Porter, David L.;
Connors, Jean M.;
Van Deerlin, Vivianna M.D.;
Duffy, Kathleen M.;
McGarigle, Carol;
Saidman, Susan L.;
Leonard, Debra G.B.;
Antin, Joseph H.
Graft-Versus-Tumor Induction With Donor Leukocyte Infusions as Primary Therapy for Patients With Malignancies
You can manage bookmarks using lists, please log in to your user account for this.
Media type:
E-Article
Title:
Graft-Versus-Tumor Induction With Donor Leukocyte Infusions as Primary Therapy for Patients With Malignancies
Contributor:
Porter, David L.;
Connors, Jean M.;
Van Deerlin, Vivianna M.D.;
Duffy, Kathleen M.;
McGarigle, Carol;
Saidman, Susan L.;
Leonard, Debra G.B.;
Antin, Joseph H.
Published:
American Society of Clinical Oncology (ASCO), 1999
Published in:
Journal of Clinical Oncology, 17 (1999) 4, Seite 1234-1234
Language:
English
DOI:
10.1200/jco.1999.17.4.1234
ISSN:
0732-183X;
1527-7755
Origination:
Footnote:
Description:
PURPOSE: Histocompatible allogeneic donor leukocyte infusions (DLIs) were administered as primary cancer therapy in a phase I trial to determine (1) whether mixed chimerism could be detected without a prior allogeneic transplantation, (2) the toxicity of primary DLI, and (3) whether a graft-versus-tumor (GVT) reaction could be observed. PATIENTS AND METHODS: Eighteen patients were studied. Patients received interferon alfa-2b for a minimum of 4 weeks, followed by DLI (level 1). Patients with no toxicity or engraftment were eligible to receive cytarabine or cyclophosphamide followed by another course of DLI (level 2). Engraftment was determined using polymerase chain reaction amplification of donor and host-specific DNA polymorphisms. RESULTS: Donor cells were detected in the blood in 14 of 16 assessable patients within 1 hour of DLI. Chimerism detectable 4 weeks after DLI was observed in four patients, and five patients were not assessable. Prior autologous transplantation was associated with late chimerism (P = .0014). Acute graft-versus-host disease (GVHD) occurred in four of 16 assessable patients (grade 1, two patients; grade 2, one patient; grade 4, one patient). One patient with grade 4 acute GVHD developed pancytopenia. Only the four patients treated after prior autologous transplantation developed acute GVHD (P = .0005). Three of four patients with acute GVHD and late chimerism responded to primary DLI, and one patient was not assessable for response. CONCLUSION: Allogeneic adoptive immunotherapy resulted in sustained chimerism, acute GVHD, and a GVT response in heavily pretreated patients. This indicates that it may be possible to generate a direct GVT response for patients with malignancies without the need for intensive conditioning therapy immediately before DLI. Immunosuppression may be required for sustained donor cell engraftment.