Myeloablative Versus Reduced-Intensity Hematopoietic Cell Transplantation for Acute Myeloid Leukemia and Myelodysplastic Syndromes

被引:465
|
作者
Scott, Bart L. [1 ]
Pasquini, Marcelo C. [2 ]
Logan, Brent R. [2 ]
Wu, Juan [3 ]
Devine, Steven M. [4 ]
Porter, David L. [5 ]
Maziarz, Richard T. [6 ]
Warlick, Erica D. [7 ]
Fernandez, Hugo F. [9 ]
Alyea, Edwin P. [10 ]
Hamadani, Mehdi [2 ]
Bashey, Asad [11 ]
Giralt, Sergio [12 ]
Geller, Nancy L. [13 ]
Leifer, Eric [13 ]
Le-Rademacher, Jennifer [8 ]
Mendizabal, Adamm M. [3 ]
Horowitz, Mary M. [2 ]
Deeg, H. Joachim [1 ]
Horwitz, Mitchell E. [14 ]
机构
[1] Fred Hutchinson Canc Res Ctr, 1100 Fairview Ave N,D1-100,POB 19024, Seattle, WA 98109 USA
[2] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[3] Emmes Corp, Rockville, MD USA
[4] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[5] Univ Penn, Philadelphia, PA 19104 USA
[6] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[7] Univ Minnesota, Minneapolis, MN USA
[8] Mayo Clin, Rochester, MN USA
[9] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[10] Dana Farber Canc Inst, Boston, MA 02115 USA
[11] Northside Hosp Canc Inst, Atlanta, GA USA
[12] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[13] NHLBI, Bldg 10, Bethesda, MD 20892 USA
[14] Duke Univ, Durham, NC USA
基金
美国国家卫生研究院;
关键词
ACUTE MYELOGENOUS LEUKEMIA; VERSUS-HOST-DISEASE; NON-RELAPSE MORTALITY; 1ST REMISSION; ALLOGENEIC TRANSPLANTATION; HEMATOLOGIC MALIGNANCIES; MARROW-TRANSPLANTATION; CONDITIONING REGIMEN; PREPARATIVE REGIMENS; THERAPY;
D O I
10.1200/JCO.2016.70.7091
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The optimal regimen intensity before allogeneic hematopoietic cell transplantation (HCT) is unknown. We hypothesized that lower treatment-related mortality (TRM) with reduced-intensity conditioning (RIC) would result in improved overall survival (OS) compared with myeloablative conditioning (MAC). To test this hypothesis, we performed a phase III randomized trial comparing MAC with RIC in patients with acute myeloid leukemia or myelodysplastic syndromes. Patients and Methods Patients age 18 to 65 years with HCT comorbidity index <= 4 and <5% marrow myeloblasts pre-HCT were randomly assigned to receive MAC (n = 135) or RIC (n = 137) followed by HCT from HLA-matched related or unrelated donors. The primary end point was OS 18 months post-random assignment based on an intent-to-treat analysis. Secondary end points included relapse-free survival (RFS) and TRM. Results Planned enrollment was 356 patients; accrual ceased at 272 because of high relapse incidence with RIC versus MAC (48.3%; 95% CI, 39.6% to 56.4% and 13.5%; 95% CI, 8.3% to 19.8%, respectively; P < .001). At 18 months, OS for patients in the RIC arm was 67.7% (95% CI, 59.1% to 74.9%) versus 77.5% (95% CI, 69.4% to 83.7%) for those in the MAC arm (difference, 9.8%; 95% CI, 20.8% to 20.3%; P = .07). TRM with RIC was 4.4% (95% CI, 1.8% to 8.9%) versus 15.8% (95% CI, 10.2% to 22.5%) with MAC (P = .002). RFS with RIC was 47.3% (95% CI, 38.7% to 55.4%) versus 67.8% (95% CI, 59.1% to 75%) with MAC (P < 01). Conclusion OS was higher with MAC, but this was not statistically significant. RIC resulted in lower TRM but higher relapse rates compared with MAC, with a statistically significant advantage in RFS with MAC. These data support the use of MAC as the standard of care for fit patients with acute myeloid leukemia or myelodysplastic syndromes. (C) 2017 by American Society of Clinical Oncology
引用
收藏
页码:1154 / 1161
页数:8
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