Intense pulsed light vs. long-pulsed dye laser treatment of telangiectasia after radiotherapy for breast cancer: a randomized split-lesion trial of two different treatments

Summary Background  Chronic radiodermatitis is a common sequela of treatment for breast cancer and potentially a psychologically distressing factor for the affected women. Objectives  To evaluate the efficacy and adverse effects of treatments with a long‐pulsed dye laser (LPDL) vs. intense pulsed li...

Full description

Saved in:
Bibliographic Details
Published inBritish journal of dermatology (1951) Vol. 160; no. 6; pp. 1237 - 1241
Main Authors Nymann, P., Hedelund, L., Hædersdal, M.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.2009
Wiley-Blackwell
Subjects
Online AccessGet full text
ISSN0007-0963
1365-2133
1365-2133
DOI10.1111/j.1365-2133.2009.09104.x

Cover

More Information
Summary:Summary Background  Chronic radiodermatitis is a common sequela of treatment for breast cancer and potentially a psychologically distressing factor for the affected women. Objectives  To evaluate the efficacy and adverse effects of treatments with a long‐pulsed dye laser (LPDL) vs. intense pulsed light (IPL) in a randomized split‐lesion trial. Methods  Thirteen female volunteers with radiodermatitis and Fitzpatrick skin types II–III were included in the study. Subjects received a series of three treatments at 6‐week intervals with half‐lesion LPDL (V‐beam Perfecta, 595 nm) and half‐lesion IPL (Ellipse Flex); the interventions were randomly assigned to left/right or upper/lower halves. Primary end‐points were reduction in telangiectasia, patient satisfaction and preferred treatment. Secondary end‐points were pain and adverse effects. Efficacy was registered by blinded photographic evaluations 3 months after the final treatment. Results  Eleven patients completed the study. Telangiectasia cleared with both treatments but the efficacy of LPDL was superior. Blinded photographic evaluations showed median vessel clearances of 90% (LPDL) and 50% (IPL) (P = 0·01). LPDL treatments were associated with lower pain scores than IPL treatments [median visual analogue scale (VAS) score 4·3 and 6·0, respectively, P < 0·01]. Patients were slightly more satisfied with LPDL (median VAS score 8) than IPL treatments (median VAS score 7; P < 0·05) and more preferred LPDL (n = 9) to IPL (n = 2) (P < 0·01). Two patients withdrew from the study because of hypopigmentation of the IPL treated areas, which slowly repigmented within 1 year. Conclusions  This study was based on two specific laser and IPL devices, and found the LPDL treatment to be advantageous compared with IPL due to superior vessel clearance and less pain.
Bibliography:ArticleID:BJD9104
ark:/67375/WNG-2PR4ZDRF-R
istex:F7E438A83BCB155A1B10E2090BC07B9936EB0AE9
Conflicts of interest
Danish Dermatologic Development, Hørsholm, Denmark and Candela Corporation, Wayland, MA, U.S.A. had no role in the design and conduct of the study, either in the collection, analysis and interpretation of data, or in the preparation of the manuscript, review or approval of the manuscript. The authors have no personal financial conflicts of interest in this article.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Undefined-3
ISSN:0007-0963
1365-2133
1365-2133
DOI:10.1111/j.1365-2133.2009.09104.x