Prevalence and predictors of chronic health conditions after hematopoietic cell transplantation: a report from the Bone Marrow Transplant Survivor Study.

Abstract:

:Long-term survival is now an expected outcome after hematopoietic cell transplantation (HCT). However, the burden of morbidity long-term after HCT remains unknown. We examined the magnitude of risk of chronic health conditions reported by 1022 HCT survivors and their siblings (n = 309). A severity score (grades 1 [mild] through 4 [life-threatening]) was assigned to each health condition using the Common Terminology Criteria for Adverse Events, Version 3. Sixty-six percent of the HCT survivors reported at least one chronic condition; 18% reported severe/life-threatening conditions; comparable values in siblings were 39% and 8%, respectively (P < .001). The cumulative incidence of a chronic health condition among HCT survivors was 59% (95% confidence interval [CI], 56%-62%) at 10 years after HCT; for severe/life-threatening conditions or death from chronic health conditions, the 10-year cumulative incidence approached 35% (95% CI, 32%-39%). HCT survivors were twice as likely as siblings to develop a chronic condition (95% CI, 1.6-2.1), and 3.5 times to develop severe/life-threatening conditions (95% CI, 2.3-5.4). HCT survivors with chronic graft-versus-host disease were 4.7 times as likely to develop severe/life-threatening conditions (95% CI, 3.0-7.2). The burden of long-term morbidity borne by HCT survivors is substantial, and long-term follow-up of patients who received transplantation is recommended.

journal_name

Blood

journal_title

Blood

authors

Sun CL,Francisco L,Kawashima T,Leisenring W,Robison LL,Baker KS,Weisdorf DJ,Forman SJ,Bhatia S

doi

10.1182/blood-2009-06-229369

subject

Has Abstract

pub_date

2010-10-28 00:00:00

pages

3129-39; quiz 3377

issue

17

eissn

0006-4971

issn

1528-0020

pii

blood-2009-06-229369

journal_volume

116

pub_type

杂志文章

相关文献

BLOOD文献大全
  • Direct correlation between the load of Epstein-Barr virus-infected lymphocytes in the peripheral blood of pediatric transplant patients and risk of lymphoproliferative disease.

    abstract::The Epstein-Barr virus (EBV) is known to cause posttransplant lymphoproliferative disease (PTLD) in immunosuppressed transplant patients. The results of this pilot study showed that all EBV- patients pretransplant experienced primary EBV infection within the first 3 months after transplant surgery. Virtually all of th...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Savoie A,Perpête C,Carpentier L,Joncas J,Alfieri C

    更新日期:1994-05-01 00:00:00

  • Restoration of sensitivity to STI571 in STI571-resistant chronic myeloid leukemia cells.

    abstract::STI571 induces sustained hematologic remission in patients with chronic myeloid leukemia (CML) in chronic phase. However, in advanced phases, especially blast crisis, the leukemia usually becomes resistant within months. It has been investigated whether resistance to STI571 is stable and immutable or whether it can be...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.13.3864

    authors: Tipping AJ,Mahon FX,Lagarde V,Goldman JM,Melo JV

    更新日期:2001-12-15 00:00:00

  • Increased peripheral platelet destruction and caspase-3-independent programmed cell death of bone marrow megakaryocytes in myelodysplastic patients.

    abstract::To investigate underlying mechanisms of thrombocytopenia in myelodysplastic syndrome (MDS), radiolabeled platelet studies were performed in 30 MDS patients with platelet counts less than 100 x 10(9)/L. Furthermore, plasma thrombopoietin and glycocalicin index (a parameter of platelet or megakaryocyte destruction) were...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-06-2108

    authors: Houwerzijl EJ,Blom NR,van der Want JJ,Louwes H,Esselink MT,Smit JW,Vellenga E,de Wolf JT

    更新日期:2005-05-01 00:00:00

  • Expression of ABH and X (Lex) antigens on platelets and lymphocytes.

    abstract::We used a panel of reagents, polyclonal and monoclonal antibodies, and lectins to define the expression of the ABH- and Lewis-related specificities on platelets and lymphocytes. We also determined the expression of the alpha 2- and alpha 3-L-fucosyltransferases necessary for their biosynthesis. The antigens that could...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Mollicone R,Caillard T,Le Pendu J,François A,Sansonetti N,Villarroya H,Oriol R

    更新日期:1988-04-01 00:00:00

  • CD20+ B-cell depletion therapy suppresses murine CD8+ T-cell-mediated immune thrombocytopenia.

    abstract::Immune thrombocytopenia (ITP) is an autoimmune bleeding disorder with a complex pathogenesis, which includes both antibody- and T-cell-mediated effector mechanisms. Rituximab (an anti-human CD20 monoclonal antibody [mAb]) is one of the treatments for ITP and is known to deplete B cells but may also work by affecting t...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2015-06-655126

    authors: Guo L,Kapur R,Aslam R,Speck ER,Zufferey A,Zhao Y,Kim M,Lazarus AH,Ni H,Semple JW

    更新日期:2016-02-11 00:00:00

  • Reproductive capacity in iron overloaded women with thalassemia major.

    abstract::The pathophysiology of iron-induced compromised fertility in women with thalassemia major (TM) was evaluated in 26 adult TM females. Low gonadotropin secretion resulted in reduced ovarian antral follicle count and ovarian volume, but levels of anti-müllerian hormone (AMH), a sensitive marker for ovarian reserve indepe...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-06-360271

    authors: Singer ST,Vichinsky EP,Gildengorin G,van Disseldorp J,Rosen M,Cedars MI

    更新日期:2011-09-08 00:00:00

  • T-cell function is partially maintained in the absence of class IA phosphoinositide 3-kinase signaling.

    abstract::The class IA subgroup of phosphoinositide 3-kinase (PI3K) is activated downstream of antigen receptors, costimulatory molecules, and cytokine receptors on lymphocytes. Targeted deletion of individual genes for class IA regulatory subunits severely impairs the development and function of B cells but not T cells. Here w...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2006-07-038620

    authors: Deane JA,Kharas MG,Oak JS,Stiles LN,Luo J,Moore TI,Ji H,Rommel C,Cantley LC,Lane TE,Fruman DA

    更新日期:2007-04-01 00:00:00

  • Whole genome scanning as a cytogenetic tool in hematologic malignancies.

    abstract::Over the years, methods of cytogenetic analysis evolved and became part of routine laboratory testing, providing valuable diagnostic and prognostic information in hematologic disorders. Karyotypic aberrations contribute to the understanding of the molecular pathogenesis of disease and thereby to rational application o...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2008-02-130435

    authors: Maciejewski JP,Mufti GJ

    更新日期:2008-08-15 00:00:00

  • Transcriptional and posttranscriptional modulation of human neutrophil elastase gene expression.

    abstract::Human neutrophil elastase (NE), a 29-Kd potent serine protease stored in azurophilic granules of mature neutrophils, is coded for by the NE gene, a single copy gene with 5 exons spanning a 6-kb segment of chromosome 11 at q14. With the knowledge that the NE gene expression is limited to early myeloid cell differentiat...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Yoshimura K,Crystal RG

    更新日期:1992-05-15 00:00:00

  • The identification and characterization of zebrafish hematopoietic stem cells.

    abstract::HSCs are defined by their ability to self-renew and maintain hematopoiesis throughout the lifespan of an organism. The optical clarity of their embryos and the ease of genetic manipulation make the zebrafish (Danio rerio) an excellent model for studying hematopoiesis. Using flow cytometry, we identified 2 populations ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2010-12-327403

    authors: Ma D,Zhang J,Lin HF,Italiano J,Handin RI

    更新日期:2011-07-14 00:00:00

  • Adhesion to E-selectin promotes growth inhibition and apoptosis of human and murine hematopoietic progenitor cells independent of PSGL-1.

    abstract::Although both P- and E-selectin are constitutively expressed on bone marrow endothelial cells, their role in the regulation of hematopoiesis has only recently been investigated. We have previously shown that P-selectin glycoprotein ligand-l (PSGL-1/CD162) is expressed by primitive human bone marrow CD34+ cells, mediat...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2003-06-1921

    authors: Winkler IG,Snapp KR,Simmons PJ,Lévesque JP

    更新日期:2004-03-01 00:00:00

  • BVL-1-like VL30 promoter sustains long-term expression in erythroid progenitor cells.

    abstract::Congenital blood disorders are common and yet clinically challenging globin disorders. Gene therapy continues to serve as a potential therapeutic method to treat these disorders. While tremendous advances have been made in vivo, gene delivery protocols and vector prototypes still require optimization. Alternative cis-...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-07-2105

    authors: Staplin WR,Knezetic JA

    更新日期:2003-03-01 00:00:00

  • Determination of platelet antigens and glycoproteins in the human fetus.

    abstract::The autosomal recessive transmission of Glanzmann's thrombasthenia (GT) and Bernard-Soulier syndrome (BSS), together with requests of families who already had children with these diseases, prompted us to investigate the feasibility of their antenatal diagnosis. The preliminary step leading to the early detection of GT...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Gruel Y,Boizard B,Daffos F,Forestier F,Caen J,Wautier JL

    更新日期:1986-08-01 00:00:00

  • Lyn physically associates with the erythropoietin receptor and may play a role in activation of the Stat5 pathway.

    abstract::Protein tyrosine phosphorylation plays a crucial role in signaling from the receptor for erythropoietin (Epo), although the Epo receptor (EpoR) lacks the tyrosine kinase domain. We have previously shown that the Jak2 tyrosine kinase couples with the EpoR to transduce a growth signal. In the present study, we demonstra...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Chin H,Arai A,Wakao H,Kamiyama R,Miyasaka N,Miura O

    更新日期:1998-05-15 00:00:00

  • Observations on the binding and interaction of radioiodinated colony-stimulating factor with murine bone marrow cells in vivo.

    abstract::Radioiodinated L-cell-derived colony-stimulating factor (CSF) was used to characterize the binding reaction to murine bone marrow cells. The major increment in cell-associated radioactivity occurred over 24 hr incubation at 37 degrees C, but virtually no binding was observed at 4 degrees C. The reaction was saturable ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Pigoli G,Waheed A,Shadduck RK

    更新日期:1982-02-01 00:00:00

  • Safety and immunologic effects of IL-15 administration in nonhuman primates.

    abstract::The administration of cytokines that modulate endogenous or transferred T-cell immunity could improve current approaches to clinical immunotherapy. Interleukin-2 (IL-2) is used most commonly for this purpose, but causes systemic toxicity and preferentially drives the expansion of CD4(+)CD25(+)Foxp3(+) regulatory T cel...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-12-189266

    authors: Berger C,Berger M,Hackman RC,Gough M,Elliott C,Jensen MC,Riddell SR

    更新日期:2009-09-17 00:00:00

  • High-dose etoposide and cyclophosphamide without bone marrow transplantation for resistant hematologic malignancy.

    abstract::Seventy-five patients with resistant acute leukemia or lymphoma received high-dose cyclophosphamide and etoposide to explore the activity of this combination in resistant hematologic malignancies, and to determine the maximum doses of these drugs that can be combined without bone marrow transplantation. Etoposide was ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Brown RA,Herzig RH,Wolff SN,Frei-Lahr D,Pineiro L,Bolwell BJ,Lowder JN,Harden EA,Hande KR,Herzig GP

    更新日期:1990-08-01 00:00:00

  • CCAAT/Enhancer binding proteins repress the leukemic phenotype of acute myeloid leukemia.

    abstract::CCAAT/enhancer binding proteins (C/EBPs) are a family of factors that regulate cell growth and differentiation. These factors, particularly C/EBPalpha and C/EBPepsilon, have important roles in normal myelopoiesis. In addition, loss of C/EBP activity appears to have a role in the pathogenesis of myeloid disorders inclu...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-05-1374

    authors: Truong BT,Lee YJ,Lodie TA,Park DJ,Perrotti D,Watanabe N,Koeffler HP,Nakajima H,Tenen DG,Kogan SC

    更新日期:2003-02-01 00:00:00

  • Intracellular storage and regulated plasma membrane expression of human complement receptor type 1 in rat basophil leukemia cell transfectants.

    abstract::Polymorphonuclear neutrophils (PMN) contain multiple distinct secretory compartments that are sequentially mobilized during cell activation. Complement receptor type 1 (CR1) is a marker for a readily mobilizable secretory vesicle compartment, which can undergo exocytic fusion with the plasma membrane independently of ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Jost C,Klickstein L,Wetzler E,Kumar A,Berger M

    更新日期:1998-07-01 00:00:00

  • Soluble CD22 as a tumor marker for hairy cell leukemia.

    abstract::CD22 is an important immunotherapeutic target on B-cell malignancies, particularly hairy cell leukemia (HCL), but its soluble extracellular domain, sCD22, has not yet been reported in the blood. By immunoaffinity and enzyme-linked immunosorbent assay techniques using anti-CD22 monoclonal antibodies, we identified the ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-01-131987

    authors: Matsushita K,Margulies I,Onda M,Nagata S,Stetler-Stevenson M,Kreitman RJ

    更新日期:2008-09-15 00:00:00

  • Murine stromal cells counteract the loss of long-term culture-initiating cell potential induced by cytokines in CD34(+)CD38(low/neg) human bone marrow cells.

    abstract::Evidence has been provided recently that shows that high concentrations of cytokines can fulfill functions previously attributed to stromal cells, such as promote the survival of, and led to a net increase in human primitive progenitors initiating long-term cultures in vitro (LTC-IC) or engrafting NOD-SCID (nonobese d...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Bennaceur-Griscelli A,Tourino C,Izac B,Vainchenker W,Coulombel L

    更新日期:1999-07-15 00:00:00

  • A missense mutation in gamma-glutamyl carboxylase gene causes combined deficiency of all vitamin K-dependent blood coagulation factors.

    abstract::To identify potential mutations in the gamma-glutamyl carboxylase gene, the sequence of all exons and intron/exon borders was determined in 4 patients from a consanguineous kindred with combined deficiency of all vitamin K-dependent procoagulants and anticoagulants and results were compared with normal genomic sequenc...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Brenner B,Sánchez-Vega B,Wu SM,Lanir N,Stafford DW,Solera J

    更新日期:1998-12-15 00:00:00

  • Relationship between patterns of engraftment in peripheral blood and immune reconstitution after allogeneic bone marrow transplantation for (severe) combined immunodeficiency.

    abstract::We report the outcome of allogeneic bone marrow transplantation (BMT) as treatment for severe combined immunodeficiency disease (SCID) in 31 patients grafted from 1968 until 1992. The patients received a graft from an HLA-identical related (n = 10), an HLA-haplo-identical related (n = 19), or a closely HLA-matched unr...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:

    authors: van Leeuwen JE,van Tol MJ,Joosten AM,Schellekens PT,van den Bergh RL,Waaijer JL,Oudeman-Gruber NJ,van der Weijden-Ragas CP,Roos MT,Gerritsen EJ

    更新日期:1994-12-01 00:00:00

  • There's no such fool like an immunosenescent fool.

    abstract::In this issue of Blood, Stepensky et al provide an astute description of immunosenescence arising from deficiency in tripeptidyl peptidase II (TPPII). Senescence of T and B lymphocytes is a striking finding, which has recently come into the limelight because it can be linked to primary immunodeficiency syndromes with ...

    journal_title:Blood

    pub_type: 评论,杂志文章

    doi:10.1182/blood-2014-12-614149

    authors: Seidel MG

    更新日期:2015-01-29 00:00:00

  • Th1 and Th2 T-helper cells exert opposite regulatory effects on procoagulant activity and tissue factor production by human monocytes.

    abstract::The role of T-cell subsets in the induction of tissue factor (TF) production by human monocytes in vitro was investigated. Mitogen stimulation enabled both unfractionated T cells and their CD4+ or CD8+ subsets to promote procoagulant activity (PCA). After mitogen or antigen activation, all seven T-cell clones with Th1...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Del Prete G,De Carli M,Lammel RM,D'Elios MM,Daniel KC,Giusti B,Abbate R,Romagnani S

    更新日期:1995-07-01 00:00:00

  • Identification of a critical regulatory site in the human interleukin-3 promoter by in vivo footprinting.

    abstract::Interleukin-3 (IL-3) is involved in proliferation and differentiation of hematopoietic progenitor cells. Its expression is subject to precise, tissue-specific regulation, and has been studied extensively in the gibbon T-cell line MLA 144 by a combination of functional assays and DNA binding experiments. To extend thes...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Cameron S,Taylor DS,TePas EC,Speck NA,Mathey-Prevot B

    更新日期:1994-05-15 00:00:00

  • Development and characterization of a physiologically relevant model of lymphocyte migration in chronic lymphocytic leukemia.

    abstract::There is growing evidence that lymphocyte trafficking contributes to the clinical course of chronic lymphocytic leukemia (CLL), but to date, only static in vitro cultures have been used to study these phenomena. To address this lack of data, we have developed a dynamic in vitro model in which CLL cells experience shea...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2013-12-544569

    authors: Walsby E,Buggins A,Devereux S,Jones C,Pratt G,Brennan P,Fegan C,Pepper C

    更新日期:2014-06-05 00:00:00

  • Bifunctional role for VEGF-induced heme oxygenase-1 in vivo: induction of angiogenesis and inhibition of leukocytic infiltration.

    abstract::Heme-oxygenases (HOs) catalyze the conversion of heme into carbon monoxide and biliverdin. HO-1 is induced during hypoxia, ischemia/reperfusion, and inflammation, providing cytoprotection and inhibiting leukocyte migration to inflammatory sites. Although in vitro studies have suggested an additional role for HO-1 in a...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2003-06-1974

    authors: Bussolati B,Ahmed A,Pemberton H,Landis RC,Di Carlo F,Haskard DO,Mason JC

    更新日期:2004-02-01 00:00:00

  • Relevance of marrow fibrosis in bone marrow transplantation: a retrospective analysis of engraftment.

    abstract::A retrospective study compared posttransplant engraftment parameters in 203 patients with myelofibrosis (MF) with those in a population of 203 matched controls without MF. There were no significant differences between these groups in the proportions of patients who died without achieving engraftment and in the disease...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Soll E,Massumoto C,Clift RA,Buckner CD,Appelbaum FR,Storb R,Sale G,Hackman R,Martin P

    更新日期:1995-12-15 00:00:00

  • Molecular basis for type 1 antithrombin deficiency: identification of two novel point mutations and evidence for a de novo splice site mutation.

    abstract::Inherited type 1 antithrombin (AT) deficiency is characterized by a reduction in both immunologically and functionally detectable protein. The disorder is associated with a high risk of thromboembolic disease. We have investigated the molecular basis of type 1 AT deficiency in three unrelated families. We have used th...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Jochmans K,Lissens W,Yin T,Michiels JJ,van der Luit L,Peerlinck K,De Waele M,Liebaers I

    更新日期:1994-12-01 00:00:00