Treatment Patterns in Patients with Locally Advanced or Metastatic Non-Small-Cell Lung Cancer Treated with Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitors: Analysis of US Insurance Claims Databases.

BACKGROUND: Most patients with epidermal growth factor receptor mutation-positive (EGFRm) non-small-cell lung cancer (NSCLC) acquire resistance to first-line (1L) first- or second-generation (1G/2G) EGFR-TKIs; therefore, it is important to optimize 1L treatment to improve patient outcomes.
OBJECTIVE: To retrospectively examine treatment patterns in locally advanced/metastatic NSCLC using MarketScan® Commercial and Medicare Supplemental Databases (all US census regions). PATIENTS AND METHODS: Adults with a lung cancer diagnosis code between 1 January 2015-31 March 2018 were analyzed from diagnosis (index) through a variable-length follow-up. Patients had ≥ 1 pharmacy claim for 1G/2G EGFR-TKIs on or within 60 days post-index. Data were stratified by presence or absence of central nervous system (CNS) metastases (30 days pre-index through study end).
RESULTS: 578 patients were included (median age 63 years, 64% female). Median follow-up was 13.5 months. The most frequently prescribed 1L EGFR-TKI was erlotinib (414/578, 72%). Median time to 1L treatment discontinuation was 8.2 (95% confidence interval (CI) 6.9, 9.0) months in patients diagnosed with CNS metastases at any time, and 7.7 (95% CI 6.9, 8.9) months in patients without CNS metastases. 270/578 patients (47%) discontinued 1L EGFR-TKIs; 209/270 (77%) initiated second-line (2L) therapy, most frequently osimertinib (96/209, 46%).
CONCLUSIONS: In an analysis of US claims data, nearly half of patients discontinued 1L EGFR-TKIs, and 46% who initiated 2L received osimertinib. As nearly a quarter of patients who discontinued 1L EGFR-TKIs did not receive 2L treatment, this study highlights the need for optimal 1L treatment in EGFRm locally advanced/metastatic NSCLC.

Key Points

Introduction

Non-small-cell lung cancer (NSCLC) accounts for approximately 80–90% of all lung cancers [1]. Epidermal growth factor receptor (EGFR) mutations are observed in approximately 10–20% and 30–50% of patients with NSCLC in non-Asian and Asian populations, respectively [2, 3].

Central nervous system (CNS) metastases are observed frequently in patients with NSCLC, and are associated with a poor prognosis and high economic burden [4, 5]. Moreover, CNS metastases have been found to be more common in patients with EGFR mutation-positive (EGFRm) NSCLC, developing in approximately 70% of patients, compared with 38% among patients with negative EGFR mutation status [6].

EGFR-tyrosine kinase inhibitors (EGFR-TKIs) are the recommended first-line (1L) treatment in patients with EGFRm advanced/metastatic NSCLC [1, 7]. Despite initial responses, most patients treated in the 1L with a first- or second-generation (1G/2G) EGFR-TKI develop resistance after a median period of 8–16 months [8, 9], with the EGFR T790M resistance mutation observed in approximately 50% of patients [10].

Osimertinib, a third-generation, irreversible, EGFR-TKI, potently and selectively inhibits both EGFR-TKI-sensitizing and T790M resistance mutations and has demonstrated efficacy in NSCLC CNS metastases [11-15]. Osimertinib initially received US Food and Drug Administration (FDA) accelerated approval in November 2015 for patients with T790M mutation-positive NSCLC and disease progression on or after EGFR-TKI treatment, and was granted full approval in this setting in March 2017 based on the confirmatory phase III AURA3 study [12]. Based on the phase III FLAURA study, osimertinib was approved as 1L treatment in patients with EGFRm (Ex19del or L858R) metastatic NSCLC in April 2018 (median progression-free survival (PFS) 18.9 months with osimertinib vs. 10.2 months with comparator EGFR-TKI; hazard ratio (HR) 0.46; median overall survival (OS) 38.6 months with osimertinib vs. 31.8 months with comparator EGFR-TKI; HR 0.80) [13, 16]. Given the evolving therapeutic landscape for EGFRm NSCLC, there remains a need to define an optimal treatment strategy. Real-world data can support this through an improved understanding of current treatment patterns and associated outcomes.

To date, several observational studies have reported on sequencing and treatment patterns in patients with EGFRm NSCLC. For example, the retrospective GioTag study (NCT03370770) investigated outcomes in patients with EGFRm NSCLC receiving sequential afatinib and osimertinib in a real-world clinical practice setting. This study found sequencing with afatinib followed by osimertinib was associated with clinical benefit among patients with T790M-acquired resistance, with a median time on treatment of 27.6 months [17]. Per the inclusion criteria, all patients in the GioTag study received 1L afatinib, and second-line (2L) osimertinib after T790M testing [17, 18]. However, it was subsequently reported that at least 30–40% of patients who received 1L afatinib were ineligible for 2L osimertinib, as in many cases progression was due to T790M-independent mechanisms [18].

As some patients died during or after 1L treatment, they did not have the opportunity to initiate 2L treatment; exclusion of patients who died on 1L afatinib potentially introduced immortal time bias in the GioTag study [17].

Real-world studies have also reported that many patients with EGFRm NSCLC treated with 1L 1G/2G EGFR-TKI may not receive subsequent therapy after disease progression and many will die; as such, there is a highly variable proportion of patients in the real-world setting who receive 2L osimertinib following 1L EGFR-TKI [19-23]. Despite reimbursement, many patients may not be treated with osimertinib after they are tested for T790M, and some are not tested at all [20, 21, 23].

Therefore, there remains a need to further understand sequencing and treatment patterns in EGFRm NSCLC following 1G/2G EGFR-TKIs in a real-world setting. Furthermore, the impact of CNS metastases on treatment patterns is poorly characterized.

Through an analysis of US insurance claims data from the MarketScan® Commercial and Medicare Supplemental Databases, this study examined treatment patterns in patients with locally advanced/metastatic NSCLC receiving 1L 1G/2G EGFR-TKIs between 1 January 2015 and 30 September 2018. The influence of CNS metastases was also assessed.

Patients and Methods

Study Design

This was a retrospective observational cohort study analyzing patients newly diagnosed with locally advanced/metastatic NSCLC treated with 1L 1G/2G EGFR-TKIs. Given receipt of EGFR-TKIs approved for EGFRm NSCLC, it was presumed that these patients had EGFRm NSCLC. This presumption was made because EGFRm status, including T790M, is not available in US insurance claims databases.

Administrative claims data were extracted from the MarketScan® Commercial and Medicare Supplemental Databases, which contain data for individuals from all US census regions. These databases record inpatient (requiring overnight hospitalization) and outpatient medical claims, and outpatient pharmacy claims of patients with employer-sponsored primary health insurance or Medicare Supplemental insurance (paid for by an employer). All database records were de-identified and compliant with US patient confidentiality requirements.

The study period was 1 October 2014–30 September 2018. The follow-up period was variable in length from the date of first lung cancer diagnosis (index date) to the earliest of the following: inpatient death, end of continuous enrollment in a healthcare plan (i.e., the end of data availability) or the end of the study period, whichever occurred first.

Patients

Eligible patients (≥ 18 years old) were identified as having at least two non-diagnostic claims (i.e., claims for a professional encounter and not simply a laboratory test or imaging claim used to rule out a condition) with an International Classification of Diseases 9th or 10th edition (ICD-9-CM, ICD-10-CM; Online Supplementary Material Table 1) diagnosis code for lung cancer (within 90 days of each other) between 1 January 2015 and 31 March 2018. Patients were required to have at least one claim for receipt of a 1G/2G EGFR-TKI (erlotinib, gefitinib, or afatinib), on or within 60 days after index date, in addition to at least 3 months of continuous enrollment prior to index date. Patients were excluded if they had a claim with a diagnosis of lung cancer or claim for an EGFR-TKI (erlotinib, gefitinib, afatinib, or osimertinib) within the 3 months prior to index date (to ensure inclusion of newly diagnosed patients), or prior treatment with chemotherapy regimens commonly used in small-cell lung cancer (e.g., cisplatin and etoposide; cisplatin and irinotecan; carboplatin and etoposide; topotecan; and/or cyclophosphamide, doxorubicin, and vincristine) [24] on or within 60 days after index date.

Patients meeting the eligibility criteria were categorized into two mutually exclusive cohorts: the CNS metastases cohort and the no CNS metastases cohort. The presence of CNS metastases was defined as at least one non-diagnostic medical claim with a diagnosis code for secondary malignant neoplasm of the brain or spinal cord, between 30 days before index date until the end of the study period.

Objectives and Outcome Measures

The primary objective was to describe treatment, attrition, and sequencing patterns in patients newly diagnosed with locally advanced/metastatic NSCLC treated with 1L 1G/2G EGFR-TKIs. A key exploratory objective was to compare treatment and sequencing patterns among patients with or without CNS metastases.

Patient demographics were captured at index date, and clinical characteristics were obtained during the 3 months prior to index date.

Treatment patterns were assessed during the variable-length follow-up period, beginning at index date. Planned treatment pattern measures included: selection and timing of 1L EGFR-TKI initiation (1L therapies erlotinib, gefitinib, afatinib, prescribed as the index-TKI); use of 1L add-on therapies (treatments used in addition to 1L/index-TKI, initiated within 30 days of treatment initiation, i.e., bevacizumab, carboplatin, pemetrexed, or other chemotherapy); proportion of inpatient death after each line of therapy; proportion of patients with progression after each line of therapy; subsequent treatments received (2L therapies were medication types prescribed after 1L progression, i.e., non-index-TKI, chemotherapy, immune-oncology therapy, other medication; later line therapies were ≥ third-line (3L) medication types prescribed after ≥ 2L discontinuation); and time to discontinuation of treatments.

Time to discontinuation of treatment was measured from treatment initiation to the last day’s supply of treatment before a treatment gap (defined as 60 days). If a patient died prior to a full 60-day treatment gap, or while still on treatment, their time to discontinuation was calculated as the time until inpatient death. However, if a patient had a 60-day treatment gap and died after this, their reason for ending a treatment line was recorded as discontinuation of treatment rather than inpatient death. Patients still on therapy at the end of the follow-up period were censored in the analysis. Due to the nature of the data source, patients could disenroll from their healthcare plan. Disenrollment in the healthcare plan was considered informative to the outcome in this scenario (discontinuation of treatment). As such, in order to avoid biased estimates of treatment duration, disenrollment was considered as a discontinuation event in the analysis. In addition, a sensitivity analysis was carried out to measure discontinuation of treatment based on a treatment gap of at least 90 days after last recorded dose of treatment.

Statistical Analysis

Descriptive analyses of demographic and treatment pattern data were conducted. Data were stratified by CNS metastases status; statistical comparisons between cohorts were evaluated using Chi-squared tests for categorical variables and t tests for continuous variables, with significance reported as nominal p values. p values are provided to help interpretation of data, not to make cross-cohort comparisons. Time to event endpoints were described using the Kaplan–Meier method.

Results

A total of 578 patients identified from the databases met the eligibility criteria for study inclusion (Fig. 1). Of these, 275 patients (48%) had CNS metastases recorded at any time during the study period and 303 (52%) had no CNS metastases recorded between 30 days before index date through the end of study.

Fig. 1

Summary of patient selection. CNS central nervous system, EGFR-TKI epidermal growth factor receptor-tyrosine kinase inhibitor, SCLC small cell lung cancer, SSA US Social Security Administration

Overall, the majority of patients included were female (64%) and more were identified from the MarketScan® Commercial Database than the Medicare Supplemental Database (60% vs. 40%). Median age was 63 years (range 33–94) at index date. Patient demographics and clinical characteristics were generally similar across the CNS metastases and no CNS metastases cohorts (Table 1), with the exception that patients in the CNS metastases cohort had a median age of 61 years (range 33–91), versus no CNS metastases with a median age of 66 years (33–94). The majority of patients (74%) had an index date before 2017 (i.e., 2015 or 2016). A similar proportion of patients had pre-2017 index dates in the CNS metastases cohort (71%) as in the no CNS metastases cohort (77%).

Table 1

Patient characteristics

	All patients (N = 578)	CNS metastases status cohorts
		CNS metastases (n = 275)	No CNS metastases (n = 303)
Sex: male/female, n (%)	208 (36)/370 (64)	94 (34)/181 (66)	114 (38)/189 (62)
Age: median (range), years	63 (33–94)	61 (33–91)	66 (33–94)
Payer: commercial/Medicare, n (%)	347 (60)/231 (40)	204 (74)/71 (26)	143 (47)/160 (53)
Geographic region, n (%)
Northeast	131 (23)	70 (25)	61 (20)
North Central	126 (22)	55 (20)	71 (23)
South	203 (35)	101 (37)	102 (34)
West	116 (20)	49 (18)	67 (22)
Unknown	2 ( < 1)	0	2 ( < 1)
Index year, n (%)
2015	230 (40)	104 (38)	126 (42)
2016	196 (34)	90 (33)	106 (35)
2017	138 (24)	73 (27)	65 (21)
2018	14 (2)	8 (3)	6 (2)
Charlson Comorbidity Index, mean (SD)	2.8 (3.4)	3.2 (3.7)	2.3 (3.0)
NCI-adapted Charlson Comorbidity Index, mean (SD)	0.5 (1.0)	0.5 (0.9)	0.6 (1.1)
NSCLC-related symptoms, n (%)a
Cough	169 (29)	68 (25)	101 (33)
Shortness of breath	90 (16)	33 (12)	57 (19)
Headaches	38 (7)	29 (11)	9 (3)
Fatigue	37 (6)	20 (7)	17 (6)
Stroke/transient ischemic attack	24 (4)	9 (3)	15 (5)
Depression	24 (4)	14 (5)	10 (3)
Anxiety	21 (4)	15 (5)	6 (2)

Demographic characteristics were collected on the index date

Clinical characteristics were collected during the 3-month pre-index period

CNS central nervous system, NCI National Cancer Institute, NSCLC non-small-cell lung cancer, SD standard deviation

a≥ 5% in either patient cohort

Treatment Patterns

The median duration of follow-up from the index date was 13.5 months. Treatment patterns, measured from the time of treatment initiation to the end of follow-up, are summarized in Fig. 2.

Fig. 2

Summary of treatment patterns. Treatment patterns were assessed during the variable-length follow-up period. EGFR mutation status was inferred from receipt of EGFR-TKIs; data on EGFR T790M mutation status were not collected. CNS central nervous system, EGFR-TKI epidermal growth factor receptor-tyrosine kinase inhibitor, NSCLC non-small-cell lung cancer. *Deaths detected from claims of inpatient death. †Between discontinuation date and end of patient follow-up. ‡Targeted therapy cancer medications

First-Line Therapy

Among the 578 eligible patients, the most frequently prescribed 1L EGFR-TKI was erlotinib (72%; n = 414), followed by afatinib (26%; n = 148) and gefitinib (3%; n = 16). The proportions of patients receiving erlotinib, afatinib, and gefitinib were similar for the CNS metastases cohort (n = 275) (69%, 28%, and 3%, respectively) and no CNS metastases cohort (n = 303) (74%, 23%, and 3%, respectively).

Thirty-five of the 578 patients (6%) received an add-on therapy concurrently with 1L EGFR-TKIs; the most common were bevacizumab (3%; n = 17) and carboplatin (2%; n = 12).

In total, 47% of patients (n = 270/578) discontinued 1L EGFR-TKI treatment. The outcomes for the 53% of patients (n = 308/578) who were not recorded as discontinuing 1L treatment, including 213 patients who ended continuous enrollment in their healthcare plan, are summarized in Fig. 2. The median time to discontinuation of 1L treatment was 8.2 (95% confidence interval (CI) 6.9, 9.0) months in the CNS metastases cohort and 7.7 (95% CI 6.9, 8.9) months in the no CNS metastases cohort (Fig. 3). A sensitivity analysis with discontinuation of treatment based on a treatment gap of at least 90 days after last recorded dose of treatment did not change these results: median time to 1L treatment discontinuation was 7.9 months in the CNS metastases cohort and 7.7 months in the no CNS metastases cohort. A greater proportion of patients in the CNS metastases cohort discontinued 1L treatment (54%; n = 149/275) versus the no CNS metastases cohort (40%; n = 121/303; nominal p < 0.001).

Fig. 3

Median time to treatment discontinuation by months for patients with and without CNS metastases at any time during the study period (p = 0.0016). CNS central nervous system

Second-Line Therapy

Of the 270 patients who discontinued 1L EGFR-TKI treatment, 77% (n = 209/270) initiated 2L therapy. Twenty-three percent of patients (n = 61/270) had no claims for subsequent anti-cancer therapies between discontinuation date and end of follow-up. A significantly greater proportion of patients in the CNS metastases cohort (45%; n = 124/275) initiated 2L therapy than in the no CNS metastases cohort (28%; n = 85/303; p < 0.001).

Of the 209 patients who initiated 2L therapy, the most frequently received therapy was osimertinib (46%; n = 96/209). As a proportion of all patients receiving 1L EGFR-TKIs, 17% (n = 96/578) received 2L osimertinib. A higher proportion of patients who received 2L therapy in the CNS metastases cohort received osimertinib (52%; n = 64/124) versus the no CNS metastases cohort (38%; n = 32/85; p = 0.047).

In total, 40% of patients (n = 84/209) discontinued 2L therapy, and the outcomes for the 60% of patients (n = 125/209) who were not recorded as discontinuing their 2L therapy are summarized in Fig. 2.

Later Lines of Therapy

Of the 84 patients who discontinued 2L therapy, 74% (n = 62/84) initiated 3L. Twenty-six percent of patients (n = 22/84) had no claims for subsequent anti-cancer therapies between discontinuation date and end of follow-up. A higher proportion of patients in the CNS metastases cohort initiated 3L therapy (14%; n = 38/275) than in the no CNS metastases cohort (8%; n = 24/303; p = 0.022). Of the full study population, 3% of patients (n = 15/578) were recorded as receiving fourth-line therapy (Fig. 2).

Discussion

This retrospective insurance claims-based analysis provided real-world data on treatment patterns for patients with NSCLC who received 1L 1G/2G EGFR-TKIs. Almost half (47%) of patients discontinued 1L 1G/2G EGFR-TKI treatment and, of the patients who discontinued 1L, 23% did not initiate 2L therapy. In line with our findings, previous observational studies investigating treatment patterns in patients with EGFRm NSCLC reported that 25–30% of patients progressing on 1G/2G EGFR-TKIs do not receive 2L therapy [19-23]. Overall, the proportion of patients receiving subsequent therapy following 1L EGFR-TKIs in the real-world setting is sub-optimal [19-23]. Furthermore, a clinically relevant proportion (15–30%) of patients die prior to receiving 2L [20, 21, 23]. Given that approximately 50% of patients receiving 1G/2G EGFR-TKIs acquire the T790M resistance mutation, there is a biologically driven limit to the number of patients eligible to receive osimertinib as 2L treatment [10, 25]. Selection of 1L treatments that optimize outcomes for patients with EGFRm NSCLC is therefore a crucial consideration.

In this study, most patients (74%) initiated 1L EGFR-TKI treatment prior to 2017, when osimertinib was only indicated for T790M mutation-positive NSCLC with progression on or after 1L EGFR-TKI treatment. Osimertinib is now approved, and recommended by current guidelines, as a 1L treatment for patients with treatment-naive EGFRm (Ex19del or L858R) metastatic NSCLC, based on the FLAURA study [13, 16], but without data for patients receiving 1L osimertinib in the present study we are unable to draw conclusions on its real-world benefits. Future studies assessing the real-world effectiveness of 1L osimertinib versus 1L 1G/2G EGFR-TKIs could help to maximize outcomes for patients with EGFRm NSCLC.

The proportion of patients with CNS metastases reported here (48%) was higher than expected, but this does include patients with a diagnosis of CNS metastases at any time during the study period; timing of treatments received relative to the development of CNS metastases is not possible in this database. In a previous retrospective study, CNS metastases were reported in up to 39% of patients with EGFRm NSCLC [26]. However, the sample included 121 patients with EGFRm NSCLC from a Canadian population-based cancer registry where there may have been under-reporting of CNS metastases. Often, registry data can be incomplete as patients are not as rigorously followed as they would be during a clinical study. Therefore, there can be patients who do not present with CNS metastases at diagnosis but develop metastases during the course of their disease, which would not be captured in their records. We also observed that a greater proportion of patients with CNS metastases initiated 2L therapy during the study period than those with no CNS metastases, particularly with osimertinib, although it is not known if a patient initiated 2L therapy before or after CNS metastases diagnosis. Osimertinib has been shown to achieve significant exposure in the brain compared with other EGFR-TKIs [27-29]. In a pooled analysis of patients who had progressed following treatment with prior EGFR-TKI therapy and who received osimertinib 80 mg once daily, confirmed CNS objective response rate and disease control rate were 54% and 92%, respectively, demonstrating the clinically meaningful efficacy of osimertinib against CNS metastases in this setting [29]. Osimertinib has also demonstrated efficacy in patients with CNS metastases in the 1L setting, including a 52% reduction in the risk of CNS progression compared with gefitinib or erlotinib [13, 15].

A strength of this study was the ability to examine real-world treatment patterns among a relatively large population with advanced/metastatic NSCLC. Through utilizing the MarketScan® Commercial and Medicare Supplemental Databases, this study offered a greater diversity of patients than a claims database from a single health plan or employer. Specifically, use of the MarketScan® Commercial Database meant that a full continuum of care in all inpatient and outpatient settings, as well as retail and specialty pharmacies, was covered. The MarketScan® Commercial and Medicare Supplemental Databases also provide accurate dates of treatment initiation for first and subsequent lines of treatment enabling an accurate examination of the treatment patterns in this patient population.

Despite the advantages of claims-based analyses, several limitations should be noted. In theory, US insurance databases, such as the MarketScan® Commercial and Medicare Supplemental Databases, should provide complete claims histories for patients receiving EGFR-TKIs as they move through the US healthcare system. However, the nature of this analysis and the databases used meant that many patients were lost to follow-up due to end of continuous enrollment in their healthcare plans, and we did not have a complete claims history for all patients. This restricted the duration of time with data available on treatment patterns and sequencing and may have resulted in an underestimation of the proportion of patients initiating 2L and subsequent therapy lines during the study. Nevertheless, this highlights the realities experienced by some US patients in clinical practice, for whom loss or disruption of insurance coverage can affect access to care [30-32]. Administrative claims are designed to track healthcare services rendered by providers for administrative purposes associated with reimbursement, rather than for research. Therefore, the presence of diagnoses or medication claims is not definitive evidence of such events and there may be some patient misclassification; in some cases, medications that may have provided further indications of diagnoses might not have been recorded, such as treatments for CNS metastases. Additionally, patients included in this study were limited to those with commercial health coverage and private Medicare supplemental coverage as employees, meaning results may not be generalizable to patients with other insurance or those without health-insurance coverage. As the study was limited to US patients, it should be noted that treatment patterns in other countries may differ from those reported here due to differences in patient populations, healthcare systems, and treatment guidelines. Demographic data such as race and ethnicity, which may have affected treatment patterns, were also unavailable.

A further limitation lies in the information captured in insurance claims ICD-9-CM and ICD-10-CM codes. The identification of patients with NSCLC relied on a proximate method due to a lack of NSCLC-specific diagnosis codes in the databases, so misclassification of patients was a possibility. As the date of CNS metastasis was also captured via the insurance claims within a window post-index, these dates may not have been as accurate as from a database that uses health records with specific diagnosis dates, potentially affecting the association between CNS metastases and discontinuation; further analyses using more accurate dates of CNS metastases diagnosis will be needed in order to draw firm conclusions. In addition, all but one patients’ CNS metastases were diagnosed post-index. Similarly, EGFRm status is unavailable in insurance claims codes. The study dates were selected in order to understand real-world 2L treatment patterns, including osimertinib use, but it was not possible to assess the prevalence of T790M resistance. EGFRm status was therefore inferred from the receipt of EGFR-TKIs. However, it is possible that some patients receiving EGFR-TKIs may have had negative EGFR mutation status and would not have benefited from targeted treatments. In addition, assumptions were made on when patients stopped treatment, as discontinuation dates were not known, meaning that time to treatment discontinuation reported here may be underestimated. The limitations of claims-based analyses may be reflective of real-world challenges in clinical practice, such as treatment decision-making for patients with unavailable T790M mutation status. A final limitation of the study is that afatinib is also used to treat metastatic squamous cell carcinoma in the USA [33], but the role of EGFRm in this histological subtype of NSCLC is debated [34]. Without histology data available in this study, it is possible that some patients who received 1L afatinib had squamous histology instead of adenocarcinoma (the latter is well linked to EGFR mutations) [34], creating potential outliers to the population presumed to have EGFRm NSCLC.

Conclusion

This retrospective real-world analysis of patients identified through US insurance claims databases showed that 270 of 578 patients with NSCLC discontinued 1L 1G/2G EGFR-TKIs. Median time to 1L treatment discontinuation was 8.2 months in patients diagnosed with CNS metastases and 7.7 months in patients without CNS metastases. Patients with CNS metastases had different treatment patterns, with a greater percentage initiating 2L therapy with osimertinib. These results highlight the importance of choosing optimal 1L EGFR-TKI treatment for EGFRm NSCLC, given that not all patients who discontinued 1L 1G/2G EGFR-TKIs initiated 2L therapy.

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 15 kb)

Median time to first-line treatment discontinuation was 8.2 months in patients with CNS metastases and 7.7 months in patients without CNS metastases.

209 of the 270 patients who discontinued first-line treatment initiated second-line NSCLC therapy and of those, 46% initiated osimertinib at second line.