Use of cancer‐specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors
Year: 2010
Type: article
Abstract: Detection of recurrent somatic rearrangements routinely allows monitoring of residual disease burden in leukemias, but is not used for most solid tumors. However, next-generation sequencing now allows rapid identification of patient-specific rearrangements in solid tumors. We mapped genomic rearrangements in three cancers and showed that PCR assays for rearrangements could detect a single copy of the tumor genome in plasma without false positives. Disease status, drug responsiveness, and incipient relapse could be serially assessed. In future, this strategy could be readily established in diagnostic laboratories, with major impact on monitoring of disease status and personalizing treatment of solid tumors.
Source: Genes Chromosomes and Cancer
DOI: 10.1002/gcc.20815
Authors: David J. McBride, Arto K. Orpana, Christos Sotiriou, Heikki Joensuu, Philip J. Stephens, Laura J. Mudie, Eija Hämäläinen, Lucy A. Stebbings, Leif C. Andersson, Adrienne M. Flanagan, Virginie Durbecq, Michail Ignatiadis, Olli Kallioniemi, Caroline A. Heckman, Kari Alitalo, Henrik Edgren, P. Andrew Futreal, Michael R. Stratton, Peter J. Campbell
Language: English
Subfield: Cancer Research
Domain: Life Sciences
Open Access status: green
Funder: Wellcome Trust
OpenAlex ID: W2162144873
