Systematic evaluation of the efficacy-effectiveness gap of systemic treatments in extensive disease small cell lung cancer
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2021-04
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taverne
Abstract
Purpose: The aim of this study is to assess how clinical outcomes in real-world (effectiveness) correspond to the outcomes in clinical trials (efficacy) of systemic treatments for extensive disease small cell lung cancer (ED SCLC). Methods: All patients diagnosed with ED SCLC between 2008 and 2014 in six Dutch large teaching hospitals (Santeon network) were identified and followed-up from date of diagnosis until death or end of data collection. For every patient, an efficacy-effectiveness factor (EE factor) was calculated by dividing individual patients' overall survival (OS) by the pooled median OS assessed from clinical trials with the respective treatment. Results: From 792 diagnosed patients, 568 (72%) started with first-line treatment. Overall, the median EE factor was 0.79 (P <.001 from 1.00). Poor performance status (ECOG≥2) and a higher age at diagnosis (age ≥ 65 years) were independent predictors for a lower EE factor. The EE gap was 43% in patients with both age ≥ 65 years and ECOG ≥2 (EE factor 0.57). The mean age and the proportion of patients with ECOG≥2 in real-world were different from those in clinical trials (mean age of 66 versus 62 years, and ECOG≥2 25% versus 17%; both P <.001). Conclusion: OS of patients with ED SCLC treated with systemic therapy in real-world practice is 21% shorter than for patients included in trials. Age at diagnosis and performance status partly explain this gap.
Keywords
effectiveness, efficacy, pharmacotherapy, real-world, small cell lung cancer, survival, Taverne, Epidemiology, Pharmacology (medical), SDG 3 - Good Health and Well-being
Citation
Cramer-van der Welle, C M, Schramel, F M N H, Peters, B J M, van Putten, J W G, Klungel, O H, Groen, H J M & van de Garde, E M W 2021, 'Systematic evaluation of the efficacy-effectiveness gap of systemic treatments in extensive disease small cell lung cancer', Pharmacoepidemiology and Drug Safety, vol. 30, no. 4, pp. 445-450. https://doi.org/10.1002/pds.5179