𝔖 Bobbio Scriptorium
✦   LIBER   ✦

13q14 Deletion size and number of deleted cells both influence prognosis in chronic lymphocytic leukemia

✍ Scribed by Michele Dal Bo; Francesca Maria Rossi; Davide Rossi; Clara Deambrogi; Francesco Bertoni; Ilaria Del Giudice; Giuseppe Palumbo; Mauro Nanni; Andrea Rinaldi; Ivo Kwee; Erika Tissino; Giorgia Corradini; Alessandro Gozzetti; Emanuele Cencini; Marco Ladetto; Angela Maria Coletta; Fabrizio Luciano; Pietro Bulian; Gabriele Pozzato; Luca Laurenti; Francesco Forconi; Francesco Di Raimondo; Roberto Marasca; Giovanni Del Poeta; Gianluca Gaidano; Robin Foà; Anna Guarini; Valter Gattei


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
434 KB
Volume
50
Category
Article
ISSN
1045-2257

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Deletion at 13q14 is detected by fluorescence in situ hybridization (FISH) in about 50% of chronic lymphocytic leukemia (CLL). Although CLL with 13q deletion as the sole cytogenetic abnormality (del13q‐only) usually have good prognosis, more aggressive clinical courses are documented for del13q‐only CLL carrying higher percentages of 13q deleted nuclei. Moreover, deletion at 13q of different sizes have been described, whose prognostic significance is still unknown. In a multi‐institutional cohort of 342 del13q‐only cases and in a consecutive unselected cohort of 265 CLL, we investigated the prognostic significance of 13q deletion, using the 13q FISH probes locus‐specific identifier (LSI)‐D13S319 and LSI‐RB1 that detect the DLEU2/MIR15A/MIR16‐1 and RB1 loci, respectively. Results indicated that both percentage of deleted nuclei and presence of larger deletions involving the RB1 locus cooperated to refine the prognosis of del13q‐only cases. In particular, CLL carrying <70% of 13q deleted nuclei with deletions not comprising the RB1 locus were characterized by particularly long time‐to‐treatment. Conversely, CLL with 13q deletion in <70% of nuclei but involving the RB1 locus, or CLL carrying 13q deletion in ≥70% of nuclei, with or without RB1 deletions, collectively experienced shorter time‐to‐treatment. A revised flowchart for the prognostic FISH assessment of del13q‐only CLL, implying the usage of both 13q probes, is proposed. © 2011 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Cytogenetic, fluorescence in situ hybrid
✍ Anne C. Gardiner; Martin M. Corcoran; David G. Oscier 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 209 KB 👁 1 views

Deletions and translocations of 13q14 are the most frequent structural chromosome abnormalities found in chronic lymphocytic leukaemia (CLL). We have identified 13q14 translocations in the blood of 30 of 450 (6.6%) CLL patients by conventional cytogenetics, using tetradecanoyl phorbol 12-myristate 1

Frequent clonal abnormalities of chromos
✍ Loann C. Peterson; Leanna L. Lindquist; Stephanie Church; Neil E. Kay 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 796 KB

We performed cytogenetic analyses of peripheral blood lymphocytes from 82 Midwestern B-cell chronic lymphocytic leukemia (B-CLL) patients. The cells were cultured with mitogens for 3 4 days. At least I 5 metaphase cells were analyzed in 79 (96%) cases. Fifty (63%) of the 79 patients had clonal chrom

Alterations of multiple tumor suppressor
✍ Elizabeth W. Newcomb; Laxmi S. Rao; Sonia S. Giknavorian; Seung Y. Lee 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 528 KB

## Abstract B‐cell chronic lymphocytic leukemia (B‐CLL) samples were screened for alterations in multiple tumor suppressor genes (__p53__ (17p13), __p__16 INK^4^ (9p21), and disrupted in B‐cell malignancy (__DBM__) (13q14)) by using poly‐merase chain reaction‐based assays. Eleven percent (11 of 96)