Double productive immunoglobulin sequence rearrangements in patients with chronic lymphocytic leukemia. Issue 4 (28th February 2013)
- Record Type:
- Journal Article
- Title:
- Double productive immunoglobulin sequence rearrangements in patients with chronic lymphocytic leukemia. Issue 4 (28th February 2013)
- Main Title:
- Double productive immunoglobulin sequence rearrangements in patients with chronic lymphocytic leukemia
- Authors:
- Visco, Carlo
Moretta, Francesca
Falisi, Erika
Facco, Monica
Maura, Francesco
Novella, Elisabetta
Nichele, Ilaria
Finotto, Silvia
Giaretta, Ilaria
Ave, Elisa
Perbellini, Omar
Guercini, Nicola
Scupoli, Maria Teresa
Trentin, Livio
Trimarco, Valentina
Neri, Antonino
Semenzato, Gianpietro
Rodeghiero, Francesco
Pizzolo, Giovanni
Ambrosetti, Achille - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The immunoglobulin heavy chain variable (IGHV) gene mutational status represents a major prognostic marker in chronic lymphocytic leukemia (CLL). Usually, the prognostic implications of IGHV gene analysis can be reliably ascertained but, occasionally, double productive rearrangements have been detected. Clinical presentation and biological features of such cases are unknown. Sixty patients with morphologically and phenotypically monoclonal CLL but double productive IGHV rearrangements were retrospectively identified by mRNA analysis from three Hematology Institutions. Clinical and biological features and survival of these 60 patients were compared with a control group of patients with CLL and single IGHV rearrangement. A prospective registry was used to assess the epidemiology of double productive IGHV among incidental patients with CLL. Using standard criteria to define IGHV‐mutated (M) or unmutated (U) cases, 39 of the 60 patients (65%) with double productive IGHV rearrangement had concordant status (23 MM, 16 UU), while 21 (35%) had discordant IGHV status. As compared with M patients, the MM ones had lower CD38 expression, more favorable cytogenetics and more indolent clinical behavior. Cases with UU had similar characteristics of U patients. Discordant cases presented with adverse prognostic features and had an aggressive clinical behavior requiring early treatment, similar to U<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The immunoglobulin heavy chain variable (IGHV) gene mutational status represents a major prognostic marker in chronic lymphocytic leukemia (CLL). Usually, the prognostic implications of IGHV gene analysis can be reliably ascertained but, occasionally, double productive rearrangements have been detected. Clinical presentation and biological features of such cases are unknown. Sixty patients with morphologically and phenotypically monoclonal CLL but double productive IGHV rearrangements were retrospectively identified by mRNA analysis from three Hematology Institutions. Clinical and biological features and survival of these 60 patients were compared with a control group of patients with CLL and single IGHV rearrangement. A prospective registry was used to assess the epidemiology of double productive IGHV among incidental patients with CLL. Using standard criteria to define IGHV‐mutated (M) or unmutated (U) cases, 39 of the 60 patients (65%) with double productive IGHV rearrangement had concordant status (23 MM, 16 UU), while 21 (35%) had discordant IGHV status. As compared with M patients, the MM ones had lower CD38 expression, more favorable cytogenetics and more indolent clinical behavior. Cases with UU had similar characteristics of U patients. Discordant cases presented with adverse prognostic features and had an aggressive clinical behavior requiring early treatment, similar to U patients. The prevalence of double IGHV was 3.1%. Patients with CLL with double concordant mutational status (MM or UU) have a clinical course similar to that of the corresponding single IGHV status, while those exhibiting discordant status represent a high risk population. This may help correct stratification within clinical trials. Am. J. Hematol. 88:277–282, 2013. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- American journal of hematology. Volume 88:Issue 4(2013:Apr.)
- Journal:
- American journal of hematology
- Issue:
- Volume 88:Issue 4(2013:Apr.)
- Issue Display:
- Volume 88, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 88
- Issue:
- 4
- Issue Sort Value:
- 2013-0088-0004-0000
- Page Start:
- 277
- Page End:
- 282
- Publication Date:
- 2013-02-28
- Subjects:
- Hematology -- Periodicals
616.15 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-8652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ajh.23396 ↗
- Languages:
- English
- ISSNs:
- 0361-8609
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0824.800000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3264.xml