CD34+-enriched-CD19+-depleted autologous peripheral blood stem cell transplantation for chronic lymphoproliferative disorders: high purging efficiency but increased risk of severe infections

Exp Hematol. 2002 Jul;30(7):824-30. doi: 10.1016/s0301-472x(02)00828-7.

Abstract

Objective: The main objective of this work was to decrease the incidence of relapse after autologous stem cell transplantation with a "double purging" procedure.

Methods: We used a "positive" (CD34) and "negative" (CD19) double selection method to improve the efficacy of "single purging" of hematopoietic harvests in poor-prognosis lymphoproliferative disorders. All patients included in the study had a positive molecular marker of their disease. Minimal residual disease (MRD) was studied by flow cytometry and PCR techniques during the purging procedure and after transplantation.

Results: Twenty-six patients fulfilled entry criteria. Median age of patients was 50 years (range: 33-66); 17 were male and 9 female. Thirteen (50%) of the patients mobilized an adequate number of CD34+ cells (>or=3 x 10(6)/kg) to proceed with the double-selection protocol. Twelve of the 13 harvests became PCR negative after purging. Ten patients were grafted with the selected products and all but one engrafted without delay. After a median follow-up of 30 months, 2 of 10 patients suffered a molecular relapse at 7 and 19 months respectively. The earlier relapse was observed in the patient who received a MRD+ product. Only one patient experienced a clinical relapse. Three patients died due to obliterans bronchiolitis, pneumococcal sepsis, and septic shock of unknown origin, respectively, and three others presented life-threatening infections.

Conclusion: Therefore, CD34+/CD19+ positive/negative selection is an effective purging approach in patients with chronic lymphoproliferative disorders. This favorable effect is, however, counterbalanced by the high frequency of life-threatening infections.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antigens, CD19 / analysis*
  • Antigens, CD34 / analysis*
  • Bacterial Infections / etiology*
  • Bacterial Infections / prevention & control
  • Blood Cells / chemistry
  • Blood Cells / transplantation*
  • Bone Marrow Purging / methods*
  • Bronchiolitis Obliterans / etiology
  • Disease Susceptibility
  • Female
  • Follow-Up Studies
  • Graft Survival
  • Hematopoietic Stem Cell Mobilization
  • Hematopoietic Stem Cell Transplantation*
  • Hematopoietic Stem Cells / chemistry
  • Hematopoietic Stem Cells / classification*
  • Humans
  • Immunocompromised Host
  • Immunomagnetic Separation*
  • Leukemia, Lymphocytic, Chronic, B-Cell / complications
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology
  • Leukemia, Lymphocytic, Chronic, B-Cell / therapy*
  • Lymphoma, Follicular / complications
  • Lymphoma, Follicular / pathology
  • Lymphoma, Follicular / therapy*
  • Lymphoma, Mantle-Cell / complications
  • Lymphoma, Mantle-Cell / pathology
  • Lymphoma, Mantle-Cell / therapy*
  • Male
  • Middle Aged
  • Neoplasm, Residual
  • Prospective Studies
  • Recurrence
  • Risk
  • Sepsis / etiology
  • Shock, Septic / etiology
  • Transplantation Conditioning
  • Treatment Outcome

Substances

  • Antigens, CD19
  • Antigens, CD34