Allogeneic Transplantation for Advanced Acute Myeloid Leukemia: The Value of Complete Remission

被引:46
作者
Weisdorf, Daniel J. [1 ]
Millard, Heather R. [2 ]
Horowitz, Mary M. [2 ]
Hyare, Parvinder S. [3 ]
Champlin, Richard [4 ]
Ho, Vincent [5 ]
Mielcarek, Marco [6 ]
Rezvani, Andrew [7 ]
Stockerl-Goldstein, Keith [8 ]
Khoury, Hanna J. [9 ]
De Lima, Marcos [10 ]
Saber, Wael [2 ]
Sandmaier, Brenda [11 ,12 ]
Zhang, Mei Jie [2 ,13 ]
Eapen, Mary [2 ]
机构
[1] Univ Minnesota, Med Ctr, Dept Med, Div Hematol Oncol & Transplantat, Minneapolis, MN 55455 USA
[2] Med Coll Wisconsin, Dept Med, Ctr Int Blood & Marrow Transplantat CIBMTR, Milwaukee, WI 53226 USA
[3] Sunesis Pharmaceut, San Francisco, CA USA
[4] Univ Texas MD Anderson Canc Ctr, Div Canc Med, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
[5] Dana Farber Canc Inst, Ctr Hematol Oncol, Boston, MA 02115 USA
[6] Seattle Canc Care Alliance, Adult Blood & Marrow Transplant Program, Fred Hutchinson Canc Res Ctr, Seattle, WA USA
[7] Stanford Hlth Care, Div Blood & Marrow Transplantat, Stanford, CA USA
[8] Barnes Jewish Hosp, Div Hematol Oncol, St Louis, MO 63110 USA
[9] Emory Univ, Sch Med, Emory Univ Hosp, Hematol Oncol, Atlanta, GA USA
[10] Univ Hosp Case Med Ctr, Seidman Canc Ctr, Dept Med, Cleveland, OH USA
[11] Univ Washington, Div Med Oncol, Seattle, WA 98195 USA
[12] Fred Hutchinson Canc Res Ctr, Clin Res Div, 1124 Columbia St, Seattle, WA 98104 USA
[13] Med Coll Wisconsin, Div Biostat, Inst Hlth & Soc, Milwaukee, WI 53226 USA
关键词
acute myeloid leukemia; allogeneic transplantation; complete remission; primary induction failure; relapse; STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; CHEMOTHERAPY; SURVIVAL; THERAPY; FAILURE; RELAPSE; DONOR;
D O I
10.1002/cncr.30536
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Patients with acute myeloid leukemia (AML) without complete remission (CR) or in first relapse (Rel1) can have extended leukemia control and survival after allogeneic hematopoietic cell transplantation (HCT). For patients in Rel1 or primary induction failure (PIF), transplantation versus treatment to achieve a second CR (CR2) and subsequent HCT might yield similar outcomes, but available comparative data are scarce. METHODS: Survival was analyzed in 4682 HCT recipients according to disease status: PIF (N = 1440), Rel1 (failing >1 reinduction; N = 1256), and CR2 (N = 1986). RESULTS: Patient, disease, and transplantation characteristics were similar, except that patients in CR2 more often had performance scores of 90% to 100%, de novo AML, and longer CR1 duration. Adverse cytogenetics were more common in patients who experienced PIF. The 5-year survival rate adjusted for performance score, cytogenetic risk, and donor type for CR2 was 39% (95% confidence interval [CI], 37%-41%) compared with 18% (95% CI, 16%-20%) for HCT in Rel1 and 21% (95% CI, 19%-23%) in PIF (P < .0001). CONCLUSIONS: Although survival is superior for patients who undergo HCT in CR2, transplantation for selected patients in Rel1 or PIF may still be valuable. These data can guide decision making about additional salvage therapy versus prompt HCT for patients not in CR, but they also highlight that AML is intrinsically more treatable in patients who have favorable-risk cytogenetics, those with longer CR1 duration, and younger patients with better performance status. (C) 2017 American Cancer Society.
引用
收藏
页码:2025 / 2034
页数:10
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