Clinical relevance of minimal residual disease monitoring in non-Hodgkin's lymphomas: a critical reappraisal of molecular strategies

被引:34
作者
Corradini, P
Ladetto, M
Pileri, A
Tarella, C
机构
[1] Ist Sci HS Raffaele, Bone Marrow Transplant Unit, I-20132 Milan, Italy
[2] Univ Turin, Azienda Osped S Giovanni Battista, Div Ematol, Turin, Italy
关键词
minimal residual disease in lymphomas;
D O I
10.1038/sj.leu.2401559
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although current treatments can induce clinical complete remissions in the vast majority of patients with indolent lymphoma, most of them actually relapse, because of the persistence of residual tumor cells which are undetectable using conventional diagnostic procedures. Polymerase chain reaction (PCR)-based methods are increasingly used for minimal residual disease detection (MRD), and provide useful prognostic information. In this review, current approaches for MRD detection in indolent lymphomas are summarized. In addition, the prognostic aspects of molecular monitoring after transplantation procedures are discussed. The experience accumulated over the past decade shows that PCR analysis has a prognostic impact in several therapeutic programs including conventional and high-dose regimens. Major advantages coming from the introduction of molecular monitoring in clinical programs have been: (1) a rapid evaluation of the anti-tumor activity of innovative treatments; and (2) an early identification of patients with a high-risk of disease recurrence.
引用
收藏
页码:1691 / 1695
页数:5
相关论文
共 52 条
  • [1] Failure of immunologic purging in mantle cell lymphoma assessed by polymerase chain reaction detection of minimal residual disease
    Andersen, NS
    Donovan, JW
    Borus, JS
    Poor, CM
    Neuberg, D
    Aster, JC
    Nadler, LM
    Freedman, AS
    Gribben, JG
    [J]. BLOOD, 1997, 90 (10) : 4212 - 4221
  • [2] ARMITAGE JO, 1993, SEMIN ONCOL, V20, P136
  • [3] CLONING THE CHROMOSOMAL BREAKPOINT OF T(14-18) HUMAN LYMPHOMAS - CLUSTERING AROUND JH ON CHROMOSOME-14 AND NEAR A TRANSCRIPTIONAL UNIT ON 18
    BAKHSHI, A
    JENSEN, JP
    GOLDMAN, P
    WRIGHT, JJ
    MCBRIDE, OW
    EPSTEIN, AL
    KORSMEYER, SJ
    [J]. CELL, 1985, 41 (03) : 899 - 906
  • [4] INTENSIVE THERAPY WITH PERIPHERAL-BLOOD PROGENITOR-CELL TRANSPLANTATION IN 60 PATIENTS WITH POOR-PROGNOSIS FOLLICULAR LYMPHOMA
    BASTION, Y
    BRICE, P
    HAIOUN, C
    SONET, A
    SALLES, G
    MAROLLEAU, JP
    ESPINOUSE, D
    REYES, F
    GISSELBRECHT, C
    COIFFIER, B
    [J]. BLOOD, 1995, 86 (08) : 3257 - 3262
  • [5] Should we purge?
    Bensinger, WI
    [J]. BONE MARROW TRANSPLANTATION, 1998, 21 (02) : 113 - 115
  • [6] DETECTION OF OCCULT LYMPHOMA IN THE PERIPHERAL-BLOOD AND BONE-MARROW OF PATIENTS WITH UNTREATED EARLY-STAGE AND ADVANCED-STAGE FOLLICULAR LYMPHOMA
    BERINSTEIN, NL
    REIS, MD
    NGAN, BY
    SAWKA, CA
    JAMAL, HH
    KUZNIAR, B
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (07) : 1344 - 1352
  • [7] High-dose therapy with autologous hematopoietic rescue for follicular low-grade non-Hodgkin's lymphoma
    Bierman, PJ
    Vose, JM
    Anderson, JR
    Bishop, MR
    Kessinger, A
    Armitage, JO
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) : 445 - 450
  • [8] GENE-MARKING TO TRACE ORIGIN OF RELAPSE AFTER AUTOLOGOUS BONE-MARROW TRANSPLANTATION
    BRENNER, MK
    RILL, DR
    MOEN, RC
    KRANCE, RA
    MIRRO, J
    ANDERSON, WF
    IHLE, JN
    [J]. LANCET, 1993, 341 (8837) : 85 - 86
  • [9] Clonal evolution in B-lineage acute lymphoblastic leukemia by contemporaneous V-H-V-H gene replacements and V-H-DJ(H) gene rearrangements
    Choi, Y
    Greenberg, SJ
    Du, TL
    Ward, PM
    Overturf, PM
    Brecher, ML
    Ballow, M
    [J]. BLOOD, 1996, 87 (06) : 2506 - 2512
  • [10] DETECTION OF A 2ND T(14-18) BREAKPOINT CLUSTER REGION IN HUMAN FOLLICULAR LYMPHOMAS
    CLEARY, ML
    GALILI, N
    SKLAR, J
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (01) : 315 - 320