Positron emission tomography as an imaging biomarker
- PMID: 16829652
- DOI: 10.1200/JCO.2006.06.6068
Positron emission tomography as an imaging biomarker
Abstract
Positron emission tomography (PET) allows noninvasive, quantitative studies of various biologic processes in the tumor tissue. By using PET, investigators can study the pharmacokinetics of anticancer drugs, identify various therapeutic targets and monitor the inhibition of these targets during therapy. Furthermore, PET provides various markers to assess tumor response early in the course of therapy. A significant number of studies have now shown that changes in tumor glucose utilization during the first weeks of chemotherapy are significantly correlated with patient outcome. These data suggest that PET may be used as a sensitive test to assess the activity of new cytotoxic agents in phase II studies. Furthermore, early identification of nonresponding tumors provides the opportunity to adjust treatment regimens according to the individual chemosensitivity of the tumor tissue. However, further prospective and randomized validation of PET is still required before PET controlled chemotherapy can be used in clinical practice.
Similar articles
-
Positron emission tomography and neoadjuvant therapy of breast cancer.J Natl Cancer Inst Monogr. 2011;2011(43):111-5. doi: 10.1093/jncimonographs/lgr035. J Natl Cancer Inst Monogr. 2011. PMID: 22043055
-
Use of PET for monitoring cancer therapy and for predicting outcome.J Nucl Med. 2005 Jun;46(6):983-95. J Nucl Med. 2005. PMID: 15937310 Review.
-
18F-FDG PET as a candidate for "qualified biomarker": functional assessment of treatment response in oncology.J Nucl Med. 2006 Jun;47(6):901-3. J Nucl Med. 2006. PMID: 16741296 No abstract available.
-
Positron emission tomography for radiation treatment planning.Strahlenther Onkol. 2005 Aug;181(8):483-99. doi: 10.1007/s00066-005-1422-7. Strahlenther Onkol. 2005. PMID: 16044216 Review.
-
The Role of Positron Emission Tomography Imaging in Radiotherapy Target Delineation.PET Clin. 2020 Jan;15(1):45-53. doi: 10.1016/j.cpet.2019.08.002. PET Clin. 2020. PMID: 31735301 Review.
Cited by
-
Can Dynamic Whole-Body FDG PET Imaging Differentiate between Malignant and Inflammatory Lesions?Life (Basel). 2022 Aug 30;12(9):1350. doi: 10.3390/life12091350. Life (Basel). 2022. PMID: 36143386 Free PMC article.
-
Impact of third-line treatment with irinotecan plus cetuximab on non-tumor standardized uptake values in patients with metastatic colorectal cancer.Oncol Lett. 2012 Jul;4(1):131-134. doi: 10.3892/ol.2012.683. Epub 2012 Apr 18. Oncol Lett. 2012. PMID: 22807975 Free PMC article.
-
Compact microfluidic device for rapid concentration of PET tracers.Lab Chip. 2014 Jul 7;14(13):2293-302. doi: 10.1039/c4lc00286e. Lab Chip. 2014. PMID: 24825578 Free PMC article.
-
Future cancer research priorities in the USA: a Lancet Oncology Commission.Lancet Oncol. 2017 Nov;18(11):e653-e706. doi: 10.1016/S1470-2045(17)30698-8. Epub 2017 Oct 31. Lancet Oncol. 2017. PMID: 29208398 Free PMC article. Review.
-
High 18F-fluorodeoxyglucose uptake in cardiac tumor: A case report.Medicine (Baltimore). 2016 Nov;95(44):e4211. doi: 10.1097/MD.0000000000004211. Medicine (Baltimore). 2016. PMID: 27858836 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources