Acta Dermato-Venereologica issue 50:1 98-1CompleteContent | Page 27
116
SHORT COMMUNICATION
Photodynamic Therapy: Influence of Clinical and Procedure Variables on Treatment Response in
Basal Cell Carcinoma and Bowen Disease
Tamara GRACIA-CAZAÑA 1 , Marta MASCARAQUE 2 , Nerea SALAZAR 2 , Jesús VERA-ÁLVAREZ 3 , María PILAR FRÍAS 4 , Salvador
GONZÁLEZ 5 , Ángeles JUARRANZ 2 and Yolanda GILABERTE 4
1
Department of Dermatology, Hospital de Barbastro, Av Pirineos nº 11 1ºA, P.O. Box: 22011 – Barbastro, Huesca, 2 Departament of Biology,
Universidad Autónoma de Madrid, Madrid, 3 Department of Pathology, 4 Department of Dermatology, Hospital San Jorge, Huesca, Spain, and
5
Dermatology Service, Memorial Sloan-Kettering Cancer Center, New York, USA. E-mail: [email protected]
Accepted Jul 31, 2017; Epub ahead of print Aug 1, 2017
Photodynamic therapy (PDT) is one of the most com-
monly used non-invasive treatments in non-melanoma
skin cancer (NMSC). High rates of complete remission
can be obtained using PDT with methyl-aminolevulinate
(MAL); for basal cell carcinoma (BCC) the response rate
is 91% at 3 months and 76% at 5 years, with 5-year recur-
rence rates of 22% in superficial BCC (sBCC) and 14%
in nodular BCC (nBCC) (1, 2), and for Bowen disease
(BD) the rate ranges from 88% to 100% at 3 months with
68% to 89% of treated lesions remaining clear for 17 to
50 months, besides PDT provides excellent cosmetic
results and a high patient satisfaction rate (1–3).
The primary limiting factors for MAL-PDT are pain
during irradiation, tumoural thickness, tumour location
(reduced sustained clearance rates for H-zone lesions),
and certain histological features of BCCs such as pig-
mentary, morphoeaform, and infiltrative variants are con-
sidered contra-indications to treatment (3). Although the
PDT procedure has changed little since its introduction,
we conducted a retrospective analysis to evaluate how
individual procedural variables relating to PDT influence
the clinical response of BCC and BD.
MATERIALS AND METHODS
This retrospective observational study analysed clinical and pro-
cedural variables for all cases of BD, nBCC and sBCC treated
with MAL-PDT at San Jorge Hospital (Huesca, Spain) between
January 2006 and December 2015.
Patients were treated with MAL-PDT (Metvix ® , Galderma, La
Defense Cedex, France) following the standard procedure (3).
Patients with nBCC first underwent curettage debulking of the
lesions. After applying haemostatic pressure, MAL was applied
to the lesion and a surrounding area of 1 cm in diameter, and was
incubated for 3 h under occlusion. The treated area was illuminated
with a coherent monochromatic diode light source (630 nm, 37 J/
cm 2 , Aktilite ® , PhotoCure ASA, Norway).
The clinical records of all patients were reviewed and data
gathered for the following variables: age at onset, sex, phototype
(Fitzpatrick scale I–IV), predisposing factors, location, size and
type of tumour. The following procedural variables were conside-
red: number of PDT sessions; fluorescence emitted by the lesion
in response to a Wood’s lamp; interruption of illumination due
to pain; analgesia prior to irradiation and pain score as evaluated
using a visual analogue scale (0–10). Clinical response was eva-
luated at the end of patient follow-up.
Statistical analyses were performed using the statistical package
SPSS, version 19.0 (IBM, Armonk, NY, USA). Associations
between qualitative variables were assessed using the Pearson
chi-squared test or Fisher exact test. The normal distribution of
doi: 10.2340/00015555-2756
Acta Derm Venereol 2018; 98: 116–118
quantitative variables was evaluated using the Kolmogorov-Smir-
nov test. Depending on the data distribution, associations between
binary and quantitative variables were evaluated using either the
Student’s t-test or Mann-Whitney U-test. In cases of variables with
more than two categories, the ANOVA or the Kruskal-Wallis tests
were used. Analyses of the odds ratio (OR) of a good response to
PDT were performed using logistic regression. p-values < 0.05
were considered statistically significant.
The study protocol was approved by the Ethical Committee for
Clinical Research of Aragon, Spain (CP-CI PI12/0096).
RESULTS
The study population consisted of 472 tumours in 249
patients, with a mean ± standard deviation (SD) age of
71.7 ± 13.78 years. Of these, 59% were men and 41%
women. The majority (92.6%) had no relevant medical
history, only 6.6% had received prior radiotherapy, and
the remainder had received transplants. The mean ± SD
age of treatment responders (69.98 ± 14.27 years) was
lower than that of non-responders (74.45 ± 11.1 years)
(p < 0.01).
The majority of the lesions analysed were nBCCs
(60.4%), followed by sBCCs (25.2%), and BD lesions
(14.4%). The back was the most common tumour lo-
cation (19.3%) followed by the forehead (16.1%), it
was associated with treatment response, with a poorer
response observed for lesions located on the face. Of
non-responding patients, 70% had lesions located on
the face (p < 0.01). In the statistical analysis when we
divided the lesions according to the facial anatomical
area affected, we verified th at of the total of 71 lesions
that were located in the nose, only 63.4%, demonstrating
that the nasal localization was an independent predictor
of poor response (p = 0.01).
A complete clinical response was observed for
81.1% of patients, the mean ± SD follow-up time was
35.96 ± 23.46 months. The number of PDT sessions ad-
ministered was as follows: 1 session, 11.7% of tumours; 2
sessions, 85.6% of tumours; 3 sessions, 2.6% of tumours.
Bivariate analysis revealed a statistically significant
association between clinical response and the follo-
wing variables: age (69.98 ± 4.27 years in responders
vs 74.46 ± 11.07 years in non-responders; p = 0.01);
location, with best response rate (92%) observed for
lesions located on the trunk, and the worst response rate
(75.62%) observed for those located on the head and
This is an open access article under the CC BY-NC license. www.medicaljournals.se/acta
Journal Compilation © 2018 Acta Dermato-Venereologica.