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Hyperfractionated Treatment with 177 Lu-Octreotate Increases Tumor Response in Human Small-Intestine Neuroendocrine GOT1 Tumor Model.

Mikael ElvbornEmman ShubbarEva Forssell-Aronsson
Published in: Cancers (2022)
Radionuclide treatment of patients with neuroendocrine tumors has advanced in the last decades with favorable results using 177 Lu-octreotate. However, the gap between the high cure rate in animal studies vs. patient studies indicates a potential to increase the curation of patients. The aim of this study was to investigate the tumor response for different fractionation schemes with 177 Lu-octreotate. BALB/c mice bearing a human small-intestine neuroendocrine GOT1 tumor were either mock treated with saline or injected intravenously with a total of 30-120 MBq of 177 Lu-octreotate: 1 × 30, 2 × 15, 1 × 60, 2 × 30, 1 × 120, 2 × 60, or 3 × 40 MBq. The tumor volume was measured twice per week until the end of the experiment. The mean tumor volume for mice that received 2 × 15 = 30 and 1 × 30 MBq 177 Lu-octreotate was reduced by 61% and 52%, respectively. The mean tumor volume was reduced by 91% and 44% for mice that received 2 × 30 = 60 and 1 × 60 MBq 177 Lu-octreotate, respectively. After 120 MBq 177 Lu-octreotate, given as 1-3 fractions, the mean tumor volume was reduced by 91-97%. Multiple fractions resulted in delayed regrowth and prolonged overall survival by 20-25% for the 120 MBq groups and by 45% for lower total activities, relative to one fraction. The results indicate that fractionation and hyperfractionation of 177 Lu-octreotate are beneficial for tumor reduction and prolongs the time to regrowth.
Keyphrases
  • newly diagnosed
  • clinical trial
  • skeletal muscle
  • neuroendocrine tumors
  • metabolic syndrome
  • insulin resistance
  • pluripotent stem cells