Korean J Lab Med.  2002 Dec;22(6):441-446.

Clinical Significance of Mixed Chimerism after Hematopoietic Stem Cell Transplantation

Affiliations
  • 1Department of Laboratory Medicine, Ewha Womans University, College of Medicine, Korea. JungWonH@hitel.net
  • 2Department of Hemato-Oncology, Ewha Womans University, College of Medicine, Korea.
  • 3Seoul Clinical Laboratories, Seoul, Korea.

Abstract

BACKGROUND: Chimerism analysis used to be one of the most valuable methods for monitoring patients after allogeneic hematopoietic stem cell transplantation (SCT). The relationship between the mixed chimerism status and the risk of relapse has been controversial. We analysed the clinical significance of mixed chimerism for the prediction of relapse after SCT.
METHODS
Between October 2000 and January 2002, 16 patients with haematologic malignancies treated with SCT were included in this study. The median follow-up periods were 11.5 months (range 5-32 months) after SCT. For chimerism analysis, STR (D13S317, D5S818, D7S820) and VNTR (D1S80, D17S30) loci were amplified by PCR. Patients who exhibited complete donor hematopoiesis at all times during the follow-up period were defined as CCG (complete chimerism group) and those who showed mixed chimerism at least once at any time were definded as the MCG (mixed chimerism group). Relapse was considered based on clinical, hematologic and cytogenetic findings.
RESULTS
MCG was 63% (10/16). Relapse was observed in 80% (8/10) of MCG and none of CCG (P>0.05). Among 8 relapsed patients, two patients showed MC 1 month prior to relapse and 4 patients changed to MC from CC at relapse status. The remaining 1 patient continued to show CC.
CONCLUSIONS
Mixed chimerism seems to be associated with a high risk of relapse. For early detection of relapse, chimerism analysis may need to be performed at shorter time intervals than once a month.

Keyword

Hematopoietic stem cell transplantation; Mixed chimerism; Complete chimerism; Relapse

MeSH Terms

Chimerism*
Cytogenetics
Follow-Up Studies
Hematopoiesis
Hematopoietic Stem Cell Transplantation*
Hematopoietic Stem Cells*
Humans
Polymerase Chain Reaction
Recurrence
Tissue Donors
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