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Departments of Radiology and Medicine, University of Missouri Hospital and Clinics, and Nuclear Medicine and Research Services, Harry S. Truman Memorial Veterans Hospital, Columbia, Missouri
Correspondence: For reprints contact: Richard A. Holmes, MD, Section of Nuclear Medicine, 2N-19, One Hospital Dr., University of Missouri Hospital and Clinics, Columbia, MO 65212.
ABSTRACT
Samarium-153 ethylenediaminetetramethylene phosphonic acid ([153Sm]EDTMP) has been proposed to palliate pain resulting from osteoblastic metastatic bone cancer. Encouraging results in dogs with primary malignant bone cancer provided the catalysis for human biodistribution studies in five patients with metastatic skeletal carcinoma. The objective was to assess the preferential localization of [153Sm]EDTMP in bony lesions and compare it to the 99mTc-labeled phosphonates. Blood clearance of [153Sm]EDTMP was rapid with minimal accumulation in nonosseous tissues. Both radiopharmaceuticals showed identical lesion uptake in 23 paired lesions (p > 0.05). This indicates that the two radiopharmaceuticals concentrate in metastatic skeletal lesions by the same mechanism and since [153Sm]EDTMP emits beta radiation it maybe therapeutically useful in ameliorating metastatic bony cancer pain.
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