2000
DOI: 10.1038/sj.leu.2401669
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Minimal residual disease is common after allogeneic stem cell transplantation in patients with B cell chronic lymphocytic leukemia and may be controlled by graft-versus-host disease

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Cited by 60 publications
(49 citation statements)
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References 37 publications
(23 reference statements)
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“…This observation agrees with the delayed clearance of CLL cells after allogeneic SCT reported before. [13][14][15]18,33 In general, MRD was not detectable during later follow-up, the only exception being a patient who eventually had to be retreated. In all patients after allogeneic SCT studied in parallel by MRD flow and by ASO IgH RQ-PCR, both methods showed the same MRD kinetics.…”
Section: Figurementioning
confidence: 96%
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“…This observation agrees with the delayed clearance of CLL cells after allogeneic SCT reported before. [13][14][15]18,33 In general, MRD was not detectable during later follow-up, the only exception being a patient who eventually had to be retreated. In all patients after allogeneic SCT studied in parallel by MRD flow and by ASO IgH RQ-PCR, both methods showed the same MRD kinetics.…”
Section: Figurementioning
confidence: 96%
“…[1][2][3][4][5][6] At the same time with the advent of purine analogs, 7 monoclonal antibodies, [8][9][10] autologous 11,12 and allogeneic SCT, [13][14][15] molecular remissions became an attainable therapeutic goal. These effective therapies and the known heterogeneity of the disease increased the importance of minimal residual disease (MRD) assessment as a surrogate marker for treatment efficiency in clinical studies.…”
Section: Introductionmentioning
confidence: 99%
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“…Moreover, an increase of MRD, as assessed by the quantitative estimation by cytofluorometry of the leukemic population, was evident in further analyses of all patients in whom MRD became detectable. In the remaining five patients, no evidence of MRD was observed at last assessment, after a median follow-up of 24 months (range, [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31]. At the time of writing, six patients have had a clinical relapse at a median of 16 months (range, 9-38) after transplant.…”
Section: Response Transplant-related Mortality (Trm) and Monitoringmentioning
confidence: 99%