05; p = 0 84), log(ANC) nadir (beta = -0 03; 95% CI, -0 10 to 0 0

05; p = 0.84), log(ANC) nadir (beta = -0.03; 95% CI, -0.10 to 0.04; p = 0.40), hemoglobin

nadir (beta = -0.09; 95% CI, -0.31 to 0.14; p = 0.452), or platelet nadir (beta = -3.47; 95% CI, -10.44 to 3.50; p = 0.339).\n\nConclusions: Irradiation of BM subregions with higher F-18-FDG-PET activity was associated with hematologic toxicity, supporting the hypothesis that reducing dose to BMACT subregions could mitigate hematologic toxicity. Future investigation should seek to confirm these findings and to identify optimal SUV thresholds to define BMACT. (C) 2012 Elsevier Inc.”
“Purpose: To determine whether optical imaging can be used for in vivo therapy response monitoring as an alternative to radionuclide techniques. For this, we evaluated the known Her2 response to 17-dimethylaminoethylamino-17-demethoxygeldanamycin hydrochloride (17-DMAG) Belnacasan Apoptosis inhibitor treatment, an Hsp90 inhibitor.\n\nExperimental Design: After in vitro 17-DMAG treatment response evaluation of MCF7 parental cells and 2 HER2-transfected

clones (clone A medium, BI-D1870 in vitro B high Her2 expression), we established human breast cancer xenografts in nude mice (only parental and clone B) for in vivo evaluation. Mice received 120 mg/kg of 17-DMAG in 4 doses at 12-hour intervals intraperitonially (n = 14) or PBS as carrier control (n = 9). Optical images were obtained both pretreatment (day 0) and posttreatment (day 3, 6, and 9), always 5 hours postinjection of 500 pmol of anti-Her2 Affibody-AlexaFluor680 via tail vein (with preinjection background subtraction). Days 3 and 9 in vivo optical imaging signal was further correlated with ex vivo Her2 levels by Western blot after sacrifice.\n\nResults: Her2 expression decreased with 17-DMAG dose in vitro. In vivo optical imaging signal was reduced by 22.5% in clone B (P = 0.003) and by 9% in MCF7 parental tumors (P = 0.23) 3 days after 17-DMAG treatment; optical imaging signal recovered in both tumor types at

days 6 to 9. In the carrier group, no signal reduction was observed. Pearson correlation of in vivo optical imaging FRAX597 manufacturer signal with ex vivo Her2 levels ranged from 0.73 to 0.89.\n\nConclusions: Optical imaging with an affibody can be used to noninvasively monitor changes in Her2 expression in vivo as a response to treatment with an Hsp90 inhibitor, with results similar to response measurements in positron emission tomography imaging studies. Clin Cancer Res; 18(4); 1073-81. (C)2012 AACR.”
“Introduction: Botulinum neurotoxin (BoNT) is probably the most potent biological toxin that can affect humans. Since its discovery by Justinus Kerner, BoNT has seen use in a wide range of cosmetic and non-cosmetic conditions such as cervical dystonia, cerebral palsy, migraines and hyperhidrosis. We tried to trace its history from its inception to its recent urological applications. Materials and Methods: Historical articles about botulinum toxin were reviewed and a Medline search was performed for its urological utility.

Comments are closed.