Original article
100% Complete response rate in patients with cutaneous metastatic melanoma treated with intralesional interleukin (IL)-2, imiquimod, and topical retinoid combination therapy: Results of a case series

https://doi.org/10.1016/j.jaad.2015.06.060Get rights and content
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Background

Patients with cutaneous melanoma metastases have experienced excellent responses to intralesional interleukin (IL)-2. This has led to its recent inclusion into the US National Comprehensive Cancer Network guidelines for management of cutaneous melanoma metastases. Despite this, intralesional IL-2 has not been highlighted in the US literature nor have US physicians adopted it.

Objective

We sought to evaluate the effectiveness of intralesional IL-2 combined with topical imiquimod and retinoid for treatment of cutaneous metastatic melanoma.

Methods

A retrospective case series of 11 patients with cutaneous metastatic melanoma were treated with intralesional IL-2 combined with topical imiquimod and retinoid.

Results

A 100% complete local response rate with long-term follow-up (average of 24 months) was seen in all 11 patients treated with this proposed regimen. Biopsy specimens of treated sites confirmed absence of malignant cells. The most common treatment-related adverse event was rigors.

Limitations

Small number of patients, retrospective review of charts, and lack of a comparison group were limitations.

Conclusion

Intralesional IL-2 administered concomitantly with topical imiquimod and a retinoid cream is a promising therapeutic option for managing cutaneous melanoma metastases. The regimen was well tolerated and should be considered as a reasonable alternative to surgical excision.

Key words

imiquimod
interleukin
intralesional
metastatic melanoma
pemphigus vulgaris
retinoid

Abbreviations used

CNS
central nervous system
IL
interleukin
MDS
myelodysplastic syndrome

Cited by (0)

Drs Shi and Tran contributed to the manuscript equally and are co-first authors.

Supported by Burroughs Wellcome Fund, Howard Hughes Medical Institute, National Cancer Institute (NCI P30CA093373), and the National Institute of Health (DP2-OD009752).

Conflicts of interest: None declared.