Hemizygous p16INK4A deletion in pediatric acute lymphoblastic leukemia predicts independent risk of relapse

被引:71
作者
Carter, TL
Watt, PM
Kumar, R
Burton, PR
Reaman, GH
Sather, HN
Baker, DL
Kees, UR
机构
[1] Univ Western Australia, TVWT Inst Child Hlth Res, Div Childrens Leukaemia & Canc Res, Ctr Child Hlth Res,Fac Med & Dent, W Perth, WA 6872, Australia
[2] Univ Western Australia, TVWT Inst Child Hlth Res, Div Biostat & Genet Epidemiol, Ctr Child Hlth Res,Fac Med & Dent, W Perth, WA 6872, Australia
[3] Princess Margaret Hosp, Dept Haematol Oncol, Perth, WA, Australia
[4] George Washington Univ, Childrens Natl Med Ctr, Washington, DC USA
[5] Childrens Canc Grp, Arcadia, CA USA
[6] Univ Leicester, Dept Epidemiol & Publ Hlth, Genet Epidemiol Unit, Leicester, Leics, England
关键词
D O I
10.1182/blood.V97.2.572
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The genes at the INK4A/ARF locus at 9p21 are frequently involved in human cancer. Virtually ail p16(INK4A) exon 2 (henceforth called p16) inactivation in pediatric acute lymphoblastic leukemia (ALL) occurs by gene deletion. The results of this study illustrate that real-time quantitative polymerase chain reaction is capable of detecting gene deletion in primary patient specimens with a precision not previously achieved by conventional methods. Importantly, this assay includes the detection of hemizygous deletions, The study revealed, strikingly, that the risk ratio for relapse for hemizygous deletion compared with no deletion was 6.558 (P = .00687) and for homozygous deletion was 11.558 (P = .000539). These results confirm and extend the authors' previous findings that homozygous deletion of p16 in pediatric ALL patients is an independent prognostic indicator of outcome from therapy. (C) 2001 by The American Society of Hematology.
引用
收藏
页码:572 / 574
页数:3
相关论文
共 15 条
  • [1] FREQUENCY OF HOMOZYGOUS DELETION AT P16/CDKN2 IN PRIMARY HUMAN TUMORS
    CAIRNS, P
    POLASCIK, TJ
    EBY, Y
    TOKINO, K
    CALIFANO, J
    MERLO, A
    MAO, L
    HERATH, J
    JENKINS, R
    WESTRA, W
    RUTTER, JL
    BUCKLER, A
    GABRIELSON, E
    TOCKMAN, M
    CHO, KR
    HEDRICK, L
    BOVA, GS
    ISAACS, W
    KOCH, W
    SCHWAB, D
    SIDRANSKY, D
    [J]. NATURE GENETICS, 1995, 11 (02) : 210 - 212
  • [2] Accommodating haploinsufficient tumour suppressor genes in Knudson's model
    Cook, WD
    McCaw, BJ
    [J]. ONCOGENE, 2000, 19 (30) : 3434 - 3438
  • [3] Review of alterations of the cyclin-dependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia-lymphoma cells
    Drexler, HG
    [J]. LEUKEMIA, 1998, 12 (06) : 845 - 859
  • [4] Gaynon PS, 1998, INT J PEDIAT HEM ONC, V5, P99
  • [5] Molecular genetics, natural history and the demise of childhood leukaemia (Reprinted from Eur J Cancer, vol 35, pg 173-185, 1999)
    Greaves, M
    [J]. EUROPEAN JOURNAL OF CANCER, 1999, 35 (14) : 1941 - 1953
  • [6] Prognostic importance of p15(INK4B) and pl6(INK4) gene inactivation in childhood acute lymphocytic leukemia
    Heyman, M
    Rasool, O
    Brandter, LB
    Liu, Y
    Grander, D
    Soderhall, S
    Gustavsson, G
    Einhorn, S
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (05) : 1512 - 1520
  • [7] Kalbfleisch J.D., 1980, The statistical analysis of failure time data
  • [8] Homozygous deletion of the p16/MTS1 gene in pediatric acute lymphoblastic leukemia is associated with unfavorable clinical outcome
    Kees, UR
    Burton, PR
    Lu, CL
    Baker, DL
    [J]. BLOOD, 1997, 89 (11) : 4161 - 4166
  • [9] Nelder JA, 1983, GEN LINEAR MODELS
  • [10] The INK4 family of cell cycle inhibitors in cancer
    Roussel, MF
    [J]. ONCOGENE, 1999, 18 (38) : 5311 - 5317