Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group.
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Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group. / Salido, Marta; Baró, Cristina; Oscier, David; Stamatopoulos, Kostas; Dierlamm, Judith; Matutes, Estela; Traverse-Glehen, Alexandra; Berger, Francoise; Felman, Pascale; Thieblemont, Catherine; Gesk, Stefan; Athanasiadou, Anastasia; Davis, Zadie; Gardiner, Anne; Milla, Fuensanta; Ferrer, Ana; Mollejo, Manuela; Calasanz, Maria José; Florensa, Lourdes; Espinet, Blanca; Luño, Elisa; Wlodarska, Iwona; Verhoef, Gregor; García-Granero, Marta; Salar, Antonio; Papadaki, Theodora; Serrano, Sergio; Piris, Miguel A; Solé, Francesc.
In: BLOOD, Vol. 116, No. 9, 9, 2010, p. 1479-1488.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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T1 - Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group.
AU - Salido, Marta
AU - Baró, Cristina
AU - Oscier, David
AU - Stamatopoulos, Kostas
AU - Dierlamm, Judith
AU - Matutes, Estela
AU - Traverse-Glehen, Alexandra
AU - Berger, Francoise
AU - Felman, Pascale
AU - Thieblemont, Catherine
AU - Gesk, Stefan
AU - Athanasiadou, Anastasia
AU - Davis, Zadie
AU - Gardiner, Anne
AU - Milla, Fuensanta
AU - Ferrer, Ana
AU - Mollejo, Manuela
AU - Calasanz, Maria José
AU - Florensa, Lourdes
AU - Espinet, Blanca
AU - Luño, Elisa
AU - Wlodarska, Iwona
AU - Verhoef, Gregor
AU - García-Granero, Marta
AU - Salar, Antonio
AU - Papadaki, Theodora
AU - Serrano, Sergio
AU - Piris, Miguel A
AU - Solé, Francesc
PY - 2010
Y1 - 2010
N2 - We conducted a retrospective collaborative study to cytogenetically characterize splenic marginal zone lymphoma (SMZL) and ascertain the prognostic value of chromosomal aberrations. Of 330 cases, 72% displayed an aberrant karyotype, 53% were complex, and 29% had a single aberration. The predominant aberrations were gains of 3/3q and 12q, deletions of 7q and 6q and translocations involving 8q/1q/14q. CD5 expression was detected in 39 of 158 cases (25%). The cytogenetic makeup of the CD5(+) group differed significantly from that of the CD5(-) group. Cases with unmutated IGHV were significantly associated with deletions of 7q and TP53. A strong association was noted between usage of the IGVH1-2 and deletion 7q, 14q alterations, and abnormal karyotype. On univariate analysis, patients with more than or equal to 2 aberrations, 14q alterations, and TP53 deletions had the shortest survival; 7q deletion did not affect survival. On multivariate analysis, cytogenetic aberrations did not retain prognostic significance; the parameters negatively affecting survival were hemoglobin and age. In conclusion, the cytogenetic profile of SMZL is distinct from other B-cell lymphomas. Complexity of the karyotype, 14q aberrations, and TP53 deletions are poor prognostic indicators and may be considered together with other clinicobiologic parameters to ascertain the prognosis of SMZL.
AB - We conducted a retrospective collaborative study to cytogenetically characterize splenic marginal zone lymphoma (SMZL) and ascertain the prognostic value of chromosomal aberrations. Of 330 cases, 72% displayed an aberrant karyotype, 53% were complex, and 29% had a single aberration. The predominant aberrations were gains of 3/3q and 12q, deletions of 7q and 6q and translocations involving 8q/1q/14q. CD5 expression was detected in 39 of 158 cases (25%). The cytogenetic makeup of the CD5(+) group differed significantly from that of the CD5(-) group. Cases with unmutated IGHV were significantly associated with deletions of 7q and TP53. A strong association was noted between usage of the IGVH1-2 and deletion 7q, 14q alterations, and abnormal karyotype. On univariate analysis, patients with more than or equal to 2 aberrations, 14q alterations, and TP53 deletions had the shortest survival; 7q deletion did not affect survival. On multivariate analysis, cytogenetic aberrations did not retain prognostic significance; the parameters negatively affecting survival were hemoglobin and age. In conclusion, the cytogenetic profile of SMZL is distinct from other B-cell lymphomas. Complexity of the karyotype, 14q aberrations, and TP53 deletions are poor prognostic indicators and may be considered together with other clinicobiologic parameters to ascertain the prognosis of SMZL.
M3 - SCORING: Zeitschriftenaufsatz
VL - 116
SP - 1479
EP - 1488
JO - BLOOD
JF - BLOOD
SN - 0006-4971
IS - 9
M1 - 9
ER -