Perspectives on the use of new diagnostic tools in the treatment of chronic lymphocytic leukemia

被引:131
作者
Binet, JL
Caligaris-Cappio, F
Catovsky, D
Cheson, B
Davis, T
Dighiero, G
Döhner, H
Hallek, M
Hillmen, P
Keating, M
Montserrat, E
Kipps, TJ
Rai, K
机构
[1] Univ Calif San Diego, Rebecca & John Moores Canc Ctr, La Jolla, CA 92093 USA
[2] Univ Cologne, Innere Med Klin 1, Cologne, Germany
[3] Hosp La Salpetriere, Ctr Ecol Cellulaire, Paris, France
[4] Univ Vita Salute San Raffaele, London, England
[5] Inst Canc Res, London, England
[6] Georgetown Univ Hosp, Lombardi Canc Ctr, Washington, DC USA
[7] Off Director, NIH, Bethesda, MD USA
[8] Inst Pasteur, Paris, France
[9] Univ Ulm, Ulm, Germany
[10] Pinderfields Gen Hosp, Wakefield, England
[11] Univ Texas, MD Anderson Canc Ctr, Dept Leukemia, Houston, TX USA
[12] Hosp Clin Barcelona, Barcelona, Spain
[13] Long Isl Jewish Med Ctr, Div Hematol Oncol, New Hyde Pk, NY USA
关键词
D O I
10.1182/blood-2005-04-1677
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recently, considerable progress has been made in the identification of molecular and cellular markers that may predict the tendency for disease progression in patients with chronic lymphocytic leukemia (CLL) or detect minimal residual disease after therapy. These developments have created uncertainty for clinicians who hope to incorporate the use of these markers and new disease-assessment tools into standard clinical practice. However, clinical trials are required to determine whether poor-prognosis leukemia-cell markers, such as expression of unmutated immunoglobulin genes or the zeta-associated protein of 70 kDa (ZAP70), can be used as the basis for determining the time or type of therapy. Pending the outcome of such trials, treatment decisions outside the context of a clinical trial still should be based on guidelines established by the most recent National Cancer Institute-sponsored Working Group.
引用
收藏
页码:859 / 861
页数:3
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