Pembrolizumab And Cryoablation In Urothelial Carcinoma

Sponsor

Massachusetts General Hospital (Other)

Overall Status

Recruiting

CT.gov ID

NCT04701918

Collaborator

Biocompatibles UK Ltd (Industry)

Enrollment

Locations

Arm

41.9

Anticipated Duration (Months)

Patients Per Site

0.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This research study is examining the effectiveness of pembrolizumab plus cryoablation on people with urothelial carcinoma, including bladder cancer, that has spread.

Condition or Disease	Intervention/Treatment	Phase
Metastatic Urothelial Carcinoma Bladder Cancer	Drug: Pembrolizumab Procedure: Cryoablation	Phase 2

Detailed Description

This is an open label Phase 2, single-arm, multi-institutional clinical trial designed to study the combination of pembrolizumab and cryoablation on people with urothelial carcinoma, including bladder cancer, that has spread.

The U.S. Food and Drug Administration (FDA) has approved both cryoablation and pembrolizumab as a treatment option for urothelial carcinoma, including bladder cancer, that has spread. However, the FDA has not yet approved the combination of the drug, pembrolizumab, and intervention, cryoablation, for urothelial carcinoma, including bladder cancer, that has spread.

Pembrolizumab is believed to work by binding to a chemical called PD-1 that is found on a special type of white blood cell in your body. This may help your body to be better at finding and destroying tumor cells. Cryoablation is an intervention which may kill cancer cells using extreme cold. It may help the immune system better recognize tumors and act against it.

The research study procedures include screening for eligibility and study treatment, including evaluations and follow up visits.

Participants will receive study treatment as long as their disease does not get worse or they do not have any unacceptable side effects for up to two years. Participants will be followed for up to 2 years after ending the study treatment.

It is expected that about 30 people will take part in this research study.

Biocompatibles UK Ltd, a device company under Boston Scientific, is supporting this research study by providing funding for the needles used in the study intervention.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

30 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Multicenter, Single-Arm Open Label Phase II Trial of Cryoablation in Combination With Pembrolizumab in Patients With Metastatic Urothelial Carcinoma

Actual Study Start Date :

Jun 4, 2021

Anticipated Primary Completion Date :

Dec 1, 2023

Anticipated Study Completion Date :

Dec 1, 2024

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Pembrolizumab + Cryoablation Participants will be given 200 mg pembrolizumab intravenously once every 3 weeks. This will continue for up to 2 years as per standard of care. Participants will receive cryoablation between the 1st and 2nd doses of pembrolizumab. Cryoablation consists of using a CT scan to guide one or more thin needles to the tumor through your skin, where extreme cold is applied.	Drug: Pembrolizumab Intravenous injection through a vein (IV) every 3 weeks Other Names: Keytruda Procedure: Cryoablation Needle inserted through the skin and into the tumor using CT guidance

Arm

Intervention/Treatment

Experimental: Pembrolizumab + Cryoablation

Participants will be given 200 mg pembrolizumab intravenously once every 3 weeks. This will continue for up to 2 years as per standard of care. Participants will receive cryoablation between the 1st and 2nd doses of pembrolizumab. Cryoablation consists of using a CT scan to guide one or more thin needles to the tumor through your skin, where extreme cold is applied.

Drug: Pembrolizumab

Intravenous injection through a vein (IV) every 3 weeks

Other Names:

Keytruda

Procedure: Cryoablation

Needle inserted through the skin and into the tumor using CT guidance

Outcome Measures

Primary Outcome Measures

Objective Response Rate [up to 2 years]
Evaluate objective response rate of non-ablated lesion(s) for combination pembrolizumab and adjunctive cryoablation per RECIST v1.1 criteria

Secondary Outcome Measures

Number of Participants With Treatment-Related Adverse Events as Assessed by CTCAE Version 5.0 [up to 2 years]
The descriptions and grading scales found in the revised NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 will be utilized for AE reporting.
Progression-Free Survival (PFS) [up to 2 years]
Defined using RECIST v1.1
Overall survival (OS) [up to 2 years]
Reported with Kaplan Meier estimates.
Duration of response (DOR) [up to 2 years]
Defined using RECIST v1.1

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

The subject has read, signed and dated the Informed Consent Form (ICF), having been advised of the risks and benefits of the trial in a language understood by the subject.
Age > 18 years at date of ICF signature having the ability to comply with the protocol.
Proof of medical insurance coverage.
Histologically or cytologically documented metastatic (M1, Stage IV) urothelial carcinoma (including renal pelvis, ureters, urinary bladder, urethra)
Measurable metastatic disease with at least one site of metastatic disease > 2 cm in size and amenable to percutaneous image-guided cryoablation based on routine Interventional Radiology criteria. Metastasis sites amenable to cryoablation to include lymph node, peritoneum, liver, soft tissue, adrenal glands, kidney, lung, and bone. Must have measurable disease (by RECIST v1.1) independent of the lesion to be ablated (ie patient must have more than one metastasis)
Life expectancy > 12 weeks.
PS ECOG 0 or 1
Laboratory requirements:
ANC > 1 x 109/L
Platelets > 75 x 109/L
ALT / AST < 5 x ULN
Total bilirubin <3 mg/dL
INR <1.7
CrCl >30 ml/min

Exclusion Criteria:

Lesion to undergo cryoablation cannot have had prior radiation therapy or other locoregional therapy
Inability to lie flat for the cryoablation procedure.
Known significant immunodeficiency due to underlying illness (e.g. HIV / AIDS) and/or blood CD4+ T cells <200/ul
History of autoimmune disease, including but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with anti-phospholipid syndrome, granulomatosis with polyangiitis, Sjogren's syndrome, Guillain- Barre syndrome, multiple sclerosis, vasculitis, or glomerulonephritis.
Patients with a history of autoimmune-related hypothyroidism on a stable dose of thyroid replacement hormone are eligible for this trial.
Patients with controlled Type I diabetes mellitus on a stable dose of insulin regimen are eligible for this trial.
Patients with history of vitiligo and controlled psoriasis are eligible for the trial.
Continued adverse events from a previously administered chemotherapeutic agents.

Grade 1 adverse events and ongoing toxicities such as alopecia are exempt

Treatment with systemic corticosteroids exceeding the equivalent of 10 mg/day of prednisone or other systemic immunosuppressive medications (including but not limited to prednisone, dexamethasone, cyclophosphamide, azathioprine, methotrexate, and anti-tumor necrosis factor [anti-TNF] agents) within 2 weeks prior to Day 1, or anticipated requirement for systemic immunosuppressive medications during the trial
Patients who receive acute, low-dose, systemic corticosteroid medications (e.g., a onetime dose of dexamethasone for nausea) or for prevention of hypersensitivity reactions to contrast agents may be enrolled in the trial.
Anticoagulant or anti-platelet medication that cannot be interrupted prior to cryoablation
Pregnant or lactating
History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins
Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicated the use of an investigational drug or that could affect the interpretation of the results or render the patient at high risk from treatment complications.
Prior treatment with immune checkpoint blockade therapies, including anti-CTLA-4, anti-PD-1, and anti-PD-L1 therapeutic antibodies
Treatment with systemic immunostimulatory agents (including but not limited to IFNs, interleukin [IL]-2) within 6 weeks or five half- lives of the drug, whichever was shorter, prior to Day 1.
Signs or symptoms clinically significant of infection within 2 weeks prior to Day 1.
Any other systemic anti-cancer treatment (including investigational agents) within 4 weeks prior to the first dose of study drug. Note: Participants must have recovered from all AEs due to previous therapies to ≤Grade 1 or baseline. Participants with ≤Grade 2 neuropathy may be eligible

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Massachusetts General Hospital Cancer Center	Boston	Massachusetts	United States	02114
2	Beth Israel Deaconess Medical Center	Boston	Massachusetts	United States	02215