Blood-based biomarkers in lung cancer: prognosis and treatment decisions
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作者:
Xu-Welliver, Meng
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Ohio State Univ, Wexner Med Ctr, Dept Radiat Oncol, Columbus, OH 43210 USAOhio State Univ, Wexner Med Ctr, Dept Radiat Oncol, Columbus, OH 43210 USA
Xu-Welliver, Meng
[1
]
Carbone, David P.
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Ohio State Univ, Dept Med, Wexner Med Ctr, Div Med Oncol, Columbus, OH 43210 USAOhio State Univ, Wexner Med Ctr, Dept Radiat Oncol, Columbus, OH 43210 USA
Carbone, David P.
[2
]
机构:
[1] Ohio State Univ, Wexner Med Ctr, Dept Radiat Oncol, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Med, Wexner Med Ctr, Div Med Oncol, Columbus, OH 43210 USA
Despite recent advances, non-small cell lung cancer ( NSCLC) remains a devastating disease with overall poor prognosis. Major contributing factors include obstacles to diagnosing the disease early in its course during the asymptomatic stage as well as diversity and complexity of its biology underlying tumorigenesis and tumor progression. Advances in molecularly targeted therapies which drives the development of personalized cancer care require precise and comprehensive understanding of tumor biology, not only at the time of diagnosis but also during treatment course and surveillance. As lung tumor tissue can be difficult to obtain without invasive and potentially risky procedures, it is difficult to monitor treatment response with serial tissue biopsies. Development of non-invasive but reliable blood based tumor markers has become an important research area. In this review, we focus on the following circulating biomarkers that have been identified in recent years: circulating tumor cells (CTCs); circulating cell-free nucleic acids, such as circulating tumor DNA (ctDNA) and microRNA (miR); and other biomarkers such as genomic and proteomic features. These biomarkers not only have prognostic values, but also can help guild treatment decisions by monitoring tumor burden, detecting minimal residual disease and/or recurrent disease, as well as monitoring evolution of genetic alterations throughout the treatment course.
机构:
Wayne State Univ, Karmanos Canc Inst, Dept Oncol, 4201 John R, Detroit, MI 48201 USAWayne State Univ, Karmanos Canc Inst, Dept Oncol, 4201 John R, Detroit, MI 48201 USA
Mamdani, Hirva
Ahmed, Shahid
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Indiana Univ, Melvin & Bren Simon Canc Ctr, Div Hematol Oncol, Indianapolis, IN 46204 USAWayne State Univ, Karmanos Canc Inst, Dept Oncol, 4201 John R, Detroit, MI 48201 USA
Ahmed, Shahid
Armstrong, Samantha
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Indiana Univ Sch Med, Internal Med, Indianapolis, IN 46202 USAWayne State Univ, Karmanos Canc Inst, Dept Oncol, 4201 John R, Detroit, MI 48201 USA
Armstrong, Samantha
Mok, Tony
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Chinese Univ Hong Kong, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R ChinaWayne State Univ, Karmanos Canc Inst, Dept Oncol, 4201 John R, Detroit, MI 48201 USA
Mok, Tony
Jalal, Shadia I.
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Indiana Univ, Melvin & Bren Simon Canc Ctr, Div Hematol Oncol, Indianapolis, IN 46204 USAWayne State Univ, Karmanos Canc Inst, Dept Oncol, 4201 John R, Detroit, MI 48201 USA
机构:
Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Harvard Med Sch, Boston, MA USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Zachariah, Marcus A.
Oliveira-Costa, Joao Paulo
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Harvard Med Sch, Boston, MA USA
Massachusetts Gen Hosp, Dept Med, Ctr Canc Res Canc Res, Boston, MA 02114 USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Oliveira-Costa, Joao Paulo
Carter, Bob S.
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机构:
Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Harvard Med Sch, Boston, MA USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Carter, Bob S.
Stott, Shannon L.
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机构:
Harvard Med Sch, Boston, MA USA
Massachusetts Gen Hosp, Dept Med, Ctr Canc Res Canc Res, Boston, MA 02114 USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Stott, Shannon L.
Nahed, Brian V.
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机构:
Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Harvard Med Sch, Boston, MA USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA