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. Author manuscript; available in PMC: 2017 Jan 15.
Published in final edited form as: Clin Cancer Res. 2016 Jan 15;22(2):284–290. doi: 10.1158/1078-0432.CCR-14-3336

Table 1. Common imaging metrics that are appropriate for application in cancer clinical trials.

Imaging Modality Parameter Interpretation Biological Strengths/Weaknesses Technical Strengths/Weaknesses Acquisition Needs Analysis Needs
Volumetric CT tumor volume volume of tumor in mm3 Provides data to immediately assess tumor burden/non-specific Only requires routinely acquired clinical data/time consuming high spatial resolution standard of care software packages; some user skill
DCE-CT tumor enhancement qualitative or semiquantitative assessment of perfusion/permeability Insight into tumor vascular properties/qualitative in nature, additional radiation dose Easy to perform in the clinical setting/does not allow for quantitative interpretation high spatial resolution, modest temporal resolution standard of care software packages
DCE-CT vessel perfusion and permeability blood flow in units of mL(blood)/mL(tissue)/min and permeability surface area product in unit of mL/s Knowledge of tumor vascular properties/mixed measure of two vascular characteristics, additional radiation dose Increased level of rigor/requires local expertise and proper software to execute properly high temporal resolution, arterial input function specialized software; close interaction with imaging core
DCE-CT volume fractions fraction of voxel that is (e.g.) blood or extravascular extracellular space Knowledge of intra-tumoral make-up/Unproven clinical value, additional radiation dose Increased level of rigor/requires local expertise and proper software to execute properly high temporal resolution, arterial input function specialized software; close interaction with imaging core
DCE-MRI tumor enhancement qualitative or semiquantitative assessment of perfusion/permeability Insight into tumor vascular properties/qualitative or semiquantitative in nature Easy to perform in the clinical setting/does not allow for quantitative interpretation does not require high temporal resolution, moderate to high spatial resolution standard of care software packages
DCE-MRI vessel perfusion and permeability contrast agent transfer rate constant in units of min-1 containing both blood flow in units of mL(100 mL tissue)-1min-1 and permeability surface area product in unit of min-1 quantitative measure of tumor vascular properties/accuracy and precision prone to variations in data acquisition and analysis Increased level of rigor in quantitative analysis/requires local or central expertise and proper software to execute properly determination of pre-contrast T1 and arterial input function, high temporal resolution specialized software (in-house, commercial, or publicly available); close interaction with imaging scientists
DCE-MRI volume fractions fraction of voxel that is (e.g.) blood or extravascular extracellular space quantitative measure of intra-tumoral make-up/accuracy and precision prone to variations in data acquisition and analysis Increased level of rigor in quantitative analysis/requires local or central expertise and proper software to execute properly determination of pre-contrast T1 and arterial input function, high temporal resolution specialized software (in-house, commercial, or publicly available); close interaction with imaging scientists
DW-MRI apparent diffusion coefficient quantitative assessment of cell density Estimates of cellularity/non-specific Straightforward to implement in clinical settings/ADC quantification can be dependent on selection of diffusion weightings multiple image sets with different diffusion weightings standard of care software packages or specialized software (in-house, commercial, or publicly available)
FDG-PET accumulation of tracer qualitative assessment of glucose utilization Well understood interpretation in context of cancer/difficult to interpret for organs with high background Easy to perform in clinical setting/quantification issues brief scan 60 minutes post injection standard of care software packages
FDG-PET SUV semi-quantitative assessment of glucose utilization Provides rough estimate of glucose utilization/unclear clinical utility Easy to perform/lacks rigor and meaning brief scan 60 minutes post injection standard of care software packages; some user skill
FDG-PET kinetic analysis quantitative assessment of delivery, retention, and utilization of glucose Well-defined interpretation/unclear clinical utility Increased level of rigor/requires local expertise and proper software to execute properly dynamic acquisition over the uptake time (∼60 min) specialized software; close interaction with imaging core
FLT-PET accumulation of tracer qualitative assessment of cell proliferation Provides rough estimate of proliferation/difficult to interpret for certain tumors Easy to perform in clinical setting/quantification issues brief scan 60 minutes post injection standard of care software packages
FLT-PET SUV semi-quantitative assessment of cell proliferation Provides rough estimate of thymidine kinase activity/unclear clinical utility Easy to perform/lacks rigor and meaning brief scan 60 minutes post injection standard of care software packages; some user skill
FLT-PET kinetic analysis quantitative assessment of delivery, retention, and utilization of cell proliferation Well-defined interpretation/unclear clinical utility Increased level of rigor/requires local expertise and proper software to execute properly dynamic acquisition over the uptake time (∼60 min) specialized software; close interaction with imaging core