Dexamethasone, carmustine, etoposide, cytarabine, and melphalan (Dexa-BEAM) followed by high-dose chemotherapy and stem cell rescue -: A highly effective regimen for patients with refractory or relapsed indolent lymphoma

被引:5
作者
Josting, A [1 ]
Reiser, M [1 ]
Wickramanayake, PD [1 ]
Rueffer, U [1 ]
Draube, A [1 ]
Söhngen, D [1 ]
Tesch, H [1 ]
Wolf, J [1 ]
Diehl, V [1 ]
Engert, A [1 ]
机构
[1] Univ Hosp Cologne, Dept Internal Med 1, D-50924 Cologne, Germany
关键词
Dexa-BEAM; high-dose chemotherapy; PBSCT; indolent non-Hodgkin's lymphoma;
D O I
10.3109/10428190009057634
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We performed a phase II study to determine the efficacy of maximal cytoreductive therapy with up to five cycles of Dexa-BEAM (dexamethasone, carmustine [BCNU], etoposide, cytarabine, and melphalan) followed by high-dose chemotherapy (HDCT) and autologous stem cell transplantation (ASCT) for patients with advanced relapsed or refractory indolent lymphoma. Thirty-two patients with primary refractory or relapsed indolent lymphoma were treated with the Dexa-BEAM regimen. Thirteen patients had primary refractory disease, 4 patients partial remission, and 15 patients first or subsequent relapse. Patients achieving PR or CR received HDCT with ASCT. The conditioning regimen used was BEAM (carmustine [BCNU], etoposide, cytarabine, and melphalan). Twenty-two patients responded to Dexa-BEAM,resulting in a response rate of 78%. Maximum response was observed after 3.2 (range 2-5) courses. One patient with progressive disease died in septic shock during neutropenia. Nineteen patients with partial or complete remission after Dexa-BEAM received HDCT. Hematopoietic stem cells (HSC) were collected after two cycles of Dexa-BEAM. The median number of CD34+ HSC reinfused was 3.1 x 10(6)/kg (range 1.6-8.2 x 10(6)/kg). There was-no transplantation-related death. All patients receiving HDCT achieved complete remission. Overall survival (OS) and freedom from treatment failure (FFTF) for all patients are estimated to be 68% and 65% at two years, respectively. With a mean follow-up of 20 months (range 8 - 42 months), 16/19 patients receiving HDCT are in continuous complete remission. The Dexa-BEAM regimen is effective in overcoming drug resistance in patients with indolent lymphoma who failed to respond to conventional treatment or who relapsed. The CR rate of 100% of those patients receiving HDCT and ASCT after maximal cytoreductive treatment with Dexa-BEAM suggests the use of HDCT at the rime of maximal response.
引用
收藏
页码:115 / 123
页数:9
相关论文
共 38 条
[1]  
ANDERSON T, 1982, CANCER-AM CANCER SOC, V50, P2708, DOI 10.1002/1097-0142(19821215)50:12<2708::AID-CNCR2820501203>3.0.CO
[2]  
2-G
[3]  
ARMITAGE JO, 1993, NEW ENGL J MED, V328, P1023
[4]   FOLLICULAR LYMPHOAMS - ASSESSMENT OF PROGNOSTIC FACTORS IN 127 PATIENTS FOLLOWED FOR 10 YEARS [J].
BASTION, Y ;
BERGER, F ;
BRYON, PA ;
FELMAN, P ;
FFRENCH, M ;
COIFFIER, B .
ANNALS OF ONCOLOGY, 1991, 2 :123-129
[5]   INTENSIVE THERAPY WITH PERIPHERAL-BLOOD PROGENITOR-CELL TRANSPLANTATION IN 60 PATIENTS WITH POOR-PROGNOSIS FOLLICULAR LYMPHOMA [J].
BASTION, Y ;
BRICE, P ;
HAIOUN, C ;
SONET, A ;
SALLES, G ;
MAROLLEAU, JP ;
ESPINOUSE, D ;
REYES, F ;
GISSELBRECHT, C ;
COIFFIER, B .
BLOOD, 1995, 86 (08) :3257-3262
[6]   High-dose therapy with autologous hematopoietic rescue for follicular low-grade non-Hodgkin's lymphoma [J].
Bierman, PJ ;
Vose, JM ;
Anderson, JR ;
Bishop, MR ;
Kessinger, A ;
Armitage, JO .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) :445-450
[7]   THE ROLE OF HIGH-DOSE THERAPY WITH HEMATOPOIETIC STEM-CELL RESCUE IN LOW-GRADE NON-HODGKINS-LYMPHOMA [J].
BISHOP, MR ;
BIERMAN, PJ ;
VOSE, JM ;
ARMITAGE, JO .
ANNALS OF ONCOLOGY, 1993, 4 :S1-S6
[8]   Comparison in low-tumor-burden follicular lymphomas between an initial no-treatment policy, prednimustine, or interferon alfa: A randomized study from the Groupe D'Etude des Lymphomes Folliculaires [J].
Brice, P ;
Bastion, Y ;
Lepage, E ;
Brousse, N ;
Haioun, C ;
Moreau, P ;
Straetmans, N ;
Tilly, H ;
Tabah, I ;
SolalCeligny, P .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (03) :1110-1117
[9]  
BRUCE WR, 1966, JNCI-J NATL CANCER I, V37, P233
[10]  
COIFFIER B, 1993, SEMIN ONCOL, V20, P89