The treatment of painful skeletal metastases is a common clinical prob
lem, and the use of therapeutic radionuclides which localize at metast
atic sites has been found to be an effective method for treatment of p
ain, especially for multiple sites for which the use of external beam
irradiation is impractical. There are currently several metastatic-tar
geted agents radiolabeled with various therapeutic radionuclides which
are in various stages of clinical investigation. Since neutron rich r
adionuclides are produced in research reactors and often decay by emis
sion of beta(-) particles, most radionuclides used for bone pain palli
ation are reactor-produced. Key examples of radionuclides produced by
single neutron capture of enriched targets include rhenium-186 and sam
arium-153. In addition, generator systems are also of interest which p
rovide therapeutic daughter radionuclides from the decay of reactor-pr
oduced parent radionuclides. One important example is rhenium-188, ava
ilable from generators via decay of reactor-produced tungsten-188. Tin
-117m is an example of a reactor-produced radionuclide which decays wi
th the emission of low-energy conversion electrons rather than by beta
(-) decay. Each of these agents and/or radionuclides has specific adva
ntages and disadvantages, however, the ideal agent for bone pain palli
ation has not yet been identified. The goal of this paper is to briefl
y review the production and use of several reactor-produced radionucli
des for bone pain palliation, and to discuss the role of the ORNL High
Flux Isotope Reactor(HFIR) for the production of many of these radion
uclides. Published by Elsevier Science Ltd.