Intensified induction chemotherapy in adult acute myeloid leukemia followed by high-dose chemotherapy and autologous peripheral blood stem cell transplantation: an Eastern Cooperative Oncology Group trial (E4995)

被引:17
作者
Cassileth, PA
Lee, SJ
Litzow, MR
Miller, KB
Stadtmauer, EA
Tallman, MS
Lazarus, HM
Bennett, JM
Paietta, E
Dewald, GW
Rowe, JM
机构
[1] Univ Miami, Sylvester Comprehens Canc Ctr, Miami, FL 33136 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Mayo Clin, Rochester, MN USA
[4] Tufts Univ New England Med Ctr, Boston, MA USA
[5] Univ Penn, Ctr Canc, Philadelphia, PA 19104 USA
[6] Northwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Miami, FL USA
[7] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[8] Univ Rochester, Ctr Canc, Rochester, NY USA
[9] Our Lady Mercy Med Ctr, Bronx, NY USA
[10] Technion Israel Inst Technol, Rambam Med Ctr, Haifa, Israel
关键词
AML; intensive therapy; high-dose cytarabine; autologous stem cell transplantation;
D O I
10.1080/10428190412331283288
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The feasibility of intensified therapy in adults 561-years-old with de novo acute myeloid leukemia (AML) was evaluated by adding high-dose cytarabine ( HDAC) to conventional induction therapy and in post-remission therapy prior to peripheral blood stem cell transplantation (PBSCT). Patients were treated with conventional induction therapy ( daunorubicin days 1-3 and cytarabine days 1-7), followed by HDAC (2 gm/M-2) every 12 h ( x 6) on days 8-10. Patients in complete remission (CR) with HLA-matched siblings were assigned to allogeneic PBSCT; the others received two courses of HDAC (3 gm/M-2 every 12 h on days 1, 3, and 5) given 1 month apart. Peripheral blood stem cells were then harvested and infused after high-dose chemotherapy. Of 62 eligible, evaluable patients, 47 (76%) achieved CR. The mortality rate was 10% (6 patients); no deaths occurred during the two post-remission courses of HDAC. Fifteen patients were assigned to allogeneic PBSCT and 32 to autologous PBSCT. All surviving patients have been followed for more than 4 years. Including all patients scheduled to receive autoPBSCT in an intent-to-treat analysis, after a median 5-year follow-up the current, non-actuarial, four-year event-free and overall survival was 47% and 47%, respectively. Intensified induction therapy was associated with more toxicity than conventional induction therapy, and the CR rate did not improve. Nevertheless, intensive post-remission therapy was well tolerated, no treatment-related mortality occurred with autologous PBSCT, and disease-free survival and overall survival were lengthy.
引用
收藏
页码:55 / 61
页数:7
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