Modified Delphi panel consensus recommendations for management of severe aplastic anemia

被引:4
作者
Babushok, Daria, V [1 ]
DeZern, Amy E. [2 ]
de Castro, Carlos M. [3 ]
Rogers, Zora R. [4 ]
Beenhouwer, David [5 ]
Broder, Michael S. [5 ]
Fanning, Suzanne R. [6 ]
Gibbs, Sarah N. [5 ]
Hanna, Rabi [7 ]
Maciejewski, Jaroslaw P. [8 ]
Scott, Bart L. [9 ]
Tantravahi, Srinivas K. [10 ]
Wlodarski, Marcin W. [11 ]
Yermilov, Irina [5 ]
Patel, Bhumika J. [6 ]
机构
[1] Univ Penn, Dept Med, Div Hematol Oncol, Philadelphia, PA USA
[2] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD USA
[3] Duke Canc Inst, Dept Med, Div Hematol Malignancies & Cellular Therapy, Durham, NC USA
[4] Univ Texas Southwestern Med Ctr Dallas, Div Pediat Hematol Oncol, Dallas, TX USA
[5] Partnership Hlth Analyt Res, Beverly Hills, CA USA
[6] Univ South Carolina, Prisma Hlth Canc Inst, Greenville, SC USA
[7] Cleveland Clin, Dept Pediat Hematol Oncol & Bone Marrow Transplant, Cleveland, OH USA
[8] Cleveland Clin, Translat Hematol & Oncol Res Dept, Cleveland, OH USA
[9] Fred Hutchinson Canc Res Ctr, Clin Res Div, Seattle, WA USA
[10] Univ Utah, Huntsman Canc Inst, Div Hematol & Hematol Malignancies, Salt Lake City, UT USA
[11] St Jude Childrens Res Hosp, Dept Hematol, Memphis, TN USA
关键词
BONE-MARROW-TRANSPLANTATION; HIGH-DOSE CYCLOPHOSPHAMIDE; APPROPRIATE USE CRITERIA; ANTI-THYMOCYTE GLOBULIN; ANTITHYMOCYTE GLOBULIN; IMMUNOSUPPRESSIVE THERAPY; CORONARY REVASCULARIZATION; CLONAL HEMATOPOIESIS; SOMATIC MUTATIONS; FANCONI-ANEMIA;
D O I
10.1182/bloodadvances.2023011642
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Severe aplastic anemia (SAA) is a rare hematologic condition for which there is no clear management algorithm. A panel of 11 experts on adult and pediatric aplastic anemia was assembled and, using the RAND/University of California, Los Angeles modified Delphi panel method, evaluated >600 varying patient care scenarios to develop clinical recommendations for the initial and subsequent management of patients of all ages with SAA. Here, we present the panel's recommendations to rule out inherited bone marrow failure syndromes, on supportive care before and during first-line therapy, and on first-line (initial management) and second-line (subsequent management) therapy of acquired SAA, focusing on when transplant vs medical therapy is most appropriate. These recommendations represent the consensus of 11 experts informed by published literature and experience. They are intended only as general guidance for experienced clinicians who treat patients with SAA and are in no way intended to supersede individual physician and patient decision making. Current and future research should validate this consensus using clinical data. Once validated, we hope these expert panel recommendations will improve outcomes for patients with SAA.
引用
收藏
页码:3946 / 3960
页数:15
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