Efficacy and safety of bortezomib in patients with plasma cell leukemia

被引:66
作者
Musto, Pellegrino
Rossini, Fausto
Gay, Francesca
Pitini, Vincenzo
Guglielmelli, Tommasina
D'Arena, Giovanni
Ferrara, Felicetto
Filardi, Nunzio
Guariglia, Roberto
Palumbo, Antonio
机构
[1] CROB, Unit Hematol & Stem Cell Transplantat, I-85028 Rionero In Vulture, PZ, Italy
[2] S Gerardo Hosp, Dept Hematol, Monza, Italy
[3] Univ Turin, Dept Hematol, I-10124 Turin, Italy
[4] Univ Messina, Dept Med Oncol, I-98100 Messina, Italy
[5] S Luigi Gonzaga Hosp, Dept Internal Med, Orbassano, To, Italy
[6] Natl Canc Inst Pascale, Dept Hematol, Naples, Italy
[7] Cardarelli Hosp, Dept Hematol, Naples, Italy
[8] San Carlo Hosp, Dept Hematol, Potenza, Italy
关键词
bortezomib; plasma cell leukemia; multiple myeloma; survival; toxicity;
D O I
10.1002/cncr.22700
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The prognosis of patients with plasma cell leukemia (PCL), an aggressive variant of multiple myeloma (MM), is usually poor. Bortezomib is the first proteasome inhibitor approved for the treatment of advanced MM. Currently available information regarding the role of bortezomib in PCL is scanty and derives from anecdotal, single-case reports. METHODS. The authors conducted a retrospective survey of unselected Italian patients with primary or secondary PCL who were treated with bortezomib outside of clinical trials. Twelve evaluable patients were recorded who had received bortezomib for I to 6 cycles as either a single agent or variously combined with other drugs. Three patients were treated with bortezomib as frontline therapy, and 9 patients received bortezomib after 1 to 4 lines of chemotherapy, including autologous stem cell transplantation and thalidomide. RESULTS. According to the International uniform response criteria of the International Myeloma Working Group, 5 partial responses (defined as a reduction in M-protein of > 50%), 4 very good partial responses (defined as a reduction of > 90% in M-protein), and 2 complete responses (defined as negative immunofixation) were achieved, for a response rate of 92%. Responses did not appear to be influenced by previous treatments or by other clinical or biologic parameters, including chromosome 13 deletion or the combination of bortezomib with other drugs. The median progression-free and overall survivals after bortezomib were 8 months and 12 months, respectively. At the time of last follow-up, 8 patients were alive 6 to 21 months after treatment with bortezomib, 4 of whom were in very good partial or complete responses. Grade 3/4 hematologic or neurologic toxicities (graded according to the Common Terminology Criteria for Adverse Events [CTCAE; version 3]) were reported to occur in 9 patients and 1 patient, respectively, whereas 6 patients experienced possible or documented infections. CONCLUSIONS. Bortezomib appears to be an effective drug for PCL that could significantly improve the usually adverse clinical outcome of these patients.
引用
收藏
页码:2285 / 2290
页数:6
相关论文
共 37 条
[1]  
ALI R, 2006, LEUK RES
[2]   A long-lasting third complete remission after second autologous transplant followed by maintenance treatment with rituximab in a patient with diffuse large cell non-Hodgkin's lymphoma [J].
Ataergin, Selmin ;
Arpaci, Fikret ;
Beyzadeoglu, Murat ;
Safali, Mukerrem ;
Ozet, Ahmet .
AMERICAN JOURNAL OF HEMATOLOGY, 2006, 81 (12) :986-987
[3]   Cytogenetic, interphase, and multicolor fluorescence in situ hybridization analyses in primary plasma cell leukemia:: a study of 40 patients at diagnosis, on behalf of the Intergroupe Francophone du Myelome and the Groupe Francais de Cytogenetique Hematologique [J].
Avet-Loiseau, H ;
Daviet, A ;
Brigaudeau, C ;
Callet-Bauchu, E ;
Terré, C ;
Lafage-Pochitaloff, M ;
Désangles, F ;
Ramond, S ;
Talmant, P ;
Bataille, R .
BLOOD, 2001, 97 (03) :822-825
[4]   Efficacy of thalidomide in the treatment of VAD-refractory plasma cell leukaemia appearing after autologous stem cell transplantation for multiple myeloma [J].
Bauduer, F .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 117 (04) :996-997
[5]  
BERNASCONI C, 1989, EUR J HAEMATOL, V43, P76
[6]   Nonsecretory myeloma, immunoglobulin D myeloma, and plasma cell leukemia [J].
Bladé, J ;
Kyle, RA .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1999, 13 (06) :1259-+
[7]   Proteasome inhibitor bortezomib for the treatment of multiple myeloma [J].
Cavo, M. .
LEUKEMIA, 2006, 20 (08) :1341-1352
[8]   Treatment of plasma cell leukemia with vincristine, liposomal doxorubicin and dexamethasone [J].
Christou, L ;
Hatzimichael, E ;
Chaidos, A ;
Tsiara, S ;
Bourantas, KL .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2001, 67 (01) :51-53
[9]   Primary plasma cell leukaemia:: a report of 18 cases [J].
Costello, R ;
Sainty, D ;
Bouabdallah, R ;
Fermand, JP ;
Delmer, A ;
Diviné, M ;
Marolleau, JP ;
Gastaut, JA ;
Olive, D ;
Rousselot, P ;
Chaïbi, P .
LEUKEMIA RESEARCH, 2001, 25 (02) :103-107
[10]   PRIMARY PLASMA-CELL LEUKEMIA [J].
DIMOPOULOS, MA ;
PALUMBO, A ;
DELASALLE, KB ;
ALEXANIAN, R .
BRITISH JOURNAL OF HAEMATOLOGY, 1994, 88 (04) :754-759