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Pre-Treatment Deep Curettage Can Significantly Reduce Tumour Thickness in Thick Basal Cell Carcinoma While Maintaining a Favourable Cosmetic Outcome When Used in Combination with Topical Photodynamic Therapy

DOI: 10.1155/2011/240340

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Abstract:

Topical photodynamic therapy (PDT) has limitations in the treatment of thick skin tumours. The aim of the study was to evaluate the effect of pre-PDT deep curettage on tumour thickness in thick (≥2?mm) basal cell carcinoma (BCC). Additionally, 3-month treatment outcome and change of tumour thickness from diagnosis to treatment were investigated. At diagnosis, mean tumour thickness was 2.3?mm (range 2.0–4.0). Pre- and post-curettage biopsies were taken from each tumour prior to PDT. Of 32 verified BCCs, tumour thickness was reduced by 50% after deep curettage . Mean tumour thickness was also reduced from diagnosis to treatment. At 3-month followup, complete tumour response was found in 93% and the cosmetic outcome was rated excellent or good in 100% of cases. In conclusion, deep curettage significantly reduces BCC thickness and may with topical PDT provide a favourable clinical and cosmetic short-term outcome. 1. Introduction Basal cell carcinoma (BCC) is the most common cancer in the white population, and its incidence is still increasing [1, 2]. This is a slow-growing, locally invasive epidermal skin tumour that can cause considerable patient morbidity [3, 4]. BCC most often arises on sun exposed, cosmetic sensitive skin areas such as the face [4]. Among several therapeutic options available for the treatment of this tumour excision surgery is regarded as the most effective [5]. However, not all patients are qualified for surgery. Excision surgery may be challenging in certain anatomic areas, cause cosmetic disfigurement, or result in complications like scar formation and functional impairment [6]. Topical PDT, with beneficial cosmesis, may in such cases be an attractive treatment option [7, 8]. This method involves the activation of a topically applied photosensitizer by light in the presence of tissue oxygen, starting a photochemical reaction in the targeted cells [9]. Five-year clearance rates in BCC from 64 to 81% are reported [10–13]. Evidence-based guidelines support the use of topical PDT in the treatment of BCC, particularly low risk, superficial lesions [14, 15]. A challenge is the limited penetration of the photosensitizing agents down to about 1.0 to 2.0?mm depth [16–18] and also limitation of red light to penetrate the skin [9]. The treatment efficacy in BCC with thickness ≥2.0?mm may therefore be reduced. Among several strategies to increase PDT effect, pre-treatment curettage has been shown to improve treatment efficacy in nodular tumours [19]. The combination of curettage ahead of PDT is today commonly used, even though data to supports

References

[1]  D. L. Miller and M. A. Weinstock, “Nonmelanoma skin cancer in the United States: incidence,” Journal of the American Academy of Dermatology, vol. 30, no. 5, part 1, pp. 774–778, 1994.
[2]  D. H. Brewster, L. A. Bhatti, J. H. C. Inglis, E. R. Nairn, and V. R. Doherty, “Recent trends in incidence of nonmelanoma skin cancers in the East of Scotland, 1992–2003,” British Journal of Dermatology, vol. 156, no. 6, pp. 1295–1300, 2007.
[3]  S. J. Miller, “Biology of basal cell carcinoma (part I),” Journal of the American Academy of Dermatology, vol. 24, no. 1, pp. 1–13, 1991.
[4]  A. N. Crowson, “Basal cell carcinoma: biology, morphology and clinical implications,” Modern Pathology, vol. 19, supplement 2, pp. S127–S147, 2006.
[5]  F. J. Bath-Hextall, W. Perkins, J. Bong, and H. C. Williams, “Interventions for basal cell carcinoma of the skin,” Cochrane Database of Systematic Reviews, no. 1, p. CD003412, 2007.
[6]  R. I. Ceilley and J. Q. del Rosso, “Current modalities and new advances in the treatment of basal cell carcinoma,” International Journal of Dermatology, vol. 45, no. 5, pp. 489–498, 2006.
[7]  R. M. Szeimies, “Methyl aminolevulinate-photodynamic therapy for basal cell carcinoma,” Dermatologic Clinics, vol. 25, no. 1, pp. 89–94, 2007.
[8]  M. H. Lien and V. K. Sondak, “Nonsurgical treatment options for basal cell carcinoma,” Journal of Skin Cancer, vol. 2011, Article ID 571734, 6 pages, 2011.
[9]  Q. Peng, T. Warloe, K. Berg et al., “5-Aminolevulinic acid-based photodynamic therapy: clinical research and future challenges,” Cancer, vol. 79, no. 12, pp. 2282–2308, 1997.
[10]  L. E. Rhodes, M. A. de Rie, R. Leifsdottir et al., “Five-year follow-up of a randomized, prospective trial of topical methyl aminolevulinate photodynamic therapy vs surgery for nodular basal cell carcinoma,” Archives of Dermatology, vol. 143, no. 9, pp. 1131–1136, 2007.
[11]  N. Basset-Seguin, S. H. Ibbotson, L. Emtestam et al., “Topical methyl aminolaevulinate photodynamic therapy versus cryotherapy for superficial basal cell carcinoma: a 5 year randomized trial,” European Journal of Dermatology, vol. 18, no. 5, pp. 547–553, 2008.
[12]  E. Christensen, E. Skogvoll, T. Viset, T. Warloe, and S. Sundstr?m, “Photodynamic therapy with 5-aminolaevulinic acid, dimethylsulfoxide and curettage in basal cell carcinoma: a 6-year clinical and histological follow-up,” Journal of the European Academy of Dermatology and Venereology, vol. 23, no. 1, pp. 58–66, 2009.
[13]  C. S. Souza, L. B. A. Felicio, J. Ferreira et al., “Long-term follow-up of topical 5-aminolaevulinic acid photodynamic therapy diode laser single session for non-melanoma skin cancer,” Photodiagnosis and Photodynamic Therapy, vol. 6, no. 3-4, pp. 207–213, 2009.
[14]  L. R. Braathen, R. M. Szeimies, N. Basset-Seguin, et al., “Guidelines on the use of photodynamic therapy for nonmelanoma skin cancer: an international consensus,” Journal of the American Academy of Dermatology, vol. 56, no. 1, pp. 125–143, 2007.
[15]  C. A. Morton, K. E. McKenna, and L. E. Rhodes, “Guidelines for topical photodynamic therapy: update,” British Journal of Dermatology, vol. 159, no. 6, pp. 1245–1266, 2008.
[16]  Q. Peng, A. M. Soler, T. Warloe, J. M. Nesland, and K. E. Giercksky, “Selective distribution of porphyrins in skin thick basal cell carcinoma after topical application of methyl 5-aminolevulinate,” Journal of Photochemistry and Photobiology B, vol. 62, no. 3, pp. 140–145, 2001.
[17]  S. Ahmadi, P. A. McCarron, R. F. Donnelly, A. D. Woolfson, and K. McKeena, “Evaluation of the penetration of 5-aminolevulinic acid through basal cell carcinoma: a pilot study,” Experimental Dermatology, vol. 13, no. 7, pp. 445–451, 2004.
[18]  C. Sandberg, C. B. Halldin, M. B. Ericson, O. Lark?, A. L. Krogstad, and A. M. Wennberg, “Bioavailability of aminolaevulinic acid and methylaminolaevulinate in basal cell carcinomas: a perfusion study using microdialysis in vivo,” British Journal of Dermatology, vol. 159, no. 5, pp. 1170–1176, 2008.
[19]  T. Warloe, H. Heyerdahl, and K. E. Giercksky, Curettage and topical ALA-based photodynamic therapy for nodular basal cell carcinoma, Ph.D. thesis, University of Oslo, Oslo, Norway, 1995.
[20]  M. R. T. M. Thissen, C. A. Schroeter, and H. A. M. Neumann, “Photodynamic therapy with delta-aminolaevulinic acid for nodular basal cell carcinomas using a prior debulking technique,” British Journal of Dermatology, vol. 142, no. 2, pp. 338–339, 2000.
[21]  E. Christensen, T. Warloe, S. Kroon et al., “Guidelines for practical use of MAL-PDT in non-melanoma skin cancer,” Journal of the European Academy of Dermatology and Venereology, vol. 24, no. 5, pp. 505–512, 2010.
[22]  L. E. Rhodes, M. de Rie, Y. Enstr?m et al., “Photodynamic therapy using topical methyl aminolevulinate vs surgery for nodular basal cell carcinoma: results of a multicenter randomized prospective trial,” Archives of Dermatology, vol. 140, no. 1, pp. 17–23, 2004.
[23]  K. Mosterd, M. R. T. M. Thissen, P. Nelemans et al., “Fractionated 5-aminolaevulinic acid-photodynamic therapy vs. surgical excision in the treatment of nodular basal cell carcinoma: results of a randomized controlled trial,” British Journal of Dermatology, vol. 159, no. 4, pp. 864–870, 2008.
[24]  A. M. Soler, T. Warloe, A. Berner, and K. E. Giercksky, “A follow-up study of recurrence and cosmesis in completely responding superficial and nodular basal cell carcinomas treated with methyl 5-aminolaevulinate-based photodynamic therapy alone and with prior curettage,” British Journal of Dermatology, vol. 145, no. 3, pp. 467–471, 2001.
[25]  C. Vinciullo, T. Elliott, D. Francis et al., “Photodynamic therapy with topical methyl aminolaevulinate for ‘difficult-to-treat’ basal cell carcinoma,” British Journal of Dermatology, vol. 152, no. 4, pp. 765–772, 2005.
[26]  Y. Scrivener, E. Grosshans, and B. Cribier, “Variations of basal cell carcinomas according to gender, age, location and histopathological subtype,” British Journal of Dermatology, vol. 147, no. 1, pp. 41–47, 2002.
[27]  R. P. Braun, F. Klumb, C. Girard et al., “Three-dimensional reconstruction of basal cell carcinomas,” Dermatologic Surgery, vol. 31, no. 5, pp. 562–566, 2005.
[28]  E. Christensen, P. Mj?nes, O. A. Foss, et al., “Pre-treatment evaluation of basal cell carcinoma for photodynamic therapy: comparative measurement of tumour thickness in punch biopsy and excision specimens,” Acta Dermato-Venereologica, vol. 91, no. 6, pp. 651–654, 2011.
[29]  C. Curson and D. Weedon, “Spontaneous regression in basal cell carcinomas,” Journal of Cutaneous Pathology, vol. 6, no. 5, pp. 432–437, 1979.
[30]  M. J. Hunt, G. M. Halliday, D. Weedon, B. E. Cooke, and R. S. Barnetson, “Regression in basal cell carcinoma: an immunohistochemical analysis,” British Journal of Dermatology, vol. 130, no. 1, pp. 1–8, 1994.
[31]  S. M. Swetter, J. C. Boldrick, P. Pierre, P. Wong, and B. M. Egbert, “Effects of biopsy-induced wound healing on residual basal cell and squamous cell carcinomas: rate of tumor regression in excisional specimens,” Journal of Cutaneous Pathology, vol. 30, no. 2, pp. 139–146, 2003.
[32]  W. E. McDaniel, “Therapy for basal cell epitheliomas by curettage only. Further study,” Archives of Dermatology, vol. 119, no. 11, pp. 901–903, 1983.
[33]  F. Reymann, “15 years' experience with treatment of basal cell carcinomas of the skin with curettage,” Acta Dermato-Venereologica, vol. 65, supplement 120, pp. 56–59, 1985.
[34]  J. O. Barlow, M. J. Zalla, A. Kyle, D. J. DiCaudo, K. K. Lim, and J. A. Yiannias, “Treatment of basal cell carcinoma with curettage alone,” Journal of the American Academy of Dermatology, vol. 54, no. 6, pp. 1039–1045, 2006.
[35]  M. H. Jih, P. M. Friedman, L. H. Goldberg, and A. Kimyai-Asadi, “Curettage prior to Mohs' micrographic surgery for previously biopsied nonmelanoma skin cancers: what are we curetting? Retrospective, prospective, and comparative study,” Dermatologic Surgery, vol. 31, no. 1, pp. 10–15, 2005.
[36]  P. Foley, M. Freeman, A. Menter et al., “Photodynamic therapy with methyl aminolevulinate for primary nodular basal cell carcinoma: results of two randomized studies,” International Journal of Dermatology, vol. 48, no. 11, pp. 1236–1245, 2009.
[37]  F. Fantini, A. Greco, C. del Giovane et al., “Photodynamic therapy for basal cell carcinoma: clinical and pathological determinants of response,” Journal of the European Academy of Dermatology and Venereology, vol. 25, no. 8, pp. 896–901, 2011.

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