ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia

被引:192
作者
Gelsi-Boyer, Veronique [1 ,2 ,3 ]
Trouplin, Virginie [1 ]
Roquain, Julien [1 ]
Adelaide, Jose [1 ]
Carbuccia, Nadine [1 ]
Esterni, Benjamin [4 ]
Finetti, Pascal [1 ]
Murati, Anne [1 ,2 ]
Arnoulet, Christine [2 ]
Zerazhi, Hacene [5 ]
Fezoui, Hacene [6 ]
Tadrist, Zoulika [7 ]
Nezri, Meyer [8 ]
Chaffanet, Max [1 ]
Mozziconacci, Marie-Joeelle [1 ,3 ]
Vey, Norbert [3 ,9 ]
Birnbaum, Daniel [1 ]
机构
[1] Ctr Rech Cancerol Marseille, Oncol Mol Lab, UMR891, INSERM,Inst Paoli Calmettes, F-13009 Marseille, France
[2] Univ Mediterrane Aix Marseille II, Marseille, France
[3] Inst Paoli Calmettes, Dept BioPathol, Marseille, France
[4] Inst Paoli Calmettes, Bur Etudes Clin, Marseille, France
[5] Ctr Hosp Gen Avignon, Serv Med Interne Oncohematol, Avignon, France
[6] Hosp Intercommunal Toulon, Hosp Font Pre Ctr, Serv Oncohematol, Toulon, France
[7] Ctr Hosp Gen Salon de Provence, Serv Med Interne Oncohematol, Salon De Provence, France
[8] Ctr Hosp Gen Martigues, Serv Med Interne, Marseille, France
[9] Inst Paoli Calmettes, Dept Hematol, Marseille, France
关键词
array-CGH; ASXL1; chronic myelomonocytic leukaemia; mutations; gene mutation; prognosis; WORLD-HEALTH-ORGANIZATION; MYELODYSPLASTIC SYNDROMES; MYELOID-LEUKEMIA; RAS MUTATIONS; GENE MUTATION; CLASSIFICATION; FREQUENT; RUNX1; TET2; HYBRIDIZATION;
D O I
10.1111/j.1365-2141.2010.08381.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P>Chronic myelomonocytic leukaemia (CMML) is a haematological disease currently classified in the category of myelodysplastic syndromes/myeloproliferative neoplasm (MDS/MPN) because of its dual clinical and biological presentation. The molecular biology of CMML is poorly characterized. We studied a series of 53 CMML samples including 31 cases of myeloproliferative form (MP-CMML) and 22 cases of myelodysplastic forms (MD-CMML) using array-comparative genomic hybridisation (aCGH) and sequencing of 13 candidate genes including ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, PTPN11, RUNX1, TET2 and WT1. Mutations in ASXL1 and in the genes associated with proliferation (CBL, FLT3, PTPN11, NRAS) were mainly found in MP-CMML cases. Mutations of ASXL1 correlated with an evolution toward an acutely transformed state: all CMMLs that progressed to acute phase were mutated and none of the unmutated patients had evolved to acute leukaemia. The overall survival of ASXL1 mutated patients was lower than that of unmutated patients.
引用
收藏
页码:365 / 375
页数:11
相关论文
共 31 条
  • [1] Gain of CBL-interacting protein, a possible alternative to CBL mutations in myeloid malignancies
    Adelaide, J.
    Gelsi-Boyer, V.
    Rocquain, J.
    Carbuccia, N.
    Birnbaum, D. J.
    Finetti, P.
    Bertucci, F.
    Mozziconacci, M. J.
    Vey, N.
    Birnbaum, D.
    Chaffanet, M.
    [J]. LEUKEMIA, 2010, 24 (08) : 1539 - 1541
  • [2] Integrated profiling of basal and luminal breast cancers
    Adelaide, Jose
    Finetti, Pascal
    Bekhouche, Ismahane
    Repellini, Laetitia
    Geneix, Jeannine
    Sircoulomb, Fabrice
    Jauffret, Emmanuelle Charafe
    Cervera, Nathalie
    Desplans, Jerome
    Parzy, Daniel
    Schoenmakers, Eric
    Viens, Patrice
    Jacquemier, Jocelyne
    Birnbaum, Daniel
    Bertucci, Francois
    Chaffanet, Max
    [J]. CANCER RESEARCH, 2007, 67 (24) : 11565 - 11575
  • [3] Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA
    Barrett, MT
    Scheffer, A
    Ben-Dor, A
    Sampas, N
    Lipson, D
    Kincaid, R
    Tsang, P
    Curry, B
    Baird, K
    Meltzer, PS
    Yakhini, Z
    Bruhn, L
    Laderman, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (51) : 17765 - 17770
  • [4] THE CHRONIC MYELOID LEUKEMIAS - GUIDELINES FOR DISTINGUISHING CHRONIC GRANULOCYTIC, ATYPICAL CHRONIC MYELOID, AND CHRONIC MYELOMONOCYTIC LEUKEMIA - PROPOSALS BY THE FRENCH-AMERICAN-BRITISH-COOPERATIVE-LEUKEMIA-GROUP
    BENNETT, JM
    CATOVSKY, D
    DANIEL, MT
    FLANDRIN, G
    GALTON, DAG
    GRALNICK, H
    SULTAN, C
    COX, C
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1994, 87 (04) : 746 - 754
  • [5] BENNETT JM, 1982, BRIT J HAEMATOL, V51, P189, DOI 10.1111/j.1365-2141.1982.tb08475.x
  • [6] Alterations of NFIA in chronic malignant myeloid diseases
    Bernard, F.
    Gelsi-Boyer, V.
    Murati, A.
    Giraudier, S.
    Trouplin, V.
    Adelaide, J.
    Rey, J.
    Olschwang, S.
    Vainchenker, W.
    Chaffanet, M.
    Vey, N.
    Mozziconacci, M. J.
    Birnbaum, D.
    [J]. LEUKEMIA, 2009, 23 (03) : 583 - 585
  • [7] High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression
    Boultwood, J.
    Perry, J.
    Zaman, R.
    Fernandez-Santamaria, C.
    Littlewood, T.
    Kusec, R.
    Pellagatti, A.
    Wang, L.
    Clark, R. E.
    Wainscoat, J. S.
    [J]. LEUKEMIA, 2010, 24 (06) : 1139 - 1145
  • [8] Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia
    Boultwood, J.
    Perry, J.
    Pellagatti, A.
    Fernandez-Mercado, M.
    Fernandez-Santamaria, C.
    Calasanz, M. J.
    Larrayoz, M. J.
    Garcia-Delgado, M.
    Giagounidis, A.
    Malcovati, L.
    Della Porta, M. G.
    Jadersten, M.
    Killick, S.
    Hellstrom-Lindberg, E.
    Cazzola, M.
    Wainscoat, J. S.
    [J]. LEUKEMIA, 2010, 24 (05) : 1062 - 1065
  • [9] Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias
    Carbuccia, N.
    Trouplin, V.
    Gelsi-Boyer, V.
    Murati, A.
    Rocquain, J.
    Adelaide, J.
    Olschwang, S.
    Xerri, L.
    Vey, N.
    Chaffanet, M.
    Birnbaum, D.
    Mozziconacci, M. J.
    [J]. LEUKEMIA, 2010, 24 (02) : 469 - 473
  • [10] Mutations of ASXL1 gene in myeloproliferative neoplasms
    Carbuccia, N.
    Murati, A.
    Trouplin, V.
    Brecqueville, M.
    Adelaide, J.
    Rey, J.
    Vainchenker, W.
    Bernard, O. A.
    Chaffanet, M.
    Vey, N.
    Birnbaum, D.
    Mozziconacci, M. J.
    [J]. LEUKEMIA, 2009, 23 (11) : 2183 - 2186