Donor Lymphocyte Infusion in Treating Patients With Recurrent or Persistent Hematologic Cancer After Donor Stem Cell Transplant

You may be eligible if

• DISEASE CHARACTERISTICS:
• Has undergone allogeneic stem cell transplantation (ASCT) for hematologic malignancy at least 30 days ago
• * No failure to engraft following transplant
• * No active acute or chronic graft-versus-host disease (GVHD)
• * Minimal GVHD allowed
• Persistent or relapsed disease after ASCT, including 1 of the following:
• * Chronic myelogenous leukemia (CML), meeting any of the following criteria:
• * Molecular relapse (may be treated with imatinib mesylate after transplant), as defined by any of the following:
• * ASCT was non-T-cell depleted, a negative bcr/abl was documented by PCR post-transplant, and bcr/abl is now detectable by 2 consecutive PCR determinations \> 30 days apart
• * ASCT was non-T-cell depleted and bcr/abl is detectable by PCR at any time after day 180 post-transplant
• * Cytogenetic relapse after 3-6 months of imatinib mesylate
• * Relapsed chronic phase, accelerated phase, or blastic phase CML after 3-6 months of imatinib mesylate
• * Must currently be in chronic phase or accelerated phase CML only
• * Patients with blastic phase CML must attain a second chronic phase
• * Acute myeloid leukemia, acute lymphoblastic leukemia, or myelodysplastic syndromes, meeting any of the following criteria:
• * Molecular relapse, as evidenced by \< 5% blasts in the bone marrow and the patient's leukemia-specific molecular abnormality detectable by PCR
• * Cytogenetic relapse, as evidenced by \< 5% blasts in the bone marrow and the patient's leukemia-specific chromosome abnormality detectable by standard cytogenetics at any time after day 60 post-transplant
• * Hematologic relapse, as evidenced by \> 20% blasts in bone marrow or soft tissue recurrence
• * Must be treated with chemotherapy after transplant, but before study donor lymphocyte infusion (DLI)
• * Multiple myeloma
• * Relapsed disease or recurrence of M-protein after thalidomide or other salvage treatment
• * Prior post-transplant documentation of disappearance of M-protein by immunofixation
• * Residual or progressive disease
• * Rising M-protein level at any time post-transplant (measured at 3-month intervals)
• * Original M-protein detectable at 6 months post-transplant
• * Immune protein electrophoresis (IPEP) is required to show that M-component is the same on day 60 post-transplant as pre-transplant
• * Residual (\> 5%) plasma cells in bone marrow
• * Relapsed non-Hodgkin lymphoma or Hodgkin lymphoma
• * Relapse or progression of disease must be evidenced within 3 months prior to donor lymphocyte infusion by physical exam, radiographic studies, or molecular studies
• * Tumor should be re-biopsied to determine histology
• * If Epstein-Barr virus (EBV) lymphoma is suspected, peripheral blood must be assayed for EBV genome (i.e., EBV DNA testing by PCR) within the past 30 days
• * EBV infection with associated pancytopenia
• * Persistent or refractory pancytopenia with EBV genome detected by PCR in the peripheral blood
• * Refractory pancytopenia is defined as pancytopenia that is poorly responsive to growth factors and/or transfusions
• * EBV lymphoproliferative disorder
• * Clonal lymphadenopathy that is refractory to standard therapy with acyclovir and immunoglobulin (DLI may be given with rituximab)
• Not a candidate for repeat ASCT
• * Chimerism status is not required for determining eligibility for DLI
• Patients eligible for allogeneic ASCT, but for whom DLI is offered as the first option, should have full donor chimerism at relapse or after therapy for relapsed disease
• Patients with relapsed underlying disease after transplant who achieved remission after chemotherapy are allowed
• No CNS recurrence that is not cleared by standard chemotherapy
• * CNS remission status must be maintained for 2 weeks
• Original hematopoietic progenitor stem cell donor must be available for cell donation
• * No syngeneic donors
• PATIENT CHARACTERISTICS:
• Karnofsky performance status 60-100%
• Life expectancy ≥ 8 weeks
• Creatinine \< 3 mg/dL
• ABO/Rh and CMV IgG/IgM status known
• No HIV1 and HIV2 antibody
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception during and for 3 months (males) or 6 months (females) after completion of study treatment
• PRIOR CONCURRENT THERAPY:
• See Disease Characteristics