Status: Open
Specialty: Bladder
Date Opened: 06/07/2022
Planned Close Date: 01/11/2023
Sponsor: Pfizer Inc.
Principal Investigator: Prof. Alison Birtle
Study Title: A multi-centre non-interventional study to describe the early clinical experience of avelumab used as monotherapy for the first-line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma who are progression-free following platinum-based chemotherapy
The purpose of this non-interventional study is to describe the early clinical real-world outcomes of patients treated with avelumab as monotherapy for the 1L maintenance treatment of locally advanced or metastatic urothelial carcinoma (UC) who are progression-free following platinum-based chemotherapy. As of September 2020, patients in the UK meeting the UC indication have been provided access to avelumab via an Early Access to Medicines Scheme (EAMS) and subsequently via a company supported Managed Access Programme. This study aims to investigate
patients who received avelumab in secondary/tertiary care in the UK through either the EAMS, EAMS extension or through NHS commissioning. The primary objective of this study is to estimate real-world overall survival in this real world Cohort.
Outcomes and characteristics relating to overall survival will be extracted from records of adult patients. The collected data are entered as part of routine care into electronic patient records and paper-based charts. Approximately 100 patients will be recruited across 10-12 geographically-spread selected centres and followed-up for up to 24 months after avelumab initiation. These patients will be above 18 years and have a confirmed diagnosis of locally advanced or metastatic stage IV UC, they would have received a platinum-based chemotherapy which they had response to or achieved a stable disease state and they should also have received maintenance avelumab.
Patients must meet all the following criteria to be eligible for inclusion in the study:
1. Patients with a diagnosis of locally advanced or metastatic UC, either de novo or relapsed
2. Patients received 1L platinum-based chemotherapy and had stable disease, partial response, or complete response to this treatment
3. Patients received avelumab as indicated as a monotherapy for the first-line maintenance treatment of adult patients with locally advanced or metastatic UC who are progression-free following platinum-based chemotherapy
4. Patients aged ≥18 years on the date that they commenced avelumab
Patients meeting any of the following criteria will be excluded from the study:
1. Patients whose hospital records are not available for review
2. Patients who are receiving an investigational medicinal product as part of a clinical trial at the time of maintenance therapy with avelumab
Clinical Trials Coordinator: Samuel Almond (x8475) Samuel.Almond@lthtr.nhs.uk
Link to EDGE