell carcinoma: a comprehensive review. Int J Mol Sci 2020; 21: 5572.

13 

Finnane A, Dallest K, Janda M et al. Tele-dermatology for the diagnosis and management of skin cancer: a systematic review. JAMA Dermatol 2017; 153: 319-327.

14 

Drucker AM, Adam GP, Rofeberg V et al. Treatments of primary basal cell carcinoma of the skin. Ann Intern Med 2018; 169: 156-166.

15 

Van Lee CB, Roorda BM, Wakkee M et al. Recurrence rates of cutaneous squamous cell carcinoma of the head and neck after Mohs micrographic surgery vs. standard excision: a retrospective cohort study. Br J Dermatol 2019; 181: 338-343.

16 

Patel R, Strimling R, Doggett S et al. Comparison of electronic brachytherapy and Mohs micrographic surgery for the treatment of early-stage non-melanoma skin cancer: a matched pair cohort study. J Contemp Brachytherapy 2017; 9: 338-344.

17 

US Department of Health and Human Services, National Institutes of Health, National Cancer Institute. Common Terminology Criteria Adverse Events (CTCAE) Version 5.0. November 27, 2017.

18 

Squamous Cell Skin Cancer: NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) v.2.2022 (accessed September 23, 2022).

19 

Kasper ME, Chaudhary AA. Novel treatment options for non-melanoma skin cancer: focus on electronic brachytherapy. Med Devices (Auckl) 2015; 26: 493-502.

20 

Caccialanza M, Piccinno R, Moretti D et al. Radiotherapy of carcinomas of the skin overlying the cartilage of the nose: results in 405 lesions. Eur J Dermatol 2003; 13: 462-465.

21 

Bhatnagar A. Electronic brachytherapy for the treatment of non-melanoma skin cancer: results up to four years. Int J Radiat Oncol Biol Phys 2014; 90 Suppl: S756.

22 

Orton CG. Uses of therapeutic x rays in medicine. Health Phys 1995; 69: 662-676.

23 

Silverman MK, Kopf AW, Gladstein AH et al. Recurrence rates of treated basal cell carcinomas. Part 4: X-ray therapy. J Dermatol Surg Oncol 1992; 18: 549-554.

24 

Zaorsky NG, Lee CT, Zhang E. Hypo-fractionated radiation therapy for basal and squamous cell skin cancer: A meta-analysis. Radiother Oncol 2017; 125: 13-20.

25 

Doggett S, Willoughby M, Willoughby C et al. Incorporation of electronic brachytherapy for skin cancer into a community dermatology practice. J Clin Aesthet Dermatol 2015; 8: 28-32.

26 

Paravati AJ, Hawkins PG, Martin AN et al. Clinical and cosmetic outcomes in patients treated with high-dose-rate electronic brachytherapy for nonmelanoma skin cancer. Pract Radiat Oncol 2015; 5: e659-e664.

27 

Bittner GC, Cerci FB, Kubo EM et al. Mohs micrographic surgery: a review of indications, technique, outcomes, and considerations. Ann Bras Dermatol 2021; 96: 263-277.

28 

Miller K. Electronic brachytherapy: understanding the technology and identifying appropriate use. Pract Dermatol 2015; 47-48.

29 

Scholten LA, Kedilioglu MA, Huizinga PM et al. LT recurrence rates of whole specimen intraop frozen section analysis in BCC face with WIFSA. J Surg Oncol 2019; 119: 103-108.

30 

Seidl-Philipp M, Frischhut N, Höllweger N et al. Known and new facts on basal cell carcinoma. J Dtsch Dermatol Ges 2021; 19: 1021-1041.

Copyright: © 2023 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
 
Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.