Publication: Reporting of somatic variants in clinical cancer care: recommendations of the Swiss Society of Molecular Pathology
Reporting of somatic variants in clinical cancer care: recommendations of the Swiss Society of Molecular Pathology
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Christinat, Y., Hamelin, B., Alborelli, I., Angelino, P., Barbié, V., Bisig, B., Dawson, H., Frattini, M., Grob, T., Jochum, W., Nienhold, R., McKee, T., Matter, M., Missiaglia, E., Molinari, F., Rothschild, S., Sobottka-Brillout, A. B., Vassella, E., Zoche, M., & Mertz, K. D. (2024). Reporting of somatic variants in clinical cancer care: recommendations of the Swiss Society of Molecular Pathology. Virchows Archiv, 485(6), 1033–1039. https://doi.org/10.1007/s00428-024-03951-0
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Somatic variant testing through next-generation sequencing (NGS) is well integrated into Swiss molecular pathology laboratories and has become a standard diagnostic method for numerous indications in cancer patient care. Currently, there is a wide variation in reporting practices within our country, and as patients move between different hospitals, it is increasingly necessary to standardize NGS reports to ease their reinterpretation. Additionally, as many different stakeholders-oncologists, hematologists, geneticists, pathologists, a
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Christinat, Y., Hamelin, B., Alborelli, I., Angelino, P., Barbié, V., Bisig, B., Dawson, H., Frattini, M., Grob, T., Jochum, W., Nienhold, R., McKee, T., Matter, M., Missiaglia, E., Molinari, F., Rothschild, S., Sobottka-Brillout, A. B., Vassella, E., Zoche, M., & Mertz, K. D. (2024). Reporting of somatic variants in clinical cancer care: recommendations of the Swiss Society of Molecular Pathology. Virchows Archiv, 485(6), 1033–1039. https://doi.org/10.1007/s00428-024-03951-0