Heterogeneous prognostic impact of derivative chromosome 9 deletions in chronic myelogenous leukemia.

Abstract:

:Derivative chromosome 9 deletions are seen in 10% to 15% of patients with chronic myelogenous leukemia and have been associated with a poor prognosis; however, no studies have been performed in the context of a randomized clinical trial. We developed a DNA-based deletion screen and investigated 339 chronic phase patients treated with interferon-alpha as first-line therapy in 3 controlled German studies with a median observation time of 7 years. Deletions were detected in pretreatment DNA of 59 of 339 (17%) patients. Of these, 21 spanned the ABL/BCR junction and 38 were centromeric (n = 20) or telomeric (n = 18) of the breakpoint. There was no significant difference in overall survival between deleted and nondeleted patients. Patients with breakpoint-spanning deletions had poorer survival compared with patients without deletions (4.7 versus 7.8 years; P = .003), but this was not significant when censored at allogeneic stem cell transplantation (n = 129) or imatinib (n = 62) treatment in the first chronic phase (P = .078). Unexpectedly, deletions that did not span the breakpoint were associated with improved survival compared with cases without deletions (P = .001). Multiple Cox regression analysis indicated that deletion status (P = .007), age (P = .018), and spleen enlargement (P < .001) were significant independent indicators of survival and confirmed that only deletions spanning the ABL/BCR breakpoint were associated with an adverse prognosis (P = .039).

journal_name

Blood

journal_title

Blood

authors

Kreil S,Pfirrmann M,Haferlach C,Waghorn K,Chase A,Hehlmann R,Reiter A,Hochhaus A,Cross NC,German Chronic Myelogenous Leukemia (CML) Study Group.

doi

10.1182/blood-2007-02-074252

subject

Has Abstract

pub_date

2007-08-15 00:00:00

pages

1283-90

issue

4

eissn

0006-4971

issn

1528-0020

pii

blood-2007-02-074252

journal_volume

110

pub_type

杂志文章

相关文献

BLOOD文献大全
  • JAK2V617F homozygosity arises commonly and recurrently in PV and ET, but PV is characterized by expansion of a dominant homozygous subclone.

    abstract::Subclones homozygous for JAK2V617F are more common in polycythemia vera (PV) than essential thrombocythemia (ET), but their prevalence and significance remain unclear. The JAK2 mutation status of 6495 BFU-E, grown in low erythropoietin conditions, was determined in 77 patients with PV or ET. Homozygous-mutant colonies...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2012-05-431791

    authors: Godfrey AL,Chen E,Pagano F,Ortmann CA,Silber Y,Bellosillo B,Guglielmelli P,Harrison CN,Reilly JT,Stegelmann F,Bijou F,Lippert E,McMullin MF,Boiron JM,Döhner K,Vannucchi AM,Besses C,Campbell PJ,Green AR

    更新日期:2012-09-27 00:00:00

  • Mcl-1 expression in human neutrophils: regulation by cytokines and correlation with cell survival.

    abstract::Human neutrophils possess a very short half-life because they constitutively undergo apoptosis. Cytokines, such as granulocyte-macrophage colony-stimulating factor (GM-CSF), and other agents can rescue neutrophils from apoptosis but the molecular mechanisms involved in this rescue are undefined. Here, we show by Weste...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Moulding DA,Quayle JA,Hart CA,Edwards SW

    更新日期:1998-10-01 00:00:00

  • Prediction of T-cell reconstitution by assessment of T-cell receptor excision circle before allogeneic hematopoietic stem cell transplantation in pediatric patients.

    abstract::The extent and rapidity with which T cells are regenerated from graft-derived precursor cells directly influences the incidence of infection and the T-cell-based graft-versus-tumor effect. Measurement of T-cell receptor excision circles (TRECs) in peripheral blood is a means of quantifying recent thymic T-cell product...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-04-1405

    authors: Chen X,Barfield R,Benaim E,Leung W,Knowles J,Lawrence D,Otto M,Shurtleff SA,Neale GA,Behm FG,Turner V,Handgretinger R

    更新日期:2005-01-15 00:00:00

  • The impact of CYP2C9 and VKORC1 genetic polymorphism and patient characteristics upon warfarin dose requirements: proposal for a new dosing regimen.

    abstract::Current dosing algorithms do not account for genetic and environmental factors for warfarin dose determinations. This study investigated the contribution of age, CYP2C9 and VKORC1 genotype, and body size to warfarin-dose requirements. Studied were 297 patients with stable anticoagulation with a target international no...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2005-03-1108

    authors: Sconce EA,Khan TI,Wynne HA,Avery P,Monkhouse L,King BP,Wood P,Kesteven P,Daly AK,Kamali F

    更新日期:2005-10-01 00:00:00

  • The Kit-activating mutation D816V enhances stem cell factor--dependent chemotaxis.

    abstract::The D816V mutation of c-kit has been detected in patients with mastocytosis. This mutation leads to constitutive tyrosine kinase activation of Kit. Because stem cell factor (SCF), the ligand for Kit (CD117(+)), is a chemoattractant for CD117(+) cells and one feature of mastocytosis is an abnormal collection of mast ce...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.4.1195

    authors: Taylor ML,Dastych J,Sehgal D,Sundstrom M,Nilsson G,Akin C,Mage RG,Metcalfe DD

    更新日期:2001-08-15 00:00:00

  • CD4(+), CD56(+) DC2 acute leukemia is characterized by recurrent clonal chromosomal changes affecting 6 major targets: a study of 21 cases by the Groupe Français de Cytogénétique Hématologique.

    abstract::CD4(+), CD56(+) DC2 malignancies constitute a novel disease entity, which has recently been shown to arise from a transformed lymphoid-related plasmacytoid dendritic cell (DC2). Diagnosis is primarily based on a particular immunophenotype with tumor cells expressing CD4 and CD56 antigens in the absence of common lymph...

    journal_title:Blood

    pub_type: 杂志文章,多中心研究

    doi:10.1182/blood.v99.11.4154

    authors: Leroux D,Mugneret F,Callanan M,Radford-Weiss I,Dastugue N,Feuillard J,Le Mée F,Plessis G,Talmant P,Gachard N,Uettwiller F,Pages MP,Mozziconacci MJ,Eclache V,Sibille C,Avet-Loiseau H,Lafage-Pochitaloff M

    更新日期:2002-06-01 00:00:00

  • T-cell leukemias with rearrangement of the gamma but not beta T-cell receptor genes.

    abstract::beta and gamma T cell receptor (TCR) gene configuration was studied in 12 patients with large granular lymphocyte T cell leukemia (LGL-leukemia). Both genes were found rearranged in ten cases. In the remaining two patients TCR beta was found in germline configuration. In one of them rearrangement of T cell-rearranging...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Foroni L,Matutes E,Foldi J,Morilla R,Rabbitts T,Luzzatto L,Catovsky D

    更新日期:1988-02-01 00:00:00

  • Gene involved in the 3q27 translocation associated with B-cell lymphoma, BCL5, encodes a Krüppel-like zinc-finger protein.

    abstract::Chromosomal translocations involving band 3q27 are the recently described nonrandom cytogenetic abnormalities in B-cell malignancies. We have previously cloned the breakpoint region of 3q27, designated as the BCL5 locus, from the B-cell line carrying the t(3;22). The cDNA for the BCL5 gene was cloned from the human li...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Miki T,Kawamata N,Hirosawa S,Aoki N

    更新日期:1994-01-01 00:00:00

  • Anti-factor VIII antibodies of hemophiliac patients are frequently directed towards nonfunctional determinants and do not exhibit isotypic restriction.

    abstract::A significant proportion of hemophilia A patients receiving transfusions of factor VIII (FVIII) develop a specific antibody response towards FVIII. These antibodies are usually detected by assays in which they inhibit the function of the molecule, such as the Bethesda clotting test. We have prepared anti-FVIII antibod...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Gilles JG,Arnout J,Vermylen J,Saint-Remy JM

    更新日期:1993-10-15 00:00:00

  • Human CD34+ hematopoietic progenitors have low, cytokine-unresponsive O6-alkylguanine-DNA alkyltransferase and are sensitive to O6-benzylguanine plus BCNU.

    abstract::Human bone marrow (BM) cells contain low levels of the DNA repair protein, O6-alkylguanine-DNA alkyltransferase, which may explain their susceptibility to nitrosourea-induced cytotoxicity and the development of secondary leukemia after nitrosourea treatment. Isolated CD34+ myeloid progenitors were also found to have l...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Gerson SL,Phillips W,Kastan M,Dumenco LL,Donovan C

    更新日期:1996-09-01 00:00:00

  • Factors influencing the development of an anti-factor IX (FIX) immune response following administration of adeno-associated virus-FIX.

    abstract::The present study sought to determine the impact of the route of administration of an adeno-associated virus (AAV) vector encoding human factor IX (hFIX) on the induction of an immune response against the vector and its xenogenic transgene product, hFIX. Increasing doses of AAV-hFIX were administered by different rout...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v97.12.3733

    authors: Ge Y,Powell S,Van Roey M,McArthur JG

    更新日期:2001-06-15 00:00:00

  • Risk score to predict event-free survival after hematopoietic cell transplant for sickle cell disease.

    abstract::We developed a risk score to predict event-free survival (EFS) after allogeneic hematopoietic cell transplantation for sickle cell disease. The study population (n = 1425) was randomly split into training (n = 1070) and validation (n = 355) cohorts. Risk factors were identified and validated via Cox regression models....

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.2020005687

    authors: Brazauskas R,Scigliuolo GM,Wang HL,Cappelli B,Ruggeri A,Fitzhugh CD,Hankins JS,Kanter J,Meerpohl JJ,Panepinto JA,Rondelli D,Shenoy S,Walters MC,Wagner JE,Tisdale JF,Gluckman E,Eapen M

    更新日期:2020-07-30 00:00:00

  • Monocyte Fc gamma receptor recognition of cell-bound and aggregated IgG.

    abstract::Monocyte and macrophage Fc gamma receptors are important components in the recognition of IgG-coated cells and IgG-containing immune complexes. Two proteins have been identified on human peripheral blood monocytes that can function as Fc gamma receptors, Fc gamma RI (70 Kd) and Fc gamma RII (40 Kd). We studied the rol...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Gomez F,Chien P,King M,McDermott P,Levinson AI,Rossman MD,Schreiber AD

    更新日期:1989-08-15 00:00:00

  • Induction of proliferation and blast transformation by interferon in human malignant and non-malignant lymph node B cells.

    abstract::The influence of interferon (IFN) on cellular proliferation, blast transformation, and differentiation was studied in lymph node cells from 17 patients with B-cell lymphomas, one patient with T-cell lymphoma, and eight patients with enlarged, non-malignant lymph nodes. The effects of IFN on lymph node cells were compa...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Ostlund L,Biberfeld P,Robèrt KH,Christensson B,Einhorn S

    更新日期:1989-06-01 00:00:00

  • Immunologic and clinical effects of repeated blood exchange in familial erythrophagocytic lymphohistiocytosis.

    abstract::Depressed cellular immune function and increased susceptibility to infection characterize familial erythrophagocytic lymphohistiocytosis (FEL), a usually fatal autosomal recessive disease. One component of the immunodeficiency is plasma-mediated inhibition of lymphocyte proliferation. We have tested whether repeated p...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Ladisch S,Ho W,Matheson D,Pilkington R,Hartman G

    更新日期:1982-10-01 00:00:00

  • Harvesting and enrichment of hematopoietic progenitor cells mobilized into the peripheral blood of normal donors by granulocyte-macrophage colony-stimulating factor (GM-CSF) or G-CSF: potential role in allogeneic marrow transplantation.

    abstract::To explore the use of stem/progenitor cells from peripheral blood (PB) for allogeneic transplantation, we have studied the mobilization of progenitor cells in normal donors by growth factors. Normal subjects were administered either granulocyte-macrophage colony-stimulating factor (GM-CSF) at 10 micrograms/kg/d, or G-...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Lane TA,Law P,Maruyama M,Young D,Burgess J,Mullen M,Mealiffe M,Terstappen LW,Hardwick A,Moubayed M

    更新日期:1995-01-01 00:00:00

  • Adiponectin, a new member of the family of soluble defense collagens, negatively regulates the growth of myelomonocytic progenitors and the functions of macrophages.

    abstract::We investigated the functions of adiponectin, an adipocyte-specific secretory protein and a new member of the family of soluble defense collagens, in hematopoiesis and immune responses. Adiponectin suppressed colony formation from colony-forming units (CFU)-granulocyte-macrophage, CFU-macrophage, and CFU-granulocyte, ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Yokota T,Oritani K,Takahashi I,Ishikawa J,Matsuyama A,Ouchi N,Kihara S,Funahashi T,Tenner AJ,Tomiyama Y,Matsuzawa Y

    更新日期:2000-09-01 00:00:00

  • Unaltered repopulation properties of mouse hematopoietic stem cells transduced with lentiviral vectors.

    abstract::Recent studies of retroviral-mediated gene transfer have shown that retroviral integrations themselves may trigger nonmalignant clonal expansion of hematopoietic stem cells (HSCs) in transplant recipients. These observations suggested that previous conclusions of HSC dynamics based on gamma-retroviral gene marking sho...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-03-142661

    authors: Gonzalez-Murillo A,Lozano ML,Montini E,Bueren JA,Guenechea G

    更新日期:2008-10-15 00:00:00

  • Role for CCG-trinucleotide repeats in the pathogenesis of chronic lymphocytic leukemia.

    abstract::Chromosome 11q deletions are frequently observed in chronic lymphocytic leukemia (CLL) in association with progressive disease and a poor prognosis. A minimal region of deletion has been assigned to 11q22-q23. Trinucleotide repeats have been associated with anticipation in disease, and evidence of anticipation has bee...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v97.2.509

    authors: Auer RL,Jones C,Mullenbach RA,Syndercombe-Court D,Milligan DW,Fegan CD,Cotter FE

    更新日期:2001-01-15 00:00:00

  • Deficient lipoxin synthesis: a novel platelet dysfunction in myeloproliferative disorders with special reference to blastic crisis of chronic myelogenous leukemia.

    abstract::The capacity to convert exogenous leukotriene A4 to lipoxins (LXs) was investigated in platelet suspensions from patients with myeloproliferative disorders (MPD) (n = 22) and healthy control subjects (n = 14). Platelets isolated from the controls produced mainly LXA4, but also 6(S)-LXA4 and the all-trans isomers of li...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Stenke L,Edenius C,Samuelsson J,Lindgren JA

    更新日期:1991-12-01 00:00:00

  • Leukocyte integrin CD11b promoter directs expression in lymphocytes and granulocytes in transgenic mice.

    abstract::The human leukocyte integrin subunit CD11b is expressed predominantly on myelomonocytic cells. To identify CD11b promoter sequences important for myelomonocytic gene expression and to assess the utility of the CD11b promoter for expressing heterologous genes in vivo, we generated transgenic mice with a human CD4 repor...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Back A,East K,Hickstein D

    更新日期:1995-02-15 00:00:00

  • Single-strand conformation polymorphism analysis is a rapid and effective method for the identification of mutations and polymorphisms in the gene for glycoprotein IIIa.

    abstract::Glanzmann thrombasthenia (GT) is the most common inherited disorder of platelets. Most of the molecular defects previously identified in GT have been caused by point (or other small) mutations in the genes for glycoprotein (GP) IIb or GPIIIa. We have used single-strand conformation polymorphism (SSCP) analysis to rapi...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Jin Y,Dietz HC,Nurden A,Bray PF

    更新日期:1993-10-15 00:00:00

  • Midostaurin, enasidenib, CPX-351, gemtuzumab ozogamicin, and venetoclax bring new hope to AML.

    abstract::In 2017, 4 drugs received US Food and Drug Administration marketing approval for acute myeloid leukemia (AML) treatment: targeted therapies for mutant FLT3 and IDH2, a liposomal cytarabine-daunorubicin formulation for therapy-related AML and AML with myelodysplasia-related changes, and resurgence of an antibody-drug c...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2017-08-784066

    authors: Wei AH,Tiong IS

    更新日期:2017-12-07 00:00:00

  • Large granular lymphocyte proliferation: an analysis of T-cell receptor gene arrangement and expression and the effect of in vitro culture with inducing agents.

    abstract::The status of the T cell receptor beta and gamma genes in natural killer (NK) cells was investigated in two patients with a marked expansion of CD2+, CD3- NK cells. Both genes were found to be in the germline state. The T alpha and complete T beta gene transcripts were not detected, but a 1.0-kilobase T beta gene tran...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Chan WC,Dahl C,Waldmann T,Link S,Mawle A,Nicholson J,Bach FH,Bongiovanni K,McCue PA,Winton EF

    更新日期:1988-01-01 00:00:00

  • Initial bone marrow reticulin fibrosis in polycythemia vera exerts an impact on clinical outcome.

    abstract::We examined the prevalence and prognostic relevance of bone marrow reticulin fibrosis in 526 patients with World Health Organization-defined polycythemia vera evaluated at the time of initial diagnosis. Seventy-four patients (14%) displayed mostly grade 1 reticulin fibrosis, with only 2 cases showing higher-grade fibr...

    journal_title:Blood

    pub_type: 杂志文章,多中心研究

    doi:10.1182/blood-2011-11-393819

    authors: Barbui T,Thiele J,Passamonti F,Rumi E,Boveri E,Randi ML,Bertozzi I,Marino F,Vannucchi AM,Pieri L,Rotunno G,Gisslinger H,Gisslinger B,Müllauer L,Finazzi G,Carobbio A,Gianatti A,Ruggeri M,Nichele I,D'Amore E,Rambald

    更新日期:2012-03-08 00:00:00

  • Cognitive and behavioral abnormalities in children after hematopoietic stem cell transplantation for severe congenital immunodeficiencies.

    abstract::Hematopoietic stem cell transplantation (HSCT) is a highly successful treatment for severe congenital immunodeficiencies. However, some studies have suggested that children may experience cognitive difficulties after HSCT. This large-scale study assessed cognitive and behavioral function for the cohort of children tre...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-04-151332

    authors: Titman P,Pink E,Skucek E,O'Hanlon K,Cole TJ,Gaspar J,Xu-Bayford J,Jones A,Thrasher AJ,Davies EG,Veys PA,Gaspar HB

    更新日期:2008-11-01 00:00:00

  • Synchronized integrin engagement and chemokine activation is crucial in neutrophil extracellular trap-mediated sterile inflammation.

    abstract::There is emerging evidence that neutrophil extracellular traps (NETs) play important roles in inflammatory processes. Here we report that neutrophils have to be simultaneously activated by integrin-mediated outside-in- and G-protein-coupled receptor (GPCR) signaling to induce NET formation in acute lung injury (ALI), ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2013-07-516484

    authors: Rossaint J,Herter JM,Van Aken H,Napirei M,Döring Y,Weber C,Soehnlein O,Zarbock A

    更新日期:2014-04-17 00:00:00

  • Mitochondrial dysfunction in antiphospholipid syndrome: implications in the pathogenesis of the disease and effects of coenzyme Q(10) treatment.

    abstract::The exact mechanisms underlying the role of oxidative stress in the pathogenesis and the prothrombotic or proinflammatory status of antiphospholipid syndrome (APS) remain unknown. Here, we investigate the role of oxidative stress and mitochondrial dysfunction in the proatherothrombotic status of APS patients induced b...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-12-400986

    authors: Perez-Sanchez C,Ruiz-Limon P,Aguirre MA,Bertolaccini ML,Khamashta MA,Rodriguez-Ariza A,Segui P,Collantes-Estevez E,Barbarroja N,Khraiwesh H,Gonzalez-Reyes JA,Villalba JM,Velasco F,Cuadrado MJ,Lopez-Pedrera C

    更新日期:2012-06-14 00:00:00

  • Mast cell hyperplasia, B-cell malignancy, and intestinal inflammation in mice with conditional expression of a constitutively active kit.

    abstract::Signaling through the receptor tyrosine kinase kit controls proliferation and differentiation of hematopoietic precursor cells and mast cells. Somatic point mutations of the receptor that constitutively activate kit signaling are associated with mastocytosis and various hematopoietic malignancies. We generated a Cre/l...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-11-189605

    authors: Gerbaulet A,Wickenhauser C,Scholten J,Peschke K,Drube S,Horny HP,Kamradt T,Naumann R,Müller W,Krieg T,Waskow C,Hartmann K,Roers A

    更新日期:2011-02-10 00:00:00

  • Isolation and characterization of an age-related antigen present on senescent human red blood cells.

    abstract::Autologous membrane-bound IgG was isolated from a subpopulation of human red blood cells (RBC) with specific density greater than 1.110, by affinity chromatography of purified RBC membrane glycoprotein preparations using immobilized wheat germ agglutinin and immobilized anti-human immunoglobulin (Ig) as immunoabsorben...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Alderman EM,Fudenberg HH,Lovins RE

    更新日期:1981-08-01 00:00:00