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12th Congress of the European Hematology ... - Haematologica

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12 th <strong>Congress</strong> <strong>of</strong> <strong>the</strong> <strong>European</strong> <strong>Hematology</strong> Association<br />

to be added to B12 <strong>the</strong>rapy in AIHA and DIC, respectively, for patients<br />

to respond. In woman with MAHA and very high serum homocysteine,<br />

112 µmol/L, B12 dose had to be doubled. After red cell transfusion, <strong>the</strong>re<br />

were a doubling <strong>of</strong> LDH in AIHA and an eightfold increase <strong>of</strong> D-dimer<br />

in DIC. Conclusions. In CDA with greatly elevated serum LDH and low<br />

normal folate fur<strong>the</strong>r search for o<strong>the</strong>r causes <strong>of</strong> hemolysis is warranted.<br />

AIHA, DIC and MAHA must be taken into account and when confirmed<br />

a <strong>the</strong>rapy modified.<br />

Table 1. CDA with hemolysis related to o<strong>the</strong>r causes than B12 deficiency<br />

alone.<br />

1379<br />

CLINICAL AND ECONOMIC INEFFICIENCY OF ROUTINELY HARVEST AUTOLOGOUS STEM<br />

CELL AT FIRST COMPLETE REMISSION IN PATIENTS OF INTERMEDIATE AND HIGH RISK<br />

AML<br />

Y.M. Liao<br />

China Medical University Hospital, TAICHUNG, Taiwan<br />

Background. For patients <strong>of</strong> intermediate and high risk adult AML, <strong>the</strong><br />

relapse rate after standard induction and consolidation chemo<strong>the</strong>rapy<br />

remains high. Once relapse <strong>of</strong> AML developed and HLA-matched allogeneic<br />

donor is not available, <strong>the</strong> treatment is limited and <strong>the</strong> outcome<br />

is dismal. Autologous stem cell can be an alternative in this situation.<br />

However, it is difficult to harvest autologous stem cell <strong>of</strong> good quality<br />

when leukemia had already relapsed. Aims. To evaluate <strong>the</strong> feasibility <strong>of</strong><br />

routinely harvest and cryopreserved autologous peripheral blood stem<br />

cell (APBSC) at first complete remission (CR) in patients <strong>of</strong> intermediate<br />

and high risk AML and having no HLA-matched allogeneic donors.<br />

Once relapse <strong>of</strong> AML developed, <strong>the</strong> patients may <strong>the</strong>n receive autologous<br />

transplantation. Methods. Patients <strong>of</strong> intermediate or high risk AML<br />

and had no HLA-matched donors received conventional induction<br />

chemo<strong>the</strong>rapy (I3A7 regimen) followed by consecutive 2 courses <strong>of</strong> high<br />

dose Ara-C (18g/sq.m in each course)/Mitoxantrone consolidation<br />

chemo<strong>the</strong>rapy (in-vivo purging). APBSCs were routinely collected<br />

immediately after recovery from nadir phase <strong>of</strong> <strong>the</strong> second course consolidation<br />

chemo<strong>the</strong>rapy. At relapse, <strong>the</strong> patients were treated with high<br />

dose chemo<strong>the</strong>rapy or chemoradio<strong>the</strong>rapy followed by in vivo-purged<br />

APBSCT. For patient with first CR longer than 1 year, ano<strong>the</strong>r course <strong>of</strong><br />

salvage chemo<strong>the</strong>rapy with high dose Ara-C will be given to induce<br />

second CR. Results. Of <strong>the</strong> consecutive 26 patients enrolled, sufficient<br />

APBSC (2 ? 106 /kg BW) was successfully harvested in 17 (65.4%) and <strong>the</strong><br />

result was not associated with age, gender, disease nature (intermediate<br />

or high risk), lapse time between diagnosis and stem cell harvest, and<br />

lapse time between second course consolidation chemo<strong>the</strong>rapy and<br />

stem cell harvest. However, a lower nadir white blood cell count (

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