TY - JOUR
T1 - Frontline chemotherapy with bortezomib-containing combinations improves response rate and survival in primary plasma cell leukemia
T2 - A retrospective study from GIMEMA Multiple Myeloma Working Party
AU - D'Arena, G.
AU - Valentini, C. G.
AU - Pietrantuono, G.
AU - Guariglia, R.
AU - Martorelli, M. C.
AU - Mansueto, G.
AU - Villani, O.
AU - Onofrillo, D.
AU - Falcone, A.
AU - Specchia, G.
AU - Semenzato, G.
AU - Di Renzo, N.
AU - Mastrullo, L.
AU - Venditti, A.
AU - Ferrara, F.
AU - Palumbo, A.
AU - Pagano, L.
AU - Musto, P.
PY - 2012
Y1 - 2012
N2 - Background: The best therapeutic approach for primary plasma cell leukemia (PPCL) remains unknown so far. In very limited studies, the poor clinical outcome of this aggressive variant of multiple myeloma seemed to be ameliorated by the use of the proteasome inhibitor bortezomib. Aiming to provide more consolidated data, this multicenter retrospective survey focused on unselected and previously untreated PPCL patients who had received bortezomib as frontline therapy. Patients and methods: Twenty-nine patients with PPCL were collected. Bortezomib was given at standard doses and schedules, in various combinations with dexamethasone, thalidomide, doxorubicin, melphalan, prednisone, vincristine, and cyclophosphamide. Results: An overall response rate of 79% was observed, with 38% of at least very good partial remission. Grade 3-4 hematological, neurological, infectious, and renal toxic effects occurred in 20%, 21%, 16%, and 4% of patients, respectively. After a median follow-up of 24 months, 16 patients were alive (55%), 12 of whom were in remission phase and 4 relapsed. The best long-term results were achieved in patients who received stem-cell transplantation after bortezomib induction. Conclusion: Bortezomib, used as initial therapy, is able to increase the percentage and the quality of responses in PPCL patients, producing a significant improvement of survival.
AB - Background: The best therapeutic approach for primary plasma cell leukemia (PPCL) remains unknown so far. In very limited studies, the poor clinical outcome of this aggressive variant of multiple myeloma seemed to be ameliorated by the use of the proteasome inhibitor bortezomib. Aiming to provide more consolidated data, this multicenter retrospective survey focused on unselected and previously untreated PPCL patients who had received bortezomib as frontline therapy. Patients and methods: Twenty-nine patients with PPCL were collected. Bortezomib was given at standard doses and schedules, in various combinations with dexamethasone, thalidomide, doxorubicin, melphalan, prednisone, vincristine, and cyclophosphamide. Results: An overall response rate of 79% was observed, with 38% of at least very good partial remission. Grade 3-4 hematological, neurological, infectious, and renal toxic effects occurred in 20%, 21%, 16%, and 4% of patients, respectively. After a median follow-up of 24 months, 16 patients were alive (55%), 12 of whom were in remission phase and 4 relapsed. The best long-term results were achieved in patients who received stem-cell transplantation after bortezomib induction. Conclusion: Bortezomib, used as initial therapy, is able to increase the percentage and the quality of responses in PPCL patients, producing a significant improvement of survival.
KW - Bortezomib
KW - Chemotherapy
KW - Multiple myeloma
KW - Primary plasma cell leukemia
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U2 - 10.1093/annonc/mdr480
DO - 10.1093/annonc/mdr480
M3 - Article
C2 - 22039089
AN - SCOPUS:84861735445
SN - 0923-7534
VL - 23
SP - 1499
EP - 1502
JO - Annals of Oncology
JF - Annals of Oncology
IS - 6
ER -