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Roche announced today that the European Medicines Management Agency (EMA) Committee for Medicinal human use (CHMP) has recommended approval of the Tecentriq® (atezolizumab) as a high expression of PD-L1 and no epidermal growth factor receptor (EGFR) or anaplastic lymphoma First-line therapy for metastatic non-small cell lung cancer ( NSCLC ) with abnormal genomic tumors of ALK .
Managing lymphoma NSCLC
The CHMP recommendations are based on data from the Phase III IMpower110 study, which showed that Tecentriq monotherapy can increase overall survival (OS) by 7.
The study showed that compared with chemotherapy, Tecentriq monotherapy can increase overall survival (OS) by 7.
If approved, Tecentriq will provide a new treatment option without the adverse reactions associated with chemotherapy.
It will also be the first and only single-dose cancer immunotherapy with three modes of administration , allowing for once every two, three or four weeks to give doctors and patients the flexibility to manage treatment.
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