Acute myeloid leukemia in the older patient

被引:22
作者
Godwin, JE [1 ]
Smith, SE [1 ]
机构
[1] Loyola Univ, Cardinal Bernardin Canc Ctr, Maywood, IL 60153 USA
关键词
acute myeloid leukemia; growth factors; G-CSF; GM-CSF; AML pathogenesis; AML biology;
D O I
10.1016/j.critrevonc.2003.04.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Acute myeloid leukemia (AML) is an extremely heterogeneous disorder. The biology of AML is incompletely understood, but much data indicates that older patients have a more biologically diverse and chemotherapy resistant form of AML that is quite different from that seen in the younger patients. Approximately 60% of AML cases are in patients greater than 60 years of age, so the predominant burden is in older patients. This problem will be magnified in the future, because the US population is both growing and aging. When one examines the treatment outcomes of older ANIL patients over the last three decades, there is little progress in long-term survival. Nine major published randomized placebo controlled trials of myeloid growth factors given during induction for AML have been conducted. All of these trials with one exception demonstrated no significant impact on the clinical outcomes of complete response (CR) rate, disease-free, and overall survival. However, the duration of neutropenia was consistently and uniformly reduced by the use of growth factor in all nine of these trials. Because of the favorable impact of the colony-stimulating factors (CSFs) on resource use, antibiotic days, hospital days, etc., it can be more economical and beneficial to use CSFs in ANIL than to withhold use. The overall dismal outlook for the older AML patient can only be altered by clinical trials with new therapeutic agents. New cellular and molecularly targeted agents are entering clinical trials and bring hope for progress to this area of cancer therapy. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:S17 / S26
页数:10
相关论文
共 53 条
[31]  
Leith CP, 1997, BLOOD, V89, P3323
[32]   The stem cell in the pathogenesis and treatment of myelogenous leukemia: a perspective [J].
Lichtman, MA .
LEUKEMIA, 2001, 15 (10) :1489-1494
[33]  
Lowenberg B, 1997, J CLIN ONCOL, V15, P3496
[34]  
Lowenberg B, 1997, BLOOD, V90, P2952
[35]   INTENSIVE POSTREMISSION CHEMOTHERAPY IN ADULTS WITH ACUTE MYELOID-LEUKEMIA [J].
MAYER, RJ ;
DAVIS, RB ;
SCHIFFER, CA ;
BERG, DT ;
POWELL, BL ;
SCHULMAN, P ;
OMURA, GA ;
MOORE, JO ;
MCINTYRE, OR ;
FREI, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (14) :896-903
[36]  
McCulloch EA, 1997, CLIN CANCER RES, V3, P2676
[37]   Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia [J].
Meshinchi, S ;
Woods, WG ;
Stirewalt, DL ;
Sweetser, DA ;
Buckley, JD ;
Tjoa, TK ;
Bernstein, ID ;
Radich, JP .
BLOOD, 2001, 97 (01) :89-94
[38]  
OHNO R, 1994, BLOOD, V83, P2086
[39]   EFFECT OF GRANULOCYTE COLONY-STIMULATING FACTOR AFTER INTENSIVE INDUCTION THERAPY IN RELAPSED OR REFRACTORY ACUTE-LEUKEMIA [J].
OHNO, R ;
TOMONAGA, M ;
KOBAYASHI, T ;
KANAMARU, A ;
SHIRAKAWA, S ;
MASAOKA, T ;
OMINE, M ;
OH, H ;
NOMURA, T ;
SAKAI, Y ;
HIRANO, M ;
YOKOMAKU, S ;
NAKAYAMA, S ;
YOSHIDA, Y ;
MIURA, AB ;
MORISHIMA, Y ;
DOHY, H ;
NIHO, Y ;
HAMAJIMA, N ;
TAKAKU, F .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (13) :871-877
[40]   2000 update of recommendations for the use of hematopoietic colony-stimulating factors: Evidence-based, clinical practice guidelines [J].
Ozer, H ;
Armitage, JO ;
Bennett, CL ;
Crawford, J ;
Demetri, GD ;
Pizzo, PA ;
Schiffer, CA ;
Smith, TJ ;
Somlo, G ;
Wade, JC ;
Wade, JL ;
Winn, RJ ;
Wozniak, AJ ;
Somerfield, MR .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (20) :3558-3585