Minimal residual disease (MRD) can be easily studied in hematological malig
nancies by analyser of various fusion transcripts or tumor-specific immunog
lobulin heavy-chain or T-cell receptor rearrangements as markers of disease
. Correlation between MRD and prognosis has been extensively investigated m
ostly in acute leukemia and chronic myeloid leukemia. Quantitative aspect s
eems an essential criterion but the current absence of standardization make
s difficult clinical decision according to MRD results. Development of real
time quantitative PCR techniques would probably overcome these limitations
. Only follicular non-Hodgkin's lymphomas are currently routinely analyzed
using BCL2-J(H) PCR but signification of results obtained in complete remis
sion remains uncertain. Analyses of tumor-specific immunoglobulin heavy-cha
in or T-cell receptor rearrangements allow physiological study and evaluati
on of bone marrow purgin system efficacy but are of limited interest in cur
rent clinical practice.