Effect of a 188 Re-SSS lipiodol/131I-lipiodol mixture, 188 Re-SSS lipiodol alone or 131I-lipiodol alone on the survival of rats with hepatocellular carcinoma

• Published in: Nuclear medicine communications Vol. 27; no. 4; p. 363
• Main Authors: Garin, Elienne, Rakotonirina, Hervé, Lejeune, Florence, Denizot, Benoit, Roux, Jerome, Noiret, Nicolas, Mesbah, Habiba, Herry, Jean-Yues, Bourguet, Patrick, Lejeune, Jean-Jacques
• Format: Journal Article
• Language: English
• Published: England 01.04.2006
• Subjects: Animals; Carcinoma, Hepatocellular - radiotherapy; Drug Combinations; Female; Iodine Radioisotopes - administration & dosage; Iodized Oil - administration & dosage; Liver Neoplasms - radiotherapy; Organometallic Compounds - administration & dosage; Prognosis; Radiopharmaceuticals - administration & dosage; Rats; Rats, Sprague-Dawley; Survival Analysis; Survival Rate; Treatment Outcome
• ISSN: 0143-3636

It has been shown that the use of a cocktail of isotopes of different ranges of action leads to an increase in the effectiveness of metabolic radiotherapy. The purpose of the present study was to compare with a control group the effectiveness of three different treatments in rats bearing hepatocellular carcinoma (HCC), using (1) a mixture of lipiodol labelled with both I and Re, (2) lipiodol labelled with I alone and (3) lipiodol labelled with Re alone. Four groups were made up, each containing 14 rats with the N1-S1 tumour cell line. Group 1 received a mixture composed of 22 MBq of Re-SSS lipiodol and 7 MBq I-lipiodol. Group 2 received 14 MBq I-lipiodol. Group 3 received 44 MBq of Re-SSS lipiodol and group 4 acted as the control. The survival of the various groups was compared by a non-parametric test of log-rank, after a follow-up of 60, 180 and 273 days. Compared with the controls, the rats treated with a mixture of Re-SSS lipiodol and I-lipiodol show an increase in survival, but only from day 60 onwards (P=0.05 at day 60 and 0.13 at days 180 and 273). For the rats treated with I-lipiodol, there was a highly significant increase in survival compared with the controls at day 60, day 180 and day 273 (P=0.03, 0.04 and 0.04, respectively). There is no significant increase in survival for the rats treated with Re-SSS lipiodol, irrespective of the follow-up duration (P=0.53 at day 60, 0.48 at day 180, and 0.59 at day 273). In this study, I-lipiodol is the most effective treatment in HCC-bearing rats, because this is the only method that leads to a prolonged improvement of survival. These results cannot necessarily be extrapolated to humans because of the relatively small size and unifocal nature of the lesions in this study. It appears necessary to carry out a study in humans with larger tumours in order to compare these three treatments, particularly with a view to replacing I-labelled lipiodol by Re-labelled lipiodol. However, this study clearly demonstrated that, for small tumours, as in an adjuvant setting for example, I-labelled lipiodol should be a better option than Re-labelled lipiodol.