Biomarkers in patients with metastatic breast cancer and the praegnant study network. Fasching, P. A., Brucker, S. Y., Fehm, T. N., Overkamp, F., Janni, W., Wallwiener, M., Hadji, P., Belleville, E., Häberle, L., Taran, F. A., Lüftner, D., Lux, M. P., Ettl, J., Müller, V., Tesch, H., Wallwiener, D., & Schneeweiss, A. Geburtshilfe und Frauenheilkunde, 75(1):41–50, February, 2015. Publisher: Georg Thieme Verlag \KG\![Biomarkers in patients with metastatic breast cancer and the praegnant study network [link]](https://bibbase.org/img/filetypes/link.svg "link")
Paper doi abstract bibtex Progress has been made in the treatment of metastatic breast cancer in recent decades, but very few therapies use patient or tumor-specific characteristics to tailor individualized treatment. More than ten years after the publication of the reference human genome sequence, analysis methods have improved enormously, fostering the hope that biomarkers can be used to individualize therapies and offer precise treatment based on tumor and patient characteristics. Biomarkers at every level of the system (genetics, epigenetics, gene expression, micro-RNA, proteomics and others) can be used for this. This has led to changes in clinical study designs, with drug developments often only focusing on small or very small subgroups of patients and tumors. The screening and registration of patients and their molecular tumor data has therefore become very important for the successful completion of clinical studies. This new form of medicine presents particular challenges for patients and physicians. Even in this new age of genome-wide analysis, the focus should still be on the patientsquality of life. This review summarizes recent developments and describes how the PRAEGNANT study network manages the aforementioned medical challenges and changes to create a professional infrastructure for patients and physicians.
@article{fasching_biomarkers_2015,
title = {Biomarkers in patients with metastatic breast cancer and the praegnant study network},
volume = {75},
issn = {14388804},
url = {https://doi.org/10.1055%2Fs-0034-1396215},
doi = {10.1055/s-0034-1396215},
abstract = {Progress has been made in the treatment of metastatic breast cancer in recent decades, but very few therapies use patient or tumor-specific characteristics to tailor individualized treatment. More than ten years after the publication of the reference human genome sequence, analysis methods have improved enormously, fostering the hope that biomarkers can be used to individualize therapies and offer precise treatment based on tumor and patient characteristics. Biomarkers at every level of the system (genetics, epigenetics, gene expression, micro-RNA, proteomics and others) can be used for this. This has led to changes in clinical study designs, with drug developments often only focusing on small or very small subgroups of patients and tumors. The screening and registration of patients and their molecular tumor data has therefore become very important for the successful completion of clinical studies. This new form of medicine presents particular challenges for patients and physicians. Even in this new age of genome-wide analysis, the focus should still be on the patientsquality of life. This review summarizes recent developments and describes how the PRAEGNANT study network manages the aforementioned medical challenges and changes to create a professional infrastructure for patients and physicians.},
number = {1},
journal = {Geburtshilfe und Frauenheilkunde},
author = {Fasching, P. A. and Brucker, S. Y. and Fehm, T. N. and Overkamp, F. and Janni, W. and Wallwiener, M. and Hadji, P. and Belleville, E. and Häberle, L. and Taran, F. A. and Lüftner, D. and Lux, M. P. and Ettl, J. and Müller, V. and Tesch, H. and Wallwiener, D. and Schneeweiss, A.},
month = feb,
year = {2015},
note = {Publisher: Georg Thieme Verlag \{KG\}},
keywords = {\#nosource, PRAEGNANT, biomarker, breast cancer, metastasis, mutation, prognosis},
pages = {41--50},
}
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