TY - JOUR
T1 - Characterizing tumors using metabolic imaging
T2 - PET imaging of cellular proliferation and steroid receptors
AU - Mankoff, David A.
AU - Dehdashti, Farrokh
AU - Shields, Anthony F.
N1 - Funding Information:
Address all correspondence to: Dr. David A. Mankoff, MD, PhD, Division of Nuclear Medicine, Box 356113, Room NN203, UWMC, 1959 NE Pacific Street, Seattle, WA 98195. 1This work was supported by NIH grants CA42045, CA72064, CA25386, CA39566, and CA82645 and DOE grant DE FG02 - 84ER60218. Received 24 September 1999; Accepted 3 November 1999.
PY - 2000
Y1 - 2000
N2 - Treatment decisions in oncology are increasingly guided by information on the biologic characteristics of tumors. Currently, patient-specific information on tumor biology is obtained from the analysis of biopsy material. Positron emission tomography (PET) provides quantitative estimates of regional biochemistry and receptor status and can overcome the sampling error and difficulty in performing serial studies inherent with biopsy. Imaging using the glucose metabolism tracer, 2-deoxy-2-fluoro-D-glucose (FDG), has demonstrated PET's ability to guide therapy in clinical oncology. In this review, we highlight PET approaches to imaging two other aspects of tumor biology: cellular proliferation and tumor steroid receptors. We review the biochemical and biologic processes underlying the imaging, positron- emitting radiopharmaceuticals that have been developed, quantitative image- analysis considerations, and clinical studies to date. This provides a basis for evaluating future developments in these promising applications of PET metabolic imaging.
AB - Treatment decisions in oncology are increasingly guided by information on the biologic characteristics of tumors. Currently, patient-specific information on tumor biology is obtained from the analysis of biopsy material. Positron emission tomography (PET) provides quantitative estimates of regional biochemistry and receptor status and can overcome the sampling error and difficulty in performing serial studies inherent with biopsy. Imaging using the glucose metabolism tracer, 2-deoxy-2-fluoro-D-glucose (FDG), has demonstrated PET's ability to guide therapy in clinical oncology. In this review, we highlight PET approaches to imaging two other aspects of tumor biology: cellular proliferation and tumor steroid receptors. We review the biochemical and biologic processes underlying the imaging, positron- emitting radiopharmaceuticals that have been developed, quantitative image- analysis considerations, and clinical studies to date. This provides a basis for evaluating future developments in these promising applications of PET metabolic imaging.
KW - Cellular proliferation
KW - Estrogen receptors
KW - Oncology
KW - PET
KW - Response
UR - http://www.scopus.com/inward/record.url?scp=0034087594&partnerID=8YFLogxK
U2 - 10.1038/sj.neo.7900075
DO - 10.1038/sj.neo.7900075
M3 - Review article
C2 - 10933070
AN - SCOPUS:0034087594
SN - 1522-8002
VL - 2
SP - 71
EP - 88
JO - Neoplasia
JF - Neoplasia
IS - 1-2
ER -