Pembrolizumab Plus Lenvatinib In Second Line and Third Line Malignant Pleural mesotheLioma Patients

Mesotheliomas Pleural Clinical Trial

— PEMMELA  

Official title:

PEMbrolizumab Plus Lenvatinib In Second Line And Third Line Malignant Pleural MEsotheLiomA Patients(PEMMELA)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04287829
• Other study ID #: N19PEM
• Status: Recruiting
• Phase: Phase 2
• Start date: March 1, 2021
• Est. completion date: December 5, 2024

Study information

• Verified date: September 2022
• Source: The Netherlands Cancer Institute
• Contact: S Burgers, PhD
• Phone: 0031205129111
• Email: s.burgers[@]nki.nl
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There is no standard second line treatment in malignant pleural mesothelioma (MPM). Pembrolizumab has shown to be active in in small phase II studies in MPM. Its activity however, is limited, with a response rate up to 20%. Since the arrival of nivolumab plus ipilimumab as first line standard of care treatment in mesothelioma, no treatment options are investigated in this group of patients in the second line. So, there is a need for new treatment combinations with drugs that might exhibit a synergistic interaction with pembrolizumab.

Description:

There is no standard second line treatment in malignant pleural mesothelioma (MPM). Pembrolizumab has shown to be active in in small phase II studies in MPM. Its activity however, is limited, with a response rate up to 20%. So, there is a need for new treatment combinations with drugs that might exhibit a synergistic interaction with pembrolizumab. The mechanisms of actions of lenvatinib, which has a broad spectrum of activities, predicts many synergistic interactions with PD-1 blocking. The aim of this study is to characterize the potential clinical activity, toxicity and biomarkers of outcome of pembrolizumab - lenvatinib in patients with recurrent MPM.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 58
• Est. completion date: December 5, 2024
• Est. primary completion date: December 5, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Histologically or cytologically diagnosed malignant pleural mesothelioma, age at least 18 years

2. Progressive disease after at least 1 and maximal 2 prior systemic treatment lines:

• Cohort 1: patients, in which one of the lines contains a platinum-based doublet (both cisplatin and carboplatin are allowed) for unresectable MPM (CLOSED)

• Cohort 2: patients with only in which one of the lines contains nivolumab-ipilimumab immunotherapy as first line treatment for unresectable MPM. No prior chemotherapy.

3. Measurable disease. At least one measurable lesion according to Modified RECIST 1.1 for pleural mesothelioma. Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions

4. WHO-ECOG performance status of 0 to 1. Evaluation of ECOG is to be performed within 7 days prior to date of allocation

5. Adequate organ function

6. Ability to understand the study and give signed informed consent (or legally acceptable representative if applicable) prior to beginning of protocol specific procedures including the approval of the thoracoscopy or transthoracic pleural biopsy before the first treatment cycle and an optional biopsy before the third treatment cycle

7. No presence of clinically relevant treatment-related toxicity from previous chemotherapy, targeted therapy and/or radiotherapy. Note: Participates must have recovered from all AEs due to previous therapies to =Grade 1 or baseline. Participants with =2 neuropathy may be eligible

8. No active uncontrolled infection, severe cardiac dysfunction (i.e. unstable angina, history of myocardial infarction within the past 12 months prior to screening, congestive heart failure > NYHA II, serious cardiac arrhythmia), unstable peptic ulcer, unstable diabetes mellitus or other seriously disabling condition

9. Adequately controlled blood pressure (BP) with or without antihypertensive medications, defined as BP =150/90 mmHg at screening ad no change in hypertensive medication within 1 week before the cycle 1/day1.

10. No prior therapy with an anti-PD-1, anti-PD-L1, or anti PD L2 agent or with another agent agents direct to another stimulatory or co-inhibitory T-cell receptor (eg CTLA-4, OC-40, CD137) or TKI or antibody targeting angiogenesis in the first cohort. Patients who have been treated with autologous tumor cell vaccination (eg. Dendritic cell-based immunotherapy) will be eligible in the first cohort. (First cohort is closed).

11. No concomitant administration to any other experimental drugs under investigation = 4 weeks prior to first admission of pembrolizumab- lenvatinib

12. No prior radiotherapy within 2 weeks before start of study treatment. Participants must have recovered from all radiation-related toxicities, not require corticosteroids as therapy for radiation induced toxicities. A 1-week washout is permitted for palliative radiation (=2 weeks of radiotherapy) to non-CNS disease.

13. No major injuries and/or surgery within the past 4 weeks prior to first study dose with incomplete wound healing

Exclusion Criteria:

1. presence of clinically relevant treatment-related toxicity from previous chemotherapy, targeted therapy and/or radiotherapy. Note: Participates must have recovered from all AEs due to previous therapies to 5Grade 1 or baseline. Participants with 52 neuropathy may be eligible

2. active uncontrolled infection, severe cardiac dysfunction (i.e. unstable angina, history of myocardial infarction within the past 12 months prior to screening, congestive heart failure > NYHA II, serious cardiac arrhythmia), unstable peptic ulcer, unstable diabetes mellitus or other seriously disabling condition

3. prior therapy with an anti-PD-1, anti-PD-L1, or anti PD L2 agent or with another agent agents direct to another stimulatory or co-inhibitory T-cell receptor (eg CTLA-4, OC-40, CD137) or TKI or antibody targeting angiogenesis in the first cohort. Patients who have been treated with autologous tumor cell vaccination (eg. Dendritic cell-based imnnunotherapy) will be eligible in the first cohort. (CLOSED)

4. concomitant administration to any other experimental drugs under investigation 5 4 weeks prior to first admission of pembrolizumab- lenvatinib

Related Conditions & MeSH terms

• Mesothelioma
• Mesothelioma, Malignant
• Mesotheliomas Pleural

Intervention

Drug:
• Pembrolizumab
Infusion
• Lenvatinib
Capsule

Locations

Country	Name	City	State
Netherlands	Antoni van Leeuwenhoekziekenhuis (NKI-AVL)	Amsterdam	Noord-Holland

Sponsors (2)

Lead Sponsor	Collaborator
The Netherlands Cancer Institute	Merck Sharp & Dohme LLC

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Immunological status	The immunological status in the tumors before study and after 6 weeks of treatment with pembrolizumab +lenvatinib. This research will include PD-L1 status, mutational load and other potential biomarkers (e.g. micro vessel density count).	before study and after 6 weeks of treatment
Primary	Objective response rate defined by Modified RECIST 1.1 criteria for pleural mesothelioma	Complete response and partial response	Through study completion, an average of 1 year
Secondary	Safety of pembrolizumab- lenvatinib	Number of participants with treatment-related adverse events as assessed by CTCAE v5.0	Up to 90 days after last study drug intake
Secondary	Describe the disease control rate (DCR) at 3 and 6 months	a percentage of the total number of patients in the study who are evaluable for the primary endpoint who have best overall response of CR or PR or SD.	From date of registration until 6 months
Secondary	Objective response rate (ORR)	Number of patients with a partial or complete response	Assessed up to 60 months
Secondary	Progression-free survival	To describe PFS by independent radiological review	From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months