why quantitative i-131 robert e. zimmerman joint program in nuclear medicine harvard medical

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Why Quantitative I-131 http://www.med.harvard.edu/physics/WhyQuantitativ eI-131_2.ppt Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical School Brigham & Women’s Hospital Dana Farber Cancer Institute The Children Hospital Boston MA

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Page 1: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Why Quantitative I-131http://www.med.harvard.edu/physics/WhyQuantitativeI-131_2.ppt

Robert E. ZimmermanJoint Program in Nuclear Medicine

Harvard Medical SchoolBrigham & Women’s HospitalDana Farber Cancer Institute

The Children HospitalBoston MA

Page 2: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Reason

Page 3: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

I-131

• “Magic Bullet” – Very specific for thyroid or thyroid mets

– Usually cleared rapidly with 2-3 day Teff

– 8 day T1/2 leaves time for to deposit its energy

– 364 kev -ray allows imaging

Page 4: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Thyroid ablation

• Very effective

• Doses to 6000-20000 rads to the thyroid

• Minimal dose to other organs

Page 5: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

But there are complications in some cases

• Mets in lung and resultant dose to lung tissue

• Dose to blood marrow

• Dose to salivary glands

• Other?– Complex distribution

Page 6: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Goals

• Limit dose to marrow to < 200 rads

• Limit dose to lungs to < 2000 rads

• Estimate dose to bladder, salivary glands, other organs with significant uptake

Page 7: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Selected History

• Benua 1962 based on MSK experience gives these guidelines to limit bone marrow dose :– < 200 rads to blood – < 120 mCi retained at 48 hr (80 mCi with

diffuse lung mets)

Page 8: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

I-131 can be imaged quantitatively but..

– scatter– penetration– sensitivity– attenuation– time

…all complicate the task of getting meaningful numbers

Page 9: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Generally accepted procedure

• Dual-head planar gamma camera imaging w/standard source

• ROI for selected organs• Obtain geometric mean of Ant and Post counts • Measure attenuation using gamma camera and

area source (e.g. Co-57 sheet source)• Obtain blood samples to estimate marrow dose• Follow long enough (e.g 4 days)• Use MIRD dose calculation techniques

Page 10: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Resource intensive

• Imaging:– ~3 hr first day

• Attenuation scan

• 2 hr pre void scan + blood

• 4 hr post void scan + blood

– 1 hr day 2, 3 and 4 + bloods

• Blood samples to count • ROI to draw and calculate• Dosimetry calculation• Dose plan

Page 11: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Attenuation scan w/ Co-57 sheet source

Blank scan previously acquired

Page 12: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

2 hr & 24 hr

Page 13: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

48 hr & 72 hr

Page 14: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Aids

• MIRD – tables, models, data

• MIRDOSE 1, 2, 3 by Stabin

• RADAR by Stabin(http://www.doseinfo-radar.com/RADARHome.html)

• Olinda by Stabin• NucliDose Erwin & Groch (includes MIRDOSE2)

• Gamma camera ROI tools

• Spreadsheets

Page 15: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

MIRD

Medical Internal Radiation Dose

Subcommittee of the

Society of Nuclear Medicine

Page 16: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

• MIRD Publication - MIRD Dose Estimate Report #19: Radiation Absorbed Dose Estimates from 18F-FDG

• MIRD Publication - MIRD Supplement 1999: Foreword, MIRD Perspective, Pamphlets 14 Revised, 15, 16, and 17

• MIRD Publication - MIRD Dose Estimate Report #13: Radiation Absorbed Dose from Technetium-99m-labeled bone imaging agents

• MIRD Publication - MIRD Pamphlet #11: S, Absorbed Dose per Unit Cumulated Activity for Selected Radionuclides and Organs (PART 1)

• MIRD Publication - MIRD Pamphlet #11: S, Absorbed Dose per Unit Cumulated Activity for Selected Radionuclides and Organs (PART 2)

• MIRD Publication - MIRD Pamphlet #11: S, Absorbed Dose per Unit Cumulated Activity for Selected Radionuclides and Organs (PART 3)

• MIRD Publication - MIRD Pamphlet #13: Specific Absorbed Fractions for Photon Sources Uniformly Distributed in the Heart Chambers and Heart Wall of Heterogeneous Phantom

• MIRD Publication - MIRD Pamphlet #5 Revised: Estimates of Absorbed Fractions for Monoenergetic Photon Sources Uniformly Distributed in Various Organs of a Heterogeneous Phantom

Page 17: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

MIRDOSE

• A series (v1, v2, v3) of software programs that ran on PCs circa 1985-1998 by Michael Stabin then of Oak Ridge Associated Universities and Oak Ridge National Laboratories

• Eventually FDA stopped distribution of the software since it was a medical device!

Page 18: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

RADARWeb site

RAdiation Dose Assessment Resource

By Michael Stabin and colleagues

Difficult to use for individual dosimetry.

Page 19: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

OLINDA/EXM

Organ Level INternal Dose Assessment/EXponential Modeling

By Michael Stabin of Vanderbilt.

Has FDA 510(k) exemption

Page 20: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Summary of dose estimates for xxx

11/Mar/01

OrganAdministered dose (mCi)

rad/mCi 100 120 140 160 180 200 220 240 260 280 300 320 340 360

MIRD:

Lungs 4 388 466 543 621 698 776 854 931 1009 1086 1164 1242 1319 1397

T.Body 0.34 34 41 47 54 61 68 75 81 88 95 102 108 115 122

Bladder 2.71 271 325 379 434 488 542 596 650 705 759 813 867 921 976

Benua:

Bld(Marrow) 0.59 59 71 83 95 107 119 131 143 155 167 178 190 202 214

48hr retain (mCi) 25 30 35 40 45 50 55 60 65 70 75 80 85 90

The amount retained at 48 hr should be <80 mCi

Amount in lungs should be < 2000 rads

Page 21: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Brigham & Women's HospitalDivision of Nuclear Medicine

 Whole Body Dosimetry Study with 131I 

Indications: Quantitative estimate of 131I in metastases or thyroid remnants requiring complete dosimetry to protect critical organs. Patient Preparation: This exam should not be performed if the patient has had any iodinemedications which will interfere with the study or any iodinated contrast media within the last 6 weeks. TSH level should be evaluated prior to radiopharmaceutical administration. Levels should be greater than 50 uU/ml. The patient should be fasting for 1 hour prior to ingestion of the radiopharmaceutical and should not eat for at least 30 min. following. Radiopharmaceutical: 131I solution Dose: 3 mCiWritten directive form must be signed by Attending Physician prior to administration. Route of Administration: oral

Page 22: Why Quantitative I-131  Robert E. Zimmerman Joint Program in Nuclear Medicine Harvard Medical

Imaging: 1.      WB Blank scan with 57Co sheet source: Use acquisition protocol BWH WB Co-57 Blank Scan. Prior to radiopharmaceutical administration a 57Co WB blank scan must be performed. Mark the table for patient re-positioning for all imaging sessions by placing a piece of tape on the table corresponding to the location of the top of the patient’s head. Place 57Co sheet source on detector 2 of e.cam or MS2 with high energy collimators in place. Use both detectors and peak for 57Co. Do blank scan with no patient on table starting where top of head will be located to end of feet.  2.      WB transmission scan is be performed next.  Use acquisition protocol BWH Co-57 Transmission Scan. Leave the 57 Co sheet source on detector 2. Place the patient on table at location of tape. Do anterior WB sweep from head to toe for 20 min. (8 cm/min). 3.      Administer the radiopharmaceutical. The patient must not void between administration and first imaging session. 4.      Prepare standard of 50-100 Ci of I-131 in 250 ml tissue culture flask. Label flask with name, time, date and activity. 5.      Use acquisition protocol BWH I131 WB scan. Perform WB sweep anterior/posterior 60-120 minutes post administration of I-131. Scan for 20 min. (8 cm/min) and include standard in field of view (e.g. between feet or lower legs). 6.      Repeat WB sweeps at 24, 48 and 72 hours post administration of 131I. Increase imaging time at later time points to 40 min (16 cm/min) and include standard in all imaging sessions. 7.      Spot views of head and neck may be required by Nuclear Med physician. 8.      Draw 2 cc of blood at each imaging session, excluding transmission session. Recordname of patient, time and date of blood drawing on each tube and on patient jacket. All samples will be counted on the last day of imaging. 9.      Processing using Nuclidose on ICON/IDL system will be done by the physicist. ROIs corresponding to each source organ will be drawn. Time activity curves will be obtained. Dose calculations will be performed to obtain rads/mCi. Adapted from CH protocol REZ5 Dec 2000