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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1999-3-11
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pubmed:abstractText |
Conventional chromosome analysis (CCA) and interphase fluorescence in situ hybridization (FISH) was performed in 42 patients with mantle-cell lymphoma (MCL), with BCL1 rearrangement. The t(11;14)(q13;q32) or 11q abnormalities were detected by CCA in 34 cases, 20 of which had additional aberrations. A normal karyotype was observed in 8 cases. Probes detecting the chromosome aberrations that were observed in at least 3 cases by CCA, ie, +12, 13q14 deletion, and 17p deletion, were used for interphase FISH analysis. FISH detected total or partial +12, 13q14 deletion and 17p- in 28.5%, 52.4%, and 26% of the cases, respectively. The presence of these anomalies was not a function of karyotype complexity. Based on the results of CCA/FISH, three groups of increasing karyotype complexity were recognized: group 1, including 11 patients without detectable aberrations in addition to BCL1 rearrangement; group 2, including 14 patients with 1 to 2 additional anomalies; and group 3, including 17 patients with three or more additional anomalies. Clinical parameters associated with shorter survival were male sex (P =.006) and primary lymph-node involvement compared with primary bone marrow involvement (P =.015). Trisomy 12 was the only single cytogenetic parameter predictive of a poor prognosis (P =.006) and the best prognostic indicator was the derived measure of karyotype complexity (P <.0001), which maintained statistical significance in multivariate analysis (P<.0001). We arrived at the following conclusions: 13q14 deletion occurs at a high incidence in MCL; 17p deletion and total/partial +12 are relatively frequent events in MCL, the latter aberration being associated with a shorter survival; and the degree of karyotype complexity has a strong impact on prognosis in this neoplasia.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0006-4971
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pubmed:author |
pubmed-author:BardiAA,
pubmed-author:BigoniRR,
pubmed-author:BirgFF,
pubmed-author:BullrichFF,
pubmed-author:CastoldiGG,
pubmed-author:CrochDD,
pubmed-author:CuneoAA,
pubmed-author:DöhnerHH,
pubmed-author:HagemeijerAA,
pubmed-author:MilanoLL,
pubmed-author:PivaNN,
pubmed-author:RigolinG MGM,
pubmed-author:RobertiM GMG,
pubmed-author:VeroneseM LML
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
93
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1372-80
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9949181-Adult,
pubmed-meshheading:9949181-Aged,
pubmed-meshheading:9949181-Aged, 80 and over,
pubmed-meshheading:9949181-Cell Lineage,
pubmed-meshheading:9949181-Chromosomes, Human, Pair 11,
pubmed-meshheading:9949181-Chromosomes, Human, Pair 14,
pubmed-meshheading:9949181-Cyclin D1,
pubmed-meshheading:9949181-Female,
pubmed-meshheading:9949181-Gene Rearrangement,
pubmed-meshheading:9949181-Humans,
pubmed-meshheading:9949181-Lymphoma,
pubmed-meshheading:9949181-Male,
pubmed-meshheading:9949181-Middle Aged,
pubmed-meshheading:9949181-Translocation, Genetic
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pubmed:year |
1999
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pubmed:articleTitle |
Cytogenetic profile of lymphoma of follicle mantle lineage: correlation with clinicobiologic features.
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pubmed:affiliation |
Department of Biomedical Sciences-Hematology Section, University of Ferrara, Italy. sse@dns.unife.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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