Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2022 Aug 17;29(8):5833-5845.
doi: 10.3390/curroncol29080460.

Real-World Testing Practices, Treatment Patterns and Clinical Outcomes in Patients from Central Eastern Europe with EGFR-Mutated Advanced Non-Small Cell Lung Cancer: A Retrospective Chart Review Study (REFLECT)

Affiliations
Observational Study

Real-World Testing Practices, Treatment Patterns and Clinical Outcomes in Patients from Central Eastern Europe with EGFR-Mutated Advanced Non-Small Cell Lung Cancer: A Retrospective Chart Review Study (REFLECT)

Urška Janžič et al. Curr Oncol. .

Abstract

The targeted therapy with tyrosine kinase inhibitors (TKIs) against the epidermal growth factor receptor mutation (EGFRm) in advanced non-small cell lung cancer (NSCLC) changed the treatment paradigm. REFLECT study (NCT04031898) explored EGFR/T790M testing and treatment patterns in EGFRm NSCLC patients receiving first- or second-generation (1G/2G) EGFR TKIs as front-line (1L) in eight countries. Pooled data from Central Eastern Europe (CEE) countries from this study (Bulgaria, Poland, Romania, Slovenia) are presented here. This physician-led chart review study was conducted in patients with confirmed-EGFRm NSCLC initiating 1L 1G/2G EGFR TKIs between 2015-2018. The CEE cohort included 389 patients receiving 1L erlotinib (37%), afatinib (34%), and gefitinib (29%). Overall, 320 (82%) patients discontinued 1L, and 298 (77%) progression events were registered. Median progression free survival on 1L TKIs was 14.0 (95% CI: 12.6-15.6) months. Median overall survival from 1L start was 26.6 (95% CI: 24.1-29.0) months. Attrition rate between 1L and next line was 30%. Among patients with 1L progression, 200 (67%) were tested for T790M and 58% were positive. This first CEE analysis of treatments and outcomes in EGFRm NSCLC patients highlights the importance of using the most efficacious therapies currently available in 1L to reduce attrition and improve patient outcomes.

Keywords: EGFR T790M mutation; advanced non-small cell lung cancer; real-world retrospective study.

PubMed Disclaimer

Conflict of interest statement

U.J. declares honoraria (self) from AstraZeneca, Boehringer Ingelheim, MSD, Roche, Pfizer, and honoraria (institution) from AstraZeneca, Boehringer Ingelheim, MSD, Roche, Pfizer, Novartis, BMS; N.T. declares honoraria (self) from AstraZeneca, BMS, Boehringer Ingelheim, MSD, Pfizer, Roche, and honoraria (institution) from AstraZeneca, BMS, Boehringer Ingelheim, MSD, Novartis, Pfizer, Roche; M.D. declares honoraria for consultancy and speaking fee from Astellas, AstraZeneca, Aventis, Amgen, BMS, Eli Lilly, Janssen, MSD, Novartis, Pfizer, Roche, Sandoz, Servier; I.S.D. declares honoraria (self) from AstraZeneca, MSD, Roche, Pfizer; T.E.C. declares honoraria for advisory/consultancy from AD Pharma, Amgen, Astellas, AstraZeneca, Boehringer Ingelheim, Bristol-Myers Squibb, Eli Lilly, Janssen, Merck Serono, Merck Sharp & Dohme, Novartis, Pfizer, Roche, Sanofi, Servier; A.P. declares honoraria (self) from AstraZeneca, BMS, Boehringer Ingelheim, MSD, Roche; R.L. and G.T. are AstraZeneca employees and have been involved in the review of the manuscript and in the decision to publish the results.

Figures

Figure 1
Figure 1
Treatment distribution in EGFRm NSCLC patients across first-, second- and third-lines of therapy. Note: multiple therapies could have been selected in one patient. a targeted therapy besides afatinib, erlotinib or gefitinib. 1L, first line therapy; 2L, second line therapy; 3L, third line therapy; N, number of patients initiating each therapy line; n, number of patients receiving specific treatments; ChemoT, chemotherapy; EGFRm, epidermal growth factor receptor mutation; IO, immunotherapy; NSCLC, non-small cell lung cancer; TT, targeted therapy; -, not applicable at the time of our study.
Figure 2
Figure 2
Reasons to discontinue first-, second- and third-line of therapy and attrition rates. Notes: Due to rounding, percentages may not always be 100%. a Deceased patients on each specific line have been excluded from the count. 1L, first line therapy; 2L, second line therapy, 3L, third line therapy; N, number of patients initiating each therapy line.

References

    1. Gridelli C., Rossi A., Carbone D.P., Guarize J., Karachaliou N., Mok T., Petrella F., Spaggiari L., Rosell R. Non-small-cell lung cancer. Nat. Rev. Dis. Primers. 2015;1:15009. doi: 10.1038/nrdp.2015.9. - DOI - PubMed
    1. Bertuccio P., Alicandro G., Malvezzi M., Carioli G., Boffetta P., Levi F., La Vecchia C., Negri E. Cancer mortality in Europe in 2015 and an overview of trends since 1990. Ann. Oncol. 2019;30:1356–1369. doi: 10.1093/annonc/mdz179. - DOI - PubMed
    1. WHO GLOBOCAN 2021. [(accessed on 23 December 2021)]. Available online: https://gco.iarc.fr/today/data/factsheets/cancers/15-Lung-fact-sheet.pdf.
    1. Zhang Y.L., Yuan J.Q., Wang K.F., Fu X.H., Han X.R., Threapleton D., Yang Z.Y., Mao C., Tang J.L. The prevalence of EGFR mutation in patients with non-small cell lung cancer: A systematic review and meta-analysis. Oncotarget. 2016;7:78985–78993. doi: 10.18632/oncotarget.12587. - DOI - PMC - PubMed
    1. Szumera-Ciećkiewicz A., Olszewski W.T., Tysarowski A., Kowalski D.M., Głogowski M., Krzakowski M., Siedlecki J.A., Wągrodzki M., Prochorec-Sobieszek M. EGFR mutation testing on cytological and histological samples in non-small cell lung cancer: A Polish, single institution study and systematic review of European incidence. Int. J. Clin. Exp. Pathol. 2013;6:2800–2812. - PMC - PubMed

Publication types

MeSH terms

Associated data