19.01.2023

Paul Pharoah, MD, PhD

A variety of technologies have been developed in recent years that enable the detection of multiple different site-specific cancers using a single blood test.  These multi-modal tests have been promoted as possible tests for the early detection of cancer that could be used in people without symptoms of cancer as a cancer screening test.  While these tests are promising there are several potential problems with their application in a screening setting. I will use the ‘Galleri’ test developed by Grail to illustrate both the potential of these tests and to outline the potential problems and the questions that will need to be answered before they can be used in clinical practice.

Multi-modal cancer screening tests: hype or hope? 

Video | Slides | Transcript

02.02.2023

Jack Wilkinson, PhD

Systematic reviews of health interventions synthesise evidence from all RCTs addressing a particular research question, and are considered very high-quality evidence. Unfortunately, it has become clear that some RCTs included in systematic reviews are not authentic and may have been entirely fabricated. We call trials subject to data falsification, fabrication, or other serious research integrity issues “problematic studies”, and recent examples can be found amongst studies included in systematic reviews of ivermectin for the treatment of COVID-19. However, there is no consensus around how to identify these problematic studies when undertaking a systematic review, and often no checks are performed at all.

In the first half of this talk, I will present the NIHR-funded INSPECT-SR project, which aims to develop a tool for identifying and excluding problematic RCTs from systematic reviews. The project will combine empirical evidence and consensus science approaches to develop a tool, which will then be refined through testing. I will outline the project, deliver interim results, and provide information about how to participate in the development of the tool.

In the second half of the talk, I will describe some of the analytic methods which are employed to assess the authenticity of RCT datasets.

The INSPECT SR project requires input from various stakeholders. This includes people with expertise and experience in research integrity, to participate in a Delphi study, and systematic reviewers who would be willing to test the tool in the production of new systematic reviews and review updates. Contact Jack if you are interested.

16.02.2023

Ivan Oransky, MD

Retractions -- the nuclear option of scientific correction -- have grown more than 100-fold in the past 20 years. Why? And is that good news, or bad news? We'll discuss fake data, paper mills, as well as ways forward.

Video | Slides | Transcript

02.03.2023

Kevin Knopf, MD

De-escalation implies readjusting cancer care to that which is appropriate for optimal patient outcome. This talk reviews how and why cancer care has escalated over time as well as how this can be harmful for patients and society. This talk discusses de-escalation efforts in surgery, imaging, radiation oncology, and chemotherapy and how these efforts can preserve outcome and improve health equity.

16.03.2023

 Nathan I Cherny MBBS, FRACP, FRCP

Prof Nathan Cherny presents an approach to the systematic critical evaluation of clinical studies to identify  some of the common issues that bias the outcomes of clinical research in oncology. 

The talk will highlight issues related to:

1.      surrogate endpoints and their predictive reliability for true clinical benefit

2.      study design and implementation issues that may exaggerate overall survival

3.      issues related post hoc and subgroup analyses and the important distinction between confirmatory and conjectural findings

Video  | Slides | Transcript

13 April 2023 4pm BST

Ben Mol, MD, PhD

Trustworthiness of medical publications can depend on either good faith or verifiable data. In recent years, it has increasingly become apparent that good faith alone is not enough, with estimates of fabricated research being 30% of published randomised clinical trials. I will discuss the role of authors and their institutes, peer review pre-and post publication and the role of publishers in this problem.

11 May 2023 17:00 BST

Daniel Lakens, PhD

Should scientists be allowed to perform studies that are a waste of time? If it is clear from the outset that the methods they use will not be able to answer the question they are asking, should they be told to redesign their study or adjust their research question? Methodological review boards provide one way to check the methodological quality of studies before data collection. Collaboratively performed methodological review can help to improve research practices and prevent research waste.

22.06.2023

Lex Bouter, PhD

The trustworthiness of research findings is threatened when researchers don’t do their utmost best to get it right and engage in questionable research practices or worse. By adopting open science practices, research becomes transparent and accountable. Only then it is possible to verify whether trust in research findings is justified. The magnitude of the issue will be explored, as well as why researchers regularly engage in behaviours that harm the validity and trustworthiness of their work.

31 August 2023

Nathan Cherny

The very high cost of new cancer medicines is threatening the sustainability of cancer care and is harming health care systems and patients. This talk explores the global economic factors underlying this phenomenon addressing critical questions like “Is this the cost of innovation or exploitative profiteering?”  and exploring global public health initiatives to address this problem.