Pembrolizumab Plus Lenvatinib in Previously Treated Classic Kaposi Sarcoma

Trial Title: Pembrolizumab Plus Lenvatinib in Previously Treated Classic Kaposi Sarcoma

NCT ID: NCT05846724

Condition: Kaposi Sarcoma
Classic Kaposi Sarcoma
Refractory Kaposi Sarcoma

Conditions: Official terms:
Sarcoma, Kaposi
Sarcoma
Pembrolizumab
Lenvatinib

Study type: Interventional

Study phase: Phase 2

Overall status: Not yet recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Pembrolizumab + Lenvatinib
Description: single-arm study of pembrolizumab plus lenvatinib
Arm group label: Single Arm

Summary: Phase II study of Pembrolizumab plus Lenvatinib in relapsed/refractory Classic Kaposi Sarcoma (CKS). After a screening phase of up to 28 days, each participant will receive study intervention of pembrolizumab plus lenvatinib until reaching a discontinuation criterion: disease progression; unacceptable adverse event(s) (AEs); intercurrent illness that prevents further administration of treatment; participant withdraws consent; pregnancy of participant; non-compliance with study intervention or procedure requirements; or administrative reasons requiring cessation of treatment. After the end of treatment, each participant will be followed for the occurrence of AEs and spontaneously reported pregnancy. Participants who discontinue for reasons other than PD will have post-treatment follow-up for disease status until PD is documented clinically by a team of committed dermatologists, and/or radiographically per RECIST 1.1, a non-study anticancer treatment is initiated, consent is withdrawn, or the participant becomes lost to follow-up. All participants will be followed for overall survival (OS) until death, withdrawal of consent,lost to follow-up, or the end of the study. The end of the study will be when the last participant completes the last study-related telephone call or visit,withdraws from the study, or is lost to follow-up.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Have a histologically confirmed diagnosis of classic (or endemic) KS 2. Progression or inadequate response to at least one prior systemic chemotherapy 3. Presence of measurable disease by PET-CT scan and/or dermatological examination 4. KS with at least 10 cutaneous and/or mucosal lesions, or involving more than one limb segment or with involvement >3% body surface 5. KS with at least 4 lesions ≥ 5mm 6. KS with at least 1 superficial lesion willing to provide tissue from cutaneous and/or mucosal biopsy at baseline 7. At least 4 weeks washout for all KS specific therapies including chemotherapy (both systemic and intralesional) and radiotherapy 8. Be ≥ 18 years of age at the time of signing informed consent 9. Have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1 10. Have adequately controlled blood pressure (BP) with or without antihypertensive medications, defined as BP ≤150/90 mm Hg and no change in antihypertensive medications within 1 week prior to randomization. Exclusion Criteria: 1. Has a known history of human immunodeficiency virus (HIV) infection (HIV 1/2 antibodies detected at screening). 2. Has a known history of Hepatitis B (defined as Hepatitis B surface antigen [HBsAg] reactive) or known active Hepatitis C virus (defined as HCV RNA [qualitative] is detected) infection. Note: no testing for Hepatitis B and Hepatitis C is required unless mandated by local health authority. 3. Has active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (eg., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment. Patients with vitiligo, type I diabetes mellitus, hypothyroidism, psoriasis not requiring systemic treatment are permitted to enroll. 4. Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent, or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, CTLA-4, OX 40, CD137). 5. Has received prior radiotherapy within 2 weeks of start of study intervention. Participants must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Start date: February 1, 2024

Completion date: February 1, 2030

Lead sponsor:
Agency: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Agency class: Other

Source: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05846724