Pharmacokinetics and dosimetry of an α-particle emitter labeled antibody: 213Bi-HuM195 (anti-CD33) in patients with leukemia Journal Article


Authors: Sgouros, G.; Ballangrud, Å M.; Jurcic, J. G.; McDevitt, M. R.; Humm, J. L.; Erdi, Y. E.; Mehta, B. M.; Finn, R. D.; Larson, S. M.; Scheinberg, D. A.
Article Title: Pharmacokinetics and dosimetry of an α-particle emitter labeled antibody: 213Bi-HuM195 (anti-CD33) in patients with leukemia
Abstract: Data from nine patients with leukemia participating in a phase I activity-escalation study of HUM195, labeled with the α-particle emitter 213Bi (half-life = 45.6 min), were used to estimate pharmacokinetics and dosimetry. This is the first trial using an α-particle emitter in humans. The linear energy transfer of particles is several hundredfold greater than that of β emissions. The range in tissue is approximately 60-90 μm. Methods: The activity administered to patients ranged from 0.6 to 1.6 GBq. Patient imaging was initiated at the start of each injection. Thirty 1-min images followed by ten 3-min images were collected in dynamic mode; a 20% photopeak window centered at 440 keV was used. Blood samples were collected until 3 h postinjection and counted in a gamma counter. Contours around the liver and spleen were drawn on the anterior and posterior views and around a portion of the spine on the posterior views. No other organs were visualized. Results: The percentage injected dose in the liver and spleen volumes increased rapidly over the first 10-15 min to a constant value for the remaining hour of imaging, yielding a very rapid uptake followed by a plateau in the antibody uptake curves. The kinetic curves were integrated to yield cumulated activity. The mean energy emitted per nuclear transition for 213Bi and its daughters, adjusted by a relative biologic effectiveness of 5 for α emissions, was multiplied by the cumulated activity to yield the absorbed dose equivalent. Photon dose to the total body was determined by calculating a photon-absorbed fraction. The absorbed dose equivalent to liver and spleen volumes ranged from 2.4 to 11.2 and 2.9 to 21.9 Sv, respectively. Marrow (or leukemia) mean dose ranged from 6.6 to 12.2 Sv. The total-body dose (photons only) ranged from 2.2 x 10-4 to 5.8 x 10-4 Gy. Conclusion: This study shows that patient imaging of 213Bi, an α-particle emitter, labeled to HUM195 is possible and may be used to derive pharmacokinetics and dosimetry. The absorbed dose ratio between marrow, liver and spleen volumes and the whole body for 213Bi-HuM195 is 1000-fold greater than that commonly observed with β-emitting radionuclides used for radioimmunotherapy.
Keywords: leukemia; unclassified drug; antineoplastic agents; radiation dose; animals; mice; radiotherapy dosage; antibodies, monoclonal; dosimetry; leukemia, myeloid; gamma cameras; drug absorption; drug half life; radioimmunotherapy; radioisotopes; photon; radioisotope decay; acute disease; cd33 antigen; electron; hum195; antibody labeling; alpha radiation; bismuth; alpha particles; linear energy transfer; bismuth 213; monoclonal antibody m 195; humans; human; priority journal; article; 213bi; α particle
Journal Title: Journal of Nuclear Medicine
Volume: 40
Issue: 11
ISSN: 0161-5505
Publisher: Society of Nuclear Medicine  
Date Published: 1999-11-01
Start Page: 1935
End Page: 1946
Language: English
PUBMED: 10565792
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 16 August 2016 -- Source: Scopus
Citation Impact
MSK Authors
  1. George Sgouros
    146 Sgouros
  2. Ronald D Finn
    279 Finn
  3. Michael R Mcdevitt
    144 Mcdevitt
  4. Joseph G Jurcic
    134 Jurcic
  5. John Laurence Humm
    437 Humm
  6. Yusuf E Erdi
    118 Erdi
  7. Steven M Larson
    960 Larson
  8. Bipin M Mehta
    36 Mehta