A disease risk index for patients undergoing allogeneic stem cell transplantation

被引:315
作者
Armand, Philippe [1 ]
Gibson, Christopher J. [2 ]
Cutler, Corey [1 ]
Ho, Vincent T. [1 ]
Koreth, John [1 ]
Alyea, Edwin P. [1 ]
Ritz, Jerome [1 ]
Sorror, Mohamed L. [4 ]
Lee, Stephanie J.
Deeg, H. Joachim
Storer, Barry E. [3 ,5 ]
Appelbaum, Frederick R.
Antin, Joseph H. [1 ]
Soiffer, Robert J. [1 ]
Kim, Haesook T. [6 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[2] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[3] Fred Hutchinson Canc Res Ctr, Div Clin Res, Clin Stat Program, Seattle, WA 98104 USA
[4] Univ Washington, Sch Med, Dept Med, Div Med Oncol, Seattle, WA 98195 USA
[5] Univ Washington, Dept Biostat, Sch Publ Hlth, Seattle, WA 98195 USA
[6] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
ACUTE MYELOGENOUS LEUKEMIA; PROGRESSION-FREE SURVIVAL; NON-HODGKIN-LYMPHOMA; MALIGNANT DISEASES; COMORBIDITY INDEX; INTENSITY; RELAPSE; PREDICTORS; EXPERIENCE; MORTALITY;
D O I
10.1182/blood-2012-03-418202
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The outcome of allogeneic HSCT varies considerably by the disease and remission status at the time of transplantation. Any retrospective or prospective HSCT study that enrolls patients across disease types must account for this heterogeneity; yet, current methods are neither standardized nor validated. We conducted a retrospective study of 1539 patients who underwent transplantation at Dana-Farber Cancer Institute/Brigham and Women's Hospital from 2000 to 2009. Using multivariable models for overall survival, we created a disease risk index. This tool uses readily available information about disease and disease status to categorize patients into 4 risk groups with significantly different overall survival and progression-free survival on the basis of primarily differences in the relapse risk. This scheme applies regardless of conditioning intensity, is independent of comorbidity index, and was validated in an independent cohort of 672 patients from the Fred Hutchinson Cancer Research Center. This simple and validated scheme could be used to risk-stratify patients in both retrospective and prospective HSCT studies, to calibrate HSCT outcomes across studies and centers, and to promote the design of HSCT clinical trials that enroll patients across diseases and disease states, increasing our ability to study nondisease-specific outcomes in HSCT. (Blood. 2012;120(4):905-913)
引用
收藏
页码:905 / 913
页数:9
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