Samarium Sm-153 lexidronam is a medium energy beta-emitting radioisoto
pe chelated to the tetraphosphate, ethylenediaminetetramethylenephosph
onic acid (EDTMP). Sm-153 has a physical half-life of 1.9 days. Samari
um Sm-153 lexidronam concentrates in bone tissue and has a metastatic
lesion : normal bone ratio of 4. Clearance of nonskeletal radioactivit
y after administration of samarium Sm-153 lexidronam is rapid, and is
almost complete from the blood and urine within 1 and 6 hours, respect
ively. Some degree of pain relief was achieved in 72% of patients with
bone metastases after a single dose of samarium Sm-153 lexidronam 1 m
Ci/kg (37 MBq/kg) compared with 44% of placebo recipients (p < 0.025).
Relief was generally attained within 2 weeks and lasted for a median
of 8 to 15 weeks. After recurrence of pain, a second dose of samarium
Sm-153 lexidronam may produce further pain relief. in some patients. 1
53 The dose-limiting toxicity of samarium Sm-153 lexidronam is reversi
ble myelosuppression.