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The implication of follicular lymphoma patients receiving allogeneic stem cell transplantation from donors carrying t(14;18)-positive cells

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We performed real-time quantitative polymerase chain reaction (RQ-PCR) in peripheral blood (PB) and/or bone marrow (BM) samples collected pre- and post transplant from 23 recipient–donor pairs receiving allogeneic stem cell transplantation (allo-SCT) for follicular lymphoma (FL). Of 23 donors, 11 had a PB and/or BM sample positive for t(14;18) (BCL2/IGH fusion) at low levels (<one t(14;18) cell in 10K total cells). Recipients from donors with (n=11) and those without (n=12) detectable t(14:18) cells were similar in age, sex, and disease status pretransplant. No differences in the incidence of graft-versus-host-disease (GVHD), delayed engraftment, relapse rate, disease-free survival and overall survival were identified between the groups. Two recipients without detectable t(14;18) cells pre-transplant showed detectable t(14;18) cells at 2 and 11 years after receiving grafts from donors with t(14:18) cells. Neither patient developed FL 1.5 and 2 years after the emergence of t(14;18) cells. Although the sample size is relatively small, our findings suggest that individuals carrying t(14;18) cells may not be excluded as donors given the lack of an association of t(14;18) detected in donors with adverse clinical outcome. It may be necessary to screen for the donor's t(14;18) status before using t(14;18) for monitoring minimal residual disease by RQ-PCR to exclude the possibility of confounding donor's t(14;18) clone.

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References

  1. Turner GE, Ross FM, Krajewski AS . Detection of t(14;18) in British follicular lymphoma using cytogenetics, Southern blotting and the polymerase chain reaction. Br J Haematol 1995; 89: 223–225.

    Article  CAS  Google Scholar 

  2. Pappa VI, Wilkes S, Salam A et al. Use of the polymerase chain reaction and direct sequencing analysis to detect cells with the t(14;18) in autologous bone marrow from patients with follicular lymphoma, before and after in vitro treatment. Bone Marrow Transplant 1998; 22: 553–558.

    Article  CAS  Google Scholar 

  3. Aster JC, Longtine JA . Detection of BCL2 rearrangements in follicular lymphoma. Am J Pathol 2002; 160: 759–763.

    Article  CAS  Google Scholar 

  4. Yasukawa M, Bando S, Dolken G et al. Low frequency of BCL-2/J(H) translocation in peripheral blood lymphocytes of healthy Japanese individuals. Blood 2001; 98: 486–488.

    Article  CAS  Google Scholar 

  5. Ladetto M, Drandi D, Compagno M et al. PCR-detectable nonneoplastic Bcl-2/IgH rearrangements are common in normal subjects and cancer patients at diagnosis but rare in subjects treated with chemotherapy. J Clin Oncol 2003; 21: 1398–1403.

    Article  CAS  Google Scholar 

  6. Ji W, Qu GZ, Ye P et al. Frequent detection of bcl-2/JH translocations in human blood and organ samples by a quantitative polymerase chain reaction assay. Cancer Res 1995; 55: 2876–2882.

    CAS  Google Scholar 

  7. Summers KE, Goff LK, Wilson AG et al. Frequency of the Bcl-2/IgH rearrangement in normal individuals: implications for the monitoring of disease in patients with follicular lymphoma. J Clin Oncol 2001; 19: 420–424.

    Article  CAS  Google Scholar 

  8. Tsimberidou AM, Jiang Y, Ford RJ et al. Quantitative real-time polymerase chain reaction for detection of circulating cells with t(14;18) in volunteer blood donors and patients with follicular lymphoma. Leuk Lymphoma 2002; 43: 1589–1598.

    Article  CAS  Google Scholar 

  9. Fuscoe JC, Setzer RW, Collard DD, Moore MM . Quantification of t(14;18) in the lymphocytes of healthy adult humans as a possible biomarker for environmental exposures to carcinogens. Carcinogenesis 1996; 17: 1013–1020.

    Article  CAS  Google Scholar 

  10. Liu Y, Hernandez AM, Shibata D, Cortopassi GA . BCL2 translocation frequency rises with age in humans. Proc Natl Acad Sci USA 1994; 91: 8910–8914.

    Article  CAS  Google Scholar 

  11. Dolken G, Illerhaus G, Hirt C, Mertelsmann R . BCL-2/JH rearrangements in circulating B cells of healthy blood donors and patients with nonmalignant diseases. J Clin Oncol 1996; 14: 1333–1344.

    Article  CAS  Google Scholar 

  12. Finke J . The role of stem cell transplantation in the treatment of follicular lymphoma. Semin Cancer Biol 2003; 13: 233–239.

    Article  Google Scholar 

  13. van Besien K, Loberiza Jr FR, Bajorunaite R et al. Comparison of autologous and allogeneic hematopoietic stem cell transplantation for follicular lymphoma. Blood 2003; 102: 3521–3529.

    Article  CAS  Google Scholar 

  14. Juckett M, Rowlings P, Hessner M et al. T cell-depleted allogeneic bone marrow transplantation for high-risk non-Hodgkin's lymphoma: clinical and molecular follow-up. Bone Marrow Transplant 1998; 21: 893–899.

    Article  CAS  Google Scholar 

  15. Stein RS, Greer JP, Goodman S et al. High-dose therapy with autologous or allogeneic transplantation as salvage therapy for small cleaved cell lymphoma of follicular center cell origin. Bone Marrow Transplant 1999; 23: 227–233.

    Article  CAS  Google Scholar 

  16. Chang CC, Bredeson C, Juckett M et al. Tumor load in patients with follicular lymphoma post stem cell transplantation may correlate with clinical course. Bone Marrow Transplant 2003; 32: 287–291.

    Article  Google Scholar 

  17. Rosenblum MD, Drobyski WR, Keever-Taylor C, Chang CC . Concurrent presence of both patient and donor t(14;18) in a follicular lymphoma patient after undergoing allogeneic BMT: implications for minimal residual disease detection post-transplant. Bone Marrow Transplant 2003; 31: 947–949.

    Article  CAS  Google Scholar 

  18. Dolken L, Schuler F, Dolken G . Quantitative detection of t(14;18)-positive cells by real-time quantitative PCR using fluorogenic probes. Biotechniques 1998; 25: 1058–1064.

    Article  CAS  Google Scholar 

  19. Hirt C, Dolken G . Quantitative detection of t(14;18)-positive cells in patients with follicular lymphoma before and after autologous bone marrow transplantation. Bone Marrow Transplant 2000; 25: 419–426.

    Article  CAS  Google Scholar 

  20. Ladetto M, Sametti S, Donovan JW et al. A validated real-time quantitative PCR approach shows a correlation between tumor burden and successful ex vivo purging in follicular lymphoma patients. Exp Hematol 2001; 29: 183–193.

    Article  CAS  Google Scholar 

  21. Mandigers CM, Meijerink JP, Mensink EJ et al. Lack of correlation between numbers of circulating t(14;18)-positive cells and response to first-line treatment in follicular lymphoma. Blood 2001; 98: 940–944.

    Article  CAS  Google Scholar 

  22. Keever-Taylor CA, Craig A, Molter M et al. Complement-mediated T-cell depletion of bone marrow: comparison of T10B9.1A-31 and Muromonab-Orthoclone OKT3. Cytotherapy 2001; 3: 467–481.

    Article  CAS  Google Scholar 

  23. Viardot A, Barth TF, Moller P et al. Cytogenetic evolution of follicular lymphoma. Semin Cancer Biol 2003; 13: 183–190.

    Article  Google Scholar 

  24. Caporaso N, Marti GE, Goldin L . Perspectives on familial chronic lymphocytic leukemia: genes and the environment. Semin Hematol 2004; 41: 201–206.

    Article  CAS  Google Scholar 

  25. Mandigers CM, Meijerink JP, Raemaekers JM et al. Graft-versus-lymphoma effect of donor leucocyte infusion shown by real-time quantitative PCR analysis of t(14;18). Lancet 1998; 352: 1522–1523.

    Article  CAS  Google Scholar 

  26. Sarris AH, Jiang Y, Tsimberidou AM et al. Quantitative real-time polymerase chain reaction for monitoring minimal residual disease in patients with advanced indolent lymphomas treated with rituximab, fludarabine, mitoxantrone, and dexamethasone. Semin Oncol 2002; 29 (1 Suppl. 2): 48–55.

    Article  CAS  Google Scholar 

  27. Summers KE, Davies AJ, Matthews J et al. The relative role of peripheral blood and bone marrow for monitoring molecular evidence of disease in follicular lymphoma by quantitative real-time polymerase chain reaction. Br J Haematol 2002; 118: 563–566.

    Article  CAS  Google Scholar 

  28. Jenner MJ, Summers KE, Norton AJ et al. JH probe real-time quantitative polymerase chain reaction assay for Bcl-2/IgH rearrangements. Br J Haematol 2002; 118: 550–558.

    Article  CAS  Google Scholar 

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Correspondence to C-C Chang.

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McGregor, D., Keever-Taylor, C., Bredeson, C. et al. The implication of follicular lymphoma patients receiving allogeneic stem cell transplantation from donors carrying t(14;18)-positive cells. Bone Marrow Transplant 35, 1049–1054 (2005). https://doi.org/10.1038/sj.bmt.1704969

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  • DOI: https://doi.org/10.1038/sj.bmt.1704969

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