An open-label expanded access program of afatinib in EGFR tyrosine kinase inhibitor-naïve patients with locally advanced or metastatic non-small cell lung cancer harboring EGFR mutations

Background Afatinib is approved globally for EGFR-TKI treatment-naïve patients with EGFR mutation-positive non-small cell lung cancer (NSCLC). In this Korean expanded access program, we evaluated its ‘real-world’ safety and efficacy. Methods EGFR-TKI treatment-naïve patients with EGFR mutation-positive NSCLC received afatinib 40 mg/day until disease progression or other withdrawal criteria. Dose reductions were permitted for adverse events (AEs). The primary endpoint was the number of patients with AEs (CTCAE version 3.0). Other endpoints included progression-free survival (PFS), overall response rate (ORR), duration of response (DOR), and changes in investigator-assessed cancer-related symptoms. Results Eighty-eight patients received afatinib, including 27 (31%) with brain metastases and 16 (18%) with uncommon EGFR mutations. Median PFS was 17.0 months (95% confidence interval [CI] 12.9–23.3 months). Grade 3 treatment-related AEs (TRAEs) were reported in 51 (58%) patients; the most common were diarrhea (22%) and rash/acne (20%). No grade > 3 TRAEs were reported. AEs leading to dose reduction occurred in 49 (56%) patients. Treatment discontinuation due to TRAEs occurred in 4 (5%) patients. ORR was 81% overall, 89% in patients with brain metastases, and 55% in patients with uncommon mutations (excluding T790M/exon 20 insertions). Median DOR was 15.1 months (95% CI 12.4–21.4 months). Cancer-related symptoms were improved/unchanged/worsened in 34–66%/36–66%/0–3% of patients over the first year. Conclusions No unexpected safety signals for afatinib were observed. AEs were manageable; the treatment discontinuation rate was low. Afatinib showed encouraging efficacy in a broad patient population including those with brain metastases or tumors harboring uncommon EGFR mutations. Trials registration ClinicalTrials.gov NCT01931306; 29/08/2013. Supplementary Information The online version contains supplementary material available at 10.1186/s12885-021-08445-9.

In randomized trials, first-line afatinib has demonstrated improved progression-free survival (PFS) compared with chemotherapy (LUX-Lung 3 and 6 [7,8]) and gefitinib (LUX-Lung 7 [9]) in patients with EGFR mutation-positive NSCLC. Of note, in both LUX-Lung 3 and 6, prespecified analysis demonstrated that afatinib significantly improved overall survival (OS) versus chemotherapy in patients with tumors carrying a Del19 EGFR mutation [10]. In LUX-Lung 7, median OS was numerically longer with afatinib versus gefitinib, but did not achieve statistical significance [11]. Across clinical trials, afatinib was well tolerated [7][8][9]. Treatmentrelated adverse events (TRAEs) with afatinib were predominantly class-related gastrointestinal and cutaneous events. While certain TRAEs (e.g., diarrhea) were more common than generally observed with first-and thirdgeneration TKIs, they were manageable with dose reductions, which did not compromise clinical activity [12,13]. Consequently, treatment discontinuations due to TRAEs were rare (< 10%). Together, these observations support the use of afatinib for patients with EGFR mutation-positive NSCLC. In phase III trials, both dacomitinib (exploratory analysis) [14] and osimertinib [15] have demonstrated prolonged OS benefit versus firstgeneration EGFR TKIs. However, as the efficacy and safety of afatinib, dacomitinib, and osimertinib have never been directly compared in prospective trials, optimal first-line treatment choice remains an open question, particularly in Asian patients, as there was no evidence of OS benefit with osimertinib over erlotinib/ gefitinib in this subgroup. Therefore, it is important to assess the efficacy and safety of EGFR TKIs in broader 'real-world' patient populations that are more representative of routine practice than clinical trials [16]. Here, we describe the results of an expanded access program performed in South Korea.

Study design
This was an open-label, single-arm, expanded access, phase IIIb trial conducted at eight centers in South Korea. The objectives were to evaluate the tolerability and activity of afatinib in EGFR TKI-naïve patients with EGFR mutation-positive NSCLC.

Patients and treatment
Patients were ≥ 18 years old with locally advanced or metastatic EGFR mutation-positive NSCLC, were EGFR TKI-naïve (one previous line of chemotherapy was permitted), and had an Eastern Cooperative Oncology Group performance status (ECOG PS) of 0-2 and adequate organ function. Main exclusion criteria were hypersensitivity to afatinib, hormonal anticancer treatment or radiotherapy within 14 days and surgery within 4 weeks prior to study start, cardiovascular abnormalities, pre-existing interstitial lung disease (ILD), active chronic infections, previous/concomitant malignancies, and symptomatic brain metastases. Patients received oral afatinib 40 mg daily in 28-day cycles until disease progression, lack of tolerability, or other study withdrawal criteria. Treatment with afatinib was permitted beyond disease progression if deemed beneficial during assessment. Treatment interruptions and dose reductions were permitted for the management of TRAEs (see the Supporting methods section in the Additional file 1).
At each center, ethical approval was given by an Institutional Review Board or and Independent Ethics Committee. The study was performed in accordance with the Declaration of Helsinki, Good Clinical Practice, and local laws. Written informed consent was given by all patients.

Endpoints, assessments and statistical considerations
The primary endpoint was the frequency of adverse events (AEs), coded using the Medical Dictionary for Regulatory Activities (MedDRA) version 21.1 and graded by the Common Terminology Criteria for Adverse Events (CTCAE) version 3. Treatment-emergent adverse events (TEAEs), TRAEs, and serious AEs (SAEs) were reported. MedDRA preferred terms for AEs of a similar nature were grouped; grouped terms included rash/acne, stomatitis, and renal insufficiency. Other endpoints included PFS, tumor response, and assessment of cancer-related symptoms (see the Supporting methods section in the Additional file 1). Cancer-related symptoms were recorded in the electronic case report form based on investigator judgment as either improved, unchanged, or 'worsening of symptoms due to cancer'. Patients were categorized every 4 weeks and at the end-of-treatment (EOT) visit. EGFR mutations were detected according to the methodology at each participating site.
Analyses were performed on all patients who received at least one dose of afatinib (treatment set). Kaplan-Meier estimates and 95% confidence intervals (CIs) were calculated for time-to-event endpoints using Greenwood's standard error estimate. Two-sided 95% CIs were calculated for the overall response rate (ORR) using the exact 95% Clopper-Pearson CI. Post hoc analyses of treatment outcomes were performed in patient subgroups based on age (< 65 years and ≥ 65 years), presence of brain metastases (yes and no), EGFR mutation status (common [Del19 only or L858R only] and uncommon), and dose interruptions within the first 6 months (yes and no).

Cancer-related symptoms
Over the first year of treatment, the maximum percentage of patients deemed to have improved symptoms was 66% (week 8) and the minimum percentage was 34% (week 52; Fig. 3). Patients deemed to have unchanged symptoms ranged from 36% (week 8) to 66% (week 36). A maximum of 3% of patients had worsening of symptoms due to cancer. At the EOT, 1% of patients had improved symptoms, 72% had unchanged symptoms, and 27% had a worsening of symptoms due to cancer.

Discussion
Real-world data are increasingly recognized by regulatory bodies as an important source of information for the monitoring the safety of approved agents, and to support approvals of agents in development [16]. In this study, patient characteristics were similar to those previously reported in studies of EGFR TKIs used in routine clinical practice in Asia, including Korea [17]. The present study included subsets that are generally underrepresented in clinical trials, such as patients with central nervous system (CNS) involvement (31%) and patients with uncommon EGFR mutations (18%). In this diverse cohort of patients, the tolerability profile of afatinib was predictable and in line with previous randomized controlled trials [7][8][9] and real-world studies [16,18]. However, the rate of TRAEs with afatinib in the current study was higher than observed in randomized controlled trials, possibly reflecting the heterogeneity of patients included the study. While the most common TRAEs were EGFR TKI class-related toxicities (diarrhea, rash/acne and stomatitis) and were not unexpected, the overall rate of grade ≥ 3 TRAEs was 58% compared with 31-49% in the LUX Lung 3, 6 and 7 studies (diarrhea: 5-14%; rash/acne: 9-16%; stomatitis: 4-9%). As expected, given the existence of multiple tablet strengths and previous clinical experience, dose reductions due to AEs were common (56%). Previous analyses of clinical trials [12,13], and real-world observations [19] have demonstrated that dose reductions of afatinib facilitate the management of TRAEs without significantly affecting activity. The rate of permanent treatment discontinuation due to TRAEs in the current study was low (5%) and was comparable to other studies performed in routine clinical practice (≤ 5%) and randomized clinical trials, (6-8%), suggesting that the use of tolerability-guided dose adjustment in real-world clinical practice can help mitigate common TRAEs [7][8][9]16].
In the current study, afatinib stabilized or improved on-treatment cancer-related symptoms in the majority patients. These observations are consistent with clinical trials. For example, in LUX-Lung 3 and 6, afatinib  improved global health status and quality of life (QoL) versus chemotherapy and conferred better control of certain key symptoms [20,21]. Of note, nearly three quarters of patients treated with afatinib had stable, or improved symptoms at the EOT, suggesting that the majority of patients would be sufficiently fit enough to undertake subsequent treatment. This assertion is supported by recent pooled analysis of LUX-Lung 3, 6, and 7 which showed that approximately 70% of patients treated with first-line afatinib subsequently received further systemic therapy [13]. Uptake of subsequent therapy was around 90% in countries with comprehensive reimbursement policies.
In this study, afatinib demonstrated encouraging activity in Korean patients with a median PFS of 17.0 months and an ORR of 81%. Sixty-seven percent of patients responded within 8 weeks. These findings generally compare favorably with afatinib activity reported in Asian patients treated in routine clinical practice (median PFS 12.2-19.1 months) [16] and in LUX-Lung 6 (median PFS 11.0 months, ORR 67%) [8]. Afatinib was observed in patient subgroups, including those with CNS metastases, rare EGFR mutations, and the elderly (≥ 65 years). In patients with uncommon mutations, median PFS was 9.0 months (15.6 months when patients with T790M or exon 20 insertions were excluded). These data are in line with other studies. Preclinical data indicate that afatinib has a broad inhibitory profile against a wide range of EGFR mutations, including compound mutations [22]. Indeed, some categories of uncommon mutations, such as exon 18 mutations, appear to be more sensitive to second-generation EGFR TKIs than first-or thirdgeneration EGFR TKIs in vitro, suggesting that afatinib could be a preferred treatment option in this setting [23]. In a retrospective analysis of LUX-Lung 2, 3, and 6, median PFS with afatinib in patients with rare EGFR exon 18-21 mutations was 10.7 months [24]. Based on these data, afatinib's label was broadened to include tumors with uncommon activating EGFR mutations, including G719X, L861Q, and S768I. Activity of afatinib against these mutations has also been demonstrated in other 'real-world' Asian studies [16]. Osimertinib has also demonstrated activity against uncommon activating EGFR mutations in a single-arm phase II study [25]. Treatment options for exon 20 mutations remain an unmet need, but several agents are in clinical development such as poziotinib and mobocertinib which has shown promise in phase II trials [26,27].
Recent preclinical data indicate that the CNS penetration of different EGFR TKIs varies and the blood-brainbarrier is more permeable to osimertinib than first-and second-generation EGFR TKIs [28]. Accordingly, subanalysis of the phase III FLAURA trial demonstrated greater CNS activity with osimertinib than erlotinib or gefitinib [29]. Although no head-to-head data versus osimertinib are available, clinical studies have shown that afatinib is also active in patients with EGFR mutationpositive NSCLC and CNS metastases [16,30]. The current study also demonstrated encouraging activity of afatinib (median PFS 14.0 months, ORR 89%) in patients with CNS metastases (n = 27). Preclinical studies have demonstrated that afatinib can cross the blood brain barrier so that pharmacologically relevant concentrations reach brain lesions. Indeed, activity against CNS lesions has been demonstrated in patients [31,32]. Also, data indicate that afatinib may be able to protect against CNS progression. Competing risk analysis of LUX-Lung 3 and 6 showed that 24-month risk of de novo CNS progression was 5% and risk of non-CNS progression was 71% [31].
This study has a number of weaknesses. As it was a single-arm, exploratory study with a small sample size, data should be interpreted with caution. Also, mutational analysis of tumors at the point of acquired resistance was not mandated in this study and postprogression therapy was not documented. However, data from other studies indicate that the T790M resistance mutation emerges in around 50-70% of afatinib-treated tumors [33][34][35], with particularly high detection rates if sensitive plasma-based assays are used [36]. Given that osimertinib is highly active against T790M-positive tumors [37], a sequential regimen of afatinib followed by osimertinib could be considered in many patients with EGFR mutation-positive NSCLC, which may delay the requirement for chemotherapy. In a recent global observational study of 203 patients, this sequence conferred median OS of 41.3 months (90% CI 36.8-46.3 months) and median time to treatment failure of 28.1 months (90% CI 26.8-30.3 months) [38]. Further data are required regarding outcomes with afatinib, or dacomitinib, followed by osimertinib, both in clinical trial and realworld settings. In this regard, data from the ongoing phase 2 trials, Heat on Beat (afatinib versus osimertinib [39]), CAPLAND (NCT04811001; dacomitinib/osimertinib versus osimertinib/dacomitinib) and NCT03810807 (dacomitinib followed by osimertinib/chemotherapy versus osimertinib followed by dacomitinib/chemotherapy) are eagerly anticipated. Of note, a recent phase 2 trial of 12 patients indicated that dacomitinib has limited activity on patients who progress on first-line osimertinib (ORR: 17%; median PFS: 1.8 months) [40]. Ultimately, consideration of sequential EGFR TKI regimens will require routine testing for T790M at the point of acquired resistance. Recent real-world evidence in the USA suggests that T790M testing rates may be low (< 20%) in an everyday clinical practice setting [41], although this will vary from country to country. Testing rates may be improved in the future with implementation of liquid biopsy methodologies [42].
In conclusion, afatinib administered to Korean patients treated in routine clinical practice was well tolerated with no unexpected safety signals. TRAEs were detected early, usually within the first few weeks of treatment, predictable, and manageable. Active management of AEs facilitated the encouraging clinical activity of afatinib observed in this study. Afatinib was active in the overall cohort and in selected patient subgroups including those with uncommon EGFR mutations or asymptomatic brain metastases at baseline.
Additional file 1: Supporting methods. Table S1. EGFR mutations in the treated set. Table S2. Treatment-emergent adverse events.

Acknowledgments
We thank the patients, their families, the investigators, and staff who participated in the study. Medical writing support for the development of this manuscript, under the direction of the authors, was provided by Lynn Pritchard, of Ashfield MedComms, an Ashfield Health company, and funded by Boehringer Ingelheim.
Authors' contributions KP: Study concepts, study design, data acquisition, data analysis and interpretation, manuscript preparation, manuscript editing, and manuscript review. JSK: Data acquisition, manuscript editing, and manuscript review. JHK: Data acquisition, manuscript editing, and manuscript review. YCK: Data acquisition, manuscript editing, and manuscript review. HGK: Data acquisition, manuscript editing, and manuscript review. EKC: Data acquisition, manuscript editing, and manuscript review. JYJ: Data acquisition, manuscript editing, and manuscript review. MK: Study design, quality control of data and algorithms, data analysis and interpretation, statistical analysis, manuscript preparation, manuscript editing, and manuscript review. AM: Study design, quality control of data and algorithms, data analysis and interpretation, statistical analysis, manuscript preparation, manuscript editing, and manuscript review. JHK: Study concepts, data acquisition, manuscript editing, and manuscript review. The author(s) read and approved the final manuscript.

Funding
This work was supported by Boehringer Ingelheim.

Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. If necessary, documents will be redacted and deidentified to protect confidentiality of study participants and personnel. Further details are available at https://trials.boehringer-ingelheim.com/data_sharing/ sharing.html#accordion-1-2. Researchers should use https://vivli.org/ to request access to raw data from this study.

Declarations
Ethics approval and consent to participate At each center, ethical approval was given by an Institutional Review Board or and Independent Ethics Committee. All experimental protocols were approved by the Independent Ethics Committee of the Samsung Medical Centre, Seoul, South Korea on 16th August 2013. The study was performed in accordance with the Declaration of Helsinki, Good Clinical Practice, and local laws. Written informed consent was given by all patients.

Consent for publications
Not applicable.