Ultralow Dose Chest CT with MBIR

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Ultralow Dose Chest CT with MBIR Ella A. Kazerooni, M.D. Professor & Director Cardiothoracic Radiology Associate Chair for Clinical Affairs University of Michigan

Disclosures Consultant: GE Healthcare

Low dose vs ultra low dose chest CT 2 3 msv LDCT FBP 0.2 msv ultraldct : MBIR

MBIR model based iterative reconstruction Advanced modeling of system statistics & optics to: reduce noise increase spatial resolution increase contrast resolution at the same (or lower) radiation doses MBIR (Veo) approved by US FDA September 2011

MBIR model based iterative reconstruction NIH funded collaboration: PI Jeff Fessler PhD UM School of Engineering, GE Global Research and U of M Radiology Mitch Goodsitt PhD CT physicist & Ella Kazerooni MD Thoracic Radiology

Ultralow Dose Chest CT Lung is a great target for low dose CT efforts Inherent contrast between lung (air) and tissue (vessels & airways) Tissues extracted as arborizing structures Lung segmentation straightforward At or near CXR exposure CT exams Trade off may be quantitative analysis lowest exposure vs. most accurate measurement

National Lung Cancer Screening Trial 20% lung cancer mortality reduction 6.9% all cause mortality reduction screen 320 individuals to save 1 from lung cancer death

Lung Cancer CT Screening Limitations false positives: NLST: 40% of subjects had 1 FP over 3 years Mayo: 75% of subjects had 1 FP over 5 years radiation concerns: from screening LDCT exams serial CT used as the primary tool to further evaluate small nodules, PET/CT, etc indeterminate lung nodules

Radiation Exposure Radiation Risks Potentially Associated with Low Dose Screening Brenner DJ et al. Radiology 2004;231:440 445 assumptions: entire US population current/former smokers age 50 75 years annual CT until age 75 (5.2 ± 0.9 mgy to lung; 60 mas) 50% compliance rate atomic bomb survivor cohort for predicting risk expect 1.9 million lung cancers 36,000 additional lung cancers attributed to CT 1.8% increase in lung cancer (95% CI 0.5 5.5%)

NLST CT Technique Chart - 2002-06 Parameter GE-VCT(64) 64 slice 0.5 sec Siemens Sensation 64 64 x 0.0.6 Phillips MX8000 16 slice 0.5 sec 16 x.75 Toshiba Aquillon 16 slice 0.5 sec kv 120 120 120 120 Gantry Rotation Time 0.5 sec 0.5 sec 0.5 sec 0.5 sec ma (Regular-Large Patient) 50-100 50-100 75-15- 80-160 mas (Regular-Large) 25-50 25-50 37.5-75 40-80 Scanner Effective mas (Reg-Large) 27-53 25-50 25-50 26.7-53.3 Detector Collimation (mm): T 0.625 mm 0.6 mm.75 mm 2 mm Number of Active Channels: N 64 32 16 16 Detector configuration: N x T 64 x 0.625 mm 32 x 0.6 mm 16 x 0.75 16 x 2 MODE (Thick/Speed) or Console Collimation 1.625/.984/39.37 64 x 0.6 mm N/A N/A Table Incrementation (mm/rotation): I 39.37 mm 19.2 mm 18 mm 48 mm Pitch ([mm/rotation]/configuration): I/NT 0.984 1.0 1.5 1.5 Table speed (mm/second) 78.74 mm/sec 38.4 mm/sec 36 mm/sec 96 mm/sec Scan time (40 cm thorax) 5.1 sec 11 sec 11 sec 4.2 sec Max Nominal Reconstructed Slice Width 2.5 mm 2 mm 2 mm 2 mm Reconstruction Interval 2.0 mm 1.8 mm 1.8 mm 1.8 mm Reconstruction Algorithm STD B30f B or C FC 10 # Images/Data set (40 cm Thorax) 200 223 223 223 CTDIvol Dose in mgy (Regular-Large) 2.2-2.4 mgy 1.9-3.8 mgy 1.9-3.8 mgy 2.7-5.4 mgy

Lung Nodule CT Tasks Detection Characterization Qualitative - Descriptive: ground glass, solid etc Semi quantitative - Caliper sizing Quantitative - Volumetric measurement Follow up

MBIR Lung CT for Nodules

MBIR Lung CT for Nodules Yamada et al. Invest Radiol 2012;8:482-489 Keio University School of Medicine, Tokyo Compared noise, subjective image quality & lung nodule 52 subjects dual chest CT acquisitions March May 2011 LDCT 50 mas screening eff dose 2.1 mgy uldct 4 mas eff dose 0.17 mgy Reconstructions LDCT filtered back projection LDCT FBP uldct filtered back projection uldct FBP uldct MBIR uldct MBIR 2 blinded readers detection on 1.25 mm axial images

MBIR Lung CT for Nodules Yamada et al. Invest Radiol 2012;8:482-489 Keio University School of Medicine, Tokyo blotchy pixelated appearance on all uldct MBIRs 1 = none; 2 = present not impacting screening results 3 = impacting screening results

blotchy pixelated appearance

blotchy pixelated appearance

MBIR Lung CT for Nodules Yamada et al. Invest Radiol 2012;8:482-489 Keio University School of Medicine, Tokyo Subjective image noise uldct MBIR = LDCT FBP uldct MBIR < uldct FBP (p < 0.001)

MBIR Lung CT for Nodules Yamada et al. Invest Radiol 2012;8:482-489 Keio University School of Medicine, Tokyo Artifacts uldct FBP > uldct MBIR > LDCT FBP p < 0.001 Image sharpness uldct MBIR & uldct FBP equivalent LDCT FBP significantly more sharp (p < 0.001)

Artifacts with MBIR

MBIR Lung CT for Nodules Yamada et al. Invest Radiol 2012;8:482-489 Keio University School of Medicine, Tokyo Nodule detection LDCT FBP used as truth Calcified nodules (n = 26, 2 10 mm diameter) uldct MBIR & uldct FBP detected all nodules Non calcified nodules (n = 184, 1 30 mm, mean 4±3 uldct MBIR > uldct FBP (p < 0.002) TPF all 0.905 0.804 TPF 4 mm 0.944 0.833 TPF < 4 mm 0.884 0.789 FPR all* 0.125 0.202 * Upon review of misses reviewed due to noise and artifacts

MBIR Lung CT for Nodules Yamada et al. Invest Radiol 2012;8:482-489 Keio University School of Medicine, Tokyo The patients Age 38 84 years (mean 66.3) Weight range: 37 84 kg (82 185 lbs) mean: 55.9 ± 11.9 kg (123 ± 26 lbs) BMI* range: 15.4 30.7 mean: 21.7 ± 3.5 *healthy weight 18.5 25; overweight 25 30; moderately obese 30 35

MBIR Lung CT for Nodules Matsura et al. Eur Rad 2012;8:1613-1623 University of Tokyo 100 subjects dual chest CT acquisitions July 2011 LDCT uldct Reconstructions LDCT filtered back projection with ASIR uldct filtered back projection ASIR uldct MBIR uldct MBIR eff dose 4.04 mgy eff dose 0.55 mgy LDCT ASIR50 uldct ASIR50 2 blinded readers Compared noise, subjective image quality & lung nodule detection on 0.625 mm axial images

MBIR Lung CT for Nodules Matsura et al. Eur Rad 2012;8:1613-1623 University of Tokyo

MBIR Lung CT for Nodules Matsura et al. Eur Rad 2012;8:1613-1623 University of Tokyo LDCT ASIR uldct ASIR uldct MBIR

MBIR Lung CT for Nodules Matsura et al. Eur Rad 2012;8:1613-1623 University of Tokyo Nodule detection not studied

MBIR Lung CT for Nodules Matsura et al. Eur Rad 2012;8:1613-1623 University of Tokyo The patients Age mean 65.6 ± 12.4 years Weight range: not reported mean: 58 ± 13 kg (128 ± 29 lbs) 1 std dev 99 157 lbs (approx 68% of subjects) 2 std dev 70 186 lbs (approx 95% of subjects) BMI not reported

MBIR Lung CT for Nodules Neroladaki et al. Eur Radiol 2012 Geneva University Hospital 42 subjects SDCT or LDCT (11.2 or 2.7 msv) uldct (0.16 msv) (in the range of 2view CXR) Reconstructions SDCT or LDCT filtered back projection uldct filtered back projection uldct ASIR uldct MBIR uldct MBIR better image quality than uldct ASIR or FBP; quality inferior for ground glass and emphysema BMI mean 25.8 males, 27.8 females; overweight

LDCT LDCT with ASIR LDCT with MBIR 255 lbs, BMI 34

ultraldct uldct with ASIR 255 lbs, BMI 34 uldct with MBIR

LDCT LDCT FBP with ASIR LDCT with MBIR 255 lbs, BMI 34

ultraldct uldct FBP with ASIR 255 lbs, BMI 34 uldct with MBIR

LDCT vs uldct LDCT ASIR LDCT MBIR uldct ASIR uldct MBIR

LDCT vs uldct 255 lbs BMI 34 LDCT ASIR uldct ASIR LDCT MBIR uldct MBIR

LDCT vs uldct - GGO 200 lbs BMI 36.6 LDCT ASIR LDCT MBIR uldct ASIR uldct MBIR

Impact of MBIR on Nodule Volume?TBD Low dose CT (conventional low dose) underestimates small nodule volume compared to standard dose chest CT (de Jong et al; 2012 Oct AJR) LDCT vs contrast enhanced standard chest CT CTDIvol 2.2 vs 5.5 20 mgy 200 mm 3 threshold or approx 8 mm below which nodules were undersized by approx 14 16%

MBIR Lung CT for Nodules Substantial radiation exposure reduction Reduces noise back to standard low dose CT levels Blotchy pixelated appearance does not appear to subjectively impact diagnostic quality of chest CTs Not validated in US patient population size cohort More work on diagnostic accuracy and impact on nodule quantification is needed

Ultralow Dose Chest CT with MBIR Ella A. Kazerooni, M.D. Professor & Director Cardiothoracic Radiology Associate Chair for Clinical Affairs University of Michigan