M. Aas et al., Internal radionuclide therapy of primary osteosarcoma in dogs, using Sm-153-ethylene-diamino-tetramethylenephosphonate (EDTMP), CLIN CANC R, 5(10), 1999, pp. 3148S-3152S
Fifteen dogs were referred because of a spontaneous bone tumor, lameness, a
nd local pain. The osteosarcoma diagnosis was established by clinical exami
nation, X-ray, bone scintigraphy, and histological examination of biopsy ma
terial. The tumors were located in the extremities (n = 12), scapula (n = 1
), maxilla (n = 1), and the frontal bone (n = 1). The dogs were given one t
o four i.v. injections of Sm-153-labeled ethylene-diamino-tetramethylene-ph
osphonate (Sm-153-EDTMP; 36-57 MBq/kg body weight). Three dogs had surgery
in addition to the radionuclide treatment, Platelet and WBC counts showed a
moderate and transient decrease. No other toxicity was observed. Average t
umor doses after a single injection were similar to 20 Gy, considerably hig
her in some areas because of inhomogeneous uptake. Macroscopically distant
metastases were detected in seven dogs at autopsy. One dog died from an int
ercurrent disease, free of cancer, 5 months after the radionuclide treatmen
t. None of the dogs was cured. The median and mean survival times from the
first treatment to death or euthanasia were 150 and 252 days, respectively.
Nine of the dogs had obvious pain relief, and five of them seemed pain-fre
e: one for 20 months and one for 48 months. It is concluded that high tumor
doses may be deposited in dog osteosarcomas by Sm-153-EDTMP, and the ratio
between tumor dose and the dose to surrounding tissues is favorable. The t
reatment gives pain relief and in some cases tumor growth delay. In combina
tion with surgery, Sm-153-EDTMP may prolong life significantly and possibly
cure the disease because the development of metastases are seemingly postp
oned. No serious side effects were observed.