Speaker
Dr
Laurent MENARD
(Laboratoire Imagerie et Modélisation en Neurobiologie et cancérologie (UMR 8165) - Université Paris 7)
Description
Surgery is still considered the primary therapeutic procedure for high grade gliomas
and several recent clinical studies have shown that gross total tumor resection is
directly associated with longer and better survival when compared to subtotal
resection. In order to refine the resection especially in the boundaries of gliomas,
we are developing an intraoperative probe specifically dedicated to the localization
of residual tumor labeled with positron emitters. The probe was designed to be
compact and electrically safe in order to be directly coupled to the excision tool
leading to simultaneous detection and removal of tumor tissues. The detection head of
the intraoperative beta-probe consists of plastic scintillating fibers held in a
close packed annular arrangement ensheathing the excision tool. This head is
connected to an optic fiber bundle that exports the scintillating light to a
multi-channel photomultiplier. The annihilation gamma ray background generated by the
annihilation of beta+ in tissues is eliminated by a real-time subtraction method.
Validation of the technical choice and optimization of the probe geometry were
performed by preliminary measurements and Monte Carlo simulations. Simulations were
realized using MCNP code and an anthropomorphic brain phantom filled with different
radiotracer activities. Optimal performances were obtained with a detection head
composed of 2-mm diameter and 0.5-mm long scintillating beta-sensitive fibers
associated to 2-mm diameter and 2-mm long beta-shielded fibers for the gamma ray
background rejection. The theoretical probe sensitivity was found to be 1.95
cps/kBq/ml with a gamma ray rejection efficiency of 99.6%. The expected minimum
radiotracer detectable concentration for 18F-FET was 3.7 kBq/ml. When compared to the
10.7 kBq/ml average concentration in the bulk of the tumor, this value demonstrate
the ability of the probe to define more accurately the extent of brain tumor resection.
Following these results, a first prototype of the probe based on seven detection
elements was developed. Characterization of the device including uniformity of the
signal gain and of the beta and gamma sensitivity among the detection elements,
spatial resolution and gamma ray rejection efficiency will be presented. The ability
of the prototype to localize small amounts of beta+-emitting radiopharmaceuticals
will be also demonstrated using a brain phantom simulating a surgical cavity after
excision of the bulk of the tumor labeled with 18F.
Author
Mr
Sébastien BONZOM
(Laboratoire Imagerie et Modélisation en Neurobiologie et cancérologie (UMR 8165) - Université Paris 7)
Co-authors
Dr
Laurent MENARD
(Laboratoire Imagerie et Modélisation en Neurobiologie et cancérologie (UMR 8165) - Université Paris 7)
Dr
Laurent PINOT
(Laboratoire Imagerie et Modélisation en Neurobiologie et cancérologie (UMR 8165))
Dr
Marie-Alix DUVAL
(Laboratoire Imagerie et Modélisation en Neurobiologie et cancérologie (UMR 8165) - Université d'Evry Val d'Essone)
Dr
Rainer SIEBERT
(Laboratoire Imagerie et Modélisation en Neurobiologie et cancérologie (UMR 8165))
Dr
Stéphane PALFI
(Service de neurochirurgie, CHU Henri Mondor , 94010 Créteil Cedex, France et URA CEA-CNRS 2210, 4 place du général Leclerc, 91401 Orsay Cedex)
Dr
Stéphanie PITRE
(Laboratoire Imagerie et Modélisation en Neurobiologie et cancérologie (UMR 8165))
Prof.
Yves CHARON
(Laboratoire Imagerie et Modélisation en Neurobiologie et cancérologie (UMR 8165) - Université Paris 7)