Phosphamide/fludarabine (CF) is active in the treatment of mantle cell lymphoma

被引:54
作者
Cohen, BJ [1 ]
Moskowitz, C [1 ]
Straus, D [1 ]
Noy, A [1 ]
Hedrick, E [1 ]
Zelenetz, A [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Lymphoma Serv, Div Hematol, New York, NY 10021 USA
关键词
mantle cell lymphoma; MCL; cyclophosphamide; fludarabine; non-Hodgkins lymphoma; indolent;
D O I
10.3109/10428190109097721
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this study was to determine the efficacy and toxicity of the cyclophosphamide and fludarabine (CF) regimen in patients with newly diagnosed and relapsed/refractory mantle cell lymphoma (MCL). Thirty patients with pathologically confirmed MCL were treated with the CF regimen. Ten (33%) had no prior therapy, six (20%) had one previous regimen, and 14 (47%) received two or more prior regimens. Ninety cycles of CF with a median of 3 cycles/patient (range, 1-5 cycles) were administered to patients with MCL. Nine patients (30%) had a complete response (CR) and 10 (33%) had a partial response (PR) for an overall response rate (RR) of 63%. The median failure-free survival (FFS) and overall survival (OS) was 4.8 months and 17.5 months, respectively. When patients were analyzed based upon the number of previous treatments (0,1, or 2 or more), those with no previous treatment (n=10) had an overall response of 100%, with 70% CR. The median FFS was 28.1 months and the median OS for this group has not been reached at 42.3+ months. Hematologic and infectious toxicity were the major toxicities encountered with the CF regimen. Grade 3-4 neutropenia, thrombocytopenia and anemia were seen in 50%, 37%, and 36% of patients, respectively. There were 13 episodes of grade 3 infections, There was no treatment related mortality. In conclusion, the high response rate associated with the CIF regimen merits further investigation in previously untreated patients with MCL, particularly in those who are not candidates for aggressive therapy.
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收藏
页码:1015 / +
页数:9
相关论文
共 26 条
  • [1] Mantle cell lymphoma: A clinicopathologic study of 80 cases
    Argatoff, LH
    Connors, JM
    Klasa, RJ
    Horsman, DE
    Gascoyne, RD
    [J]. BLOOD, 1997, 89 (06) : 2067 - 2078
  • [2] New approach to classifying non-hodgkin's lymphomas: Clinical features of the major histologic subtypes
    Armitage, JO
    Weisenburger, DD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) : 2780 - 2795
  • [3] Bosch F, 1998, CANCER, V82, P567, DOI 10.1002/(SICI)1097-0142(19980201)82:3<567::AID-CNCR20>3.0.CO
  • [4] 2-Z
  • [5] Campo E, 1999, SEMIN HEMATOL, V36, P115
  • [6] Report of an international workshop to standardize response criteria for non-Hodgkin's lymphomas
    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
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (04) : 1244 - 1253
  • [7] Phase II trial of fludarabine monophosphate in patients with mantle-cell lymphomas
    Decaudin, D
    Bosq, J
    Tertian, G
    Nedellec, G
    Bennaceur, A
    Venuat, AM
    Bayle, C
    Carde, P
    Bendahmane, B
    Hayat, M
    Munck, JN
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) : 579 - 583
  • [8] DORFMAN DM, 1994, MODERN PATHOL, V7, P326
  • [9] A CLINICAL ANALYSIS OF 2 INDOLENT LYMPHOMA ENTITIES - MANTLE CELL LYMPHOMA AND MARGINAL ZONE LYMPHOMA (INCLUDING THE MUCOSA-ASSOCIATED LYMPHOID-TISSUE AND MONOCYTOID B-CELL SUBCATEGORIES) - A SOUTHWEST-ONCOLOGY-GROUP STUDY
    FISHER, RI
    DAHLBERG, S
    NATHWANI, BN
    BANKS, PM
    MILLER, TP
    GROGAN, TM
    [J]. BLOOD, 1995, 85 (04) : 1075 - 1082
  • [10] Fludarabine and cyclophosphamide with filgrastim support in patients with previously untreated indolent lymphoid malignancies
    Flinn, IW
    Byrd, JC
    Morrison, C
    Jamison, J
    Diehl, LF
    Murphy, T
    Piantadosi, S
    Seifter, E
    Ambinder, RF
    Vogelsang, G
    Grever, MR
    [J]. BLOOD, 2000, 96 (01) : 71 - 75