Efficacy of Photodynamic Therapy with Chlorine-Based Photosensitizer in the Treatment of Basal Cell Carcinomas
- Authors
-
-
T.P. Artsemyeva
Department of Hyperthermia and Photodynamic Therapy, N.N. Alexandrov National Cancer Center of Belarus, Lesnoy, Republic of Belarus -
D.A. Tzerkovsky
Laboratory of Morphology, Molecular and Cellular Biology with Group of Experimental Medicine, N.N. Alexandrov National Cancer Center of Belarus, Lesnoy, Republic of Belarus
-
- Keywords:
- Basal cell carcinoma, chlorine-based photosensitizer, photodynamic therapy, tolerability, safety and antitumor efficacy
- Abstract
-
The aim of this study is to evaluate a safety and antitumor efficacy of photodynamic therapy (PDT) with chlorine-based photosensitizer (PS) for treatment patients with basal cell skin carcinomas (BCC).
Material and Methods: The work was performed on the basis of the Department of hyperthermia and photodynamic therapy. The object of the study were 172 patients with a verified diagnosis of BCC (T1N0M0, I stage), who received treatment from 2007 to 2022. PS «Photolon» (RUE «Belmedpreparaty», Republic of Belarus) was administrated intravenously at a dose of 2.0-2.5 mg/kg. The session of PDT was performed 2.5-3 h after intravenous injection of PS using semiconductor lasers (λ=660±5 nm) with exposure doses 50-250 J/cm² and power density – 0.15-0.5 W/cm². Frequency and severity of side effects after treatment session was assessed based on the criteria CTCAE (Version 4.03; 2010). The antitumor efficacy was evaluated 3 months after treatment. Clinical outcome was evaluated visually and morphologically by cytological or histopathological examination. Performance criteria were as follows (according to WHO, 1979).
Results: The phenomenon of skin phototoxicity due to violation of the light regime (hyperemia, burning, slight swelling of the soft tissues of the face; CTCAE, I-II grades) was registered in 5.8% of cases (n=10). Serious adverse reactions (anaphylactic shock, Quincke's edema, severe pain syndrome) after the administration of PS and photoirradiation were not identified. Complete and partial regressions of tumors was observed in 93.0% and 4.7% of patients, respectively. The objective answer was 97.7%. The frequency of local relapses of the disease 1, 2, 3, 4 and 5 years after PDT was 3.1%, 3.1%, 4.6%, 4.6% and 6.9%, respectively.
Сonclusion: PDT is a well-tolerated and highly effective therapeutic option in patients with BCC.
- References
-
Dika E, Scarfì F, Ferracin M, et al. Basal cell carcinoma: a comprehensive review. Int J Mol Sci 2020; 21(15): 5572. https://doi.org/10.3390/ijms21155572
Lomas A, Leonardi-Bee J, Bath-Hextall F. A systematic review of worldwide incidence of nonmelanoma skin cancer. Br J Dermatol 2012; 166: 1069-80. https://doi.org/10.1111/j.1365-2133.2012.10830.x
Tzerkovsky DA. Photodynamic therapy for patients with basal cell carcinoma: N.N. Alexandrov national cancer center experience. Arch Gen Intern Med 2017; 1: 22-4.
Basset-Segun N, Herms F. Update on the management of basal cell carcinoma. Acta Derm Venereol 2020; 100(11): 5750. https://doi.org/10.2340/00015555-3495
Rodriguez-Vigil T, Vázquez-López F, Perez-Oliva N. Recurrence rates of primary basal cell carcinoma in facial risk areas treated with curettage and electrodesiccation. J Am Acad Dermatol 2007; 56(1): 91-5. https://doi.org/10.1016/j.jaad.2006.07.007
Kim SE, Lee KS, Cho JE. Photodynamic therapy combined with cryotherapy for the treatment of nodular basal cell carcinoma. Oncol Lett 2013; 6: 939-41. https://doi.org/10.3892/ol.2013.1504
Agostinis P, Berg K, Cengel KA, et al. Photodynamic therapy of cancer: an update. CA: A Cancer J Clin 2011; 61: 250-81. https://doi.org/10.3322/caac.20114
Kwiatkowski S, Knap B, Przystupski D, et al. Photodynamic therapy – mechanisms, photosensitizers and combinations. Biomed Pharmacother 2018; 106: 1098-107. https://doi.org/10.1016/j.biopha.2018.07.049
Wang BC, Fu C, Qin L, et al. Photodynamic therapy with methyl-5-aminolevulinate for basal cell carcinoma: A systematic review and meta-analysis. Photodiagnosis Photodyn Ther 2020; 29: 101667. https://doi.org/10.1016/j.pdpdt.2020.101667
Mpourazanis G, Mpourazanis P, Stogiannidis G, et al. The effectiveness of photodynamic therapy and cryotherapy on patients with basal cell carcinoma: A systematic review and meta-analysis. Dermatol Ther 2020; 33(6): e13881. https://doi.org/10.1111/dth.13881
Rodrigues JA, Correia JH. Enhanced photodynamic therapy: a review of combined energy sources. Cells 2022; 11(24): 3995. https://doi.org/10.3390/cells11243995
Kessel D, Reiners JJ. Photodynamic therapy: autophagy and mitophagy, apoptosis and paraptosis. Autophagy 2020; 16(11): 2098-101. https://doi.org/10.1080/15548627.2020.1783823
Kessel D. Death pathways associated with photodynamic therapy. Photochem Photobiol 2021; 97(5): 1101-103. https://doi.org/10.1111/php.13436
Wang Y, Lin Y, Zhang HG, et al. A photodynamic therapy combined with topical 5-aminolevulinic acid and systemic hematoporphyrin derivative is more efficient but less phototoxic for cancer. J Cancer Res Clin Oncol 2016; 142(4): 813-21. https://doi.org/10.1007/s00432-015-2066-3
Zou Y, Zhao Y, Yu J, et al. Photodynamic therapy versus surgical excision to basal cell carcinoma: meta-analysis. J Cosmet Dermatol 2016; 15(4): 374-82. https://doi.org/10.1111/jocd.12236
Nguyen KP, Knuiman GJ, Blokx WAM, et al. Is a single day patient friendly methyl aminolevulinate photodynamic therapy illumination scheme for superficial basal cell carcinoma feasible? A randomized multicenter pilot trial. J Dermatolog Treat 2019; 30(2): 194-99. https://doi.org/10.1080/09546634.2018.1484558
Filonenko E, Kaprin A, Urlova A, et al. Topical 5-aminolevulinic acid-mediated photodynamic therapy for basal cell carcinoma. Photodiagnosis Photodyn Ther 2020; 30: 101644. https://doi.org/10.1016/j.pdpdt.2019.101644
Woźniak Z, Trzeciakowski W, Chlebicka I, et al. Photodynamic diagnosis and photodynamic therapy in basal cell carcinoma using a novel laser light source. Photodiagnosis Photodyn Ther 2020; 31: 101883. https://doi.org/10.1016/j.pdpdt.2020.101883
Gómez C, Cobos P, Alberdi E. Methyl aminolevulinate photodynamic therapy after partial debulking in the treatment of superficial and nodular basal cell carcinoma: 3-years follow-up. Photodiagnosis Photodyn Ther 2021; 33: 102176. https://doi.org/10.1016/j.pdpdt.2021.102176
Hellen R, Dhonncha EN, Havelin A, et al. An open-label prospective study to assess short incubation time white LED light photodynamic therapy in the treatment of superficial basal cell carcinoma. Photodermatol Photoimmunol Photomed 2022; 38(4): 322-27. https://doi.org/10.1111/phpp.12750
Sukhova TE. The efficacy of photodynamic therapy for basal cell carcinoma with intralesional injection of radachlorine. Biomed Photonics 2015; 3: 24-8 (in Russian). https://doi.org/10.24931/2413-9432-2015-4-3-24-28
Sukhova TE Intralesional injection of fotolon for photodynamic therapy of basal cell carcinoma. Biomed Photonics 2016; 5(1): 15-21 (in Russian). https://doi.org/10.24931/2413-9432-2016-5-1-15-21
Kapinus VN, Kaplan MA, Yaroslavtseva-Isayeva EV, et al. Photodynamic therapy for head and neck basal cell skin cancer with additional interstitial laser irradiation. Biomed Photonics 2017; 6(4): 20-6 (in Russian). https://doi.org/10.24931/2413-9432-2017-6-4-20-26
Kapinus VN, Kaplan MA, Yaroslavtseva-Isayeva EA, et al. Chlorine e6-photodynamic therapy basal cell carcinoma. Res Pract Med J 2021; 8(4): 33-43. https://doi.org/10.17709/2410-1893-2021-8-4-3
- Downloads
- Published
- 2023-04-03
- Issue
- Vol. 12 (2023)
- Section
- Articles
- License
-

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
Similar Articles
- Novoa Vargas Arturo, Neoadyuvant Hormonotherpy for Posmenopausics Women with Locallity Advanced Breast Cancer , Journal of Analytical Oncology: Vol. 2 No. 1 (2013)
- Radu Radulescu, Alexandra Totan, Bogdan Calenic, Cosmin Totan , Maria Greabu, Biomarkers of Oxidative Stress, Proliferation, Inflammation and Invasivity in Saliva from Oral Cancer Patients , Journal of Analytical Oncology: Vol. 4 No. 1 (2015)
- Arun Chairmadurai, Harish Chandra Goel, Sandeep Jain, Aklank Jain, Hridayesh Prakash, Ra-SBRT is Potential Immune Adjuvant for Innate Immune Cell Populations in Advance Stage NSCLC Patients , Journal of Analytical Oncology: Vol. 8 (2019)
- Palak Lunkad, Deepika Malik, Sahil Shah, Mohini Gurjar, Virendra Bhandari, Incidental Diagnosis of Leptomeningeal Disease in Breast Cancer with Brain Metastases- a Case Report with Review of Literature , Journal of Analytical Oncology: Vol. 14 (2025)
- Pedro Salinas Hernández, Rafael Trujillo Vilchez, Antonio Arriví García-Ramos, Rosana Grande Ladron de Guevara, Angeles Rodríguez Jaraiz, Pedro Gallurt Moreira, Jose Maria Vieitez de Prado, Miguel Ruiz López de Tejada, Antonio Irigoyen Medina, Juan Manuel Campos Cervera, Juan Carlos Cámara Vicario, Uriel Bohn Sarmiento, Pedro López Tendero, Juan Domingo Alonso Lajara, Ana León Carbonero, Marisa García de Paredes, Juan de Alvaro Liaño, Asunción Juarez Marroquí, Luis López Gómez , Diego Soto de Prado Otero, Bevacizumab Plus Chemotherapy as First-Line Treatment for Patients with Metastatic Colorectal Cancer: Results from a Spanish Observational Study , Journal of Analytical Oncology: Vol. 2 No. 3 (2013)
- Kenneth K. Wu, Tryptophan Metabolism and Cancer Progression , Journal of Analytical Oncology: Vol. 10 (2021)
- Paola Castro-Garcia, Carmen Gil-Gas, Paloma Honrubia-Gómez, Carmen Belen Alvarez-Simón, Jesús-José Ferré-Fernández, Francisco Sánchez-Sánchez, Jose Luis Sánchez-Sánchez, Jose Mª Garcia-Bueno, Sebastiá Sabater, Guadalupe Aparicio, Luis Miguel Antón-Aparicio, Carmen Ramírez-Castillejo, C-Terminal-PEDF Reduces IC50 Doses and Chemoresistant Population of CD133 and BCRP1-Positve Cancer Stem Like Cells , Journal of Analytical Oncology: Vol. 2 No. 4 (2013)
- Mudathir Ahmed, Mohammed Ibrahim, Fawzia E.M. Elbashir, Neazar Bagdadi, Fathi Awad, Iron Oxide Nanoparticles Functionalized with Macrocycle Antagonists for CXCR4 Receptor Targeting in Cancer Cells , Journal of Analytical Oncology: Vol. 13 (2024)
- Loren Pickart, Jessica M. Vasquez-Soltero, Francoise D. Pickart , John Majnarich , GHK, the Human Skin Remodeling Peptide, Induces Anti-Cancer Expression of Numerous Caspase, Growth Regulatory, and DNA Repair Genes , Journal of Analytical Oncology: Vol. 3 No. 2 (2014)
- Maria Caffo, Lucia Merlo, Valeria Barresi, Ema Tot, Gerardo Caruso, Brain Metastases: State of the Art and Innovative Targeted Therapies , Journal of Analytical Oncology: Vol. 4 No. 3 (2015)
You may also start an advanced similarity search for this article.
Most read articles by the same author(s)
- D.A. Tzerkovsky, A.N. Mazurenko, F.F. Borychevsky, D.V. Shashkouski, Radiodynamic Therapy with Photosensitizers: Mini-Review of Experimental and Clinical Studies , Journal of Analytical Oncology: Vol. 11 (2022)
- F.F. Borichevsky, I.S. Lioubichtchev, A.E. Sahun, A.S. Trus, D.A. Tzerkovsky, Magnetotherapy in Experimental and Clinical Neuro-Oncology: A Review , Journal of Analytical Oncology: Vol. 12 (2023)
- D.A. Tzerkovsky, A.N. Mazurenko, D.I. Kozlovsky, F.F. Borychevsky, Radiodynamic Therapy with Chlorine-Based Photosensitizer on Pliss Lymphosarcoma Solid Tumor: In Vivo Experiment , Journal of Analytical Oncology: Vol. 11 (2022)
