Radiation dosimetry for radionuclide therapy in a nonmyeloablative strategy

Gerald L Denardo, Christine L. Hartmann Siantar, Sally J. DeNardo

Research output: Contribution to journalArticlepeer-review

16 Scopus citations


Radionuclide therapy extends the usefulness of radiation from localized disease to multifocal disease by combining radionuclides with disease-seeking drugs such as antibodies or custom-designed synthetic agents. Like conventional radiotherapy the effectiveness of targeted radionuclides is ultimately limited by the amount of undesired radiation given to a critical dose-limiting normal tissue most often the bone marrow. Because radionuclide therapy relies on biological delivery of radiation its optimization and characterization are necessarily different than for conventional radiation therapy. However the principals of radiobiology and of absorbed radiation dose remain important for predicting radiation effects. Fortunately most radionuclides emit gamma rays that allow the measurement of isotope concentrations in both tumor and normal tissues in the body. By administering a small "test dose" of the intended therapeutic drug the clinician can predict the radiation dose distribution in the patient. This can serve as a basis to predict therapy effectiveness optimize drug selection and select the appropriate drug dose in order to provide the safest most effective treatment for each patient. Although treatment planning for individual patients based upon tracer radiation dosimetry is an attractive concept and opportunity practical considerations may dictate simpler solutions under some circumstances. There is agreement that radiation dosimetry (radiation absorbed dose distribution cGy) should be utilized to establish the safety of a specific radionuclide drug during drug development but it is less generally accepted that absorbed radiation dose should be used to determine the dose of radionuclide (radioactivity GBq) to be administered to a specific patient (i.e. radiation dose-based therapy). However radiation dosimetry can always be utilized as a tool for developing drugs assessing clinical results and establishing the safety of a specific radionuclide drug. Bone marrow dosimetry continues to be a "work in progress." Blood-derived and/or body-derived marrow dosimetry may be acceptable under specific conditions but clearly do not account for marrow and skeletal targeting of radionuclide. Marrow dosimetry can be expected to improve significantly but no method for marrow dosimetry seems likely to account for decreased bone marrow reserve.

Original languageEnglish (US)
Pages (from-to)107-118
Number of pages12
JournalCancer Biotherapy and Radiopharmaceuticals
Issue number1
StatePublished - 2002


  • Cancer
  • Dosimetry
  • Radionuclide
  • Radiotherapy
  • Therapy

ASJC Scopus subject areas

  • Oncology
  • Radiology Nuclear Medicine and imaging
  • Pharmacology
  • Cancer Research


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