TY - JOUR
T1 - Development of a semi-conductor sequencing-based panel for genotyping of colon and lung cancer by the Onconetwork consortium
AU - Tops, Bastiaan B.J.
AU - Normanno, Nicola
AU - Kurth, Henriette
AU - Amato, Eliana
AU - Mafficini, Andrea
AU - Rieber, Nora
AU - Le Corre, Delphine
AU - Rachiglio, Maria M.
AU - Reiman, Anne
AU - Sheils, Orla
AU - Noppen, Christoph
AU - Lacroix, Ludovic
AU - Cree, Ian A.
AU - Scarpa, Aldo
AU - Ligtenberg, Marjolijn J.L.
AU - Laurent-Puig, Pierre
N1 - Publisher Copyright:
© 2015 Tops et al.
PY - 2015/1/31
Y1 - 2015/1/31
N2 - Background: The number of predictive biomarkers that will be necessary to assess in clinical practice will increase with the availability of drugs that target specific molecular alterations. Therefore, diagnostic laboratories are confronted with new challenges: costs, turn-around-time and the amount of material required for testing will increase with the number of tests performed on a sample. Our consortium of European clinical research laboratories set out to test if semi-conductor sequencing provides a solution for these challenges. Methods: We designed a multiplex PCR targeting 87 hotspot regions in 22 genes that are of clinical interest for lung and/ or colorectal cancer. The gene-panel was tested by 7 different labs in their own clinical setting using ion-semiconductor sequencing. Results: We analyzed 155 samples containing 112 previously identified mutations in the KRAS, EGFR en BRAF genes. Only 1 sample failed analysis due to poor quality of the DNA. All other samples were correctly genotyped for the known mutations, even as low as 2%, but also revealed other mutations. Optimization of the primers used in the multiplex PCR resulted in a uniform coverage distribution over the amplicons that allows for efficient pooling of samples in a sequencing run. Conclusions: We show that a semi-conductor based sequencing approach to stratify colon and lung cancer patients is feasible in a clinical setting.
AB - Background: The number of predictive biomarkers that will be necessary to assess in clinical practice will increase with the availability of drugs that target specific molecular alterations. Therefore, diagnostic laboratories are confronted with new challenges: costs, turn-around-time and the amount of material required for testing will increase with the number of tests performed on a sample. Our consortium of European clinical research laboratories set out to test if semi-conductor sequencing provides a solution for these challenges. Methods: We designed a multiplex PCR targeting 87 hotspot regions in 22 genes that are of clinical interest for lung and/ or colorectal cancer. The gene-panel was tested by 7 different labs in their own clinical setting using ion-semiconductor sequencing. Results: We analyzed 155 samples containing 112 previously identified mutations in the KRAS, EGFR en BRAF genes. Only 1 sample failed analysis due to poor quality of the DNA. All other samples were correctly genotyped for the known mutations, even as low as 2%, but also revealed other mutations. Optimization of the primers used in the multiplex PCR resulted in a uniform coverage distribution over the amplicons that allows for efficient pooling of samples in a sequencing run. Conclusions: We show that a semi-conductor based sequencing approach to stratify colon and lung cancer patients is feasible in a clinical setting.
KW - Colorectal cancer
KW - Ion torrent
KW - Multiplex PCR
KW - Next-generation sequencing
KW - Non-small cell lung cancer
KW - Semi-conductor sequencing
UR - http://www.scopus.com/inward/record.url?scp=84924139134&partnerID=8YFLogxK
U2 - 10.1186/s12885-015-1015-5
DO - 10.1186/s12885-015-1015-5
M3 - Article
C2 - 25637035
AN - SCOPUS:84924139134
SN - 1471-2407
VL - 15
JO - BMC Cancer
JF - BMC Cancer
IS - 1
M1 - 26
ER -