Abstract
Abstract 2241Poster Board II-218 Introduction:T-LGL has the phenotype characteristics of a post-thymus mature T cell. Expansion of T-LGL has been reported to occur in association with viral infections, autoimmune diseases, lymphoproliferative malignancy and HSCT. The clinical significance of finding T-LGL expansion post HSCT is unclear. We recently reviewed the incidence of T-LGL expansion in patients who underwent allogeneic HSCT in our institution. We specifically asked whether T-LGL expansion was associated with increased viral infections, stable chimerism, graft-versus-host disease (GvHD), recurrence of primary disease, and overall survival. Patients and Methods:A retrospective analysis was done on all adult patients who underwent allogeneic HSCT at the Karmanos Cancer Institute between January 1, 2004 to June 30, 2009. In patients with persistent lymphocytosis (>3000 cells/mm3) post HSCT, expansion of T-LGL phenotype was identified by flow cytometry (CD2, CD3, CD5, CD7, CD8 and CD57 positive) and clonality was confirmed by T cell receptor beta and/or gamma gene rearrangement (TCR-GR) using southern blot analysis and polymerase chain reaction (PCR). Results:A total of 547 patients underwent allogeneic HSCT during the study period. We identified T-LGL expansion in 24 patients with persistent lymphocytosis using flow cytometry. Median age of patients with T-LGL expansion was 50 years (range 24-68 years). Median time to diagnosis was 275 days post HSCT (range 69-1454 days) and median duration of follow-up was 811 days (range 85-1701 days). All 24 patients achieved full donor chimerism post transplantation by STR analysis. Fourteen out of 24 patients with T-LGL expansion had positive TCR-GR, in 2 patients TCR-GR was not done and the remainder was negative. Twenty out of 24 patients had cytomegalovirus (CMV) viremia confirmed by PCR before the onset of T-LGL expansion; the remainder had no CMV viremia. In all patients with T-LGL expansion there was no subsequent recurrence of CMV viremia or infection. All 24 patients had documented graft versus host disease (GvHD). In the group with T-LGL expansion only 2 patients relapsed with primary disease and only one patient died (due to a cardiac event). The cumulative incidence of T-LGL expansion was 4.4% at the end of the study period. Conclusion: To our knowledge, this is the largest reported series of T-LGL expansion post allogeneic HSCT. T-LGL expansion was associated with an interesting sequence of CMV viremia preceding T-LGL expansion and subsequent lack of recurrence of CMV viremia or infection. We also observed a very low number of relapse of primary disease or death in patients with T-LGL expansion. One hypothesis is that T-LGL expansion may be a result of specific stimulation with CMV antigens post allogeneic HSCT. An alternate hypothesis is that T-LGL expansion is a surrogate marker for accelerated immune reconstitution. At present, it is also unclear if T-LGL expansion is a marker of ‘graft-versus-leukemia' effect with respect to relapse of primary disease warranting further research.T-LGL expansionTCR-GR PositiveTCR-GR Negative/Not doneNo. of patients1410Type of transplantationUnrelated 6 ; Related 8Unrelated 7 ; Related 3Pre-transplantation diagnosisAML 3AML 4NHL 5NHL 2CLL 2ALL 2ALL 3CML 1MM 1MM 1GVHD ProphylaxisTAC/CELL 11TAC/CELL 9CSA 1ATG/TAC/SIRO 1ATG/ TAC/ SIRO 2CMV statusD-/R+ 8D-/R+ 3D+/R+ 6D+/R+ 6D+/R- 1CMV viremia by PCRPositive 13; Negative 1Positive 7; Negative 3GVHDPresent 14; Absent 0Present 10; Absent 0Median lymphocyte count at diagnosis (cells per mm3)3900 (range 1600-16,800)4000 (range 3100-8600)Median time to diagnosis (Days post HSCT)188 (range 69-1280)575 (range 154-1454)AML- Acute myeloid leukemia; NHL- Non-Hodgkin's lymphoma; CLL- Chronic lymphocytic leukemia; ALL- Acute lymphocytic leukemia; MM- Multiple myelomaTAC- Tacrolimus; CELL- Mycophenolate mofetil; CSA- Cyclosporine; ATG- Anti-thymocyte globulin; Siro- Sirolimus Disclosures:Lum:Transtarget Corporation: Founder
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