Additional prognostic impact of the percentage of erythroid cells in the bone marrow of patients with myelodysplastic syndromes

被引:0
|
作者
Neukirchen-Strapatsas, Judith [1 ]
Tuechler, Heinz [2 ]
Della Porta, Matteo [3 ,4 ]
Fenaux, Pierre [5 ]
Guerci, Agnes [6 ]
Haas, Rainer [1 ]
Rossi, Marianna [3 ,4 ]
Sapena, Rosa [7 ]
Sperr, Wolfgang R. [8 ,9 ]
Strupp, Corinna [1 ]
Stamatoullas, Aspasia [10 ]
Valent, Peter [8 ,9 ]
Germing, Ulrich [1 ]
Bennett, John M. [11 ,12 ]
机构
[1] Heinrich Heine Univ Duesseldorf, Dept Hematol Oncol & Clin Immunol, Dusseldorf, Germany
[2] Hanusch Hosp, Boltzmann Inst Leukemia Res, Vienna, Austria
[3] Humanitas Res Hosp, Canc Ctr, Milan, Italy
[4] Humanitas Univ, Milan, Italy
[5] Hop St Louis, Hematol Clin Senior, Paris, France
[6] Univ Hosp, Hematol Dept, Nancy, France
[7] GFM, Paris, France
[8] Med Univ Vienna, Div Hematol & Hemostaseol, Dept Internal Med 1, Vienna, Austria
[9] Med Univ Vienna, Ludwig Boltzmann Cluster Oncol, Vienna, Austria
[10] Ctr Henri Becquerel, INSERM U1245, Rouen, France
[11] Univ Rochester, Med Ctr, Dept Pathol, Hematopathol Unit, Rochester, NY 14642 USA
[12] Univ Rochester, Med Ctr, James P Wilmot Canc Inst, Rochester, NY 14642 USA
关键词
MDS; IPSS-R; AML; Erythroid precursors; Prognosis; SCORING SYSTEM; CLASSIFICATION;
D O I
10.1016/j.leukres.2018.12.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In patients with myelodysplastic syndromes (MDS) the impact of the percentage of erythroid precursors in the bone marrow has been the subject of considerable debate, especially with regard to prognosis. We examined the prognostic impact of the percentage of erythroid cells in the bone marrow (bmery) in 2453 primary untreated MDS patients in a retrospective multi-center analysis. Bmery were quantified in bone marrow smears at the time of diagnosis and were correlated with overall survival (OS) and AML evolution. We identified three distinct risk categories: "<=10% bmery" (poor), "11-25 or >45% bmery" (intermediate), and "26-45% bmery" (good) with distinct OS of 23, 40 and 48 months, respectively. The percentage of bmery showed prognostic significance concerning OS (Dxy=0.08, p<0.001) and AML-free survival (Dxy=0.15, p<0.001). Considering the IPSS-R by stratification, the Dxy were 0.09 for survival, and 0.18 for transformation (p<0.001). Added to the IPSS-R, bmery enhances the prognostic power for both survival (Dxy=0.39) and time to AML (Dxy=0.59). Survival and time to AML differ in MDS according to the percentage of bmery. The best outcome was found in those who had normal or near normal bmery counts. Moreover, adding bmery as differentiating feature to the IPSS-R may enhance its prognostic significance.
引用
收藏
页码:8 / 13
页数:6
相关论文
共 50 条
  • [21] Bone marrow immune microenviroment in patients with myelodysplastic syndromes
    Tsakiraki, Z.
    Papageorgiou, S.
    Spathis, A.
    Gouloumis, A. R.
    Pouliakis, A.
    Bouchla, A.
    Thomopoulos, T.
    Angelopoulou, E.
    Panayiotides, I.
    Pappa, V.
    Foukas, P.
    VIRCHOWS ARCHIV, 2021, 479 (SUPPL 1) : S116 - S116
  • [22] The proliferation index of bone marrow cells from myelodysplastic syndromes is associated with the diagnostic and prognostic of the disease
    Matarraz, S.
    Teodosio, C.
    Fernandez, C.
    Albors, M.
    Jara-Acevedo, M.
    Lopez, A.
    Gonzalez-Gonzalez, M.
    Gutierrez, M. L.
    Flores-Montero, J.
    Cervero, C.
    LEUKEMIA RESEARCH, 2013, 37 : S87 - S87
  • [23] PROGNOSTIC IMPLICATION OF SEQUENTIAL BONE-MARROW CULTURES IN THE MYELODYSPLASTIC SYNDROMES
    YOSHIDA, Y
    YOSHIDA, C
    TOHYAMA, K
    OHMORI, S
    OHMORI, M
    UEDA, Y
    TANIGUCHI, Y
    UCHINO, H
    LEUKEMIA RESEARCH, 1989, 13 (11) : 967 - 972
  • [24] Bone marrow fibrosis impact on response to azacitidine in myelodysplastic syndromes
    Shahidi, Roya
    Mohamed, Muhajir
    Sharma, Archana
    Heenan, Jessica
    Gardner, Julia
    Hitchins, Sam
    PATHOLOGY, 2022, 54 (06) : 763 - 767
  • [25] PROGNOSTIC IMPACT OF ADDITIONAL CHROMOSOMAL ABERRATIONS TO 5Q-IN PATIENTS WITH PRIMARY MYELODYSPLASTIC SYNDROMES
    Mallo, M.
    Cervera, J.
    Schanz, J.
    Espinet, B.
    Such, E.
    Luno, E.
    Steidl, C.
    Martin, M. L.
    Germing, U.
    Granada, I.
    Pfeilstoecker, M.
    Hernandez, J. M.
    Noesslinger, T.
    Calasanz, M. J.
    Valent, P.
    Collado, R.
    Fonatsch, C.
    Bureo, E.
    Luebbert, M.
    Rios, R.
    Stauder, R.
    Arranz, E.
    Hildebrandt, B.
    Cigudosa, J. C.
    Pedro, C.
    Salido, M.
    Arenillas, L.
    Sanz, G. F.
    Sanz, M. A.
    Valencia, A.
    Florensa, L.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 : 360 - 361
  • [26] Bone marrow lymphocytosis in myelodysplastic syndromes
    Horny, HP
    LEUKEMIA RESEARCH, 2002, 26 (06) : 531 - 531
  • [27] Bone marrow niches in myelodysplastic syndromes
    Tosato, Giovanna
    Feng, Jing-Xin
    Ohnuki, Hidetaka
    Sim, Minji
    JOURNAL OF CANCER METASTASIS AND TREATMENT, 2021, 7
  • [28] Myelodysplastic syndromes with bone marrow fibrosis
    Della Porta, Matteo Giovanni
    Malcovati, Luca
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2011, 96 (02): : 180 - 183
  • [29] Bone marrow niche in the myelodysplastic syndromes
    Cogle, Christopher R.
    Saki, Najmaldin
    Khodadi, Elahe
    Li, June
    Shahjahani, Mohammad
    Azizidoost, Shirin
    LEUKEMIA RESEARCH, 2015, 39 (10) : 1020 - 1027
  • [30] Myelodysplastic syndromes and bone marrow microenvironment
    Della Porta, Matteo Giovanni
    LEUKEMIA RESEARCH, 2011, 35 (11) : 1442 - 1443