Diphenylcyclopropenone for the treatment of cutaneous in-transit melanoma metastases - results of a prospective, non-randomized, single-centre study

被引:18
|
作者
Read, T. [1 ,2 ,3 ]
Webber, S. [4 ]
Tan, J. [4 ]
Wagels, M. [1 ,2 ]
Schaider, H. [4 ,5 ]
Soyer, H. P. [4 ,5 ]
Smithers, B. M. [1 ,2 ]
机构
[1] Queensland Hlth, Princess Alexandra Hosp, Queensland Melanoma Project, Brisbane, Qld, Australia
[2] Univ Queensland, Discipline Surg, Sch Med, Brisbane, Qld, Australia
[3] Griffith Univ, Sch Med, Gold Coast, Qld, Australia
[4] Queensland Hlth, Princess Alexandra Hosp, Dept Dermatol, Brisbane, Qld, Australia
[5] Univ Queensland, Dermatol Res Ctr, Sch Med, Translat Res Inst, Brisbane, Qld, Australia
关键词
ISOLATED LIMB INFUSION; MALIGNANT-MELANOMA; TOPICAL DIPHENCYPRONE; IMMUNOTHERAPY; LYMPHADENECTOMY; IPILIMUMAB; EXTREMITY;
D O I
10.1111/jdv.14422
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BackgroundCurrent treatments for in-transit melanoma (ITM) metastases are frequently invasive and do not improve overall survival. Recently, there has been increasing investigation into the use of topical agents. Diphenylcyclopropenone or diphencyprone (DPCP) is a novel, topical therapy that has been reported to have immune-sensitizing properties useful in the treatment of ITM. ObjectiveTo assess the clinical outcomes of patients treated within a prospective, non-randomized, non-comparative study using DPCP for cutaneous ITM metastases. MethodsA review was conducted assessing the outcomes of 58 patients prospectively treated using DPCP. Patients had satellite or in-transit disease (stage IIIB+), with all lesion morphology types included. The patients were treated through a single, specialized clinic with regular outpatient follow-up. DPCP was topically applied as an aqueous cream in 0.005-1% concentrations once to twice per week for up to 24-48 h of duration. To assess variables associated with response, a per-protocol statistical analysis was performed. ResultsFifty-four patients were treated who satisfied eligibility criteria for analysis. The overall response rates were as follows: complete response 22%, partial response 39%, stable disease 24% and progressive disease 15%. The mean time to complete response was 10.5 months, mean duration (disease-free interval) 12.3 months and recurrence rate in complete responders 41%. Lesion morphology was predictive of clinical benefit with a higher response in epidermotropic disease (P < 0.05). ConclusionsDPCP provided a well-tolerated, convenient and efficacious treatment for cutaneous ITM metastases. Identifying patterns of response may assist treatment selection and improve patient-rated outcomes.
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收藏
页码:2030 / 2037
页数:8
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