TY - JOUR
T1 - Lung cancer biomarker testing: Perspective from Europe
AU - Thunnissen, Erik
AU - Weynand, Birgit
AU - Udovicic-Gagula, Dalma
AU - Brcic, Luka
AU - Szolkowska, Malgorzata
AU - Hofman, Paul
AU - Smojver-Ježek, Silvana
AU - Anttila, Sisko
AU - Calabrese, Fiorella
AU - Kern, Izidor
AU - Skov, Birgit
AU - Perner, Sven
AU - Dale, Vibeke G.
AU - Eri, Zivka
AU - Haragan, Alex
AU - Leonte, Diana
AU - Carvallo, Lina
AU - Prince, Spasenja Savic
AU - Nicholson, Siobhan
AU - Sansano, Irene
AU - Ryska, Ales
PY - 2020/6/1
Y1 - 2020/6/1
N2 - A questionnaire on biomarker testing previously used in central European countries was extended and distributed in Western and Central European countries to the pathologists participating at the Pulmonary Pathology Society meeting 26–28 June 2019 in Dubrovnik, Croatia. Each country was represented by one responder. For recent biomarkers the availability and reimbursement of diagnoses of molecular alterations in non-small cell lung carcinoma varies widely between different, also western European, countries. Reimbursement of such assessments varies widely between unavailability and payments by the health care system or even pharmaceutical companies. The support for testing from alternative sources, such as the pharmaceutical industry, is no doubt partly compensating for the lack of public health system support, but it is not a viable or long‐term solution. Ideally, a structured access to testing and reimbursement should be the aim in order to provide patients with appropriate therapeutic options. As biomarker enabled therapies deliver a 50% better probability of outcome success, improved and unbiased reimbursement remains a major challenge for the future.
AB - A questionnaire on biomarker testing previously used in central European countries was extended and distributed in Western and Central European countries to the pathologists participating at the Pulmonary Pathology Society meeting 26–28 June 2019 in Dubrovnik, Croatia. Each country was represented by one responder. For recent biomarkers the availability and reimbursement of diagnoses of molecular alterations in non-small cell lung carcinoma varies widely between different, also western European, countries. Reimbursement of such assessments varies widely between unavailability and payments by the health care system or even pharmaceutical companies. The support for testing from alternative sources, such as the pharmaceutical industry, is no doubt partly compensating for the lack of public health system support, but it is not a viable or long‐term solution. Ideally, a structured access to testing and reimbursement should be the aim in order to provide patients with appropriate therapeutic options. As biomarker enabled therapies deliver a 50% better probability of outcome success, improved and unbiased reimbursement remains a major challenge for the future.
UR - http://www.scopus.com/inward/record.url?scp=85090191489&partnerID=8YFLogxK
U2 - 10.21037/tlcr.2020.04.07
DO - 10.21037/tlcr.2020.04.07
M3 - Scientific review articles
AN - SCOPUS:85090191489
SN - 2218-6751
VL - 9
SP - 887
EP - 897
JO - Translational Lung Cancer Research
JF - Translational Lung Cancer Research
IS - 3
ER -