Pre- and Post-Surgery Pembrolizumab for Melanoma
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests the effectiveness of pembrolizumab, an immunotherapy, when used before and after surgery for individuals with high-risk melanoma, a type of skin cancer. The goal is to determine if using pembrolizumab both before and after surgery is more effective than using it only after surgery. Participants with stage III or IV melanoma that hasn't spread to the brain and is visible on scans or exams may be suitable candidates. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.
Will I have to stop taking my current medications?
The trial protocol does not specify if you need to stop taking your current medications. However, you must not receive any other biologic therapy, hormonal therapy, or chemotherapy while on the study. It's best to discuss your specific medications with the trial team.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research shows that pembrolizumab, a treatment for melanoma, is generally safe. Studies have found that it remains safe for long-term use when given alone for advanced melanoma, with serious side effects uncommon for most patients.
The FDA has approved pembrolizumab for treating advanced melanoma, further confirming its safety. In a large study, most participants tolerated pembrolizumab well, indicating that severe problems are rare.
Overall, pembrolizumab's history in treating melanoma suggests it is generally safe for use.12345Why are researchers excited about this study treatment for melanoma?
Unlike the standard care for melanoma, which often involves surgery followed by adjuvant treatment, pembrolizumab offers a unique approach by acting as both a neoadjuvant and adjuvant therapy. Pembrolizumab is a type of immunotherapy that works by unleashing the immune system to attack cancer cells, targeting the PD-1 pathway, which is different from traditional treatments like chemotherapy. Researchers are excited about this treatment because it could potentially shrink tumors before surgery, making them easier to remove, and help prevent the cancer from coming back after surgery. This dual approach aims to improve outcomes for patients with melanoma by using the body's own defenses in a more strategic manner.
What evidence suggests that pembrolizumab might be an effective treatment for melanoma?
Research has shown that pembrolizumab can help treat advanced melanoma. In one study, over one-third of patients with advanced melanoma were still alive 10 years after receiving pembrolizumab, outperforming those treated with ipilimumab. Another study found that pembrolizumab halted cancer progression in 43% of patients, compared to 32% with ipilimumab. Additionally, more patients experienced tumor shrinkage with pembrolizumab. In this trial, participants in Arm I will receive adjuvant pembrolizumab, while those in Arm II will receive both adjuvant and neoadjuvant pembrolizumab. The drug is also known to improve long-term survival and reduce the chance of cancer returning or spreading. Overall, pembrolizumab has shown promising results in aiding the body's immune system to fight melanoma.15678
Who Is on the Research Team?
Sapna P Patel
Principal Investigator
SWOG Cancer Research Network
Are You a Good Fit for This Trial?
This trial is for adults with high-risk melanoma (stage III-IV) that can be removed by surgery. They must not have had previous neoadjuvant immunotherapy or certain other treatments, no active infections, and no history of severe autoimmune disease or pneumonitis. Participants need functioning major organs, no brain metastases, and women of childbearing age must test negative for pregnancy.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Neoadjuvant Treatment
Participants receive pembrolizumab IV every 3 weeks for 3 cycles before surgery
Surgery
Participants undergo surgical resection
Adjuvant Treatment
Participants receive pembrolizumab IV every 3 weeks for 15 cycles after surgery
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Pembrolizumab
- Therapeutic Conventional Surgery
Pembrolizumab is already approved in United States, European Union, United Kingdom for the following indications:
- Head and neck squamous cell carcinoma (HNSCC) with PD-L1 CPS ≥1
- Melanoma
- Non-small cell lung cancer (NSCLC)
- Urothelial carcinoma
- Colorectal cancer
- Gastric cancer
- Hepatocellular carcinoma
- Renal cell carcinoma
- Cervical cancer
- Endometrial carcinoma
- Head and neck squamous cell carcinoma (HNSCC) with PD-L1 CPS ≥1
- Melanoma
- Non-small cell lung cancer (NSCLC)
- Urothelial carcinoma
- Colorectal cancer
- Gastric cancer
- Hepatocellular carcinoma
- Renal cell carcinoma
- Cervical cancer
- Endometrial carcinoma
- Untreated metastatic or unresectable recurrent head and neck squamous cell carcinoma (HNSCC) with PD-L1 CPS ≥1
Find a Clinic Near You
Who Is Running the Clinical Trial?
National Cancer Institute (NCI)
Lead Sponsor