Quantitative detection of t(14;18)-positive cells in patients with follicular lymphoma before and after autologous bone marrow transplantation

Authors
Citation
C. Hirt et G. Dolken, Quantitative detection of t(14;18)-positive cells in patients with follicular lymphoma before and after autologous bone marrow transplantation, BONE MAR TR, 25(4), 2000, pp. 419-426
Citations number
42
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Journal title
BONE MARROW TRANSPLANTATION
ISSN journal
02683369 → ACNP
Volume
25
Issue
4
Year of publication
2000
Pages
419 - 426
Database
ISI
SICI code
0268-3369(200002)25:4<419:QDOTCI>2.0.ZU;2-5
Abstract
The aim of this study was to evaluate whether a quantitative analysis of ci rculating t(14;18)-positive cells is of prognostic significance in patients with follicular lymphoma (FL) after myelo-ablative therapy supported by AB MT, We tested DNA from primary lymphoma tissue as well as PBMC before and a fter ABMT from 15 patients for the presence of the t(14;18) translocatican. Nine patients showed a t(14;18) translocation, six patients were t(14;18)- negative. Circulating t(14;18)positive cells of seven patients were quantit atively determined by limiting dilution assays combined with a two-step PCR and by real-time quantitative PCR, The results of both methods correlate v ery well. The number of circulating t(14;18)-positive cells decreased signi ficantly in all patients after myeloablative therapy and ABMT, t(14;18)-neg ative blood samples were found in five of seven patients. In all patients c irculating t(14;18)positive cells reappeared within 2 years after ABMT show ing two different patterns. During continuous CR the numbers of circulating t(14;18)-positive cells were found to be stable within one order of magnit ude. In contrast, in one patient the relapse was accompanied by a logarithm ic increase of t(14;18)-positive cells. In a second patient the enlargement of lymph nodes developing over a period of 12 months was accompanied by ve ry slowly increasing numbers of t(14;18)-positive cells. In all cases where diagnostic lymph node tissue was available, the same t(14;18) translocatio n was found at first diagnosis and after ABMT as shown by nucleotide sequen ce analysis. We conclude that the quantitative detection of circulating t(1 4;18)-positive cells during follow-up of patients with FL after ABMT reflec ts the clinical course of the disease. Relapses are associated with increas ing numbers of circulating t(14;18)-positive cells and continuous complete remissions with stable cell counts.