M. Taniwaki et al., NONRANDOM CHROMOSOMAL REARRANGEMENTS AND THEIR IMPLICATIONS IN CLINICAL-FEATURES AND OUTCOME OF MULTIPLE-MYELOMA AND PLASMA-CELL LEUKEMIA, Leukemia & lymphoma, 21(1-2), 1996, pp. 25
Rearrangements of bands 14q32.3 and 19p13.3 and preferential deletion
of the short arm of chromosome 1 were nonrandom chromosomal abnormalit
ies in MM and PCL, warranting further investigation at the molecular l
evel. From the viewpoint of clinical relevance, chromosome 14q32 trans
location seems to be associated with leukemic manifestation, level of
LDH, and shorter survival period from the time of chromosomal analysis
. However, these results were obtained from patients with advanced dis
ease, most of whom had already been treated with alkylating agents pri
or to cytogenetic analysis. To investigate the karyotypes of MM in the
early stage and to determine correlations with clinical features, non
-dividing cells should be analyzed, For this purpose, interphase FISH
and/or comparative genomic hybridization are promising procedures to d
etect genomic alterations in early multiple myeloma.