Sequential intensive treatment with the F-MACHOP regimen (+/-radiotherapy) and autologous stem cell transplantation for primary systemic CD30 (Ki-1)-positive anaplastic large cell lymphoma in adults

被引:9
作者
Fanin, R
Silvestri, F
Geromin, A
Cerno, M
Infanti, L
Zaja, F
Barillari, G
Savignano, C
Rinaldi, C
Damiani, D
Baccarani, M
机构
[1] UNIV HOSP, DEPT BONE MARROW TRANSPLANT, UDINE, ITALY
[2] GEN HOSP, UDINE, ITALY
关键词
autologous transplantation; anaplastic large cell lymphoma;
D O I
10.3109/10428199709039026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Most of the adult patients with primary systemic CD30 (Ki-1)-positive anaplastic large cell lymphoma (ALCL) reported in the literature have been treated with combination chemotherapy (CHT), with only an occasional patient being autotransplanted, mostly after relapse. Here we report a series of 19 patients treated at our Institution with a sequential intensive therapeutic program including CHT (the F-MACHOP regimen given for 6 cycles), radiotherapy (RT), and autologous stem cell transplantation (ASCT) after conditioning with the BAVC regimen. Eleven of 19 (58%) patients achieved a complete remission (CR) after CHT; 3 after RT and 4 after ASCT (1 patient is still not evaluable for response to ASCT). The actuarial overall survival is 100% at a median of 49 months from diagnosis and the actuarial disease free survival is 100% at a median of 41 months from the time CR was reached. These data suggest that ALCL can be successfully managed with a sequential intensive treatment that prevents early relapses and projects these patients as long-term survivors.
引用
收藏
页码:369 / 377
页数:9
相关论文
共 48 条
  • [1] KI-1 POSITIVE LARGE CELL LYMPHOMA - A MORPHOLOGIC AND IMMUNOLOGICAL STUDY OF 19 CASES
    AGNARSSON, BA
    KADIN, ME
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1988, 12 (04) : 264 - 274
  • [2] BELJAARDS RC, 1993, CANCER, V71, P2097, DOI 10.1002/1097-0142(19930315)71:6<2097::AID-CNCR2820710626>3.0.CO
  • [3] 2-7
  • [4] MORPHOLOGY IN KI-1(CD30) - POSITIVE NON-HODGKINS-LYMPHOMA IS CORRELATED WITH CLINICAL-FEATURES AND THE PRESENCE OF A UNIQUE CHROMOSOMAL ABNORMALITY, T(2 - 5)(P23 - Q35)
    BITTER, MA
    FRANKLIN, WA
    LARSON, RA
    MCKEITHAN, TW
    RUBIN, CM
    LEBEAU, MM
    STEPHENS, JK
    VARDIMAN, JW
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1990, 14 (04) : 305 - 316
  • [5] CARBONE PP, 1971, CANCER RES, V31, P1860
  • [6] ANAPLASTIC LARGE CELL KI-1 LYMPHOMA - DELINEATION OF 2 MORPHOLOGICAL TYPES
    CHAN, JKC
    NG, CS
    HUI, PK
    LEUNG, TW
    LO, ESF
    LAU, WH
    MCGUIRE, LJ
    [J]. HISTOPATHOLOGY, 1989, 15 (01) : 11 - 34
  • [7] KI-1-POSITIVE LARGE CELL LYMPHOMA - A CLINICOPATHOLOGICAL STUDY OF 41 CASES
    CHOTT, A
    KASERER, K
    AUGUSTIN, I
    VESELY, M
    HEINZ, R
    OEHLINGER, W
    HANAK, H
    RADASZKIEWICZ, T
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1990, 14 (05) : 439 - 448
  • [8] DAMIANI D, 1996, UNPUB BLOOD
  • [9] De Vita Ferdinando, 1994, Recenti Progressi in Medicina, V85, P278
  • [10] DIFFERENCES IN CLINICAL BEHAVIOR AND IMMUNOPHENOTYPE BETWEEN PRIMARY CUTANEOUS AND PRIMARY NODAL ANAPLASTIC LARGE-CELL LYMPHOMA OF T-CELL OR NULL-CELL PHENOTYPE
    DEBRUIN, PC
    BELJAARDS, RC
    VANHEERDE, P
    VANDERVALK, P
    NOORDUYN, LA
    VANKRIEKEN, JHJM
    KLUINNELEMANS, JC
    WILLEMZE, R
    MEIJER, CJLM
    [J]. HISTOPATHOLOGY, 1993, 23 (02) : 127 - 135