NSCLC molecular testing in Central and Eastern European countries
- PMID: 29523116
- PMCID: PMC5845184
- DOI: 10.1186/s12885-018-4023-4
NSCLC molecular testing in Central and Eastern European countries
Abstract
Background: The introduction of targeted treatments for subsets of non-small cell lung cancer (NSCLC) has highlighted the importance of accurate molecular diagnosis to determine if an actionable genetic alteration is present. Few data are available for Central and Eastern Europe (CEE) on mutation rates, testing rates, and compliance with testing guidelines.
Methods: A questionnaire about molecular testing and NSCLC management was distributed to relevant specialists in nine CEE countries, and pathologists were asked to provide the results of EGFR and ALK testing over a 1-year period.
Results: A very high proportion of lung cancer cases are confirmed histologically/cytologically (75-100%), and molecular testing of NSCLC samples has been established in all evaluated CEE countries in 2014. Most countries follow national or international guidelines on which patients to test for EGFR mutations and ALK rearrangements. In most centers at that time, testing was undertaken on request of the clinician rather than on the preferred reflex basis. Immunohistochemistry, followed by fluorescent in situ hybridization confirmation of positive cases, has been widely adopted for ALK testing in the region. Limited reimbursement is a significant barrier to molecular testing in the region and a disincentive to reflex testing. Multidisciplinary tumor boards are established in most of the countries and centers, with 75-100% of cases being discussed at a multidisciplinary tumor board at specialized centers.
Conclusions: Molecular testing is established throughout the CEE region, but improved and unbiased reimbursement remains a major challenge for the future. Increasing the number of patients reviewed by multidisciplinary boards outside of major centers and access to targeted therapy based on the result of molecular testing are other major challenges.
Keywords: ALK rearrangements; Central eastern European region; EGFR mutations; Molecular testing; Non-small cell lung cancer.
Conflict of interest statement
Ethics approval and consent to participate
Ethics Committee approval was not needed as the data are purely descriptive and epidemiological. Tables 3 and 5 include retrospective data on the results of prior routine diagnostic molecular testing; no patient level data are included and no additional procedures, tests or samples were required. All respondents were clearly informed that the information collected was to form the basis for a manuscript describing molecular testing for NSCLC in the CEE region.
Consent for publication
Not applicable.
Competing interests
AR reports receiving grants and personal fees from AstraZeneca and MSD, honoraria for advisory board participation AstraZeneca, MSD, Novartis, Boehringer Ingelheim and personal fees and honoraria for advisory board participation and lectures from BMS, outside the submitted work. PB reports receiving honoraria from AstraZeneca, Boehringer Ingelheim, Pfizer, MSD, and Roche, and has participated at advisory boards for Boehringer Ingelheim, Pfizer, and MSD. LB reports receiving personal fees from Roche, AstraZeneca, Pfizer, Boehringer Ingelheim, outside the submitted work. TC reports receiving consulting fees from Pfizer, Boehringer Ingelheim, BMS outside the submitted work. RD reports personal fees from Pfizer, Roche, AstraZeneca, Boehringer Ingelheim, Novartis, outside the submitted work. MG reports receiving consulting fees from Pfizer, Boehringer Ingelheim, BMS, MSD. IK reports receiving personal fees from Pfizer (participation in 2015 advisory board preparing the manuscript) related to the work under consideration. WO reports receiving honoraria or consulting fees from MSD, Boehringer Ingelheim, Pfizer and Abbott outside the submitted work. OB reports receiving consulting fees from Pfizer, Boehringer Ingelheim, BMS and MSD outside the submitted work. LP reports receiving grants from Slovak Research and Development Agency, Pfizer Slovakia, Ministry of Health Slovakia related to the work under consideration and grants from Novartis Slovakia, Takeda Slovakia, and AstraZeneca Slovakia outside the submitted work. JT reports receiving personal fees from BMS, Lilly, Pfizer, Roche, and Boehringer Ingelheim outside the submitted work. All authors report receiving financial support from Pfizer and non-financial support from SuccinctChoice Medical Communications (funded by Pfizer) related to the work under consideration.
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