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Bortezomib (velcade)-thalidomide-dexamethasone (VTD) is superior to thalidomide-dexamethasone (TD) in patients with multiple myeloma (MM) progressing or relapsing after autologous transplantation

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GARDERET L. IACOBELLI S. MOREAU P. DIB M. CAILLOT D. NIEDERWIESER D. MASSZI T. FONTAN J. MICHALLET M. GRATWOHL A. MILONE G. DOYEN C. PEGOURIE B. HÁJEK Roman CASASSUS P. KOLB B. CHALETEIX C. HERTENSTEIN B. ONIDA F. HEINZ L. VEKEMANS MC. KETTERER N. DAGUENEL A. KOENECKE C. MOHTY M. GORIN NC. HAROUSSEAU JL. DE WITTE T. MORRIS C. GAHRTON G.

Rok publikování 2011
Druh Konferenční abstrakty
Citace
Popis An IFM and EBMT prospective, randomized, open label phase III, multicenter study, comparing VTD (arm A) with TD (arm B) for MM patients in first progression/relapse after at least one autologous transplantation. Primary end point:TTP. Bortezomib 1.3 mg/m2 on days 1, 4, 8 and 11, followed by a 10-day rest period (8 cycles) and then on days 1, 8, 15 and 22, followed by a 20-day rest period (4 cycles). In both arms:thalidomide:200mg/day for 1 year, dexamethasone:40 mg/day for 4 days every 3 weeks for 1 year. 267 patients (135 in arm A, 132 in arm B) and 157 events. Median age:61 years (range 29-76), ISS: I in 56 %, II in 27 %, III in 17 %, previous autologous transplants:one in 71 vs 69 patients and two or more in 64 vs 63 patients(A and B). Median followup:27 mo, median TTP:19.5 vs 13.8 mo (A and B), with a CI of relapse/progression at 2 years of 56% vs 71% (p=0.0011). Median PFS:18.6 vs 12.7 mo with a CI at 2 years of 37% vs 23% (A vs B, p=0.0011). First two years OS:72% vs 68% (p=0.18). First year CR and CR+PR:32% vs 12% and 90% vs 69% with VTD and TD (p=0.0001,and p=0.0001). Mean number of treatment cycles for the first 8 cycles:6.25 vs 6.88 and for the 12 cycles, 7.56 vs 9.93 (VTD and TD). Treatment discontinuation due to toxicity: 48 patients (VTD= 36, TD=12). 33 death during treatment period (VTD= 14, TD= 19). Thrombo-embolism; 6.6% vs 5.2%, p=ns while thrombocytopenia:16% vs 7%, p= 0.025 (events >= grade 3,VTD vs TD). VTD resulted in significantly longer TTP and PFS in patients relapsing after ASCT with an acceptable toxicity. Protocol EUDRACT number: 2005-001628-35.

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