FDA
approves osimertinib for first-line treatment of metastatic NSCLC with most
common EGFR mutations
On April 18, 2018, the Food and Drug Administration
approved osimertinib (Tagrisso, AstraZeneca Pharmaceuticals LP) for the
first-line treatment of patients with metastatic non-small cell lung cancer
(NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19
deletions or exon 21 L858R mutations, as detected by an FDA-approved test.
Approval was based on a multicenter, international, randomized,
double-blind, active-controlled trial (FLAURA, NCT02296125) conducted in 556
patients with EGFR exon 19 deletion or exon 21 L858R mutation-positive,
unresectable or metastatic NSCLC who had not received previous systemic
treatment for advanced disease. Patients were randomized (1:1) to receive
osimertinib 80 mg orally once daily or “standard-of-care (SOC)” treatment of
gefitinib 250 mg or erlotinib 150 mg orally once daily. Of those randomized to
SOC, 20% received osimertinib as the next line of antineoplastic therapy.
The estimated median progression-free survival (PFS) was 18.9 months (95%
CI: 15.2, 21.4) in the osimertinib arm and 10.2 months (95% CI: 9.6, 11.1) in
the SOC arm (hazard ratio 0.46 (95% CI: 0.37, 0.57), p<0.0001). The
confirmed overall response rate was 77% for the osimertinib arm and 69% for the
SOC arm. The estimated median response durations for the osimertinib and SOC
arms were 17.6 and 9.6 months, respectively. At the time of the primary PFS
analysis, there were too few deaths to estimate or compare survival outcomes.
The most common adverse reactions (occurring in at least 20% of patients
treated with osimertinib) were diarrhea, rash, dry skin, nail toxicity,
stomatitis, and decreased appetite. Serious adverse reactions were reported in
4% of patients treated with osimertinib. The most common serious adverse
reactions (≥1%) were pneumonia (2.9%), ILD/pneumonitis (2.1%), and pulmonary
embolism (1.8%).
The recommended dose of osimertinib is 80 mg orally once daily, with or
without food.
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