1570P - ‘Research’ vs ‘real world’ patients: the representativeness of clinical trial participants

Date 10 October 2016
Event ESMO 2016 Congress
Session Poster display
Topics Translational Research
Presenter Yasemin Karanis
Citation Annals of Oncology (2016) 27 (6): 526-544. 10.1093/annonc/mdw392
Authors Y.B. Karanis1, F.A. Bermudez Canta1, L. Mitrofan2, H. Mistry1, C. Anger1
  • 1Global Oncology, IMS Health, N1 9JY - London/GB
  • 2Global Oncology, IMS Health, 92088 - La Defence/FR



Randomized Clinical Trials (RCTs) are the gold standard in assessing the efficacy of new treatments as they allow for the analysis of a homogenous study population. However restricting the eligibility criteria may result in cherry-picking RCT participant thus compromising the generalisability. We have investigated differences in certain prognostic factors between trial and non-trial patients to see if this has an effect on how long patients stay on cytotoxic or targeted treatments.


IMS Health Oncology Analyzer™, a patient database collected through a quarterly physician panel survey was used. Data includes Stage IV, NSCLC, Colorectal (CRC) and Pancreatic Cancer (PC) patients within EU5 (France, Germany, Italy, Spain, UK) reported between 2013 and 2015. For the initial analysis the prognostic factors compared are ECOG, Co-morbidities and Age. For the secondary analysis cytotoxic and targeted treatments were grouped and the average duration of treatments (DOTs) were compared.


Based on the results displayed above, patients enrolled in clinical trials are more likely to be Younger (1), Fitter (2) and with No-Comorbidities (3) versus ‘Real World’ patients. Similar DOTs (4) were observed for the two patient groups in CRC and NSCLC. Sample number for PC patients with DOT information were too low to analyse.

Non-Trial n = 10,534 Trial n = 439 Non-Trial n = 6,260 Trial n = 265 Non-Trial n = 4,081 Trial n = 41
(1) Age
65 Years of age 46% 39% 54% 45% 55% 39%
(2) Performance Status
ECOG 0-1 78% 85% 84% 89% 66% 71%
ECOG 2-4 22% 15% 16% 11% 34% 29%
(3) Co-Morbidities
No Co-morbidities 40% 55% 49% 64% 39% 66%
4) Average DOT (months)
Cytotoxic Treatments 3.7 3.8 6.3 6.4 4.8 -
Targeted Treatments 7.6 7.3 7.6 7.2 6.4 -


Our data supports the existence of prognostic differences between ‘Trial’ and ‘Real World’ patients. Even though we have not observed an effect of this on DOT, further analysis is required to study the array of clinical and survival outcomes that prognostic differences are likely to impact. The next step is a comparison of parameters such as response to therapy, adverse events and Progression Free Survival to further analyse the representativeness of RCTs.

Clinical trial identification

Legal entity responsible for the study

IMS Health


IMS Health


All authors have declared no conflicts of interest.