Ifosfamide, gemcitabine, and vinorelbine: a now induction regimen for refractory and relapsed Hodgkin's lymphoma

被引:161
作者
Santoro, Armando
Magagnoli, Massimo
Spina, Michele
Pinotti, Graziella
Siracusano, Licia
Michieli, Mariagrazia
Nozza, Andrea
Sarina, Barbara
Morenghi, Emanuela
Castagna, Luca
Tirelli, Umberto
Balzarotti, Monica
机构
[1] Ist Clin Humanitas, Dept Med Oncol & Hematol, I-20089 Milan, Italy
[2] Ctr Riferimento Oncol, Dept Med Oncol, I-33081 Aviano, Italy
[3] Osped Circolo Varese, Div Med Oncol, Varese, Italy
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2007年 / 92卷 / 01期
关键词
Hodgkin's lymphoma; salvage chemotherapy; complete remission; CD34(+) cell mobilization;
D O I
10.3324/haematol.10661
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives Response to pre-transplant salvage chemotherapy remains the most important prognostic factor for outcome in refractory or relapsed Hodgkin's lymphoma. Results of a new induction regimen are reported in terms of response rates, toxicity, and stem cell mobilization. Design and Methods Ninety-one patients with refractory or relapsed Hodgkin's lymphoma were treated prospectively with a salvage regimen consisting of ifosfamide 2000 mg/m(2) on days 1 to 4, gemcitabine 800 mg/m(2) on days 1 and 4, vinorelbine 20 mg/m(2) on day 1, and prednisolone 100 mg on days 1 to 4 (IGEV). Results Forty-nine patients (53.8%) achieved a complete remission and 25 (27.5%) a partial response for an overall response rate of 81.3%. In the multivariate analysis response to the last chemotherapy (p < 0.0001) and involvement of 3 sites (p < 0.049) were the most important prognostic factors for response. Adequate CD34(+) cell collection was achieved in 78 out of 79 (98.7%) mobilized patients. So far, no treatment-related death has been documented. Thirteen (4.2%) and 27 (8.6%) out of 313 evaluated cycles had to be delayed or reduced, respectively, mainly because of neutropenia and thrombocytopenia. No grade 4 non-hematologic toxicity was observed, except for one episode of mucositis. Interpretation and Conclusions The high response rate, in particular the complete remission rate, the low toxicity profile, and the very high mobilizing potential of the IGEV regimen strongly suggest that patients with relapsed/refractory Hodgkin's lymphoma may benefit from the use of this salvage induction regimen.
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收藏
页码:35 / 41
页数:7
相关论文
共 32 条
[1]   ESHAP plus fixed dose G-CSF as autologous peripheral blood stem cell mobilization regimen in patients with relapsed or refractory diffuse large cell and Hodgkin's lymphoma: a single institution result of 127 patients [J].
Akhtar, S ;
Tbakhi, A ;
Humaidan, H ;
El Weshi, A ;
Rahal, M ;
Maghfoor, I .
BONE MARROW TRANSPLANTATION, 2006, 37 (03) :277-282
[2]   Gemcitabine, dexamethasone and cisplatin is an active and non-toxic chemotherapy regimen in relapsed or refractory Hodgkin's disease: a phase II study by the National Cancer Institute of Canada Clinical Trials Group [J].
Baetz, T ;
Belch, A ;
Couban, S ;
Imrie, K ;
Yau, J ;
Myers, R ;
Ding, K ;
Paul, N ;
Shepherd, L ;
Iglesias, J ;
Meyer, R ;
Crump, M .
ANNALS OF ONCOLOGY, 2003, 14 (12) :1762-1767
[3]  
Bonfante V, 1998, BRIT J HAEMATOL, V103, P533
[4]   Outcome of patients with Hodgkin's disease failing after primary MOPP-ABVD [J].
Bonfante, V ;
Santoro, A ;
Viviani, S ;
Devizzi, L ;
Balzarotti, M ;
Soncini, F ;
Zanini, M ;
Valagussa, P ;
Bonadonna, G .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) :528-534
[5]   Feasibility of tandem autologous stem-cell transplantation (ASCT) in induction failure or very unfavorable (UF) relapse from Hodgkin's disease (HD) [J].
Brice, P ;
Divine, M ;
Simon, D ;
Coiffier, B ;
Leblond, V ;
Simon, M ;
Voilat, L ;
Devidas, A ;
Morschhauser, F ;
Rohrlich, P ;
André, M ;
Lepage, E ;
Ferme, C .
ANNALS OF ONCOLOGY, 1999, 10 (12) :1485-1488
[6]   Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas [J].
Cheson, BD ;
Horning, SJ ;
Coiffier, B ;
Shipp, MA ;
Fisher, RI ;
Connors, JM ;
Lister, TA ;
Vose, J ;
Grillo-López, A ;
Hagenbeek, A ;
Cabanillas, F ;
Klippensten, D ;
Hiddemann, W ;
Castellino, R ;
Harris, NL ;
Armitage, JO ;
Carter, W ;
Hoppe, R ;
Canellos, GP .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) :1244-1253
[7]   MINI-BEAM AS SALVAGE THERAPY FOR RELAPSED OR REFRACTORY HODGKINS-DISEASE BEFORE INTENSIVE THERAPY AND AUTOLOGOUS BONE-MARROW TRANSPLANTATION [J].
COLWILL, R ;
CRUMP, M ;
COUTURE, F ;
DANISH, R ;
STEWART, AK ;
SUTTON, DMC ;
SCOTT, JG ;
SUTCLIFFE, SB ;
BRANDWEIN, JM ;
KEATING, A .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (02) :396-402
[8]   VINORELBINE - AN ACTIVE-DRUG FOR THE MANAGEMENT OF PATIENTS WITH HEAVILY PRETREATED HODGKINS-DISEASE [J].
DEVIZZI, L ;
SANTORO, A ;
BONFANTE, V ;
VIVIANI, S ;
BALZARINI, L ;
VALAGUSSA, P ;
BONADONNA, G .
ANNALS OF ONCOLOGY, 1994, 5 (09) :817-820
[9]   THE MINE REGIMEN AS INTENSIVE SALVAGE CHEMOTHERAPY FOR RELAPSED AND REFRACTORY HODGKINS-DISEASE [J].
FERME, C ;
BASTION, Y ;
LEPAGE, E ;
BERGER, F ;
BRICE, P ;
MOREL, P ;
GABARRE, J ;
NEDELLEC, G ;
REMAN, O ;
CHERON, N ;
OBERLIN, O ;
COIFFIER, B .
ANNALS OF ONCOLOGY, 1995, 6 (06) :543-549
[10]   High-dose therapy and autologous hematopoietic progenitor cell transplantation for recurrent or refractory Hodgkin's disease: Analysis of the Stanford University results and prognostic indices [J].
Horning, SJ ;
Chao, NJ ;
Negrin, RS ;
Hoppe, RT ;
Long, GD ;
Hu, WW ;
Wong, RM ;
Brown, BW ;
Blume, KG .
BLOOD, 1997, 89 (03) :801-813