Molecular quantification of viral load in plasma allows for fast and accurate prediction of response to therapy of Epstein-Barr virus-associated lymphoproliferative disease after allogeneic stem cell transplantation

Br J Haematol. 2001 Jun;113(3):814-21. doi: 10.1046/j.1365-2141.2001.02789.x.

Abstract

Epstein-Barr virus lymphoproliferative disease (EBV-LPD) following allogeneic stem cell transplantation (allo-SCT) has a poor prognosis. We used a sensitive real-time polymerase chain reaction (PCR) assay for quantitative detection of EBV-DNA in plasma and serially measured EBV-DNA levels to assess the response to treatment in allo-SCT recipients with EBV-LPD. Fourteen allo-SCT recipients with EBV-LPD who received a T cell-depleted (TCD) sibling (n = 5) or matched unrelated donor (n = 9) graft were monitored from the time of EBV-LPD diagnosis, during therapy and assessment of clinical response. Seven patients had complete responses of EBV-LPD to therapy, of whom 21% (3 out of 14) survived beyond 6 months from EBV-LPD diagnosis. Clinically responding patients showed a rapid decline of EBV-DNA plasma levels within 72 h from the start of therapy. In contrast, all clinical non-responders showed an increase of EBV-DNA levels. Absolute EBV-DNA levels at the time of EBV-LPD diagnosis did not predict for response, but the pattern of EBV-DNA levels within 72 h from the start of therapy (> 50% decrease versus increase) strongly predicted for clinical response (P = 0.001). Quantitative monitoring of EBV-DNA levels from the start of and during therapy for EBV-LPD rapidly and accurately predicts for response to therapy as early as within 72 h. It may thus provide a powerful tool to adjust and select treatment in individuals with EBV-LPD following allo-SCT.

MeSH terms

  • Acute Disease
  • Adult
  • Anemia, Aplastic / mortality
  • Anemia, Aplastic / surgery
  • Anemia, Aplastic / virology
  • DNA, Viral / blood*
  • Female
  • Follow-Up Studies
  • Hematopoietic Stem Cell Transplantation*
  • Herpesvirus 4, Human / genetics*
  • Humans
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / mortality
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / surgery
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / virology
  • Leukemia, Myeloid / mortality
  • Leukemia, Myeloid / surgery
  • Leukemia, Myeloid / virology
  • Leukemia, Myelomonocytic, Chronic / mortality
  • Leukemia, Myelomonocytic, Chronic / surgery
  • Leukemia, Myelomonocytic, Chronic / virology
  • Lymphoproliferative Disorders / mortality
  • Lymphoproliferative Disorders / surgery*
  • Lymphoproliferative Disorders / virology*
  • Male
  • Middle Aged
  • Multiple Myeloma / mortality
  • Multiple Myeloma / surgery
  • Multiple Myeloma / virology
  • Polymerase Chain Reaction / methods
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / mortality
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / surgery
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / virology
  • Prognosis
  • Survival Rate
  • Transplantation, Homologous
  • Viral Load

Substances

  • DNA, Viral