Skip to main content
Wiley Open Access Collection logoLink to Wiley Open Access Collection
. 2015 Mar 31;57(1):24–28. doi: 10.1111/ajd.12295

Treatment of face and scalp solar (actinic) keratosis with daylight‐mediated photodynamic therapy is possible throughout the year in Australia: Evidence from a clinical and meteorological study

Lynda Spelman 1,14,, Diana Rubel 14,2, Dedee F Murrell 6, Jo‐Ann See 7, Daniel Hewitt 9, Peter Foley 14,3,4,5, Robert Salmon 11, Delphine Kerob 12, Thierry Pascual 13, Stephen Shumack 14,10, Pablo Fernandez‐Penas 8
PMCID: PMC6667998  PMID: 25827200

Abstract

Background/Objectives

Solar (actinic) keratosis (AK) is an emergent concern worldwide and is associated with an increased risk of development of non‐melanoma skin cancer, especially squamous cell carcinoma. Daylight‐mediated photodynamic therapy (DL‐PDT) using methyl aminolaevulinate cream has proved to be an effective, nearly painless, and more convenient alternative to conventional PDT for the treatment of AK. In a phase III, randomised, controlled trial performed in Australia, the mean irradiance (light intensity) received by patients during DL‐PDT treatment, assessed via a spectroradiometer, was 305 W/m2 (min. 40 to max. 585 W/m2) with similar efficacy irrespective of intensity or dose. The objective of the present meteorological study was to assess the suitability of natural daylight to perform DL‐PDT for the treatment of face and scalp AK during different periods of the year and different geographical locations and latitudes across Australia.

Methods

To determine daylight irradiance during a complete year in eight different geographical locations throughout Australia, we used meteorological software (Meteonorm, Meteotest, Bern, Switzerland), and available solar radiation and weather data from 1986–2005.

Results

The average daily irradiance remained within the levels (40–585 W/m2) measured during the clinical DL‐PDT study in Australia, throughout the year and in all geographical locations investigated (yearly average from Darwin 548 W/m2 to Hobart 366 W/m2).

Conclusions

DL‐PDT for the treatment of face and scalp AK in Australia can be performed effectively throughout the entire year as long as weather conditions permit daylight exposure and allow participants to remain under direct light for 2 h.

Keywords: Australia, daylight irradiance, daylight‐mediated photodynamic therapy, meteorological study, methyl aminolaevulinate, solar (actinic) keratosis


Abbreviations

AK

actinic keratosis

c‐PDT

conventional photodynamic therapy

DL‐PDT

daylight‐mediated photodynamic therapy

MAL

methyl aminolaevulinate cream

MICB

minimum irradiance inducing clinical benefit

PpIX

protoporphyrin IX

Introduction

Solar (actinic) keratosis (AK) is a concern worldwide with a prevalence of approximately 13% among the Caucasian population in Brazil,1 15% in England,2 and up to 60% in Australia.3 AK are common skin lesions that appear after long‐term exposure to UV radiation. The presence of AK is associated with an increased risk of developing non‐melanoma skin cancer, especially squamous cell carcinoma.

Conventional photodynamic therapy (c‐PDT) using methyl aminolaevulinate cream (MAL) under occlusion for 3 h before illumination with a red light‐emitting diode lamp is an effective procedure approved for the treatment of non‐melanoma skin cancers such as superficial and nodular basal cell carcinomas, Bowen's disease4 and thin, non‐hyperkeratotic AK on the face and scalp.5 European studies have shown that daylight‐mediated MAL PDT (DL‐PDT) is an effective, almost painless, and more convenient alternative to c‐PDT for the treatment of AK, especially in large fields of actinic damage which can easily be exposed to daylight.6, 7, 8, 9, 10 In 2012 an international consensus concluded that exposure to daylight for 2 h following skin preparation and the application of MAL would be appropriate to achieve a similar efficacy to c‐PDT.11

More recently, a phase III, multicentre, randomised controlled study performed from March to June 2012 in Australia compared the efficacy and safety of DL‐PDT with that of c‐PDT in 100 patients with mild AK on the face and scalp. The participants in this study were treated only when weather conditions permitted daylight exposure and allowed them to remain under direct light for 2 h, based on investigator's judgement. The results corroborated previous findings from European studies demonstrating that AK can be treated with DL‐PDT as effectively as with c‐PDT, while inducing significantly less treatment‐related pain, fewer treatment‐related adverse events and high patient satisfaction.12

Thus far, DL‐PDT studies have been conducted in Europe and Australia during limited periods of the year. Variations in weather conditions and the abundance of daylight in different geographical locations have raised questions over the feasibility of DL‐PDT and the applicability of the recommended treatment on a global scale. A recent study addressing these issues in Europe and Israel showed that the protoporphyrin IX (PpIX) light dose was influenced by geographical location, weather conditions and the time of year.13 Therefore, it was considered essential to investigate the feasibility of DL‐PDT in Australia according to the geographical location (latitude), weather conditions and time of the year.

Methods

The aim of this meteorological study was to determine daylight irradiance (light intensity), based on available solar radiation and weather data using meteorological software, in different locations and times of the year in Australia. These findings were compared to the irradiance measured by investigators during the recent DL‐PDT phase III study performed in the same country.12

Geographical locations

A total of eight geographical locations at different latitudes across Australia were investigated in this study, namely Darwin, Brisbane, Perth, Sydney, Adelaide, Canberra, Melbourne and Hobart (Fig. 1).

Figure 1.

Figure 1

Geographical locations investigated in this study.

Data source

Data in this study were calculated in collaboration with Meteotest (Bern, Switzerland), an expert in worldwide meteorology, environment and information technology.

For this investigation, new atmospheric and global solar radiation data were required. Data combining simulation and existing climatology databases (solar irradiance, weather conditions, and so on) were generated using Meteonorm (http://www.meteonorm.com), the reputable meteorological data software developed by Meteotest. Atmospheric parameters required for modelling irradiance at the ground level (atmospheric turbidity, water vapour and ozone) were also determined using data from the Meteonorm software.14 A specific model was developed to study and generate worldwide data for the purpose of DL‐PDT, taking into consideration the PpIX waveband and absorption spectrum. This model was able to use measurements from existing databases as well as interpolate data where measurements were not available, allowing the statistical analysis of a comprehensive dataset in this study.

Furthermore, real irradiance (light intensity) was measured by investigators during the recent DL‐PDT study performed in Australia using light measurement instruments.12

Method

During the Australian DL‐PDT clinical study, the solar irradiance and dose received by participants were measured at clinical sites by all investigators using a spectroradiometer (ILT950, International Light, Peabody, MA, USA) at each site. The instrument measured the spectrum and the amount of energy received at the time of the exposure for DL‐PDT by the participants, from 250 to 1050 nm, expressed in Watts/m2 (1 Watt = 1 joule/sec), during the 2‐hour exposure of each subject. A mean irradiance value was obtained and the final dose (mean irradiance × time) was calculated. In this study, no correlation between efficacy and dose or irradiance was observed. Therefore, the range of irradiance received by the participants during this study can be considered as suitable for DL‐PDT.

To compare the clinical study data to the meteorological data we decided to use irradiance values instead of PpIX effective irradiance or dose. Although PpIX effective irradiance (solar irradiance weighted by the PpIX absorption spectrum, that is, the irradiance of the biologically effective part of the solar spectrum) would be a better photobiological measurement, adjusting all study and meteorological data to the PpIX effective irradiance does not add value to the comparison between irradiance levels as the light source (the sun) is the same. Moreover, irradiance is a simpler measurement that can be easily recorded by the standard radiometers that dermatologists could use in their practices. Regarding dose, the reciprocity law states that different combinations of irradiance and exposure time achieving the same dose will have the same effect, but there is no evidence that DL‐PDT (like other photobiological processes) abide by this law. In fact, the transformation of MAL into PpIX requires an undetermined amount of time. If we achieve a fixed dose in less time than that required for the transformation of MAL into PpIX the treatment will be ineffective. Due to these factors, in our article we consider a 2‐h exposure as the amount of time needed to generate a good clinical response, as reported in the Australian phase III study.

Regarding meteorological data, we decided to calculate the mean solar irradiance at ground level (global horizontal irradiance) during office hours (9:00 to 18:00) for an entire year. For practical reasons the meteorological study was limited to office hours as this represents the period of the day when the patients would be visiting the dermatologist's clinic. This is also a period of the day when the influence of the sun's elevation is less likely to range into unwanted lower levels. The values were based on Meteonorm software data for the period 1986–2005. The data presented in the Table 1 are daily averages for each month over an entire year at each location.

Table 1.

Modelled daily average global radiation for each month Meteonorm data 1986–2005)

Locations Latitude Average daily irradiance in W/m2
Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Yearly Average
Darwin −12.4 507 485 547 538 538 529 554 591 601 580 583 516 548
Brisbane −27.4 635 575 551 471 358 309 344 396 497 547 584 609 489
Perth −31.9 737 668 591 410 330 285 292 392 495 591 692 739 518
Sydney −33.8 610 562 481 410 303 245 267 335 410 488 514 589 434
Adelaide −34.9 709 669 550 394 273 222 248 338 449 551 641 691 477
Canberra −35.3 654 612 528 413 295 227 252 329 419 517 599 657 458
Melbourne −37.8 604 555 485 345 227 193 211 285 387 464 555 598 408
Hobart −42.8 568 524 400 286 189 154 179 250 347 446 505 552 366

Assessment criteria

We decided to calculate the minimum irradiance that induced a clinical benefit (MICB) after 2 h of daylight exposure from the DL‐PDT study.

Results

In the Australian DL‐PDT study the mean irradiance to which participants were exposed during the 2‐h treatment was 305.8 W/m2. DL‐PDT sessions during this study were performed between March and May. The irradiance range was from 40 to 585 W/m2.12 There was no statistically significant correlation between the clinical benefit and solar irradiance and, therefore we considered the MICB to be the lowest average irradiance received during this study, that is, MICB = 40 W/m2.

Throughout the year, in all Australian geographical study locations, the average daily solar irradiance exceeded the mean irradiance level in the DL‐PDT study (305.8 W/m2). Darwin reported the highest yearly average of daily irradiance (548 W/m2) followed by Perth (518 W/m2) and Brisbane (489 W/m2). The location with the lowest yearly average of daily irradiance, although still higher than the mean irradiance in the study, was Hobart (366 W/m2) (Table 1) (Fig. 2).

Figure 2.

Figure 2

Modelled daily average global radiation for each month (Meteonorm data 1986–2005). Horizontal lines indicate light intensity levels of Australian DL‐PDT study12 (red: min. 40 W/m2; orange: max. 585 W/m2; green: average 305.8 W/m2).

Although average daily sun irradiance below the mean clinical study level (305.8 W/m2) was indeed observed, it was still much higher than the MICB (40 W/m2). These lower levels were observed in Melbourne during June (193 W/m2) and July (211 W/m2) as well as in Hobart during June (154 W/m2) and July (179 W/m2) (Table 1) (Fig. 2).

Discussion

No relationship between sun irradiance and treatment efficacy was found during the Australian DL‐PDT clinical study.12 While irradiance is influenced by geographical location, weather conditions, hour of the day and period of the year,13 the reported average irradiance levels in this meteorological study consistently exceeded the MICB received during the recent Australian DL‐PDT study.12 Therefore, the findings of this meteorological analysis suggest that weather conditions in Australia throughout the year are appropriate to perform DL‐PDT for the treatment of face and scalp AK. This also suggests that, as the procedure is feasible throughout the year, the main factor to consider before selecting DL‐PDT should be weather conditions rather than season of the year or geographical location. Weather conditions should allow patients to stay outside comfortably for 2 h.

It has previously been demonstrated that treatment effectiveness is reduced at ultra‐low irradiances using artificial daylight sources15 but a MICB has not yet been calculated for sunlight. In any case, low irradiance levels in daylight occur under deep shade or during rainy weather, and these conditions were avoided during the DL‐PDT study. Since these weather conditions lead to low levels of light and do not allow patients to stay outside comfortably for the 2 h of required exposure, DL‐PDT should be avoided under these conditions to ensure effective and convenient treatment. Of note, users should bear in mind that this publication presents average data, and that there are variations in real life. In general, sunny and rainy days will have higher and lower irradiance values, respectively, compared to average values presented in this study. Moreover, the irradiance varies throughout the day due to the sun's elevation. Therefore, for practical reasons, the patient should be exposed during office hours to minimise the potential influence of sun's elevation, especially in winter.

Collectively, these meteorological data demonstrate that both light conditions and atmospheric conditions in Australia are suitable throughout the year for the use of DL‐PDT in the treatment of face and scalp AK. During hours of increased risk for exposure to UV radiation, participants receiving treatment should use sunscreen offering adequate sun protection (SPF 30 or higher) that does not contain physical filters such as titanium dioxide, zinc oxide or iron oxide that could interfere with the visible light activation spectrum of PpIX.16 Sunscreen should be applied on all sun‐exposed areas including treated areas to protect the skin from exposure to UV radiation and damage.

DL‐PDT is dependent both on the light dose received and the exposure time. Thus, the 2‐h exposure to daylight is essential for the production and activation of PpIX. Shorter exposure to daylight may lead to the insufficient production of PpIX and impair the efficacy of treatment.

Patients are not obliged to remain for 2 h under direct sunlight. When this is uncomfortable (e.g. too hot), they may move intermittently in the shade. However, they should avoid deep shade, where there is a lack of sufficient light, as this may lead to reduced efficacy.

In conclusion, DL‐PDT for the treatment of face and scalp AK can be performed effectively throughout the entire year in Australia as long as weather conditions permit daylight exposure and allow participants to remain comfortably under direct light for 2 h, based on the judgement of the treating physician. Treatment during rainy weather should not be recommended as there are no data to support treatment efficacy under these conditions.

Acknowledgements

The authors would like to thank Sotirios Georgantopoulos, PhD, for editorial assistance.

Lynda Spelman, FACD. Diana Rubel, FACD. Dedee F Murrell, FACD. Jo‐Ann See, FACD. Daniel Hewitt, FACD. Peter Foley, FACD. Robert Salmon, FACD. Delphine Kerob, MD. Thierry Pascual, MSc. Stephen Shumack, FACD. Pablo Fernandez‐Penas, FACD.

Shared responsibility: all authors have contributed significantly and are in agreement with the content of the article.

Conflict of interest: Drs Spelman, Rubel, Murrell, See, Hewitt, Foley, Salmon, Shumack, and Fernandez‐Penas served as investigators or advisors and received investigator or advisor fees. Dr Kerob and Mr Pascual are employees of Galderma R&D.

References

  • 1. Sociedade Brasileira de Dermatologia . Data analysis of the Brazilian Society of Dermatology skin cancer prevention campaign, 1999 to 2005. An. Bras. Dermatol. 2006; 81: 529–535. [Google Scholar]
  • 2. Memon AA, Tomenson JA, Bothwell J et al Prevalence of solar damage and actinic keratosis in a Merseyside population. Br. J. Dermatol. 2000; 142: 1154–1159. [DOI] [PubMed] [Google Scholar]
  • 3. Frost C, Green A. Epidemiology of solar keratosis. Br. J. Dermatol. 1994; 131: 455–464. [DOI] [PubMed] [Google Scholar]
  • 4. Morton CA, Szeimies RM, Sidoroff A et al European guidelines for topical photodynamic therapy part 1: treatment delivery and current indications – actinic keratoses, Bowen's disease, basal cell carcinoma. J. Eur. Acad. Dermatol. Venereol. 2013; 27: 536–544. [DOI] [PubMed] [Google Scholar]
  • 5. de Berker D, McGregor JM, Hughes BR et al Guidelines for the management of actinic keratoses. Br. J. Dermatol. 2007; 156: 222–230. [DOI] [PubMed] [Google Scholar]
  • 6. Wiegell S, Hædersdal M, Philipsen P et al Continuous activation of PpIX by daylight is as effective as and less painful than conventional photodynamic therapy for actinic keratoses; a randomized, controlled, single‐blinded study. Br. J. Dermatol. 2008; 158: 740–746. [DOI] [PubMed] [Google Scholar]
  • 7. Wiegell S, Haedersdal M, Eriksen P et al Photodynamic therapy of actinic keratoses with 8% and 16% methyl aminolaevulinate and home‐based daylight exposure: a double‐blinded randomized clinical trial. Br. J. Dermatol. 2009; 160: 1308–1314. [DOI] [PubMed] [Google Scholar]
  • 8. Wiegell S, Fabricius S, Stender I et al A randomized, multicentre study of directed daylight exposure times of 1½ vs. 2½ h in daylight‐mediated photodynamic therapy with methyl aminolaevulinate in patients with multiple thin actinic keratoses of the face and scalp. Br. J. Dermatol. 2011; 164: 1083–1090. [DOI] [PubMed] [Google Scholar]
  • 9. Braathen LR. Daylight photodynamic therapy in private practice in Switzerland: gain without pain. Acta Derm. Venereol. 2012; 92: 652–653. [DOI] [PubMed] [Google Scholar]
  • 10. Wiegell SR, Fabricius S, Gniadecka M et al Daylight‐mediated photodynamic therapy of moderate to thick actinic keratoses of the face and scalp: a randomized multicentre study. Br. J. Dermatol. 2012; 166: 1327–1332. [DOI] [PubMed] [Google Scholar]
  • 11. Wiegell SR, Wulf HC, Szeimies RM et al Daylight photodynamic therapy for actinic keratosis: an international consensus: International Society for Photodynamic Therapy in Dermatology. J. Eur. Acad. Dermatol. Venereol. 2012; 26: 673–679. [DOI] [PubMed] [Google Scholar]
  • 12. Rubel DM, Spelman L, Murrell DF et al Daylight PDT with methyl aminolevulinate cream as a convenient, similarly effective, nearly painless alternative to conventional PDT in actinic keratosis treatment: a randomised controlled trial. Br. J. Dermatol. 2014; 171: 1164–1171 [DOI] [PubMed] [Google Scholar]
  • 13. Wiegell SR, Fabricius S, Heydenreich J et al Weather conditions and daylight‐mediated photodynamic therapy: protoporphyrin IX‐weighted daylight doses measured in six geographical locations. Br. J. Dermatol. 2013; 168: 186–191. [DOI] [PubMed] [Google Scholar]
  • 14. Remund J, Salvisberg E, Kunz S. Generation of hourly shortwave radiation data on tilted surfaces at any desired location. Solar Energy 1998; 62: 331–344. [Google Scholar]
  • 15. Wiegell SR, Heydenreich J, Fabricius S et al Continuous ultra‐low‐intensity artificial daylight is not as effective as red LED light in photodynamic therapy of multiple actinic keratoses. Photodermatol 2011; 27: 280–285. [DOI] [PubMed] [Google Scholar]
  • 16. Wiegell SR, Wulf HC, Szeimies RM et al Daylight photodynamic therapy for actinic keratosis: an international consensus. J. Eur. Acad. Dermatol. Venereol. 2012; 26: 673–679. [DOI] [PubMed] [Google Scholar]

Articles from The Australasian Journal of Dermatology are provided here courtesy of Wiley

RESOURCES