Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study.

نویسندگان

  • Henrik Hasle
  • Todd A Alonzo
  • Anne Auvrignon
  • Catherine Behar
  • Myron Chang
  • Ursula Creutzig
  • Alexandra Fischer
  • Erik Forestier
  • Alcira Fynn
  • Oskar A Haas
  • Jochen Harbott
  • Christine J Harrison
  • Nyla A Heerema
  • Marry M van den Heuvel-Eibrink
  • Gertjan J L Kaspers
  • Franco Locatelli
  • Peter Noellke
  • Sophia Polychronopoulou
  • Yaddanapudi Ravindranath
  • Bassem Razzouk
  • Dirk Reinhardt
  • Natalia N Savva
  • Batia Stark
  • Stefan Suciu
  • Ichiro Tsukimoto
  • David K Webb
  • Dorora Wojcik
  • William G Woods
  • Martin Zimmermann
  • Charlotte M Niemeyer
  • Susana C Raimondi
چکیده

Monosomy 7 (-7) and deletion 7q \del(7q)] are rare in childhood acute myeloid leukemia (AML). We retrospectively collected data on 258 children with AML or refractory anemia with excess blasts in transformation (RAEB-T) and -7 or del(7q) with or without other cytogenetic aberrations \+/- other]. Karyotypes included -7 (n = 90), -7 other (n = 82), del(7q) (n = 21), and del(7q) other (n = 65). Complete remission (CR) was achieved in fewer patients with -7 +/- other compared with del(7q) +/- other (61% versus 89%, P < .001). Overall, the 5-year survival rate was 39% (SE, 3%). Survival was superior in del(7q) +/- other compared with -7 +/- other (51% versus 30%, P < .01). Cytogenetic aberrations considered favorable in AML \t(8;21)(q22;q22), inv(16)(p13q22), t(15;17)(q22;q21), t(9;11)(p22;q23)] (n = 24) were strongly associated with del(7q) and a higher 5-year survival rate compared with del(7q) without favorable cytogenetics (75% versus 46%, P = .03). Patients with -7 and inv(3),-5/del(5q), or + 21 had a 5-year survival rate of 5%. Stem cell transplantation analyzed as a time-dependent variable had no impact on overall survival. However, patients not achieving CR had a 31% survival rate after stem cell transplantation. Childhood AML with chromosome 7 aberrations represents a heterogeneous group of disorders with additional cytogenetic aberrations having a major prognostic impact which should be reflected in future risk-group stratification.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

CLINICAL TRIALS AND OBSERVATIONS Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study

Henrik Hasle,1 Todd A. Alonzo,2 Anne Auvrignon,3 Catherine Behar,4 Myron Chang,5 Ursula Creutzig,6 Alexandra Fischer,7 Erik Forestier,8 Alcira Fynn,9 Oskar A. Haas,10,11 Jochen Harbott,12 Christine J. Harrison,13 Nyla A. Heerema,14 Marry M. van den Heuvel-Eibrink,15,16 Gertjan J. L. Kaspers,17 Franco Locatelli,18 Peter Noellke,7 Sophia Polychronopoulou,19 Yaddanapudi Ravindranath,20 Bassem Razz...

متن کامل

A novel cytogenetic abnormality r(7)(::p11.2->q36.3::) in a Philadelphia-positive chronic myeloid leukemia case

The so-called Philadelphia (Ph) chromosome is present in more than 90% of chronic myeloid leukemia (CML) cases. It results in juxtaposition of the 5' part of the BCR gene on chromosome 22 and the 3' part of the ABL1 gene on chromosome 9. An additional acquired monosomy 7 or deletion of 7q is associated with poor prognosis in a variety of myeloid disorders. Here we report a novel Ph chromosome p...

متن کامل

Identification of a common microdeletion cluster in 7q21.3 subband among patients with myeloid leukemia and myelodysplastic syndrome.

Monosomy 7 and interstitial deletions in the long arm of chromosome 7 (-7/7q-) is a common nonrandom chromosomal abnormality found frequently in myeloid disorders including acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), and juvenile myelomonocytic leukemia (JMML). Using a short probe-based microarray comparative genomic hybridization (mCGH) technology, we identified a common micr...

متن کامل

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis.

Loss of heterozygosity affecting chromosome 7q is common in acute myeloid leukemia and myelodysplastic syndromes, pointing toward the essential role of this region in disease phenotype and clonal evolution. The higher resolution offered by recently developed genomic platforms may be used to establish more precise clinical correlations and identify specific target genes. We analyzed a series of ...

متن کامل

Identification of Two Critically Deleted Regions within Chromosome Segment 7q35-q36 in EVI1 Deregulated Myeloid Leukemia Cell Lines

Chromosomal rearrangements involving the EVI1 proto-oncogene are a recurrent finding in myeloid leukemias and are indicative of a poor prognosis. Rearrangements of the EVI1 locus are often associated with monosomy 7 or cytogenetic detectable deletions of part of 7q. As EVI1 overexpression alone is not sufficient to induce leukemia, loss of a 7q tumour suppressor gene might be a required coopera...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Blood

دوره 109 11  شماره 

صفحات  -

تاریخ انتشار 2007