The need for core outcome sets in urological cancer research
Editorial Commentary on Expectant Management in Genitourinary Malignancies (Prostate, Bladder, Kidney)

The need for core outcome sets in urological cancer research

Steven MacLennan1,2, Paula R. Williamson3

1Academic Urology Unit, Institute of Applied Health Sciences, University of Aberdeen, Aberdeen, UK; 2European Association of Urology Guidelines Office Methodology Committee, Arnhem, The Netherlands; 3MRC North West Hub for Trials Methodology Research, University of Liverpool and Liverpool Health Partners, Liverpool, UK

Correspondence to: Steven MacLennan. Academic Urology Unit, Institute of Applied Health Sciences, University of Aberdeen, Academic Urology Unit, Health Sciences Building (2nd Floor), Foresterhill, Aberdeen, AB25 2ZD, UK. Email:

Submitted Oct 09, 2020. Accepted for publication Oct 29, 2020.

doi: 10.21037/tau-20-1323

Choosing outcomes relevant to patients and healthcare professionals is essential if clinical trial results are to be translated into practice. A frequent frustration encountered in summarising the clinical effectiveness of treatments for urological cancers is heterogeneity in the outcomes reported. This refers to two interrelated problems: inconsistency, where different outcomes are reported across different studies, and variability, where the same outcomes are reported across studies but are defined or measured differently. Outcome inconsistency and variability make comparing, contrasting, synthesising and interpreting the results of different studies on the same topic more complicated than it ought to be. The implications of outcome reporting heterogeneity come into sharp relief in systematic reviews of interventions. For instance, in a cohort of Cochrane systematic reviews, 40% of reviewers noted problems due outcome inconsistency (1). This problem is of particular importance when meta-analysis (the statistical pooling of aggregated data from two or more studies, providing more power and precision) is either not possible, or worse, done inappropriately regardless. Systematic reviews are a cornerstone of the Evidence Based Medicine (EBM) movement and are an essential component in creating clinical practice guideline (CPG) recommendations—which inform patient, clinician and policy decision-making. To arrive at CPG treatment recommendations, urology guideline making bodies such as the European Association of Urology (EAU) rely on published or commissioned systematic reviews, ideally of RCTs, but frequently incorporating various study designs. There are numerous examples of outcome reporting heterogeneity hindering guideline panels from making evidence-based recommendations throughout urology oncology and some examples from prostate and bladder cancer are outlined below.

For clinical trial results to be useful the views of a variety of stakeholders, particularly patients, must be considered. Localised prostate cancer patients and health care professionals alike prioritise oncological outcomes, such as survival and progression, as well as health related quality of life (HRQoL) outcomes, encompassing bowel, urinary and sexual function, as among the most important outcomes to be measured in prostate cancer research (2,3). Given that there is a lack of evidence on oncological superiority in currently available localised prostate cancer treatments, the EAU prostate cancer guideline panel commissioned a systematic review to ascertain HRQoL and functional outcomes after any intervention for localised prostate cancer (4). Numerous patient-reported outcome measures (PROMs) were found purporting to assess HRQoL and various aspects of the functional outcomes (e.g., EPIC, UCLA-PCI, EORTC QLQ-30/PR25, PCOS) across the 18 included studies. Not every tool covers every functional domain and the measurement scales are often non-commensurable. Meta-analysis was not possible, and interpretation was difficult. Similarly, in a Health Technology Assessment including 54 studies comparing laparoscopic with robotic prostatectomy, Ramsay et al. (5) (page 84) noted that a “…specific methodological limitation that frustrated pooled analysis was the use of differing definitions and measures of functional outcomes for both urinary and erectile dysfunction. The variety of different ways of measuring dysfunction reduced the ability to compare data or to conduct a comprehensive meta-analysis”. A further review of PROMs used in prostate cancer research found 15 disease specific or generic tools have been used and that none were established enough to be relevant for long term prostate cancer survivorship (6). The results of these three examples all point to the same conclusion: it is difficult to say anything meaningful about the comparative effectiveness of the variety of available treatments for localised prostate cancer on long term functional outcomes.

Two systematic reviews commissioned by the EAU Guidelines Office muscle invasive bladder cancer (MIBC) panel demonstrated outcome inconsistency and variability. Veskimäe et al. (7) reviewed oncological and functional outcomes of pelvic organ sparing radical cystectomy compared with standard radical cystectomy in women undergoing curative surgery and orthotopic neobladder substitution for bladder cancer. In the main results table, the column headers are ‘local recurrence’, ‘time to local recurrence’, ‘metastatic recurrence’, ‘disease specific survival’ and ‘overall survival’. Of the 15 included studies reporting on oncological outcomes, only one reported all these outcomes, and no single oncology outcome was reported in all the studies. Indeed ‘not reported’ is by far the most frequently occurring data in the table’s cells. No meta-analysis was possible, and a cumbersome narrative synthesis was required. Hernández et al. (8) systematically reviewed sexual function preserving cystectomy versus standard radical cystectomy in men. Continence was frequently measured across the 12 included studies, but the time point of measurement (6, 1–9, 12, 48 months) and the method of measurement [self-reported, number of pads, pad test (volume), voiding diary, and Bladder Cancer Index questionnaire] were variable. The data relating to these outcomes are qualitatively different from each other, so statistically combining them is not possible, and even if standardisation were possible, the differing time points would make a pooled average statistic meaningless and misleading.

The previous examples have been situated in the context of difficulties in recommendation-making for guideline panels. However, outcome heterogeneity is also problematic for initiatives seeking to address improvement through benchmarking value across providers, such as the International Consortium for Health Outcome Measurement (ICHOM) (3,9), and for big data projects such as Prostate PIONEER where consistency in outcome definitions and measurements are key considerations in data harmonisation with multiple sources such as RCTs, observational studies, institutional registries, and claims databases all contributing data (10).

Core outcome sets (COSs) are a solution to heterogeneity in outcomes reporting. A COS is an agreed standardised collection of outcomes which should be reported as a minimum in all trials for a specific clinical area (11). The Core Outcome Measures for Effectiveness Trials (COMET) initiative is a hub for COS development. They provide guidance, develop methodological standards (12) and reporting guidelines (13,14) as well as maintain a searchable database of ongoing and completed COS projects. Importantly, COMET note that where COS exist, researchers should not feel restricted to measure only the core outcomes, other outcomes may be collected additionally.

The development of a COS proceeds by first identifying what outcomes are important, then how they should be measured. An essential initial step is to define the COS scope, for which the first three elements of the Patient Intervention Comparator Outcomes (PICO) structure is useful. Consideration should also be given to the intended end uses of the COS, for example in RCTs only, routine care only, or both. Then, the COMET database ( should be checked to ensure no duplication of effort or to potentially offer collaboration where an ongoing COS is already registered.

If a new COS is to be initiated then a study protocol should be developed according to the Core Outcome Set Standard Protocol (COS-STAP) items statement and the study registered with COMET (14). Next, various research methods such as systematic reviews and stakeholder interviews are used to generate a comprehensive list of outcomes potentially important to a variety of stakeholders, such as surgeons, oncologists, nurses and patients. A consensus exercise to prioritise the most important outcomes is then recommended using methods such as a Delphi survey, and often culminating in a face-to-face consensus meeting, where a final list of core outcomes is agreed and ratified (11). Finally, the COS is usually reported in a journal manuscript and reporting according to the Core Outcome Set Standards for Reporting (COS-STAR) statement (13) is encouraged. Then attention should turn to uptake of the COS among the clinical and research communities. However, implementation is rarely linear and other efforts, such as encouraging uptake through endorsement from journal editors, trial funders, trial registries and regulatory authorities is likely to be more successful than publication alone.

Once the core outcomes are known, further review and consensus work is required to assess and recommend the most appropriate definitions and measurement tools. Definitions for clinician reported outcomes may require reviewing existing definitions used in published studies and seeking consensus from stakeholders on which of those definitions is most appropriate, and other considerations like the timepoint(s) of measurement. For PROMs additional work on assessing the psychometric properties and feasibility of use is required prior to further consensus work. Extensive guidance on systematically reviewing and evaluating PROMs is available from the COnsensus-based Standards for the selection of health Measurement Instruments (COSMIN) group (15,16).

Although COS require effort to develop, promote and engage the clinical specialty community, experience from other disciplines demonstrate that improvement is possible. For instance, the Outcome Measures in Rheumatology (OMERACT) group involved a variety of stakeholders in identifying and prioritising outcomes in antirheumatic drugs for rheumatoid arthritis (RA) trials. OMERACT published their first RA COS in 1994 (17). Since then there has been a consistent increase in the use of the RA COS and 81% of registered and completed RA trials now report the COS, and selective outcome reporting has decreased (18). Also, the CoRe Outcomes in Women’s and Newborn health (CROWN) initiative have demonstrated a targeted and organised approach to implementing their COS by facilitating a consortium of over 80 gynaecology-obstetrics related journals to publicise relevant COS through editorials, publish the various COS, and endorse the use of COS in studies submitted to their journals (19). Finally, the Cochrane Skin group, who manage Cochrane reviews in the dermatology setting, have embedded a COS initiative within their review group which aims to facilitate implementation (20).

Outcome reporting heterogeneity is problematic for urology cancer research and decision-making at many levels. COS are proposed as a solution. Fortunately, a supportive methodological hub and a wealth of applied research examples are available. Initiatives from other disciplines show that improvement is possible and there is no reason why the urology community cannot organise in a concerted effort to reduce outcome reporting inconsistency and variability, to reduce waste in research.


Funding: None.


Provenance and Peer Review: This article was commissioned by the Guest Editors (Mieke Van Hemelrijck and Netty Kinsella) for the series “Expectant Management in Genitourinary Malignancies (Prostate, Bladder, Kidney)” published in Translational Andrology and Urology. The article did not undergo external peer review.

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at The series “Expectant Management in Genitourinary Malignancies (Prostate, Bladder, Kidney)” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See:


  1. Williamson PR, de Ávila Oliveira R, Clarke M, et al. Assessing the relevance and uptake of core outcome sets (an agreed minimum collection of outcomes to measure in research studies) in Cochrane systematic reviews: a review. BMJ Open 2020;10:e036562 [Crossref] [PubMed]
  2. MacLennan S, Williamson PR, Bekema H, et al. A core outcome set for localised prostate cancer effectiveness trials. BJU Int 2017;120:E64-79. [Crossref] [PubMed]
  3. Martin NE, Massey L, Stowell C, et al. Defining a standard set of patient-centered outcomes for men with localized prostate cancer. Eur Urol 2015;67:460-7. [Crossref] [PubMed]
  4. Lardas M, Liew M, van den Bergh RC, et al. Quality of life outcomes after primary treatment for clinically localised prostate cancer: a systematic review. Eur Urol 2017;72:869-85. [Crossref] [PubMed]
  5. Ramsay C, Pickard R, Robertson C, et al. Systematic review and economic modelling of the relative clinical benefit and cost-effectiveness of laparoscopic surgery and robotic surgery for removal of the prostate in men with localised prostate cancer. Health Technol Assess 2012;16:1-313. [Crossref] [PubMed]
  6. Davies N, Gibbons E, Mackintosh A, et al. A structured review of patient-reported outcome measures (PROMs) for prostate cancer. 2009.
  7. Veskimäe E, Neuzillet Y, Rouanne M, et al. Systematic review of the oncological and functional outcomes of pelvic organ-preserving radical cystectomy (RC) compared with standard RC in women who undergo curative surgery and orthotopic neobladder substitution for bladder cancer. BJU Int 2017;120:12-24. [Crossref] [PubMed]
  8. Hernández V, Espinos EL, Dunn J, et al. Oncological and functional outcomes of sexual function-preserving cystectomy compared with standard radical cystectomy in men: a systematic review. Urol Oncol 2017;35:539.e17-29. [Crossref] [PubMed]
  9. Morgans AK, van Bommel AC, Stowell C, et al. Development of a standardized set of patient-centered outcomes for advanced prostate cancer: an international effort for a unified approach. Eur Urol 2015;68:891-8. [Crossref] [PubMed]
  10. Omar MI, Roobol MJ, Ribal MJ, et al. Introducing PIONEER: a project to harness big data in prostate cancer research. Nat Rev Urol 2020;17:351-62. [Crossref] [PubMed]
  11. Williamson PR, Altman DG, Bagley H, et al. The COMET Handbook: version 1.0. Trials 2017;18:280. [Crossref] [PubMed]
  12. Kirkham JJ, Davis K, Altman DG, et al. Core Outcome Set-STAndards for Development: The COS-STAD recommendations. PLoS Med 2017;14:e1002447 [Crossref] [PubMed]
  13. Kirkham JJ, Gorst S, Altman DG, et al. Core Outcome Set-STAndards for Reporting: The COS-STAR Statement. PLoS Med 2016;13:e1002148 [Crossref] [PubMed]
  14. Kirkham JJ, Gorst S, Altman DG, et al. Core Outcome Set-STAndardised Protocol Items: the COS-STAP Statement. Trials 2019;20:116. [Crossref] [PubMed]
  15. Prinsen CA, Vohra S, Rose MR, et al. How to select outcome measurement instruments for outcomes included in a "Core Outcome Set" - a practical guideline. Trials 2016;17:449. [Crossref] [PubMed]
  16. Mokkink LB, Prinsen C, Patrick DL, et al. COSMIN methodology for systematic reviews of patient-reported outcome measures (PROMs): user manual. 2018.
  17. Boers M, Tugwell P, Felson DT, et al. World Health Organization and International League of Associations for Rheumatology core endpoints for symptom modifying antirheumatic drugs in rheumatoid arthritis clinical trials. J Rheumatol Suppl 1994;41:86-9. [PubMed]
  18. Kirkham JJ, Clarke M, Williamson PR. A methodological approach for assessing the uptake of core outcome sets using findings from a review of randomised controlled trials of rheumatoid arthritis. BMJ 2017;357:j2262. [Crossref] [PubMed]
  19. Khan K. Chief Editors of Journals participating in The CROWN Initiative (Appendix 1). The CROWN Initiative: journal editors invite researchers to develop core outcomes in women's health. BJOG 2016;123:103-4. [Crossref] [PubMed]
  20. Prinsen CAC, Spuls PI, Kottner J, et al. Navigating the landscape of core outcome set development in dermatology. J Am Acad Dermatol 2019;81:297-305. [Crossref] [PubMed]
Cite this article as: MacLennan S, Williamson PR. The need for core outcome sets in urological cancer research. Transl Androl Urol 2021;10(6):2832-2835. doi: 10.21037/tau-20-1323

Download Citation