Pre-existing invasive fungal infection is not a contraindication for allogeneic HSCT for patients with hematologic malignancies: a CIBMTR study

被引:33
作者
Maziarz, R. T. [1 ]
Brazauskas, R. [2 ,3 ]
Chen, M. [2 ]
McLeod, A. A. [1 ]
Martino, R. [4 ]
Wingard, J. R. [5 ]
Aljurf, M. [6 ]
Battiwalla, M. [7 ]
Dvorak, C. C. [8 ]
Geroge, B. [9 ]
Guinan, E. C. [10 ]
Hale, G. A. [11 ]
Lazarus, H. M. [12 ]
Lee, J-W [13 ]
Liesveld, J. L. [14 ]
Ramanathan, M. [15 ]
Reddy, V. [16 ]
Savani, B. N. [17 ]
Smith, F. O. [18 ]
Strasfeld, L. [19 ]
Taplitz, R. A. [20 ]
Ustun, C. [21 ]
Boeckh, M. J. [22 ]
Gea-Banacloche, J. [23 ]
Lindemans, C. A. [24 ]
Auletta, J. J. [25 ,26 ,27 ]
Riches, M. L. [28 ]
机构
[1] Oregon Hlth & Sci Univ, Adult Blood & Marrow Stem Cell Transplant Program, Knight Canc Inst, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA
[2] Med Coll Wisconsin, Dept Med, CIBMTR, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Inst Hlth & Soc, Div Biostat, Milwaukee, WI 53226 USA
[4] Hosp Santa Creu & Sant Pau, Div Clin Hematol, Barcelona, Spain
[5] Univ Florida, Dept Med, Div Hematol & Oncol, Gainesville, FL USA
[6] King Faisal Specialist Hosp Ctr & Res, Dept Oncol, Riyadh, Saudi Arabia
[7] NHLBI, Hematol Branch, Bethesda, MD 20892 USA
[8] Univ Calif San Francisco, Dept Pediat, Med Ctr, San Francisco, CA USA
[9] Christian Med Coll & Hosp, Dept Hematol, Vellore, Tamil Nadu, India
[10] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[11] All Childrens Hosp, Dept Hematol Oncol, St Petersburg, FL USA
[12] Univ Hosp Case Med Ctr, Seidman Canc Ctr, Cleveland, OH USA
[13] Catholic Univ Korea, Seoul St Marys Hosp, BMT Ctr, Seoul, South Korea
[14] Univ Rochester, Med Ctr, Dept Med, Rochester, NY 14642 USA
[15] UMass Mem Med Ctr, Dept Med, Div Hematol & Oncol, Worcester, MA USA
[16] Univ Cent Florida, Coll Med, Dept Internal Med, Orlando, FL 32816 USA
[17] Vanderbilt Univ, Med Ctr, Dept Med, Div Hematol Oncol, Nashville, TN USA
[18] Univ Cincinnati, Inst Canc, Cincinnati, OH USA
[19] Oregon Hlth & Sci Univ, Infect Dis Clin, Portland, OR 97201 USA
[20] UC San Diego Hlth, Infect Dis Program, La Jolla, CA USA
[21] Univ Minnesota, Med Ctr, Div Hematol Oncol & Transplantat, Dept Med, Minneapolis, MN 55455 USA
[22] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, 1124 Columbia St, Seattle, WA 98104 USA
[23] NCI, Expt Transplantat & Immunol Branch, NIH, Bethesda, MD 20892 USA
[24] Univ Med Ctr Utrecht, Pediat Blood & Marrow Transplantat Program, Utrecht, Netherlands
[25] Nationwide Childrens Hosp, Div Hematol Oncol, Columbus, OH USA
[26] Nationwide Childrens Hosp, Div Bone Marrow Transplantat, Columbus, OH USA
[27] Nationwide Childrens Hosp, Div Infect Dis, Columbus, OH USA
[28] Univ North Carolina Chapel Hill, Div Hematol Oncol, Chapel Hill, NC USA
关键词
HEMATOPOIETIC-CELL TRANSPLANTATION; UNRELATED DONORS; ASPERGILLOSIS; RECIPIENTS; DISEASES; PROPHYLAXIS; FLUCONAZOLE; MORTALITY; VORICONAZOLE; COMBINATION;
D O I
10.1038/bmt.2016.259
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Patients with prior invasive fungal infection (IFI) increasingly proceed to allogeneic hematopoietic cell transplantation (HSCT). However, little is known about the impact of prior IFI on survival. Patients with pre-transplant IFI (cases; n = 825) were compared with controls (n = 10247). A subset analysis assessed outcomes in leukemia patients pre-and post 2001. Cases were older with lower performance status (KPS), more advanced disease, higher likelihood of AML and having received cord blood, reduced intensity conditioning, mold-active fungal prophylaxis and more recently transplanted. Aspergillus spp. and Candida spp. were the most commonly identified pathogens. 68% of patients had primarily pulmonary involvement. Univariate and multivariable analysis demonstrated inferior PFS and overall survival (OS) for cases. At 2 years, cases had higher mortality and shorter PFS with significant increases in non-relapse mortality (NRM) but no difference in relapse. One year probability of post-HSCT IFI was 24% (cases) and 17% (control, P < 0.001). The predominant cause of death was underlying malignancy; infectious death was higher in cases (13% vs 9%). In the subset analysis, patients transplanted before 2001 had increased NRM with inferior OS and PFS compared with later cases. Pre-transplant IFI is associated with lower PFS and OS after allogeneic HSCT but significant survivorship was observed. Consequently, pre-transplant IFI should not be a contraindication to allogeneic HSCT in otherwise suitable candidates. Documented pre-transplant IFI is associated with lower PFS and OS after allogeneic HSCT. However, mortality post transplant is more influenced by advanced disease status than previous IFI. Pre-transplant IFI does not appear to be a contraindication to allogeneic HSCT.
引用
收藏
页码:270 / 278
页数:9
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