I. Majolino et al., ALLOGENEIC TRANSPLANTATION OF UNMANIPULATED PERIPHERAL-BLOOD STEM-CELLS IN PATIENTS WITH MULTIPLE-MYELOMA, Bone marrow transplantation, 22(5), 1998, pp. 449-455
In multiple myeloma (MM), allogeneic bone marrow transplantation may p
roduce complete and durable responses, but is accompanied by significa
nt transplant-related mortality (TRM). To assess feasibility and possi
ble advantages offered by the use of allogeneic, growth factor-primed
PBSC instead of marrow, we analyzed the data of 10 patients with MM (I
gG = 6, IgA = 1, BJ = 2, non-secreting = 1; stage II = 1, stage III =
8, plasma-cell leukemia = 1) who received an allogeneic transplant wit
h PBSC. Their age ranged between 35 and 53 years (median 45). All were
HLA-identical to their sibling donors. Prior to allograft, six patien
ts received standard-dose chemotherapy (DAV or CY-Dexa) and four a seq
uential intensified scheme with autologous PBSC support. At the time o
f transplantation, three patients were in CR, three in PR, three had r
efractory disease, one progressive disease. Patients were conditioned
with busulfan-melphalan (n = 9) or busulfan-cyclophosphamide (rt = 1),
and were allografted with unmanipulated PBSC obtained by apheresis af
ter treatment with G-CSF alone (n = 6) or GM-CSF followed by G-CSF (n
= 4). All patients engrafted, with 0.5 x 10(9)/l PMN and 50 x 10(9)/l
platelets on (median) day 13. Four patients had greater than or equal
to grade II acute GVHD (grade II in 3, grade III in 1). Following allo
graft, CR was achieved in 71% patients. Eight are currently alive, wit
h six in CR at a median of 18.5 months (range 7-28) from the transplan
t. Two patients died, 1 and 4 months from the allograft, respectively,
and one is alive with progression. A PCR analysis of IgH rearrangemen
t showed that residual disease was no more molecularly detectable in f
our out of seven evaluated patients following allograft. The results s
uggest that PBSC may improve the therapeutic efficacy of allogeneic tr
ansplant in MM, not only by a reduction of TRM but also by an improvem
ent of rate and quality of response.