TY - JOUR
T1 - Contemporary lung cancer screening and the promise of blood-based biomarkers
AU - Von Itzstein, Mitchell S.
AU - Gerber, David E.
AU - Minna, John D.
N1 - Funding Information:
D.E. Gerber reports grants from AstraZeneca outside the submitted work and personal fees from Bristol-Myers Squibb outside the submitted work. In addition, D.E. Gerber has a patent for Prediction and Treatment of Immunotherapeutic Toxicity pending. J.D. Minna reports grants from NIH, Cancer Prevention and Research Institute of Texas, from Burroughs Wellcome Fund, and NIH during the conduct of the study; personal fees from NIH, University of Texas Southwestern Medical Center. In addition, J.D. Minna has a patent for Gene signature predicting adenocarcinoma prognosis and therapeutic response pending. No disclosures were reported by the other author.
Funding Information:
This work was supported, in part, by the University of Texas Lung Cancer Specialized Program in Research Excellence (SPORE, P50-CA-070907-08S1), the National Institute of Allergy and Infectious Disease (1U01AI156189-01), the Cancer Prevention and Research Institute of Texas (CPRIT; RP160030 and RP190052), and a UTSW Physician-Scientist Institutional Award from the Burroughs Wellcome Fund.
Publisher Copyright:
© 2021 American Association for Cancer Research.
PY - 2021/7/1
Y1 - 2021/7/1
N2 - In this issue, the study by Dagnino and colleagues represents an important addition to the maturing field of blood-based biomarkers for lung cancer screening. Their comprehensive approach to analyzing circulating inflammatory proteins identified CDCP1 as a potential biomarker for distinguishing patients with or without lung cancer, a finding that was confirmed in a validation cohort. CDCP1 blood levels, when combined with smoking history, gave an AUC receiver operator characteristic of 0.75. Analysis of transcripts in peripheral blood cells suggested a Wnt/β-catenin signaling-based mechanism for CDCP1 in tumorigenesis providing biologic plausibility. CDCP1 now joins the ranks of other potential blood-based lung cancer screening biomarkers (including epithelial tumor marker proteins, tumor-associated miRNA, antitumor antibodies, and tumor-specific DNA methylation) that need validation in future clinical trials. Further exploration of how CDCP1 levels might be integrated into current lung cancer screening programs, including both detection of lung cancer, and evaluation of the need for invasive biopsies, as well as how CDCP1 performs in different racial populations, is warranted.
AB - In this issue, the study by Dagnino and colleagues represents an important addition to the maturing field of blood-based biomarkers for lung cancer screening. Their comprehensive approach to analyzing circulating inflammatory proteins identified CDCP1 as a potential biomarker for distinguishing patients with or without lung cancer, a finding that was confirmed in a validation cohort. CDCP1 blood levels, when combined with smoking history, gave an AUC receiver operator characteristic of 0.75. Analysis of transcripts in peripheral blood cells suggested a Wnt/β-catenin signaling-based mechanism for CDCP1 in tumorigenesis providing biologic plausibility. CDCP1 now joins the ranks of other potential blood-based lung cancer screening biomarkers (including epithelial tumor marker proteins, tumor-associated miRNA, antitumor antibodies, and tumor-specific DNA methylation) that need validation in future clinical trials. Further exploration of how CDCP1 levels might be integrated into current lung cancer screening programs, including both detection of lung cancer, and evaluation of the need for invasive biopsies, as well as how CDCP1 performs in different racial populations, is warranted.
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U2 - 10.1158/0008-5472.CAN-21-0706
DO - 10.1158/0008-5472.CAN-21-0706
M3 - Article
C2 - 34252039
AN - SCOPUS:85109019091
SN - 0008-5472
VL - 81
SP - 3441
EP - 3443
JO - Cancer Research
JF - Cancer Research
IS - 13
ER -