Therapeutic advances in leukemia and myelodysplastic syndrome over the past 40 years

被引:74
作者
Kantarjian, Hagop [1 ]
O'Brien, Susan [1 ]
Cortes, Jorge [1 ]
Wierda, William [1 ]
Faderl, Stefan [1 ]
Garcia-Manero, Guillermo [1 ]
Issa, Jean-Pierre [1 ]
Estey, Elihu [1 ]
Keating, Michael [1 ]
Freireich, Emil J. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
关键词
acute leukemia; chronic leukemia myelodysplastic syndrome; survival; treatment era; prognosis;
D O I
10.1002/cncr.23655
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Major therapeutic progress has been accomplished in leukemia and myelodysplastic syndrome (MDS) over the past 40 years, which may not be fully appreciated by the larger medical community The objective of this review was to briefly highlight the treatment breakthroughs in leukemia and MDS. Therapeutic progress happened through better Understanding of disease pathophysiologies and rational development of targeted agents, like imatinib mesylate in chronic myeloid leukemia (CML), and through astute, empirical discoveries in the clinic, like all-trans retinoic acid and arsenic trioxide in acute promyelocytic leukemia (APL) and chlorodeoxyadenosine in hairy cell leukemia (HCL). Today, the 5- to 10-year Survival rates in patients with APL and HCL exceed 80%. In patients with CML, imatinib therapy has been associated with estimated 5- to 7-year survival rates from 85% to 90%. In patients with adult acute lymphocytic leukemia, modern intensive regimens have improved the 5-year survival rates from 20% up to 40%. In Patients with chronic lymphocytic leukemia, chemoimmunotherapy recently produced high rates of quality responses and improved long-term outcome. In younger patients with acute myeloid leukemia (AML), the 5-year survival rates range from 40% to 50%, although elderly AML remains a therapeutic challenge. In patients with MDS, it was recently demonstrated that epigenetic therapy with hypomethylating agents improved survival. Much therapeutic progress has been witnessed in leukemia and MDS, and Much more is expected to occur soon.
引用
收藏
页码:1933 / 1952
页数:20
相关论文
共 227 条
[1]  
Alas S, 2001, CLIN CANCER RES, V7, P709
[2]  
AOKI E, 2006, P AM SOC CLIN ONCOL, V24
[3]   PROSPECTIVE GENETICALLY RANDOMIZED COMPARISON BETWEEN INTENSIVE POSTINDUCTION CHEMOTHERAPY AND BONE-MARROW TRANSPLANTATION IN ADULTS WITH NEWLY-DIAGNOSED ACUTE MYELOID-LEUKEMIA [J].
ARCHIMBAUD, E ;
THOMAS, X ;
MICHALLET, M ;
JAUBERT, J ;
TRONCY, J ;
GUYOTAT, D ;
FIERE, D .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (02) :262-267
[4]   Molecular genetics of acute lymphoblastic leukemia [J].
Armstrong, SA ;
Look, AT .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (26) :6306-6315
[5]   Congestive heart failure is a rare event in patients receiving imatinib therapy [J].
Atallah, Ehab ;
Durand, Jean-Bernard ;
Kantarjian, Hagop ;
Cortes, Jorge .
BLOOD, 2007, 110 (04) :1233-1237
[6]   CONSOLIDATION TREATMENT OF ADULT ACUTE LYMPHOBLASTIC-LEUKEMIA - A PROSPECTIVE, RANDOMIZED TRIAL COMPARING ALLOGENEIC VERSUS AUTOLOGOUS BONE-MARROW TRANSPLANTATION AND TESTING THE IMPACT OF RECOMBINANT INTERLEUKIN-2 AFTER AUTOLOGOUS BONE-MARROW TRANSPLANTATION [J].
ATTAL, M ;
BLAISE, D ;
MARIT, G ;
PAYEN, C ;
MICHALLET, M ;
VERNANT, JP ;
SAUVAGE, C ;
TROUSSARD, X ;
NEDELLEC, G ;
PICO, J ;
HUGUET, F ;
STOPPA, AM ;
BROUSTET, A ;
SOTTO, JJ ;
PRIS, J ;
MARANINCHI, D ;
REIFFERS, J .
BLOOD, 1995, 86 (04) :1619-1628
[7]   A randomized comparison of native Escherichia coli asparaginase and polyethylene glycol conjugated asparaginase for treatment of children with newly diagnosed standard-risk acute lymphoblastic leukemia:: a Children's Cancer Group study [J].
Avramis, VI ;
Sencer, S ;
Periclou, AP ;
Sather, H ;
Bostrom, BC ;
Cohen, LJ ;
Ettinger, AG ;
Ettinger, LJ ;
Franklin, J ;
Gaynon, PS ;
Hilden, JM ;
Lange, B ;
Majlessipour, F ;
Mathew, P ;
Needle, M ;
Neglia, J ;
Reaman, G ;
Holcenberg, JS .
BLOOD, 2002, 99 (06) :1986-1994
[8]   BAALC expression and FLT3 internal tandem duplication mutations in acute myeloid leukemia patients with normal cytogenetics:: Prognostic implications [J].
Baldus, CD ;
Thiede, C ;
Soucek, S ;
Bloomfield, CD ;
Thiel, E ;
Ehninger, G .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (05) :790-797
[9]   PROPOSALS FOR THE CLASSIFICATION OF THE MYELODYSPLASTIC SYNDROMES [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
BRITISH JOURNAL OF HAEMATOLOGY, 1982, 51 (02) :189-199
[10]  
Beran M, 2001, CANCER-AM CANCER SOC, V92, P1999, DOI 10.1002/1097-0142(20011015)92:8<1999::AID-CNCR1538>3.0.CO