Bladder Cancer Clinical Trial

Evaluating Length of Treatment With PD-1/PD-L1 Inhibitor in Advanced Solid Tumors

Summary

Based on the overwhelming positive response to this survey and the large number of patients being treated with PD-1/PD-L1 therapy in the UPMC system, the investigators are proposing a trial that will randomize patients who have disease stability to stop treatment at 1 year or continue treatment until disease progression. The investigators anticipate that the results of this study will answer questions regarding the optimal duration of treatment. therapy.

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Full Description

Within the UPMC system, approximately 2,300 patients received PD-1/PD-L1 therapy for a variety of advanced solid tumors within the past year. It is anticipated that this number will increase as the clinical indications for treatment with these agents also increase. The investigators conducted a survey of 60 Medical Oncologists within the UPMC system regarding their interest in a trial that will attempt to address the question of optimal length of PD-1/PD-L1 treatment. Fifty-two (86.7%) physicians indicated that they would participate in a clinical trial that had a primary goal of determining whether it was feasible to stop immunotherapy after 1 year of treatment.

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Eligibility Criteria

Inclusion Criteria:

All patients must have an advanced solid tumor malignancy (specifically NSCLC, bladder, HNSCC, renal, melanoma, cervical, Merkel cell, MMR/MSI [colon, rectal, cholangio, esophageal, ovarian, uterine], anal, gastric and GE junction, hepatocellular, triple negative breast cancer) that is being treated with a PD-1/PD-L1 inhibitor including pembrolizumab, nivolumab, atezolizumab, durvalumab, or avelumab according to standard of care treatment.
Patients who initially started treatment with another agent in combination with the PD-1/PD-L1 inhibitor, i.e. chemotherapy, ipilumumab, are eligible.
Patients must have at least stable disease as evidenced by scans performed within 6 weeks of randomization.
Signed Informed consent allowing randomization to stopping immunotherapy at 1 year ± 4 weeks versus continued treatment beyond 1 year.
Patients can have measurable or non-measurable disease per iRECIST.
Patients cannot be enrolled in a clinical trial.

Exclusion Criteria:

Patients with documented progressive disease prior to randomization.
Patients with an immune-related toxicity preventing the continuation of treatment beyond 1 year at the treating physician's discretion.

Study is for people with:

Bladder Cancer

Phase:

Phase 3

Estimated Enrollment:

578

Study ID:

NCT04157985

Recruitment Status:

Recruiting

Sponsor:

Antoinette J Wozniak, MD

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There is 1 Location for this study

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UPMC Hillman Cancer Center
Pittsburgh Pennsylvania, 15232, United States More Info
Jennifer Ruth, BSN
Contact
412-623-8963
[email protected]
BSN
Contact
Antoinette J Wozniak, MD, FACP
Principal Investigator

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Study is for people with:

Bladder Cancer

Phase:

Phase 3

Estimated Enrollment:

578

Study ID:

NCT04157985

Recruitment Status:

Recruiting

Sponsor:


Antoinette J Wozniak, MD

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