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
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.