What's new AAPOS 2008 - The Private Eye Clinic
What's new AAPOS 2008 - The Private Eye Clinic
What's new AAPOS 2008 - The Private Eye Clinic
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Treatment of retinoblastoma: Current status and future perspectives.<br />
Rodriguez-Galindo C, Chantada GL, Haik BG, Wilson MW.<br />
Curr Treat Options Neurol 2007 Jul; 9(4):294-307.<br />
This is a good review article delineating the current treatment status for RB. <strong>The</strong>y<br />
emphasize that the treatment must always be individualized. <strong>The</strong>y review the various<br />
treatment modalities: surgery, focal therapy (photocoagulation, cryo, and<br />
thermotherapy), radiation therapy and chemotherapy. Each of the specific chemo<br />
agents is reviewed. <strong>The</strong>y touch on the emerging therapies and provide an opinion<br />
statement.<br />
<strong>Eye</strong> size in retinoblastoma: MR imaging measurements in normal and affected<br />
eyes.<br />
De Graaf P, Knol DL, Moll AC, Imhof SM et al.<br />
Radiology 2007 Jul; 244(1):273-80<br />
This is a retrospective study of 100 eyes (50 boys/50girls) with RB over a 12 year<br />
period. <strong>The</strong>y used MR imaging to measure axial length (AL), equatorial diameter ED)<br />
and eye volume (EV). Normal eyes of patients with unilateral retinoblastoma served as<br />
controls. <strong>Eye</strong>s with Rb had significantly shorter AL’s and EDs and significantly smaller<br />
EVs than normal eyes. In those eyes with Rb, the larger the tumor volume, the smaller<br />
the eye.<br />
One hit, two hits, three hits, more? Genomic changes in the development of<br />
retinoblastoma.<br />
Corson TW, Gallie BL.<br />
Genes Chromosomes Cancer 2007 Jul; 46(7):617-34.<br />
RB is initiated by the loss of both alleles of the prototypic tumor suppressor gene RB1.<br />
However a large number of cytogenetic and comparative genomic hybridization studies<br />
have shown that the M1 and M2 mutational events are not the only genomic changes in<br />
RB. <strong>The</strong> authors review these subsequent changes which are likely crucial for tumor<br />
progression. <strong>The</strong> authors provide a comprehensive summary of the genomic evidence<br />
implicating gain of 1q, 2p, 6p, and 13q and loss of 16q in RB oncogenesis. <strong>The</strong>y<br />
discuss the search for candidate oncogenes and tumor suppressor genes within these<br />
regions and their potential diagnostic, prognostic, and therapeutic implications.<br />
Outcomes of a two-drug chemotherapy regimen for intraocular retinoblastoma.<br />
Zage PE, Reitman AJ, Seshadri R, et al<br />
Pediatr Blood Cancer, 2007 Aug 29 [Epub ahead of print]<br />
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