TY - JOUR
T1 - Liquid biopsy in lung cancer
T2 - A perspective from members of the pulmonary pathology society
AU - Sholl, Lynette M.
AU - Aisner, Dara L.
AU - Allen, Timothy Craig
AU - Beasley, Mary Beth
AU - Cagle, Philip T.
AU - Capelozzi, Vera L.
AU - Dacic, Sanja
AU - Hariri, Lida P.
AU - Kerr, Keith M.
AU - Lantuejoul, Sylvie
AU - Mino-Kenudson, Mari
AU - Raparia, Kirtee
AU - Rekhtman, Natasha
AU - Roy-Chowdhuri, Sinchita
AU - Thunnissen, Eric
AU - Tsao, Ming
AU - Vivero, Marina
AU - Yatabe, Yasushi
PY - 2016/8
Y1 - 2016/8
N2 - Liquid biopsy has received extensive media coverage and has been called the holy grail of cancer detection. Attempts at circulating tumor cell and genetic material capture have been progressing for several years, and recent financially and technically feasible improvements of cell capture devices, plasma isolation techniques, and highly sensitive polymerase chain reaction- and sequencing-based methods have advanced the possibility of liquid biopsy of solid tumors. Although practical use of circulating RNA-based testing has been hindered by the need to fractionate blood to enrich for RNAs, the detection of circulating tumor cells has profited from advances in cell capture technology. In fact, the US Food and Drug Administration has approved one circulating tumor cell selection platform, the CellSearch System. Although the use of liquid biopsy in a patient population with a genomically defined solid tumor may potentially be clinically useful, it currently does not supersede conventional pretreatment tissue diagnosis of lung cancer. Liquid biopsy has not been validated for lung cancer diagnosis, and its lower sensitivity could lead to significant diagnostic delay if liquid biopsy were to be used in lieu of tissue biopsy. Ultimately, notwithstanding the enthusiasm encompassing liquid biopsy, its clinical utility remains unproven.
AB - Liquid biopsy has received extensive media coverage and has been called the holy grail of cancer detection. Attempts at circulating tumor cell and genetic material capture have been progressing for several years, and recent financially and technically feasible improvements of cell capture devices, plasma isolation techniques, and highly sensitive polymerase chain reaction- and sequencing-based methods have advanced the possibility of liquid biopsy of solid tumors. Although practical use of circulating RNA-based testing has been hindered by the need to fractionate blood to enrich for RNAs, the detection of circulating tumor cells has profited from advances in cell capture technology. In fact, the US Food and Drug Administration has approved one circulating tumor cell selection platform, the CellSearch System. Although the use of liquid biopsy in a patient population with a genomically defined solid tumor may potentially be clinically useful, it currently does not supersede conventional pretreatment tissue diagnosis of lung cancer. Liquid biopsy has not been validated for lung cancer diagnosis, and its lower sensitivity could lead to significant diagnostic delay if liquid biopsy were to be used in lieu of tissue biopsy. Ultimately, notwithstanding the enthusiasm encompassing liquid biopsy, its clinical utility remains unproven.
UR - http://www.scopus.com/inward/record.url?scp=84980332141&partnerID=8YFLogxK
U2 - 10.5858/arpa.2016-0163-SA
DO - 10.5858/arpa.2016-0163-SA
M3 - Review article
C2 - 27195432
AN - SCOPUS:84980332141
SN - 0003-9985
VL - 140
SP - 825
EP - 829
JO - Archives of Pathology and Laboratory Medicine
JF - Archives of Pathology and Laboratory Medicine
IS - 8
ER -