TY - JOUR
T1 - Temporal trends and regional variability in BRAF and KRAS genetic testing in Denmark (2010–2022)
T2 - Implications for precision medicine
AU - Frost, Matilde Grupe
AU - Jensen, Kristoffer Jarlov
AU - Jimenez-Solem, Espen
AU - Qvortrup, Camilla
AU - Kuhlmann, Tine Plato
AU - Andersen, Jon Lykkegaard
AU - Høgdall, Estrid
AU - Petersen, Tonny Studsgaard
N1 - Correction: https://doi.org/10.1002/gcc.70020
Funding Information:
Phase4CPH (to which M. G. F. and K. J. J. are affiliated) has received financial support from Amgen Inc. for a previous study on KRAS mutations and survival in Danish lung cancer patients. Amgen, or its employees, did were not involved in the present study. The authors declare that they have no further conflicts of interest.
Publisher Copyright:
© 2024 The Authors. Genes, Chromosomes and Cancer published by Wiley Periodicals LLC.
PY - 2024
Y1 - 2024
N2 - Objective: This study aims to evaluate the developments in the testing of Kirsten Rat Sarcoma viral oncogene homolog (KRAS) and v-Raf murine sarcoma viral oncogene homolog B1 (BRAF) mutations across different cancer types and regions in Denmark from 2010 to 2022. Study design and setting: Using comprehensive data from the Danish health registries, we linked molecular test results from the Danish Pathology Registry with cancer diagnoses from the Danish National Patient Registry between 2010 and 2022. We assessed the frequency and distribution of KRAS and BRAF mutations across all cancer types, years of testing, and the five Danish regions. Results: The study included records of KRAS testing for 30 671 patients and BRAF testing for 30 860 patients. Most KRAS testing was performed in colorectal (78%) and lung cancer (18%), and BRAF testing in malignant melanoma (13%), colorectal cancer (67%), and lung cancer (12%). Testing rates and documentation mutational subtypes increased over time. Reporting of wildtype results varied between lung and colorectal cancer, with underreporting in lung cancer. Regional variations in testing and reporting were observed. Conclusion: Our study highlights substantial progress in KRAS and BRAF testing in Denmark from 2010 to 2022, evidenced by increased and more specific reporting of mutational test results, thereby improving the precision of cancer diagnosis and treatment. However, persistent regional variations and limited testing for cancer types beyond melanoma, colorectal, and lung cancer highlight the necessity for a nationwide assessment of the optimal testing approach.
AB - Objective: This study aims to evaluate the developments in the testing of Kirsten Rat Sarcoma viral oncogene homolog (KRAS) and v-Raf murine sarcoma viral oncogene homolog B1 (BRAF) mutations across different cancer types and regions in Denmark from 2010 to 2022. Study design and setting: Using comprehensive data from the Danish health registries, we linked molecular test results from the Danish Pathology Registry with cancer diagnoses from the Danish National Patient Registry between 2010 and 2022. We assessed the frequency and distribution of KRAS and BRAF mutations across all cancer types, years of testing, and the five Danish regions. Results: The study included records of KRAS testing for 30 671 patients and BRAF testing for 30 860 patients. Most KRAS testing was performed in colorectal (78%) and lung cancer (18%), and BRAF testing in malignant melanoma (13%), colorectal cancer (67%), and lung cancer (12%). Testing rates and documentation mutational subtypes increased over time. Reporting of wildtype results varied between lung and colorectal cancer, with underreporting in lung cancer. Regional variations in testing and reporting were observed. Conclusion: Our study highlights substantial progress in KRAS and BRAF testing in Denmark from 2010 to 2022, evidenced by increased and more specific reporting of mutational test results, thereby improving the precision of cancer diagnosis and treatment. However, persistent regional variations and limited testing for cancer types beyond melanoma, colorectal, and lung cancer highlight the necessity for a nationwide assessment of the optimal testing approach.
KW - epidemiology
KW - genetic testing
KW - KRAS oncogene
KW - personalized medicine
KW - precision oncology
KW - proto oncogene protein B raf
U2 - 10.1002/gcc.23236
DO - 10.1002/gcc.23236
M3 - Journal article
C2 - 38656617
AN - SCOPUS:85191150135
VL - 63
JO - Genes, Chromosomes & Cancer
JF - Genes, Chromosomes & Cancer
SN - 1045-2257
IS - 4
M1 - e23236
ER -