Interphase cytogenetic analysis of chromosome 13q14 was performed in 28 patients with multiple myeloma (MM) receiving high-dose therapy followed by autologous (n=24) or allogeneic (n=4) stem cell support. Eleven (39%) patients were found to have a deletion of chromosome 13q14. Response rates to high-dose therapy were independent of the chromosome 13 status, but patients with a deletion of 13q14 had a significantly shorter progression-free (p=0.001) and overall survival (p=0.012) than patients with normal chromosome 13q14. Our results indicate that high-dose therapy appears promising in patients with normal chromosome 13, whereas in patients with a deletion of 13q14 innovative therapeutic concepts are warranted.
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http://dx.doi.org/10.1007/s002770100296 | DOI Listing |
Breast Cancer Res
November 2024
Department of Medical Genetics, Institute of Clinical Medicine, Faculty of Medicine, University of Oslo and Oslo University Hospital, Oslo, Norway.
Pediatr Res
November 2024
Department of Obstetrics & Gynecology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Am J Obstet Gynecol
September 2024
Division of Neonatology, Department of Pediatrics, Columbia University Irving Medical Center, New York City, NY. Electronic address:
J Assoc Genet Technol
January 2024
Cytogenetics Lab director, Department of Pathology, Moffitt Cancer Center, Tampa, FL.
Fluorescence in situ hybridization (FISH) is a reliable method to detect a deletion on chromosome 13q14. Currently, three commercial probes are available for FISH testing in clinical cytogenetics laboratories, RB1, D13S319, and D13S25, with the D13S319 probe most commonly used for 13q deletion. In this study, we compared FISH test results among these three probes in CLL cases with positive 13q deletion.
View Article and Find Full Text PDFCurr Issues Mol Biol
June 2024
Hepatology Unit, Department of Clinical and Experimental Medicine, Policlinico "G. Rodolico-San Marco" Hospital, University of Catania, 95123 Catania, Italy.
Wilson's disease (WD) is a biallelic disease-causing variant in the gene on chromosome 13q14.3 that results in copper accumulation in many organs, particularly the liver and brain. The phenotypic spectrum is wide and symptoms at onset can be heterogeneous.
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