Topical treatment of actinic keratoses in organ transplant recipients: a feasibility study for SPOT (Squamous cell carcinoma Prevention in Organ transplant recipients using Topical treatments)
dc.contributor.author | Zeeshaan-Ul, H. | |
dc.contributor.author | Ahmed, I. | |
dc.contributor.author | Matin, R. N. | |
dc.contributor.author | Homer, V. | |
dc.contributor.author | Lear, J. T. | |
dc.contributor.author | Ismail, F. | |
dc.contributor.author | Whitmarsh, T. | |
dc.contributor.author | Green, Adèle C | |
dc.contributor.author | Thomson, J. | |
dc.contributor.author | Milligan, A. | |
dc.contributor.author | Hogan, S. | |
dc.contributor.author | Van-de-Velde, V. | |
dc.contributor.author | Mitchell-Worsford, L. | |
dc.contributor.author | Kentley, J. | |
dc.contributor.author | Gaunt, C. | |
dc.contributor.author | Jefferson-Hulme, Y. | |
dc.contributor.author | Bowden, S. J. | |
dc.contributor.author | Gaunt, P. | |
dc.contributor.author | Wheatley, K. | |
dc.contributor.author | Proby, C. M. | |
dc.contributor.author | Harwood, C. A. | |
dc.date.accessioned | 2022-08-01T09:07:09Z | |
dc.date.available | 2022-08-01T09:07:09Z | |
dc.date.issued | 2022 | en |
dc.identifier.citation | Hasan Z, Ahmed I, Matin RN, Homer V, Lear JT, Ismail F, et al. Topical treatment of actinic keratoses in organ transplant recipients: a feasibility study for <scp>SPOT</scp> (Squamous cell carcinoma Prevention in Organ transplant recipients using Topical treatments). British Journal of Dermatology. Wiley; 2022. | en |
dc.identifier.pmid | 34988975 | en |
dc.identifier.doi | 10.1111/bjd.20974 | en |
dc.identifier.uri | http://hdl.handle.net/10541/625400 | |
dc.description.abstract | Background: The risk of cutaneous squamous cell carcinoma (cSCC) is significantly increased in organ transplant recipients (OTRs). Clearance of actinic keratoses (AKs) is generally regarded as a surrogate biomarker for cSCC prevention. OTR-cSCC chemoprevention with topical AK treatments has not been investigated in randomized controlled trials (RCTs), although there is evidence that 5% 5-fluorouracil (5-FU) may be chemoprotective in immunocompetent patients. Objectives: To assess the feasibility, activity and evaluation outcomes relevant to the design of a future phase III RCT of topical cSCC chemoprevention in OTRs. Methods: OTRs with 10 or more AKs in predefined areas were randomized 1 : 1 : 1 to topical 5-FU, 5% imiquimod (IMIQ) or sunscreen (sun-protective factor 30+) in a phase II, open-label RCT over 15 months. Feasibility outcomes included proportions of eligible OTRs randomized, completing treatment and willing to be re-treated. AK activity [AK clearance, new AK development, patient-centred outcomes (toxicity, health-related quality of life, HRQoL)] and evaluation methodology (clinical vs. photographic) were assessed. Results: Forty OTRs with 903 AKs were randomized. All feasibility outcomes were met (56% of eligible OTRs were randomized; 89% completed treatment; 81% were willing to be re-treated). AK activity analyses found 5-FU and IMIQ were superior to sunscreen for AK clearance and prevention of new AKs. 5-FU was more effective than IMIQ in AK clearance and prevention in exploratory analyses. Although toxicity was greater with 5-FU, HRQoL outcomes were similar. Conclusions: Trials of topical AK treatments in OTRs for cSCC chemoprevention are feasible and AK activity results support further investigation of 5-FU-based treatments in future phase III trials. | en |
dc.language.iso | en | en |
dc.relation.url | https://dx.doi.org/10.1111/bjd.20974 | en |
dc.title | Topical treatment of actinic keratoses in organ transplant recipients: a feasibility study for SPOT (Squamous cell carcinoma Prevention in Organ transplant recipients using Topical treatments) | en |
dc.type | Article | en |
dc.contributor.department | Department of Dermatology, Barts Health NHS Trust, London, UK. | en |
dc.identifier.journal | British Journal of Dermatology | en |
dc.description.note | en] | |
refterms.dateFOA | 2022-08-01T12:56:37Z |