National clinical quality registry for pancreatic cancerthe time is nigh Dear Editor, We note the editorial by Aitken. 1 We would like to applaud the author for raising awareness of the variability in outcomes from pancreaticoduodenectomy (PD) across Australia and for advocating for a national pancreatic cancer (PC) clinical quality registry (CQR).In fact, in 2016, Monash University developed an Upper Gastrointestinal Cancer Registry (UGICR)a CQR that adheres to the framework outlined by the Australian Commission on Safety and Quality in Health Care (ACSQHC). The UGICR is a multi-modular registry that includes a module on PC (as well as oesophagogastric, biliary and primary liver cancers). The PC module was originally piloted in 2017, and now has data on 4225 people with PC recruited from 60+ participating hospitals across Victoria and New South Wales. 2 In line with the ACSQHC framework, the PC module of the UGICR routinely collects data to monitor the quality of care provided to individuals with PC by measuring and benchmarking clinical indicators to identify variations in care to improve patient outcomes. 3 Preliminary findings using the registry data to explore compliance with clinical indicators as well as evaluate the association between compliance and survival, found that patients diagnosed in a regional area or diagnosed in a hospital with annual case volume of less than 10 had an increased risk of death in a univariate analysis. 4 The PC module of the UGICR has also been a platform for a number of research studies, including an innovative registry-based, randomized controlled trial of symptom monitoring and centralized care coordination.Funding to support existing data capture as well as expand this registry across Australia is badly needed. This would provide an opportunity to measure variation and monitor care at a national level as proposed by the authors.