期刊论文详细信息
Diagnostic Pathology
Evaluation of bone marrow aspirates in patients with acute myeloid leukemia at day 14 of induction therapy
Rodrigo D Portugal1  Marcio Nucci1  José Carlos Morais1  Wolmar Pulcheri1  Monique M Loureiro1  João Tadeu D Souto Filho2 
[1] University Hospital, Universidade Federal do Rio de Janeiro, Rua Prof. Rodolpho Paulo Rocco, 255, Sala 4A 12, Rio de Janeiro 22251-030, RJ, Brazil;Instituto Federal de Educação, Ciência e Tecnologia Fluminense, Campos dos Goytacazes, RJ, Brazil
关键词: D14;    Blasts counting;    Bone marrow;    Acute myeloid leukemia;   
Others  :  1225961
DOI  :  10.1186/s13000-015-0365-2
 received in 2015-06-08, accepted in 2015-07-15,  发布年份 2015
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【 摘 要 】

Background

Early assessment of response to chemotherapy in acute myeloid leukemia may be performed by examining bone marrow aspirate (BMA) or biopsy (BMB); a hypocellular bone marrow sample indicates adequate anti-leukemic activity. We sought to evaluate the quantitative and qualitative assessment of BMA performed on day 14 (D14) of chemotherapy, to verify the inter-observer agreement, to compare the results of BMA and BMB, and to evaluate the impact of D14 blast clearance on the overall survival (OS).

Methods

A total of 107 patients who received standard induction chemotherapy and had bone marrow samples were included. BMA evaluation was performed by two observers using two methods: quantitative assessment and a qualitative (Likert) scale. ROC curves were obtained correlating the BMA quantification of blasts and the qualitative scale, by both observers, with BMB result as gold-standard.

Results

There was a significant agreement between the two observers in both the qualitative and quantitative assessments (K w  = 0.737, p < 0.001, and r s  = 0.798, p < 0.001; ICC = 0.836, p < 0.001, respectively). The areas under the curve (AUC) were 0.924 and 0.946 for observer 1 and 0.867 and 0.870 for observer 2 for assessments of the percentage of blasts and qualitative scale, respectively. The best cutoff for blast percentage in BMA was 6 % and 7 % for observers 1 and 2, respectively. A similar analysis for the qualitative scale showed the best cutoff as “probably infiltrated”. Patients who attained higher grades of cytoreduction on D14 had better OS.

Conclusions

Evaluation of D14 BMA using both methods had a significant agreement with BMB and between observers, identifying a population of patients with poor outcome.

【 授权许可】

   
2015 Filho et al.

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【 参考文献 】
  • [1]Estey E, Dohner H. Acute myeloid leukaemia. Lancet. 2006; 368:1894-907.
  • [2]Milligan DW, Grimwade D, Cullis JO, Bond L, Swirsky D, Craddock C et al.. Guidelines on the management of acute myeloid leukaemia in adults. Br J Haematol. 2006; 135:450-74.
  • [3]Tallman MS, Gilliland DG, Rowe JM. Drug therapy for acute myeloid leukemia. Blood. 2005; 106:1154-63.
  • [4]Byrd JC, Mrozek K, Dodge RK, Carroll AJ, Edwards CG, Arthur DC et al.. Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461). Blood. 2002; 100:4325-36.
  • [5]Grimwade D, Walker H, Oliver F, Wheatley K, Harrison C, Harrison G et al.. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children’s Leukaemia Working Parties. Blood. 1998; 92:2322-33.
  • [6]Slovak ML, Kopecky KJ, Cassileth PA, Harrington DH, Theil KS, Mohamed A et al.. Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study. Blood. 2000; 96:4075-83.
  • [7]Patel JP, Gonen M, Figueroa ME, Fernandez H, Sun Z, Racevskis J et al.. Prognostic relevance of integrated genetic profiling in acute myeloid leukemia. N Engl J Med. 2012; 366:1079-89.
  • [8]Kern W, Haferlach T, Schoch C, Loffler H, Gassmann W, Heinecke A et al.. Early blast clearance by remission induction therapy is a major independent prognostic factor for both achievement of complete remission and long-term outcome in acute myeloid leukemia: data from the German AML Cooperative Group (AMLCG) 1992 Trial. Blood. 2003; 101:64-70.
  • [9]Wheatley K, Burnett AK, Goldstone AH, Gray RG, Hann IM, Harrison CJ et al.. A simple, robust, validated and highly predictive index for the determination of risk-directed therapy in acute myeloid leukaemia derived from the MRC AML 10 trial. United Kingdom Medical Research Council’s Adult and Childhood Leukaemia Working Parties. Br J Haematol. 1999; 107:69-79.
  • [10]Buchner T, Hiddemann W, Wormann B, Loffler H, Gassmann W, Haferlach T. Double induction strategy for acute myeloid leukemia: the effect of high-dose cytarabine with mitoxantrone instead of standard-dose cytarabine with daunorubicin and 6-thioguanine: a randomized trial by the German AML Cooperative Group. Blood. 1999; 93:4116-24.
  • [11]Cheson BD, Bennett JM, Kopecky KJ, Buchner T, Willman CL, Estey EH. Revised recommendations of the International Working Group for Diagnosis, Standardization of Response Criteria, Treatment Outcomes, and Reporting Standards for Therapeutic Trials in Acute Myeloid Leukemia. J Clin Oncol. 2003; 21:4642-9.
  • [12]O’Donnell MR, Tallman MS, Abboud CN, Altman JK, Appelbaum FR, Arber DA, et al. Acute Myeloid Leukemia (Version 2.2013). J Natl Compr Canc Netw. 2013;11:1047–55.
  • [13]Morra E, Barosi G, Bosi A, Ferrara F, Locatelli F, Marchetti M et al.. Clinical management of primary non-acute promyelocytic leukemia acute myeloid leukemia: Practice Guidelines by the Italian Society of Hematology, the Italian Society of Experimental Hematology, and the Italian Group for Bone Marrow Transplantation. Haematologica. 2009; 94:102-12.
  • [14]Dohner H, Estey EH, Amadori S, Appelbaum FR, Buchner T, Burnett AK et al.. Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet. Blood. 2010; 115:453-74.
  • [15]Preisler HD, Priore R, Azarnia N, Barcos M, Raza A, Rakowski I et al.. Prediction of response of patients with acute nonlymphocytic leukaemia to remission induction therapy: use of clinical measurements. Br J Haematol. 1986; 63:625-36.
  • [16]Liso V, Albano F, Pastore D, Carluccio P, Mele G, Lamacchia M et al.. Bone marrow aspirate on the 14th day of induction treatment as a prognostic tool in de novo adult acute myeloid leukemia. Haematologica. 2000; 85:1285-90.
  • [17]Xiao Z, Xue H, Li R, Zhang L, Yu M, Hao Y. The prognostic significance of leukemic cells clearance kinetics evaluation during the initial course of induction therapy with HAD (homoharringtonine, cytosine arabinoside, daunorubicin) in patients with de novo acute myeloid leukemia. Am J Hematol. 2008; 83:203-5.
  • [18]Hussein K, Jahagirdar B, Gupta P, Burns L, Larsen K, Weisdorf D. Day 14 bone marrow biopsy in predicting complete remission and survival in acute myeloid leukemia. Am J Hematol. 2008; 83:446-50.
  • [19]Yanada M, Borthakur G, Ravandi F, Bueso-Ramos C, Kantarjian H, Estey E. Kinetics of bone marrow blasts during induction and achievement of complete remission in acute myeloid leukemia. Haematologica. 2008; 93:1263-5.
  • [20]Gruppo RA, Lampkin BC, Granger S. Bone marrow cellularity determination: comparison of the biopsy, aspirate, and buffy coat. Blood. 1977; 49:29-31.
  • [21]Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, Gralnick HR et al.. Proposed revised criteria for the classification of acute myeloid leukemia. A report of the French-American-British Cooperative Group. Ann Intern Med. 1985; 103:620-5.
  • [22]Souto Filho JT, Portugal RD, Loureiro M, Pulcheri W, Nucci M. Characterization and analysis of the outcome of adults with acute myeloid leukemia treated in a Brazilian University hospital over three decades. Braz J Med Biol Res. 2011; 44:660-5.
  • [23]Likert R. A Technique for the Measurement of Attitudes. Archives of Psychology. 1932; 140:1-55.
  • [24]Landis JR, Koch GG. The measurement of observer agreement for categorical data. Biometrics. 1977; 33:159-74.
  • [25]Ludbrook J. Statistical techniques for comparing measurers and methods of measurement: a critical review. Clin Exp Pharmacol Physiol. 2002; 29:527-36.
  • [26]Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Int J Nurs Stud. 2010; 47:931-6.
  • [27]DeLong ER, DeLong DM, Clarke-Pearson DL. Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. Biometrics. 1988; 44:837-45.
  • [28]Fernandez HF, Sun Z, Yao X, Litzow MR, Luger SM, Paietta EM. Anthracycline dose intensification in acute myeloid leukemia. N Engl J Med. 2009; 361:1249-59.
  • [29]Ferrara F, Izzo T, Criscuolo C, Riccardi C, Celentano M, Mele G. Day 15 bone marrow driven double induction in young adult patients with acute myeloid leukemia: feasibility, toxicity, and therapeutic results. Am J Hematol. 2010; 85:687-90.
  • [30]Bertoli S, Bories P, Béné MC, Daliphard S, Lioure B, Pigneux A, Prognostic impact of day 15 blast clearance in risk-adapted remission induction chemotherapy for younger patients with acute myeloid leukemia: long-term results of the multicenter prospective LAM-2001 trial by the GOELAMS study group. Haematologica. 2014;99:46–53.
  • [31]Heil G, Krauter J, Raghavachar A, Bergmann L, Hoelzer D, Fiedler W et al.. Risk-adapted induction and consolidation therapy in adults with de novo AML aged ≤ 60 years: results of a prospective multicenter trial. Ann Hematol. 2004; 83(6):336-44.
  • [32]Pullarkat V, Aldoss I. Prognostic and therapeutic implications of early treatment response assessment in acute myeloid leukemia. Crit Rev Oncol Hematol. 2015; 95(1):38-45.
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