Osimertinib: A Review in Previously Untreated, EGFR Mutation-Positive, Advanced NSCLC.

Activating mutations in the epidermal growth factor receptor (EGFR) gene have been identified as key oncogenic drivers of non-small cell lung cancer (NSCLC). Osimertinib (Tagrisso®) is an orally administered, third-generation EGFR tyrosine kinase inhibitor (EGFR-TKI) that is widely approved for the first-line treatment of advanced NSCLC with activating EGFR mutations. In the pivotal phase III FLAURA trial, osimertinib significantly prolonged progression-free survival (PFS) and overall survival (OS) relative to first-generation EGFR-TKIs in patients with previously untreated, EGFR mutation-positive, advanced NSCLC. Osimertinib also significantly prolonged central nervous system (CNS) PFS in patients with CNS metastases at trial entry. Osimertinib had a generally manageable tolerability profile; the majority of adverse events considered to be possibly related to treatment were of mild to moderate severity. Osimertinib represents a valuable targeted therapeutic for use in adults with previously untreated, EGFR mutation-positive, advanced NSCLC.

Osimertinib: clinical considerations in untreated, EGFR mutation-positive, advanced NSCLC

Introduction

Non-small cell lung cancer (NSCLC) accounts for the majority (≈ 85%) of all lung cancers and is a leading contributor to cancer-related mortality; advanced NSCLC is associated with a 5-year survival rate of < 5% [1, 2]. The best-characterized oncogenic drivers of NSCLC include activating mutations in the tyrosine kinase domain of the epidermal growth factor receptor (EGFR) gene, the most common of which are exon 19 deletions and the exon 21 L858R substitution [3]. EGFR mutation prevalence varies based on ethnicity, with mutations being detected in ≈ 17% of Caucasian patients and ≈ 39% of Asian patients with NSCLC [2]. These mutations serve as both biomarkers and rational molecular targets for tailored therapy, sensitizing the tumours that harbour them to the effects of EGFR tyrosine kinase inhibitors (EGFR-TKIs) [4].

The emergence of EGFR-TKIs at the beginning of the 21st century constituted a paradigm shift in the management of EGFR mutation-positive NSCLC, heralding an era of precision medicine. Compared with traditional cytotoxic therapies, EGFR-TKIs have improved clinical outcomes and health-related quality of life in patients with advanced disease [5]. However, acquired resistance to first-generation (e.g. erlotinib, gefitinib) and second-generation (e.g. afatinib, dacomitinib) EGFR-TKIs typically develops after a median of 9–15 months, with the EGFR T790M gatekeeper mutation appearing to mediate the development of resistance in ≈ 50–60% of patients [6]. Furthermore, the aforementioned EGFR-TKIs (particularly second-generation) non-selectively inhibit wild-type EGFR and can be associated with dose-limiting toxicities [7, 8]. Third-generation EGFR-TKIs have been designed to selectively inhibit the sensitizing and T790M mutant forms of EGFR tyrosine kinase whilst largely sparing wild-type EGFR activity and thus reducing off-target toxicity relative to earlier-generation EGFR-TKIs [7, 8].

Osimertinib (Tagrisso®) is an orally administered, third-generation EGFR-TKI that is widely approved for the first-line treatment of advanced NSCLC with activating EGFR mutations (Sect. 4). This article reviews the clinical efficacy and tolerability of osimertinib in this indication. An overview of the pharmacological properties of osimertinib is provided in Table 1. While osimertinib has also been approved in other NSCLC treatment settings (e.g. in EGFR-TKI-experienced patients with advanced EGFR T790M mutation-positive NSCLC; reviewed previously [9]) in many countries, use in these indications is beyond the scope of this review.

Table 1

Pharmacological properties of osimertinib in advanced NSCLC with activating EGFR mutations

Pharmacodynamic properties

Binds irreversibly to clinically relevant mutant EGFR kinase forms (e.g. L858R, ex19del, T790M) to selectively inhibit mutant EGFR kinase activity [7, 19, 20]; potently inhibits EGFR phosphorylation in EGFR-TKI-sensitizing mutant and T790M mutant NSCLC cell lines, exhibiting less activity against wild-type cell lines [7, 20]

Produces two pharmacologically active metabolites; AZ7550 is similar to osimertinib in potency and selectivity, while AZ5104 is more potent in inhibiting both mutant EGFR and wild-type EGFR (smaller selectivity margin than osimertinib) [7, 19]

Dose-dependently induced profound and sustained tumour regression in xenograft and transgenic models of EGFR-mutant lung cancer (including those of CNS metastases) in vivo [7, 30]; exhibited potent anti-tumour activity against both L858R and L858R/T790M EGFR-mutant tumours (unlike afatinib, which was only effective against the former) in transgenic mice [7]

Exhibited anti-tumour effects in pts with NSCLC harbouring various EGFR mutations (common and uncommon) in clinical trials [10, 11, 27]; inhibited growth of CNS metastases in pts with EGFR mutation-positive NSCLC [13, 31]

Resistance to osimertinib eventually develops in pts, with various mechanisms underlying acquired resistance [32]; in a subset of pts in the phase III FLAURA trial (Sect. 2), the most common acquired resistance mechanisms identified in osimertinib recipients who experienced clinical progression and/or discontinued treatment were MET amplification (15%; 14/91) and the EGFR C797S mutation (7%; 6/91) [33]

Potential for QTc prolongation and changes in cardiac contractility [18–20]; a concentration-dependent QTc interval prolongation of 14 ms is predicted at the recommended dosage [19, 20]; in a pooled analysis of data from clinical trials (n = 1479 treated with osimertinib), a QTc increase from baseline of > 60 ms and a QTc > 500 ms occurred in 3.1% and 0.8% of pts, respectively, while an LVEF decline of ≥ 10% from baseline and to < 50% LVEF occurred in 3.2% of pts who had baseline data and ≥ 1 follow-up assessment (n = 1233) [19, 20]

Pharmacokinetic properties

Linear pharmacokinetics with dose-proportional increases in exposure (Cmax and AUC; dose range 20–240 mg) [19, 20, 34]

Slow absorption after oral administration (median Tmax 6 h) [19, 20, 34]; no clinically meaningful effects of food on osimertinib exposure in pts with EGFR mutation-positive advanced NSCLC or of omeprazole-induced gastric pH elevations on exposure in healthy volunteers [35]

Steady-state exposures reached after 15 days of once-daily administration (drug accumulation ≈ 3-fold) [19]

Extensively distributed in tissues (mean Vd 918 L at steady state) [19, 20]; high blood-brain barrier penetrance and brain exposure relative to other EGFR-TKIs in preclinical studies (brain to plasma AUC ratios ≈ 2 with oral dosing in animal models [19]) [30, 36]; achieved rapid, high and uniform brain exposure in a phase I trial in adults with EGFR mutation-positive advanced NSCLC and CNS metastases (n = 4) [31]

Main metabolic pathways are oxidation (primarily by CYP3A) and dealkylation, with two pharmacologically active metabolites found in plasma after oral administration (AZ7550 and AZ5104; each had a geometric mean exposure ≈ 10% that of osimertinib at steady state) [19, 20, 34]

Low to moderate clearance (14.2 L/h at steady state) and long half-life (≈ 50 h after single dose) in pts with advanced NSCLC [34]

Eliminated primarily in faeces (68%) and less so in urine (14%); unchanged drug represented ≈ 2% of the elimination [19, 20]

Pharmacokinetics in pts with CLcr < 15 mL/min or severe hepatic impairment (TBil 3–10 × ULN and any AST) unknown [19, 20]; in the EU, caution is required in pts with CLcr < 30 mL/min and use in pts with severe hepatic impairment is not recommended [20]

Drug interactions

Concomitant use of strong CYP3A inducers may decrease osimertinib exposure and should be avoided in the EU [20] and, if possible, in the USA (dosage adjustments required if concomitant use is unavoidable) [19]; in the EU, the co-administration of osimertinib and moderate CYP3A4 inducers should be approached with caution or, if possible, avoided [20]

In the EU, pts concomitantly using drugs with disposition dependent upon BCRP or P-gp and narrow therapeutic indices should be closely monitored for tolerability of the concomitant drug (exposure potentially increased) [20]; in the USA, pts concomitantly using BCRP or P-gp substrates should be monitored for adverse reactions of the BCRP or P-gp substrate (unless instructed otherwise in approved labelling) [19]

Effect of use with drugs known to prolong QTc interval is unknown; in the USA, co-administration of osimertinib and drugs known to prolong the QTc interval with known risk of Torsades de pointes should be avoided if feasible (or periodic ECG monitoring conducted if not) [19]

AST aspartate aminotransferase, AUC area under the plasma concentration-time curve, BCRP breast cancer resistance protein, CL creatinine clearance, C peak plasma concentration, CNS central nervous system, EGFR epidermal growth factor receptor, ex19del exon 19 deletion, LVEF left ventricular ejection fraction, NSCLC non-small cell lung cancer, P-gp P-glycoprotein, pts patients, TBil total bilirubin, TKI tyrosine kinase inhibitor, T time to peak plasma concentration, ULN upper limit of normal, V volume of distribution

Therapeutic Efficacy of Osimertinib

The therapeutic efficacy of osimertinib in the first-line treatment of EGFR mutation-positive, advanced NSCLC was evaluated in the randomized, double-blind, active-controlled, multinational phase III FLAURA trial (Fig. 1) [10]. Promising results in this treatment setting were initially seen in the phase I component of the AURA trial [11]; AURA will not be discussed further, given that phase III data are available.

Fig. 1. 

Trial design of the randomized, double-blind, multinational phase III FLAURA trial in adults with EGFR mutation-positive, advanced NSCLC [10, 12]. Efficacy results are reported in the animated figure (available online). EGFR epidermal growth factor receptor, HR hazard ratio, NSCLC non-small cell lung cancer, PFS progression-free survival, TKI tyrosine kinase inhibitor

FLAURA enrolled adults with locally advanced or metastatic NSCLC who had not previously been treated for advanced disease and were eligible for first-line treatment with a first-generation EGFR-TKI [10]. The presence of the EGFR exon 19 deletion or L858R mutation (alone or in conjunction with other EGFR mutations), confirmed locally or centrally, was also required. Patients with central nervous system (CNS) metastases were eligible if their condition was neurologically stable [10].

Patients were assigned oral osimertinib (n = 279) or an oral comparator EGFR-TKI (erlotinib or gefitinib; n = 277) [dosages provided in Table 2], with randomization stratified by tumour EGFR mutation (exon 19 deletion or L858R) and race (Asian or non-Asian) [10]. Treatment continued until disease progression (if deemed to be of clinical benefit, treatment was permitted to continue beyond the point of disease progression), unacceptable toxicity or withdrawal of consent. The primary endpoint was progression-free survival (PFS), determined by investigator assessments based on RECIST version 1.1 criteria. Efficacy analyses were conducted in the full analysis set (FAS), which included all randomized patients [10]. After the primary endpoint analysis, progression event data were no longer centrally collected [12]. A final analysis of overall survival (OS), a secondary endpoint, was planned for after ≈ 318 deaths in the FAS [12].

Table 2

Efficacy of osimertinib in the first-line treatment of EGFR mutation-positive advanced NSCLC in FLAURA

	Osimertiniba	Comparator EGFR-TKIsb
Full analysis set [10, 12]
No. of pts	279	277
Median PFSc (months)	18.9	10.2
Hazard ratio (95% CI)	0.46 (0.37–0.57)***
Median OSd (months)	38.6	31.8
Hazard ratio (95.05% CI)	0.80 (0.64–1.00)*
ORR (% of pts)	80	76
Odds ratio (95% CI)	1.27 (0.85–1.90)
CNS full analysis sete [13]
No. of pts	61	67
Median CNS PFSf (months)	NR	13.9
Hazard ratio (95% CI)	0.48 (0.26–0.86)**
CNS ORR (% of pts)	66	43
Odds ratio (95% CI)	2.5 (1.2–5.2)**

Data cut-off 12 June 2017 for all endpoints except OS (data cut-off 25 June 2019). PFS and ORR based on investigator assessment; CNS PFS and ORR based on neuroradiological BICR

BICR blinded independent central review, CNS central nervous system, EGFR epidermal growth factor receptor, NR not reached, ORR objective response rate, OS overall survival, PFS progression-free survival, pts patients, TKI tyrosine kinase inhibitor

*p = 0.046, **p ≤ 0.014, ***p < 0.001 vs comparator EGFR-TKIs

a80 mg once daily

bGefitinib 250 mg (n = 183 in full analysis set) or erlotinib 150 mg (n = 94) once daily

cPFS was primary endpoint; time from randomization to objective disease progression or death (any cause)

dAt the time of final OS analysis (alpha value 0.0495 to maintain overall 5% type 1 error rate across interim and final OS analyses)

eAll pts with baseline CNS metastases (measurable or not) by BICR

fTime from randomization to objective CNS progression or death (any cause)

Baseline characteristics were generally well balanced between treatment arms [10]. The majority of patients had metastatic disease (95%), with 35% having visceral metastases and 21% having CNS metastases. In each treatment group, 63% of patients had the EGFR exon 19 deletion at randomization and 37% had the L858R mutation [10].

Progression-Free Survival

Osimertinib significantly prolonged investigator-assessed PFS relative to comparator EGFR-TKIs (primary endpoint; Table 2) [10]. At data cut-off for the primary analysis, the median duration of follow-up for PFS was 15.0 months in the osimertinib group and 9.7 months in the comparator EGFR-TKI group; RECIST-defined progression or death had occurred in 49% of osimertinib recipients versus 74% of comparator EGFR-TKI recipients. In a sensitivity analysis, results for PFS according to blinded independent central review (BICR) were consistent with those for PFS based on investigator assessments [10].

The benefit of osimertinib over comparator EGFR-TKIs for PFS was consistent across all predefined subgroups assessed, including those based on EGFR mutation at randomization (exon 19 deletion vs L858R), known or treated CNS metastases at trial entry (yes vs no) and race (Asian vs non-Asian) [all hazard ratios (HRs) and upper limits of associated 95% CIs < 1] [10]. In patients with known or treated CNS metastases, median PFS was 15.2 months in the osimertinib group versus 9.6 months in the comparator EGFR-TKI group (HR 0.47; 95% CI 0.30–0.74; p < 0.001); in patients without CNS metastases, median PFS was 19.1 months versus 10.9 months in the corresponding groups (HR 0.46; 95% CI 0.36–0.59; p < 0.001) [10].

Overall Survival

At the time of the primary analysis of PFS, median OS could not be calculated in either group (HR for death 0.63; 95% CI 0.45–0.88; p = 0.007); in this interim OS analysis, a p-value < 0.0015 was required for statistical significance [10]. At 12 months, 89% of osimertinib recipients were alive versus 82% of comparator EGFR-TKI recipients; at 18 months, 83% versus 71% were alive [10].

Osimertinib recipients had significantly longer OS than comparator EGFR-TKI recipients at the time of the final OS analysis (Table 2) [12]. At data cut-off, the median duration of follow-up for OS was 35.8 months in the osimertinib group and 27.0 months in the comparator EGFR-TKI group. At 24 months, 74% of osimertinib recipients were alive versus 59% of comparator EGFR-TKI recipients; at 36 months, 54% versus 44% were alive. The OS benefit with osimertinib versus comparator EGFR-TKIs was generally consistent across predefined subgroups; all HRs were < 1, except for analyses in Asian patients (HR 1.00; 95% CI 0.75–1.32) and patients with the L858R mutation at randomization (HR 1.00; 95% CI 0.71–1.40) [12].

Other Outcomes

Objective response rate (ORR) did not markedly differ between osimertinib and comparator EGFR-TKI recipients (Table 2) [10]. While the median time to response was 6.1 weeks in each treatment group, the median duration of response was longer with osimertinib than with comparator EGFR-TKIs [17.2 months (95% CI 13.8–22.0) vs 8.5 months (95% CI 7.3–9.8)]. The median best percentage change in target-lesion size was −54.7% with osimertinib versus −48.5% with comparator EGFR-TKIs (p = 0.003) and disease control was achieved in 97% of osimertinib recipients versus 92% of comparator EGFR-TKI recipients [odds ratio (OR) 2.78; 95% CI 1.25–6.78; p = 0.01] [10].

Osimertinib was active against CNS metastases, significantly prolonging CNS PFS relative to comparator EGFR-TKIs in patients with CNS metastases at trial entry (Table 2) [13]. At data cut-off, the median duration of follow-up for CNS PFS was 12.4 months in the osimertinib group and 7.0 months in the comparator EGFR-TKI group. CNS progression by BICR occurred in 20% of osimertinib recipients versus 39% of comparator EGFR-TKI recipients and the CNS ORR was higher with osimertinib than with comparator EGFR-TKIs (Table 2) [13]. In the FAS, which included patients with and without CNS metastases at trial entry, investigator-assessed CNS progression events were observed in 6% of osimertinib recipients versus 15% of comparator EGFR-TKI recipients [10].

First-line osimertinib may delay the need for subsequent therapies relative to comparator EGFR-TKI therapy, with 28% of the osimertinib group versus 9% of the comparator EGFR-TKI group continuing to receive the first-line trial drug at 36 months [12]. At the time of the final analysis of OS, 48% of osimertinib recipients and 65% of comparator EGFR-TKI recipients had started a first subsequent anticancer therapy after discontinuing their randomized treatment (with 47% of the latter group having received osimertinib as their first subsequent therapy). The median time to first subsequent therapy or death was 25.5 months with osimertinib versus 13.7 months with comparator EGFR-TKIs (HR 0.48; 95% CI 0.39–0.58; p < 0.0001). Of all randomized patients, 26% of osimertinib recipients and 33% of comparator EGFR-TKI recipients received a second subsequent therapy. The median time to second subsequent therapy was 31.1 months with osimertinib versus 23.4 months with comparator EGFR-TKIs (HR 0.69; 95% CI 0.56–0.84; p = 0.0003) [12].

With respect to patient-reported outcomes, both osimertinib and comparator EGFR-TKI recipients reported improvements in key lung cancer symptoms (i.e. cough, chest pain, dyspnoea, fatigue and appetite loss), global health status/quality of life and levels of functioning from baseline to treatment discontinuation [14]. There were no statistically significant, clinically relevant differences in mean changes between treatment groups [14].

Efficacy in Asian Patients

In subsets of Asian patients (n = 162 and 160 randomized to osimertinib and comparator EGFR-TKI therapy at Asian sites) [15] and Japanese patients (n = 65 and 55 randomized to osimertinib and gefitinib) [16] in FLAURA, the efficacy of osimertinib relative to comparator EGFR-TKI therapy was generally comparable to that in the overall study population. In the Asian subset, median investigator-assessed PFS was 16.5 months in osimertinib recipients versus 11.0 months in comparator EGFR-TKI recipients (HR 0.54; 95% CI 0.41–0.72; p < 0.0001) [15]. The ORR was 80% with osimertinib and 75% with comparator EGFR-TKIs. Deaths occurred in 20% and 28% of osimertinib and comparator EGFR-TKI recipients, with OS data immature at the time of this analysis; median OS was not reached in either treatment arm. At 18 months, the survival rate was 82% with osimertinib versus 72% with comparator EGFR-TKIs (HR for death 0.65; 95% CI 0.42–1.02) [15]. In the Japanese subset, median investigator-assessed PFS was 19.1 months with osimertinib versus 13.8 months with gefitinib (HR 0.61; 95% CI 0.38– 0.99; nominal p = 0.0456) [16]. The ORR was 75% with osimertinib versus 76% with gefitinib. Deaths occurred in 14% and 18% of osimertinib and gefitinib recipients, with OS data immature at the time of analysis [16].

FLAURA China evaluated first-line osimertinib in Chinese patients with EGFR mutation-positive advanced NSCLC enrolled in either the global FLAURA study or in a China-only study following the same protocol as FLAURA (total n = 71 and 65 randomized to osimertinib and gefitinib) [17]. In FLAURA China, median investigator-assessed PFS was 17.8 months in osimertinib recipients versus 9.8 months in gefitinib recipients (HR 0.56; 95% CI 0.37–0.85; nominal p = 0.007) [primary endpoint]; median follow-up for PFS was 16.7 months and 9.8 months in the respective groups. At data cut-off for the final OS analysis, median OS was 33.1 months with osimertinib versus 25.7 months with gefitinib (HR 0.85; 95% CI 0.56–1.29). Deaths had occurred in 63% and 68% of osimertinib and gefitinib recipients. The median follow-up for OS was 31.0 months and 24.9 months in the respective groups [17].

Tolerability of Osimertinib

Osimertinib had a generally manageable tolerability profile in adults with previously untreated, EGFR mutation-positive advanced NSCLC participating in the pivotal FLAURA trial [10]. The safety of osimertinib in Asian patient subsets (including in the FLAURA China study) was generally consistent with that in the overall FLAURA population [15-17].

At data cut-off for the primary PFS analysis of FLAURA, the median duration of treatment exposure was 16.2 months for osimertinib recipients and 11.5 months for comparator EGFR-TKI recipients; 51% of osimertinib recipients versus 23% of comparator EGFR-TKI recipients continued to receive their assigned trial treatment [10]. In osimertinib recipients, the most common adverse events (AEs) assessed by the investigator as possibly related to treatment were rashes and acnes, diarrhoea, dry skin, paronychia, stomatitis, pruritus, decreased appetite, aspartate aminotransferase (AST) elevation and alanine aminotransferase (ALT) elevation (Fig. 2). Grade ≥ 3 AEs of any causality occurred in 34% of osimertinib recipients versus 45% of comparator EGFR-TKI recipients, with the most common grade 3 AE in the osimertinib group being decreased appetite (3 vs 2% with comparator EGFR-TKIs). Grade 4 AEs occurred in 2% of osimertinib recipients and 4% of comparator EGFR-TKI recipients (no grade 4 AEs in osimertinib recipients were assessed to be possibly related to treatment, while 1% of comparator EGFR-TKI recipients experienced possibly treatment-related grade 4 ALT elevations). Serious AEs occurred in 22% of osimertinib recipients versus 25% of comparator EGFR-TKI recipients and were of interstitial lung disease (ILD) in 2.2 versus 1.4%. AEs led to permanent treatment discontinuation in 13% of osimertinib recipients versus 18% of comparator EGFR-TKI recipients, dose interruption in 25% versus 24%, and dose reduction in 4% versus 5%. Fatal AEs occurred in 2% of osimertinib recipients and 4% of comparator EGFR-TKI recipients [10].

Fig. 2.

Adverse events possibly causally related to treatment and occurring in ≥ 10% of patients in either treatment arm in the FLAURA trial (n = 279 and 277 receiving osimertinib and comparator EGFR-TKIs) [10]. AEs adverse events, ALT alanine aminotransferase, AST aspartate aminotransferase, EGFR-TKIs epidermal growth factor receptor tyrosine kinase inhibitors, ϴ zero incidence of grade ≥ 3 AEs

No new safety signals were observed at the time of the FLAURA final OS analysis [12]. Despite a longer median duration of treatment exposure in the osimertinib group than the comparator EGFR-TKI group (20.7 vs 11.5 months), rates of grade ≥ 3 AEs (42 vs 47% of patients), serious AEs (27 vs 27%) and treatment discontinuation due to AEs (15 vs 18%) were comparable between treatment groups. Fatal AEs occurred in 3% of osimertinib recipients versus 4% of comparator EGFR-TKI recipients and no deaths in the osimertinib group were considered to be related to treatment (vs two in the comparator EGFR-TKI group) [12].

A comprehensive evaluation of cardiac safety data in patients with advanced NSCLC from the osimertinib global safety database did not identify any causal relationship between osimertinib and cardiac failure [18]. Across the clinical study program, most cardiac failure-related AEs were asymptomatic decreases in ejection fraction (Table 1). Generally, ejection fraction decreases resolved without treatment or dose modification of osimertinib. In FLAURA, there was one case of cardiac failure possibly related to osimertinib (occurring in a patient with a medical history of hypertension and chronic heart failure) and one case of pulmonary edema considered to be unrelated to osimertinib [18].

Various warnings pertain to the use of osimertinib and precautions must be taken to reduce the risk or severity of potential AEs [19, 20]. In the USA, cardiac monitoring should be conducted in patients with cardiac risk factors or at increased risk of QTc prolongation (e.g. due to unavoidable concomitant administration with drugs known to prolong QTc interval; Table 1) [19]. This monitoring should also be considered in the EU (and administration in patients with congenital long QT syndrome avoided where possible) [20]. Cardiac adverse reactions may necessitate withholding, dose modification or discontinuation of osimertinib (see local prescribing information) [19, 20]. In a pooled analysis of data from the FLAURA, AURA and ADAURA trials (n = 1479 treated with osimertinib), ILD or ILD-like adverse reactions (e.g. pneumonitis) occurred in 3.7% of osimertinib recipients and were fatal in 0.3% [19, 20]. Patients with worsening (or new [20]) symptoms potentially indicative of ILD (e.g. dyspnoea, fever, cough) should be carefully assessed for ILD [19, 20]. Treatment with osimertinib should be withheld during this assessment and discontinued if ILD is confirmed. Based on preclinical data and its mechanism of action, osimertinib can cause foetal harm if used during pregnancy [19, 20].

Dosage and Administration of Osimertinib

Osimertinib is approved for use in the first-line treatment of patients with EGFR mutation-positive, advanced NSCLC in several countries, including those of the EU [20] and the USA [19]. In the EU, osimertinib is indicated as monotherapy for the first-line treatment of adults with locally advanced or metastatic NSCLC with activating EGFR mutations [20]. In the USA, osimertinib is indicated for the first-line treatment of patients with metastatic NSCLC whose tumours harbour EGFR mutations (exon 19 deletions or exon 21 L858R mutations) [19]. EGFR mutation status in plasma or tumour specimens should be confirmed using a validated [20] or locally approved [19] test method. Osimertinib is available as 80 or 40 mg tablets, to be swallowed whole with water [19, 20]. The recommended dose of osimertinib is 80 mg once daily, with treatment continuing until disease progression or unacceptable toxicity. If individual safety and tolerability necessitates a dose reduction, the dose should be reduced to 40 mg once daily [19, 20]. Co-administering osimertinib with St. John’s Wort is contraindicated in the EU [20]. Consult local prescribing information for detailed information concerning the administration of osimertinib in patients who have difficulty swallowing solids, missed doses, management of adverse reactions, contraindications, warnings and precautions, and use in special populations.

Place of Osimertinib in the Management of Previously Untreated, EGFR Mutation-Positive NSCLC

EGFR-TKIs have revolutionized the treatment of EGFR mutation-positive NSCLC. Osimertinib is the first third-generation EGFR-TKI to be approved for use in the first-line treatment of patients with EGFR mutation-positive, advanced NSCLC. In the USA, osimertinib is recommended as the preferred first-line treatment option (ahead of earlier-generation EGFR-TKIs) for patients with sensitizing EGFR mutation-positive advanced NSCLC (NCCN clinical practice guidelines [21]) and patients with stage IV NSCLC harbouring the EGFR L858R or exon 19 deletion mutation with or without T790M [ASCO/OH(CCO) guidelines [22]]. The European Society for Medical Oncology also considers osimertinib to be the preferred first-line option for patients with advanced/metastatic NSCLC with sensitizing EGFR mutations [3]. Robust testing methods are available for the detection of EGFR mutations in plasma and tissue samples [23].

Osimertinib was significantly more effective than first-generation EGFR-TKIs in prolonging PFS and OS in the pivotal FLAURA trial in patients with previously untreated, EGFR mutation-positive advanced NSCLC (Sect. 2). Improvements in PFS and OS were clinically meaningful, with gains of ≈ 9 months and ≈ 7 months, respectively. EGFR mutations are more prevalent in Asian populations (Sect. 1) and the efficacy of osimertinib relative to comparator EGFR-TKIs in Asian patient subsets of FLAURA and FLAURA China (Sect. 2.4) was generally comparable to that in the overall FLAURA population. Consistent with preclinical data demonstrating relatively high blood-brain barrier penetration and CNS exposure with osimertinib versus other EGFR-TKIs (Table 1), osimertinib significantly prolonged CNS PFS relative to comparator EGFR-TKI therapy (Sect. 2.3). Activity against CNS metastases is of particular importance given the high rate of CNS metastases in patients with EGFR mutation-positive advanced NSCLC (≈ 25% at the time of diagnosis [24]). CNS-penetrant targeted therapies such as osimertinib may delay the need for cranial radiotherapy, which is associated with risks of cognitive impairment [25, 26]. While the FLAURA trial only enrolled patients with the most common EGFR mutations (exon 19 deletion and L858R), preclinical data (Table 1) and preliminary clinical results [27] indicate that the therapeutic efficacy of osimertinib is likely to extend to tumours harbouring relatively rare EGFR mutations. As with earlier-generation EGFR-TKIs, it should be noted that resistance to osimertinib does eventually develop (Table 1); trials into the mechanisms of acquired resistance are ongoing [e.g. ELIOS (NCT03239340)].

Osimertinib had a generally manageable tolerability profile in patients with previously untreated, EGFR mutation-positive advanced NSCLC (Sect. 3). The safety and tolerability of osimertinib in FLAURA was largely consistent with that established in EGFR-TKI-experienced patients with T790M mutation-positive advanced NSCLC [9]. In FLAURA, the overall tolerability of osimertinib was similar to that of comparator EGFR-TKIs, with a somewhat lower frequency of grade ≥ 3 AEs (Sect. 3). The majority of AEs possibly causally related to treatment with osimertinib were of mild to moderate severity, the most common being dermatological (e.g. acne and rash, dry skin, paronychia) or gastrointestinal (e.g. diarrhoea, decreased appetite). Patients with a history of ILD or radiation pneumonitis requiring steroid treatment, or any evidence of clinically active ILD, were excluded from clinical trials of osimertinib, as were patients with clinically important cardiac abnormalities [20].

In the absence of direct comparisons between osimertinib and the second-generation EGFR-TKIs, network meta-analyses generally suggest osimertinib has favourable efficacy compared with other first-line EGFR-TKIs (e.g. [28, 29]). Unlike osimertinib, afatinib and dacomitinib may be associated with higher risks of rash and diarrhoea than other EGFR-TKIs [28]. The results of such comparisons must be interpreted with caution, however, given their indirect nature and direct head-to-head comparative studies are desirable.

As an effective first-line treatment for EGFR mutation-positive, advanced NSCLC, with a generally manageable tolerability profile, osimertinib represents a valuable targeted therapeutic for use in adults with previously untreated, EGFR mutation-positive, advanced NSCLC.

Below is the link to the electronic supplementary material.

Supplementary file1 (PPTX 772 kb)

Digital Features for this Adis Drug Evaluation can be found at https://doi.org/10.6084/m9.figshare.14788161

Selectively inhibits mutant EGFR kinase activity

Prolongs PFS and OS relative to first-generation EGFR-TKIs

Readily penetrates blood-brain barrier and is active against CNS metastases

Most common potentially drug-related adverse events dermatological or gastrointestinal in nature