Microneedle Chemotherapy for Skin Cancer
(cSCC Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new method for treating cutaneous squamous cell carcinoma (a type of skin cancer) using small patches with tiny needles. These patches deliver low doses of doxorubicin, a chemotherapy drug, directly to the cancerous area. The trial aims to determine the safety and effectiveness of this method. Individuals with a biopsy-confirmed diagnosis of resectable stage I-III cSCC who can follow study instructions might be suitable candidates. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this innovative treatment.
Will I have to stop taking my current medications?
The trial does not specify if you need to stop taking your current medications, but you cannot be on any other investigational treatments. You also cannot receive other treatments for skin cancer, except for certain skin moisturizers without steroids or antibiotics.
What prior data suggests that this microneedle chemotherapy method is safe for skin cancer treatment?
Research has shown that the microneedle array doxorubicin (MNA-D) patch was well-tolerated in past studies. Researchers identified 50 micrograms as the highest safe dose for another type of skin cancer. This indicates that the patches are generally safe, with careful monitoring of the application site. Other studies have also demonstrated positive results in using these patches to deliver chemotherapy drugs like doxorubicin. This method allows for targeted and controlled release, which can help reduce side effects. Overall, the MNA-D patches appear to be a safe option for those considering participation in this clinical trial.12345
Why are researchers excited about this trial?
Unlike the standard treatments for skin cancer, which often involve surgical removal, radiation, or topical chemotherapy creams, the Microneedle Chemotherapy uses a microneedle array to deliver doxorubicin directly into the skin. This method is unique because it precisely targets cancer cells with minimal discomfort, reducing side effects associated with traditional chemotherapy. Researchers are excited about this approach because it potentially offers a less invasive and more localized treatment option, which could be particularly beneficial for patients with compromised immune systems.
What evidence suggests that this microneedle array is effective for skin cancer?
Studies have shown that microneedle patches containing doxorubicin can improve treatment for skin cancers like basal cell carcinoma. In this trial, participants will receive the Microneedle Array Doxorubicin (MNA-D) patch, which targets cancer more precisely than standard creams. This allows the medication to penetrate deeper into the skin and potentially enhance effectiveness. Early research using similar microneedle technology for other skin cancers has shown promising results, indicating it might also be effective for cutaneous squamous cell carcinoma (cSCC). The microneedle patches are designed to dissolve, releasing the drug slowly over time, which may reduce side effects compared to traditional chemotherapy. These encouraging findings suggest that this new method could offer a more effective and targeted way to treat skin cancer.12356
Who Is on the Research Team?
Oleg E Akilov, MD, PhD
Principal Investigator
University of Pittsburgh
Are You a Good Fit for This Trial?
This trial is for adults with a confirmed diagnosis of cutaneous squamous cell skin cancer, which can be surgically removed and measures between 5mm to less than 100mm. Participants should have an ECOG status of 0-2, meaning they are fully active or at least capable of self-care, not on other experimental treatments, and able to follow study instructions. Pregnant individuals or those with significant heart issues, autoimmune diseases (with some exceptions), recent major surgery, lung conditions caused by drugs, or active infections like HIV/hepatitis cannot join.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive the MNA-D patch on 4 subsequent visits for a 20 minute time period at each application
Rest
A rest period following the initial treatment phase
Follow-up
Participants are monitored for safety and effectiveness after treatment, including final follow-up visit and excision of remaining cSCC lesion
What Are the Treatments Tested in This Trial?
Interventions
- Doxorubicin
- Microneedle Array
Doxorubicin is already approved in United States, European Union, Canada, Japan for the following indications:
- Breast cancer
- Ovarian cancer
- Bladder cancer
- Lymphomas
- Leukemias
- Multiple myeloma
- Kaposi's sarcoma
- Soft tissue sarcomas
- Breast cancer
- Ovarian cancer
- Bladder cancer
- Lymphomas
- Leukemias
- Multiple myeloma
- Kaposi's sarcoma
- Soft tissue sarcomas
- Breast cancer
- Ovarian cancer
- Bladder cancer
- Lymphomas
- Leukemias
- Multiple myeloma
- Kaposi's sarcoma
- Soft tissue sarcomas
- Breast cancer
- Ovarian cancer
- Bladder cancer
- Lymphomas
- Leukemias
- Multiple myeloma
- Kaposi's sarcoma
- Soft tissue sarcomas
Find a Clinic Near You
Who Is Running the Clinical Trial?
Falo, Louis, MD
Lead Sponsor
National Cancer Institute (NCI)
Collaborator