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. 2017 Mar;92(3):279-285.
doi: 10.1002/ajh.24629. Epub 2017 Feb 1.

Significance of recurrence of minimal residual disease detected by multi-parameter flow cytometry in patients with acute lymphoblastic leukemia in morphological remission

Affiliations

Significance of recurrence of minimal residual disease detected by multi-parameter flow cytometry in patients with acute lymphoblastic leukemia in morphological remission

Naveen Pemmaraju et al. Am J Hematol. 2017 Mar.

Abstract

We sought to determine the significance of minimal residual disease (MRD) relapse in patients with ALL after achieving MRD negative status following induction and consolidation therapy. Between January 2003 and September 2014, 647 newly diagnosed patients were treated [HyperCVAD-based (n = 531); Augmented BFM (n = 116)]. Six hundred and one (93%) achieved complete remission (CR), and 546 (91%) became MRD negative. Fifty-five patients [HyperCVAD-based (n = 49); Augmented BFM (n = 6)] developed recurrence of MRD while still in morphological CR and are the subjects of this study. MRD was assessed by 6-color (4-color prior to 2009) multi-parameter flow cytometry (MFC) at CR and multiple time points thereafter. Their median age was 44 years (range, 18-72 years), median WBC at initial presentation was 7.3 K/µL-1 (range, 0.6-303.8 K/µL-1 ) and median bone marrow blast percentage 88% (range, 26-98%). The median time to MRD relapse was 14 months (range 3-58 months). Forty-four (80%) patients subsequently developed morphological relapse after median of 3 months (range, <1-33 months) from detection of MRD recurrence. Treatments received after MRD positivity and prior to morphological relapse: 16 continued maintenance chemotherapy; 15 received late intensification; 9 allogeneic stem cell transplant, 9 changed chemotherapy, 6 no further therapy. Only six remain alive and in CR1 and nine are alive after morphological relapse. MRD relapse detected by MFC at any time after achieving CR is associated with a high risk for morphological relapse. SCT can result in long-term remission in some patients. Prospective studies of long-term MRD assessments, together with less toxic treatment strategies to eradicate MRD, are warranted.

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Conflict of interest statement

DISCLOSURES/CONFLICTS OF INTEREST

The authors have no conflicts of interest to disclose with regards to this manuscript.

Figures

FIGURE 1
FIGURE 1
Patient disposition: study flowchart. [Color figure can be viewed at wileyonlinelibrary.com]
FIGURE 2
FIGURE 2
(a) Disease-free survival (DFS) in patients with MRD relapse (n=55) from the time of MRD relapse. (b) Complete remission duration (CRD) in patients with MRD relapse (n=55) from the time of MRD relapse. (c) Overall survival (OS) in patients with MRD relapse (n=55) from the time of MRD relapse
FIGURE 3
FIGURE 3
(a) Disease-free survival (DFS) in patients with MRD relapse from the time of MRD relapse (SCT n=9 vs. non-SCT n=46). (b) Complate remission duration (CRD) in patients with MRD relapse from the time of MRD relapse (SCT n-9 vs. non-sct n=46). (c) Overall survival (OS) in patients with MRD relapse from the time of MRD relapse (SCT n=9 vs. non-SCT n=46). [Color figure can be viewed at wileyonlinelibrary.com]

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