Pembrolizumab gives an added benefit that is non-quantifiable to patients with advanced head and neck PD-L1 expressing tumours.

‘Patients with advanced head and neck cancer could benefit from using pembrolizumab by increasing the life expectancy.’
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In an early benefit assessment, the German Institute for Quality and Efficiency in Health Care (IQWiG) has now examined whether in these patients with PD-L1 expressing tumours, the monoclonal antibody pembrolizumab offers an added benefit over individual treatment of physician's choice. According to the findings, there is a hint of an added benefit, which is non-quantifiable, however.Read More..





Only small subpopulation of the study relevant
The extent of the added benefit was rated non-quantifiable because of the small number of study participants who were treated in compliance with the approval. The drug manufacturer presented data from a study that compared pembrolizumab with three drugs: methotrexate, cetuximab, and docetaxel. Many of the 129 study participants with PD-L1 expressing tumours were planned for comparison with cetuximab and docetaxel, which are not approved for this therapeutic indication in Germany, however. Hence, only the treatment of 37 study participants concurred with the research question of this dossier assessment. In such a small subpopulation, only very large effects can reach statistical significance.
Supporting analysis of larger subpopulation
In the larger subpopulation of 129 participants, many of whom were treated in the comparator arm with drugs that are not approved for this therapeutic indication in Germany, the advantages of pembrolizumab in overall survival were statistically significant, however. The same applied to disadvantages regarding immune-related side effects.
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The consistency of the direction of the effect and the similarity of the effect size between the smaller and the larger subpopulation suggest that both the increase in life expectancy and the disadvantages in immune-related side effects of pembrolizumab compared with methotrexate are clinically relevant. In the overall consideration, there is therefore a hint of an added benefit, which is non-quantifiable due to the uncertainty of this derivation, however.
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The dossier assessment is part of the early benefit assessment according to the Act on the Reform of the Market for Medicinal Products (AMNOG) supervised by the Federal Joint Committee (G-BA). After publication of the dossier assessment, the G-BA conducts a commenting procedure and makes a final decision on the extent of the added benefit.
More English-language information will be available soon (Sections 2.1 to 2.6 of the dossier assessment as well as easily understandable information on informedhealth.org). If you would like to be informed when these documents are available, please send an e-mail to [email protected].
Source-Eurekalert