Biomarkers in Patients with Metastatic Breast Cancer and the PRAEGNANT Study Network

被引:64
作者
Fasching, P. A. [1 ]
Brucker, S. Y. [3 ]
Fehm, T. N. [4 ]
Overkamp, F. [5 ]
Janni, W. [6 ]
Wallwiener, M. [7 ]
Hadji, P. [8 ]
Belleville, E. [9 ]
Haeberle, L. [1 ,10 ]
Taran, F. -A. [2 ]
Lueftner, D. [11 ]
Lux, M. P. [1 ]
Ettl, J. [12 ]
Mueller, V. [13 ]
Tesch, H. [14 ]
Wallwiener, D. [2 ]
Schneeweiss, A. [15 ]
机构
[1] Univ Erlangen Nurnberg, Comprehens Canc Ctr Erlangen EMN, Frauenklin Univ Klinikums Erlangen, D-91054 Erlangen, Germany
[2] Univ Tubingen, Univ Frauenklin, Dept Frauengesundheit, Univ Klinikum Tubingen, Tubingen, Germany
[3] Univ Tubingen, Forschungsinst Frauengesundheit, Dept Frauengesundheit, Tubingen, Germany
[4] Univ Dusseldorf, Univ Frauenklin Dusseldorf, Dusseldorf, Germany
[5] Oncologianova GmbH Recklinghausen, Recklinghausen, Germany
[6] Univ Frauenklin Ulm, Ulm, Germany
[7] Heidelberg Univ, Univ Frauenklin Heidelberg, Heidelberg, Germany
[8] Klin Gynakol & Geburtshilfe, Krankenhaus Nordwest, Frankfurt, Germany
[9] Clin Sol GmbH, Wurzburg, Germany
[10] Univ Erlangen Nurnberg, Unit Biostat, Dept Gynecol & Obstet, Univ Hosp Erlangen, D-91054 Erlangen, Germany
[11] Charite Campus Benjamin Franklin Berlin, Med Klin Schwerpunkt Hamatol & Onkol, Berlin, Germany
[12] Tech Univ Munich, Klinikum Rechts Isar, Abt Gynakol & Geburtshilfe, D-80290 Munich, Germany
[13] Univ Klinikum Hamburg Eppendorf, Klin Gynakol, Hamburg, Germany
[14] Onkol Bethanien, Frankfurt, Germany
[15] Natl Ctr Tumorerkrankungen, Heidelberg, Germany
关键词
breast cancer; metastasis; PRAEGNANT; mutation; biomarker; prognosis; CIRCULATING TUMOR-CELLS; GENOME-WIDE ASSOCIATION; FACTOR RECEPTOR 2; ESTROGEN-RECEPTOR; MAMMOGRAPHIC DENSITY; SUSCEPTIBILITY LOCI; HER2; STATUS; CYP2D6; POLYMORPHISMS; COMMON VARIANTS; DETECT III;
D O I
10.1055/s-0034-1396215
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
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 patients' quality 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.
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页码:41 / 50
页数:10
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