HSR in Oncology: patients with non-small cell lung cancer treated with anti-PD-1/PD-L1 therapy in real-world practice. A pilot project in cooperation with Tirol Kliniken GmbH & KAGes
Geiger-Gritsch S, Absenger G, Endel F, Flickers M, Hermann A, Kocher F, Olschewski H, Pall G, Wurm R, Zechmeister M
Record ID 32018001668
Authors' objectives: Real World Evidence (RWE) complements the data of randomised clinical trials, that are based on selected, homogeneous patient populations and a limited study duration, with long-term data from clinical practice. As there has been no evaluation of immunotherapy in everyday care in Austria to date, a retrospective pilot study was conducted in six Austrian hospitals on the efficacy and safety of anti-PD-1/PDL1 monotherapy in patients with NSCLC using routine data.
Authors' results and conclusions: Results: Especially for second-line therapy with immunotherapy, a higher objective response rate and a slightly longer median overall survival could be observed compared to the clinical trials, as well as a comparable median progression-free survival. In contrast, results from pivotal clinical trials for first-line pembrolizumab monotherapy could not be confirmed. Conclusion: In summary, the present retrospective pilot study shows clinically relevant results regarding the use of immunotherapy in daily care practice and underlines the need for real world evidence to demonstrate the efficacy and safety of new therapies.
Authors' recomendations: Larger (prospective) real world studies are needed to contribute to a better understanding of the efficacy of immunotherapy in daily practice and to complement the results from randomised controlled trials to ensure the care of patients who benefit most from immunotherapy.
Authors' methods: A matched-pair analysis to compare overall survival and progression-free survival of patients receiving immunotherapy with those receiving chemotherapy from the Tyrol Lung Cancer Project ("Tyrol Study") was conducted to describe the characteristics of NSCLC patients treated with immunotherapy in everyday hospital care; to analyse overall survival (OS), progression-free survival (PFS), objective response rate (ORR) and disease control rate (DCR) as well as safety endpoints (grade 3 and 4 adverse events) and to compare patient characteristics and outcomes from everyday care with the results of the pivotal studies.
Project Status: Completed
URL for project: https://aihta.at/page/versorgungsforschung-in-der-onkologie-krebstherapien-detailanalysen-zu-einer-indikation-lunge/en
Year Published: 2021
URL for published report: https://eprints.aihta.at/1227/1/HTA-Projektbericht_Nr.126.pdf
URL for additional information: https://eprints.aihta.at/1227/
English language abstract: An English language summary is available
Publication Type: Full HTA
- Lung Neoplasms
- Pragmatic Clinical Trials as Topic
- Programmed Cell Death 1 Receptor
- Antibodies, Monoclonal
- Carcinoma, Non-Small-Cell Lung
- lung cancer
- Real World Evidence (RWE)
Organisation Name: Austrian Institute for Health Technology Assessment
Contact Address: Garnisongasse 7/20, A-1090 Vienna, Austria
Contact Name: firstname.lastname@example.org
Contact Email: email@example.com
Copyright: HTA Austria - AIHTA GmbH
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