Pembrolizumab Plus Lenvatinib in Unresectable Cutaneous Angiosarcoma Patients

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-85
SponsorNational Cancer Center, Japan

About this trial

Cutaneous angiosarcoma is a rare cancer for which effective treatment has not been developed sufficiently. Still, because it often occurs in elderly people, the number of patients is increasing due to the aging population. Cutaneous angiosarcoma is difficult to completely remove by surgery, and recurrence and metastasis after surgery are not uncommon. Therefore, chemotherapy, radiation therapy, and a combination of these are currently widely used as treatments. Traditionally, the anticancer drug used for cutaneous angiosarcoma was mainly doxorubicin. In recent years, it has been reported that cancer shrank in 18% of patients after two months of paclitaxel administration in a clinical trial. Therefore, paclitaxel has become more commonly used for cutaneous angiosarcoma. Other options include anthracycline anticancer drugs and gemcitabine. However, even with these anticancer drugs (and radiation therapy), cutaneous angiosarcoma progresses quickly, and some reports have said that the 5-year survival rate is 9%. This study is planned to develop a safer and more effective treatment for cutaneous angiosarcoma and will include 38 participants. In this study, eligible participants will receive combination chemotherapy with 200 mg of pembrolizumab (injection liquid, once every 3 weeks) and 20 mg of lenvatinib (capsule, once daily) for up to approximately two years as protocol treatment unless the criteria for termination meet. Before, during, and after the protocol treatment, participants will undergo many examinations and evaluations, including blood tests, urine tests, and imaging tests (e.g., x-ray, CT scan, or MRI) to assess the safety and efficacy of the protocol treatment.

Eligibility criteria

Qualifiers

Histologically diagnosed with cutaneous angiosarcoma.

Unresectable primary or metastatic disease.

No spinal metastases that require radiotherapy or surgical intervention.

No pericardial effusion, pleural effusion, or ascites that require treatment.

Disqualifiers

Persons previously treated with anti-PD-1, anti-PD-L1, anti-PD-L2 agents, or agents targeting other co-inhibitory T-cell receptors (e.g., CTLA-4, OX-40, CD137).

Individuals previously treated with lenvatinib or another angiogenesis inhibitor, including treatment for other cancer types.

Patients who are likely to be cured with chemoradiotherapy, at the discretion of the treating physician.

Patients who received radiation therapy within 14 days prior to enrollment or patients with radiation therapy-related toxicities at enrollment.

Trial design

Treatments tested in this trial

  • Pembrolizumab plus Lenvatinib

Treatment groups

38 Participants
are divided into 1 treatment group

Sponsors and collaborators

National Cancer Center, Japan

Lead sponsor

Merck Sharp & Dohme LLC

Collaborator