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New systemic treatment paradigms in resectable non-small cell lung cancer and variations in patient access across Europe.


ABSTRACT: The treatment landscape of resectable early-stage non-small cell lung cancer (NSCLC) is set to change significantly due to encouraging results from randomized trials evaluating neoadjuvant and adjuvant immunotherapy, as well as adjuvant targeted therapy. As of January 2024, marketing authorization has been granted for four new indications in Europe, and regulatory approvals for other study regimens are expected. Because cost-effectiveness and reimbursement criteria for novel treatments often differ between European countries, access to emerging developments may lead to inequalities due to variations in recommended and available lung cancer care throughout Europe. This Series paper (i) highlights the clinical studies reshaping the treatment landscape in resectable early-stage NSCLC, (ii) compares and contrasts approaches taken by the European Medicines Agency (EMA) for drug approval to that taken by the United States Food and Drug Administration (FDA), and (iii) evaluates the differences in access to emerging treatments from an availability perspective across European countries.

SUBMITTER: Houda I 

PROVIDER: S-EPMC10928304 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

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New systemic treatment paradigms in resectable non-small cell lung cancer and variations in patient access across Europe.

Houda Ilias I   Dickhoff Chris C   Uyl-de Groot Carin A CA   Reguart Noemi N   Provencio Mariano M   Levy Antonin A   Dziadziuszko Rafal R   Pompili Cecilia C   Di Maio Massimo M   Thomas Michael M   Brunelli Alessandro A   Popat Sanjay S   Senan Suresh S   Bahce Idris I  

The Lancet regional health. Europe 20240304


The treatment landscape of resectable early-stage non-small cell lung cancer (NSCLC) is set to change significantly due to encouraging results from randomized trials evaluating neoadjuvant and adjuvant immunotherapy, as well as adjuvant targeted therapy. As of January 2024, marketing authorization has been granted for four new indications in Europe, and regulatory approvals for other study regimens are expected. Because cost-effectiveness and reimbursement criteria for novel treatments often dif  ...[more]

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