News Release
August 6, 2015

Topical Gel Proves Safe, Effective Treatment for Patients with Skin T Cell Lymphoma, Penn Study Finds

Phase One Trial First to Show Topical Therapy Causes Systemic Immune Response, and May Eradicate Cancerous Cells from Treated and Untreated Lesions

PHILADELPHIA – Results of a phase one trial show that an investigational topical drug, resiquimod gel, causes regression of both treated and untreated tumor lesions and may completely remove cancerous cells from both sites in patients with early stage cutaneous T cell lymphoma (CTCL) – a rare type of non-Hodgkin lymphoma that affects the skin. Currently, there is no cure for CTCL aside from a bone marrow transplant. However, the new study from researchers at the Perelman School of Medicine at the University of Pennsylvania, shows that the topical gel can eliminate malignant T cells, leading to diminished lesions. Results, which build upon previous research, are giving hope to patients who have not responded to other modalities, including certain types of topical chemotherapy, phototherapy and even systemic treatment with interferon alpha and oral bexarotene. The study is published online this month in the journal Blood.

In the trial, led by principal investigator Alain Rook, MD, professor of Dermatology and director of the Cutaneous Lymphoma Program at Penn Medicine, and Joel M. Gelfand, MD, MSCE, associate professor of Dermatology and medical director of the Clinical Studies Unit at Penn Medicine, and co-led by Rachael Clark, MD, PhD, associate professor of Dermatology at Harvard Medical School, twelve patients who had previously undergone an average of six treatments for early stage CTCL were treated with topical resiquimod gel at varying doses and intervals. Patients applied specified doses (0.03 percent of 0.06 percent) to select skin lesions for 16 weeks. However, some patients using the 0.06 percent dose showed a full clearing of all malignant cells after only eight weeks.

By the final evaluation, treated lesions were significantly improved in 75 percent of patients, and 30 percent saw full resolution in all treated lesions. Unlike other treatments, resiquimod also improved untreated lesions, resulting in more than 50 percent improvement for more than 90 percent of patients. Two participants, one of whom had been living with CTCL for more than 15 years without response to treatment, saw full eradication of the disease.

“The results of the trial suggest that resiquimod is safely and effectively absorbed into the skin, and beyond diminishing treated lesions, also enhances the immune response, leading to healing of even untreated lesions,” first author and principal investigator Rook, said.. “To our knowledge, this is the first topical therapy that can clear untreated lesions and lead to complete remission in some patients.”

Using a method known as high throughput sequencing (HTS), the team was able to determine how many distinct malignant cells were present within a sample of healthy cells. The technique showed it could identify a single malignant cell amongst 100,000 healthy cells. DNA from biopsies of the same treated lesion were analyzed before treatment and eight weeks after treatment began to identify the number of malignant T cells. The percentage of malignant T cells was reduced significantly in nine of ten tested participants, three of whom had complete eradication of the malignant population, and one of whom had a 99.6 percent reduction.

“Overall, lesions responded far better to topical resiquimod than they have with other topical therapies, including some potent topical steroids and topical chemotherapy, and was extremely well tolerated by patients,” Rook said. “Building upon previous research, our study suggests resiquimod might be useful in combination with other therapies  in the treatment of more advanced CTCL. Further research with larger participant populations is needed to determine the best approach and application for these patients.”

Other Penn authors include Maria Wysocka, Andrea Troxel, Bernice Benoit, Rosalie Elenitsas, Marie Buchanan, Deborah Leahy, and Ellen Kim, from the department of Dermatology and the Center for Clinical Biostatistics and Epidemiology at Penn Medicine.

Funding for the study was provided by the National Institutes of Health (R01 CA122569, R01 AR056720, and R01 AR063962) and the Food and Drug Administration (FD-RO1-04092). Resiquimod for the trial was provided by Spirig, Inc. The authors disclose no conflict of interest.

Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation's first medical school) and the University of Pennsylvania Health System, which together form a $5.3 billion enterprise.

The Perelman School of Medicine has been ranked among the top five medical schools in the United States for the past 18 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $373 million awarded in the 2015 fiscal year.

The University of Pennsylvania Health System's patient care facilities include: The Hospital of the University of Pennsylvania and Penn Presbyterian Medical Center -- which are recognized as one of the nation's top "Honor Roll" hospitals by U.S. News & World Report -- Chester County Hospital; Lancaster General Health; Penn Wissahickon Hospice; and Pennsylvania Hospital -- the nation's first hospital, founded in 1751. Additional affiliated inpatient care facilities and services throughout the Philadelphia region include Chestnut Hill Hospital and Good Shepherd Penn Partners, a partnership between Good Shepherd Rehabilitation Network and Penn Medicine.

Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2015, Penn Medicine provided $253.3 million to benefit our community.


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