Association between the choice of the conditioning regimen and outcomes of allogeneic hematopoietic cell transplantation for myelofibrosis

被引:19
|
作者
Murthy, Guru Subramanian Guru [1 ]
Kim, Soyoung [2 ,3 ]
Estrada-Merly, Noel [3 ]
Abid, Muhammad Bilal
Aljurf, Mahmoud [4 ]
Assal, Amer [5 ]
Badar, Talha [6 ]
Badawy, Sherif M. [7 ,8 ]
Ballen, Karen [9 ]
Beitinjaneh, Amer [10 ]
Cerny, Jan [11 ]
Chhabra, Saurabh [3 ]
DeFilipp, Zachariah [12 ]
Dholaria, Bhagirathbhai [13 ]
Perez, MiguelAngel Diaz [14 ]
Farhan, Shatha [15 ]
Freytes, Cesar O. [16 ]
Gale, Robert Peter [17 ]
Ganguly, Siddhartha [18 ]
Gupta, Vikas [19 ]
Grunwald, Michael R. [20 ]
Hamad, Nada [21 ]
Hildebrandt, Gerhard C. [22 ]
Inamoto, Yoshihiro [23 ]
Jain, Tania [24 ]
Jamy, Omer [25 ]
Juckett, Mark [26 ]
Kalaycio, Matt [27 ]
Krem, Maxwell M. [28 ]
Lazarus, Hillard M. [29 ]
Litzow, Mark [30 ]
Munker, Reinhold [22 ]
Murthy, Hemant S. [31 ,32 ]
Nathan, Sunita [33 ]
Nishihori, Taiga [34 ]
Orti, Guillermo [35 ]
Patel, Sagar S. [36 ]
van der Poel, Marjolein [37 ]
Rizzieri, David A. [38 ]
Savani, Bipin N. [39 ]
Seo, Sachiko [40 ]
Solh, Melhem [41 ]
Verdonck, Leo F. [42 ]
Wirk, Baldeep [43 ]
Yared, Jean A. [44 ]
Nakamura, Ryotaro [45 ]
Oran, Betul [46 ]
Scott, Bart [47 ]
Saber, Wael [3 ]
机构
[1] Med Coll Wisconsin, Div Hematol & Oncol, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Inst Hlth & Equ, Div Biostat, Milwaukee, WI USA
[3] Med Coll Wisconsin, CIBMTR Ctr Int Blood & Marrow Transplant Res, Dept Med, Milwaukee, WI USA
[4] King Faisal Specialist Hosp Ctr & Res, Dept Oncol, Riyadh, Saudi Arabia
[5] Columbia Univ, Dept Med Bone Marrow Transplant & Cell Therapy Pro, Irving Med Ctr, New York, NY USA
[6] Mayo Clin, Jacksonville, FL USA
[7] Ann & Robert H Lurie Childrens Hosp Chicago, Div Hematol Oncol & Stem Cell Transplantat, Chicago, IL USA
[8] Northwestern Univ, Dept Pediat, Feinberg Sch Med, Chicago, IL USA
[9] Univ Virginia Hlth Syst, Div Hematol Oncol, Charlottesville, VA USA
[10] Univ Miami Hosp &Clin, Slyvester Comprehens Canc Ctr, Div Transplantat & Cellular Therapy, Miami, FL USA
[11] Univ Massachusetts, Dept Med, Div Hematol Oncol, Med Ctr, Worcester, MA USA
[12] Massachusetts Gen Hosp, Hematopoiet Cell Transplant & Cellular Therapy Pro, Boston, MA USA
[13] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[14] Univ Nino Jesus, Hosp Infantil, Dept Hematol Oncol, Madrid, Spain
[15] Henry Ford Hlth Syst, Stem Cell Transplant & Cellular Therapy Program, Detroit, MI USA
[16] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX USA
[17] Imperial Coll London, Hematol Res Ctr, Dept Immunol & Inflammat, London, England
[18] Univ Kansas Hlth Syst, Div Hematol Malignancy & Cellular Therapeut, Kansas City, KS USA
[19] Univ Toronto, Princess Margaret Canc Ctr, MPN Program, Toronto, ON, Canada
[20] Atrium Hlth, Levine Canc Inst, Dept Hematol Oncol & Blood Disorders, Charlotte, NC USA
[21] St Vincent Hosp, Darlinghurst, NSW, Australia
[22] Univ Kentucky, Markey Canc Ctr, Lexington, KY USA
[23] Natl Canc Ctr, Div Hematopoiet Stem Cell Transplantat, Tokyo, Japan
[24] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[25] Univ Alabama Birmingham, Birmingham, AL USA
[26] Univ Minnesota, Blood & Marrow Transplant Program Adults, Minneapolis, MN USA
[27] Cleveland Clin, Taussig Canc Inst, Cleveland, OH USA
[28] Kansas City VA Med Ctr, Kansas City, MO USA
[29] Case Western Reserve Univ, Univ Hosp Cleveland Med Ctr, Cleveland, OH USA
[30] Mayo Clin Rochester, Div Hematol, Rochester, MN USA
[31] Mayo Clin, Blood & Marrow Transplantat Program, Div Hematol Oncol, Jacksonville, FL USA
[32] Mayo Clin Rochester, Transplant Ctr, Rochester, MN USA
[33] Rush Univ, Sect Bone Marrow Transplant & Cell Therapy, Med Ctr, Chicago, IL USA
[34] H Lee Moffitt Canc Ctr & Res Inst, Dept Blood & Marrow Transplant & Cellular Immunoth, Tampa, FL USA
[35] Vall dHebron Univ Hosp, Barcelona, Spain
[36] Univ Utah, Huntsman Canc Inst, Blood & Marrow Transplant Program, Salt Lake City, UT USA
[37] Masstricht Univ, GROW Sch Oncol & Dev Biol, Dept Internal Med, Div Hematol,Med Ctr, Maastricht, Netherlands
[38] Duke Univ, Div Hematol Malignancies & Cellular Therapy, Durham, NC USA
[39] Vanderbilt Univ, Dept Med, Div Hematol Oncol, Med Ctr, Nashville, TN USA
[40] Dokkyo Med Univ, Dept Hematol & Oncol, Mibu, Tochigo, Japan
[41] Northside Hosp, Blood & Marrow Transplant Grp Georgia, Atlanta, GA USA
[42] Isala Clin, Dept Hematol Oncol, Zwolle, Netherlands
[43] Penn State Canc Inst, Bone Marrow Transplant Program, Hershey, PA USA
[44] Univ Maryland, Greenebaum Comprehens Canc Ctr, Dept Med, Div Hematol Oncol,Transplantat & Cellular Therapy, Baltimore, MD USA
[45] City Hope Natl Med Ctr, Dept Hematol & Hematopoiet Cell Transplantat, Duarte, CA USA
[46] Univ Texas MD Anderson Canc Ctr Houston, Dept Stem Cell Transplantat, Div Canc Med, Houston, TX USA
[47] Fred Hutchinson Canc Res Ctr, Seattle, WA USA
关键词
INTERNATIONAL-BLOOD;
D O I
10.3324/haematol.2022.281958
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Allogeneic hematopoietic cell transplantation (allo-HCT) remains the only curative treatment for myelofibrosis. However, the optimal conditioning regimen either with reduced-intensity conditioning (RIC) or myeloablative conditioning (MAC) is not well known. Using the Center for International Blood and Marrow Transplant Research database, we identified adults aged & GE;18 years with myelofibrosis undergoing allo-HCT between 2008-2019 and analyzed the outcomes separately in the RIC and MAC cohorts based on the conditioning regimens used. Among 872 eligible patients, 493 underwent allo-HCT using RIC (fludara-bine/busulfan n=166, fludarabine/melphalan n=327) and 379 using MAC (fludarabine/busulfan n=247, busulfan/cyclophospha-mide n=132). In multivariable analysis with RIC, fludarabine/melphalan was associated with inferior overall survival (hazard ratio [HR]=1.80; 95% confidenec interval [CI]: 1.15-2.81; P=0.009), higher early non-relapse mortality (HR=1.81; 95% CI: 1.12-2.91; P=0.01) and higher acute graft -versus-host disease (GvHD) (grade 2-4 HR=1.45; 95% CI: 1.03-2.03; P=0.03; grade 3-4 HR=2.21; 95%CI: 1.28-3.83; P=0.004) compared to fludarabine/busulfan. In the MAC setting, busulfan/cyclophosphamide was associated with a higher acute GvHD (grade 2-4 HR=2.33; 95% CI: 1.67-3.25; P<0.001; grade 3-4 HR=2.31; 95% CI: 1.52-3.52; P<0.001) and inferior GvHD-free relapse-free survival (GRFS) (HR=1.94; 95% CI: 1.49-2.53; P<0.001) as compared to fludarabine/busulfan. Hence, our study suggests that fludarabine/busulfan is associated with better outcomes in RIC (better overall survival, lower early non-relapse mortality, lower acute GvHD) and MAC (lower acute GvHD and better GRFS) in myelofibrosis.
引用
收藏
页码:1900 / 1908
页数:9
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