TAGRISSO (osimertinib)
Reason for request
Favourable opinion for reimbursement as monotherapy in the first-line treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with activating epidermal growth factor receptor (EGFR) mutations.
TAGRISSO provides a therapeutic improvement compared to other anti-EGFR TKIs in the treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) with mutations (EGFR).
In the treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with activating epidermal growth factor receptor (EGFR) mutations, when the use of an anti-EGFR TKI isconsidered, osimertinib is the first-line treatment of choice due to demonstration of an improvement in overall survival compared to erlotinib and gefitinib with a safety profile judged to be acceptable.
The Committee reiterates that patients with EGFR mutations other than exon 19 deletion or exon 21 (L858R) activating mutations (in particular the T790M mutation for which osimertinib has an MA and a specific Committee opinion) were not assessed in the FLAURA study. Exons 19 or 21 mutations represent the majority of all EGFR mutations (85%)[1] [2]
Clinical Benefit
Substantial |
The clinical benefit of TAGRISSO (osimertinib) is substantial in this MA indication extension.
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Clinical Added Value
moderate |
Considering:
the Committee considers that TAGRISSO (osimertinib) provides a moderate clinical added value (CAV III) compared to the anti-EGFR TKIs TARCEVA (erlotinib) and IRESSA (gefitinib) in the first-line treatment of locally advanced or metastatic non-small cell lung cancer (NSCLC) with activating EGFR mutations.
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