Biobanking in Molecular Biomarker Research for the Early Detection of Cancer
Although population-wide screening programs for several cancer types have been implemented in multiple countries, screening procedures are invasive, time-consuming and often perceived as a burden for patients. Molecular biomarkers measurable in non-invasively collected samples (liquid biopsies) coul...
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Published in | Cancers Vol. 12; no. 4; p. 776 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Abstract | Although population-wide screening programs for several cancer types have been implemented in multiple countries, screening procedures are invasive, time-consuming and often perceived as a burden for patients. Molecular biomarkers measurable in non-invasively collected samples (liquid biopsies) could facilitate screening, as they could have incremental value on early diagnosis of cancer, but could also predict prognosis or monitor treatment response. Although the shift towards biomarkers from liquid biopsies for early cancer detection was initiated some time ago, there are many challenges that hamper the development of such biomarkers. One of these challenges is large-scale validation that requires large prospectively collected biobanks with liquid biopsies. Establishing those biobanks involves several considerations, such as standardization of sample collection, processing and storage within and between biobanks. In this perspective, we will elaborate on several issues that need to be contemplated in biobanking, both in general and for certain specimen types specifically, to be able to facilitate biomarker validation for early detection of cancer. |
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AbstractList | Although population-wide screening programs for several cancer types have been implemented in multiple countries, screening procedures are invasive, time-consuming and often perceived as a burden for patients. Molecular biomarkers measurable in non-invasively collected samples (liquid biopsies) could facilitate screening, as they could have incremental value on early diagnosis of cancer, but could also predict prognosis or monitor treatment response. Although the shift towards biomarkers from liquid biopsies for early cancer detection was initiated some time ago, there are many challenges that hamper the development of such biomarkers. One of these challenges is large-scale validation that requires large prospectively collected biobanks with liquid biopsies. Establishing those biobanks involves several considerations, such as standardization of sample collection, processing and storage within and between biobanks. In this perspective, we will elaborate on several issues that need to be contemplated in biobanking, both in general and for certain specimen types specifically, to be able to facilitate biomarker validation for early detection of cancer. |
Author | Lommen, Kim Smits, Kim M Odeh, Selena Theije, Chiel C de |
AuthorAffiliation | 1 Department of Pathology, GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands; k.lommen@maastrichtuniversity.nl (K.L.); s.odeh@maastrichtuniversity.nl (S.O.) 2 Central Biobank Maastricht UMC, 6229 ER Maastricht, The Netherlands; chiel.detheije@biobank.nl |
AuthorAffiliation_xml | – name: 1 Department of Pathology, GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands; k.lommen@maastrichtuniversity.nl (K.L.); s.odeh@maastrichtuniversity.nl (S.O.) – name: 2 Central Biobank Maastricht UMC, 6229 ER Maastricht, The Netherlands; chiel.detheije@biobank.nl |
Author_xml | – sequence: 1 givenname: Kim orcidid: 0000-0002-1118-6379 surname: Lommen fullname: Lommen, Kim organization: Department of Pathology, GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, 6229HX Maastricht, The Netherlands – sequence: 2 givenname: Selena surname: Odeh fullname: Odeh, Selena organization: Department of Pathology, GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, 6229HX Maastricht, The Netherlands – sequence: 3 givenname: Chiel C de surname: Theije fullname: Theije, Chiel C de organization: Central Biobank Maastricht UMC, 6229 ER Maastricht, The Netherlands – sequence: 4 givenname: Kim M surname: Smits fullname: Smits, Kim M organization: Department of Pathology, GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, 6229HX Maastricht, The Netherlands |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32218259$$D View this record in MEDLINE/PubMed |
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Title | Biobanking in Molecular Biomarker Research for the Early Detection of Cancer |
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