T-cell prolymphocytic leukemia (T-PLL)

1999-10-01 Martin Yuille Affiliation

1.Academic Department of Haematology, Cytogenetics Institute of Cancer Research, 15 Cotswold Road, SUTTON Surrey SM2 5NG, UK
2.Department of Hematology and Center for Human Genetics Cliniques Universitaires Saint Luc Avenue Hippocrate 10 1200 Brussels, Belgium

Clinics and Pathology

Disease

chronic T-cell lymphoproliferative syndrome

Phenotype stem cell origin

disease affecting mature T-cells; T-cell prolymphocytes usually express CD3, CD5 and CD7; they have either a T-helper (CD4+/CD8-) or a T-suppressor (CD4-/CD8+) phenotype; a small number of cases may co-express CD4 and CD8; this finding is more prevalent in the small cell variant of T-PLL than in classic T-PLL

Epidemiology

very rare disease; represents 20% of prolymphocytic leukemias; the disease occurs at advanced age, typically in the 7th or 8th decade; slight male predominance

Clinics

splenomegaly is common; lymphadenopathy at presentation is unusual but more frequent than in B-PLL; blood data: high leucocyte counts usually exceeding 100x10⁹/l; T-cell prolymphocytes have the same morphologic features than B-cell prolymphocytes; a small cell variant of T-PLL has been described

Prognosis

evolution: progresses rapidly and is generally more aggressive than B-PLL; prognosis: poor response to chemotherapy is observed; median survival is approximatively 7 months from diagnosis

Genes Involved and Proteins

Note

as with other T-cell neoplasms, T-PLL exhibits clonal rearrangement of T-cell receptor genes; translocation t(X;14)(q28;q11) may result into fusion of MTCP1 with TRA/Dgenes; finally, the TCL1 locus on chromosome 14q32 might also been involved

in Ataxia Telangiectasia- a rare recessive pleiotropic disease (including elevated cancer predisposition) mapping to 11q23 and caused by mutations of theATM gene - a recurrent malignancy is observed that is similar to T-PLL; its frequency in A-T patients is higher than in the non-A-T related form; A-T related TPLL has a similar course, a similar immunophenotype and similar cytogenetics (with the notable exception that 11q23 breakpoints are recurrent in the sporadic but not the A-T related form of the disease); an initial report of ATM mutations in T-PLL demonstrated the principle that ATM was a candidate cancer gene in sporadic forms of malignancies prevalent in A-T; the identification of lesions in ATM associated with T-PLL has shown that:

homozygous truncating mutations are present in some cases; this suggests ATM can appear to act like a conventional tumour suppressor with biallelic inactivation in the tumour cell

missense mutations cluster in the carboxy-terminal phosphatidyl-3-kinase (PIK) domain; this suggests impairment of this domain can contribute to - and may constitute a distinct step in - tumourigenesis

rearrangement of the gene is frequent; some rearrangements are consistent with a translocation event, in agreement with cytogenetic data implicating 11q23 in T-PLL; others involve transposition of a segment of the ATM gene elsewhere in the genome.

one allele only is mutated (by rearrangement) in some cases; this is probably not associated with a concomitant epigenetic event such as abnormal promoter methylation

no T-PLL case has been reported with germline ATM mutation; this may reflect the small numbers investigated; all the same, the hypothesis is excluded that this rare disease is due solely to germline ATM mutation

Article Bibliography

Pubmed ID	Last Year	Title	Authors
2738163	1989	Proposals for the classification of chronic (mature) B and T lymphoid leukaemias. French-American-British (FAB) Cooperative Group.	Bennett JM et al
1913594	1991	Inversions and tandem translocations involving chromosome 14q11 and 14q32 in T-prolymphocytic leukemia and T-cell leukemias in patients with ataxia telangiectasia.	Brito-Babapulle V et al
8247530	1993	The chromosomal translocation t(X;14)(q28;q11) in T-cell pro-lymphocytic leukaemia breaks within one gene and activates another.	Fisch P et al
7987802	1994	Multiple karyotypic abnormalities in three cases of small cell variant of T-cell prolymphocytic leukemia.	Heinonen K et al
9622061	1998	Ataxia-telangiectasia and T-cell leukemias: no evidence for somatic ATM mutation in sporadic T-ALL or for hypermethylation of the ATM-NPAT/E14 bidirectional promoter in T-PLL.	Luo L et al
8634440	1996	Expression of p13MTCP1 is restricted to mature T-cell proliferations with t(X;14) translocations.	Madani A et al
9614908	1998	Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization.	Maljaei SH et al
1742486	1991	Clinical and laboratory features of 78 cases of T-prolymphocytic leukemia.	Matutes E et al
7918072	1994	Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T-prolymphocytic leukaemia: four new cases and a review of the literature.	Mossafa H et al
8286748	1994	Cytogenetic findings in peripheral T-cell lymphomas as a basis for distinguishing low-grade and high-grade lymphomas.	Schlegelberger B et al
8361760	1993	MTCP-1: a novel gene on the human chromosome Xq28 translocated to the T cell receptor alpha/delta locus in mature T cell proliferations.	Stern MH et al
9334731	1997	Biallelic mutations in the ATM gene in T-prolymphocytic leukemia.	Stilgenbauer S et al
9573030	1998	Inactivation of the ATM gene in T-cell prolymphocytic leukemias.	Stoppa-Lyonnet D et al
8152252	1994	A gene on chromosome Xq28 associated with T-cell prolymphocytic leukemia in two patients with ataxia telangiectasia.	Thick J et al
8415691	1993	Chromosome walking on the TCL1 locus involved in T-cell neoplasia.	Virgilio L et al
9288106	1997	Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia.	Vorechovský I et al
9488043	1998	ATM is usually rearranged in T-cell prolymphocytic leukaemia.	Yuille MA et al

Citation

Martin Yuille

T-cell prolymphocytic leukemia (T-PLL)

Atlas Genet Cytogenet Oncol Haematol. 1999-10-01

Online version: http://atlasgeneticsoncology.org/haematological/2042/css/gene-explorer/gene-fusions-explorer/hgnc

Historical Card

1997-10-01 T-cell prolymphocytic leukemia (T-PLL) by Lucienne Michaux Affiliation

Department of Hematology and Center for Human Genetics Cliniques Universitaires Saint Luc Avenue Hippocrate 10 1200 Brussels, Belgium