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FLAURA: What the Lung Cancer Trial Found
FLAURA compared osimertinib with the older EGFR pills as first treatment for EGFR-mutated lung cancer. It nearly doubled the time before the cancer grew; the survival gain arrived three years later and only just reached the mark.
Original commentary from the Cancer Explained editorial team.

Please note: this page is educational only — it is not medical advice, and it does not speculate about anyone’s health beyond reliable public reporting. For questions about your own health, talk with your healthcare team.
The question was which EGFR pill to go first
By 2014, lung cancer with an EGFR mutation was already treated with a targeted pill rather than chemotherapy. Gefitinib and erlotinib were the usual choices.
Osimertinib was designed for a later problem. When those first-generation pills stop working, it is often because the cancer has acquired a second change called T790M, and osimertinib blocks that as well. FLAURA asked whether the newer drug should be used from the start instead of being held in reserve.
Who was enrolled
| Field | Detail |
|---|---|
| Trial | FLAURA |
| Identifier | NCT02296125 |
| Phase | Phase 3 |
| Design | Randomised, double-blind |
| Cancer type | Untreated advanced non-small-cell lung cancer with an EGFR mutation |
| Comparator | Osimertinib 80 mg daily against gefitinib 250 mg or erlotinib 150 mg daily |
| Primary endpoint | Progression-free survival, assessed by the investigator |
These are the amounts the trial compared. Your own prescription governs what you swallow, and it can be lowered for side effects.
556 people were randomised, half to each side. All had advanced disease not yet treated, and all carried one of the two common EGFR mutations: an exon 19 deletion or L858R. Neither patients nor doctors knew which pill was which.
Note the primary endpoint. It was time before the cancer grew. Survival was a secondary measure, and had to wait.
Nearly nine extra months before the cancer grew
Median progression-free survival was 18.9 months with osimertinib and 10.2 months with the older pills. The hazard ratio was 0.46 (95% CI 0.37 to 0.57, p<0.001).
At an interim look, 83% of the osimertinib group and 71% of the comparator group were alive at 18 months (hazard ratio 0.63, 95% CI 0.45 to 0.88, p=0.007) — a p-value that did not count as significant at that stage of the trial.
Why the response rate is the wrong thing to look at
Tumours shrank in 80% of the osimertinib group and 76% of the comparator group. That difference was not significant (odds ratio 1.27, 95% CI 0.85 to 1.90, p=0.24).
Both drugs, in other words, worked at first for roughly the same share of people. What separated them was how long it lasted: a median response duration of 17.2 months (95% CI 13.8 to 22.0) against 8.5 months (95% CI 7.3 to 9.8). Osimertinib did not start better. It held longer.
Severe side effects, grade 3 or higher, were less common with osimertinib: 34% against 45%.
The survival number came later, and only just
The final survival analysis was published in 2020. Median overall survival was 38.6 months (95% CI 34.5 to 41.8) with osimertinib and 31.8 months (95% CI 26.6 to 36.0) with the comparator. The hazard ratio for death was 0.80, with a 95.05% confidence interval of 0.64 to 1.00 and a p-value of 0.046.
That interval touches 1.00. The result cleared the line by a very small margin, on a secondary endpoint. It is supportive evidence, not the trial's main claim.
By three years, 28% of the osimertinib group were still on their assigned drug, against 9% of the comparator group. Grade 3 or higher side effects at that point were 42% against 47%, despite far longer exposure on osimertinib.
What this trial cannot tell you
- How osimertinib compares with today's alternatives. The comparator was gefitinib or erlotinib alone. Combinations of an EGFR drug with chemotherapy, and other newer approaches, were not in this trial.
- What to expect with an uncommon EGFR mutation. Only exon 19 deletions and L858R were eligible.
- Whether the survival gain is solid. A p-value of 0.046 on a secondary endpoint should be read with care.
- What to do when it stops working. FLAURA tested first treatment, not what comes after.
Questions about EGFR-mutated lung cancer
- Which EGFR mutation do I have, and was it one of the two studied here?
- Is the plan a pill alone, or a pill with something added?
- When this stops working, will you biopsy again to see why?
Sources
This article was written from the sources below, which were checked on the source-check date shown above.
- NEJM: Osimertinib in Untreated EGFR-Mutated Advanced NSCLC (FLAURA) (primary)
- NEJM: Overall Survival with Osimertinib in Untreated, EGFR-Mutated Advanced NSCLC (FLAURA) (primary)
How this article was prepared
Prepared by Cancer Explained's AI-assisted editorial system and checked against the sources listed below. This article has not been reviewed by a healthcare professional unless a named reviewer is specifically shown.
Cancer Explained is published by the National Cancer Information Foundation as a nonprofit-oriented public-interest education project. It is not a diagnostic service, does not recommend treatments, and is not for emergencies.
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Prevention, possible warning signs, screening, and diagnosis
This story relates to Lung cancer. The information below is general: it does not reveal anything else about a public person’s health, and not every point applies to every cancer. Personal advice depends on age, symptoms, family history, exposures, and medical history.
Prevention and risk reduction
Not every cancer can be prevented. Avoiding tobacco, protecting skin from ultraviolet radiation, limiting alcohol, staying active, and receiving recommended HPV or hepatitis B vaccination can lower the risk of certain cancers. A risk factor is not a prediction or a cause in one individual.
Symptoms and possible early signs
Possible signs vary and are often caused by conditions other than cancer. Changes worth discussing include a new lump, unexplained bleeding or weight loss, a persistent cough, lasting bowel or bladder changes, a changing skin spot, or symptoms that persist or worsen. Some early cancers cause no symptoms.
Screening and early detection
Screening looks for certain cancers before symptoms begin. Recommended tests exist only for some cancers and depend on age and risk. Screening can have benefits and harms; it is not the same as evaluating a new symptom, and there is no single routine scan or blood test that reliably screens for every cancer.
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