Donor Stem Cell Transplant in Treating Patients With High-Risk Hematologic Cancer

Diagnosis of one of the following hematological malignancies:

• CML, with 1 of the following:

  • In first CP AND failed imatinib mesylate therapy, defined as failure to obtain a hematologic remission at 3 months or a major cytogenetic response (i.e., Ph+ cells < 35%) at 6 months or demonstrated clonal evolution or disease progression during therapy
  • In accelerated phase with < 15% blasts
  • In blast crisis that has entered into a second CP following induction chemotherapy

• AML, with 1 of the following:

  • In second or subsequent complete remission (CR) (i.e., < 5% blasts by morphology, no residual leukemia by flow cytometry, and absence of cytogenetic abnormalities)
  • Failed primary induction chemotherapy, but subsequently entered into a CR with ≤ 2 subsequent re-induction chemotherapy treatment(s)
  • In first CR with intermediate-risk or poor-risk cytogenetics

• ALL with 1 of the following:

  • In second or subsequent CR
  • In first CR AND presence of t(9;22)

• MDS, with the following:

  • High-risk disease, defined by IPSS score of ≥ 1.5 at diagnosis AND meets 1 of the following criteria:

    • ≤ 10% blasts at diagnosis
    • In morphologic CR (< 5% blasts) following cytoreductive chemotherapy

• CMML, with 1 of the following:

  • ≤ 10% blasts at diagnosis
  • In morphologic CR (< 5% blasts) following cytoreductive chemotherapy

• CLL/PLL with the following:

  • Rai stage I-IV disease
  • Failed ≥ 1 prior chemotherapy regimen (including fludarabine phosphate) or ASCT
  • Documented chemosensitive or stable, non-bulky disease prior to transplant, defined as < 20% bone marrow involvement AND lymph node size < 3 cm in axial diameter
  • No bulky tumor masses, elevated lactate dehydrogenase (LDH), B symptoms, or progressive disease prior to transplant

• Low-grade non-Hodgkin lymphoma (NHL) (i.e., small lymphocytic lymphoma, follicular center lymphoma [grade 1 or 2], marginal zone lymphoma, or B-cell lymphoma), with the following criteria:

  • Failed ≥ 1 prior chemotherapy regimen or ASCT
  • Documented chemosensitive or stable, non-bulky disease prior to transplant, defined as < 20% bone marrow involvement AND lymph node size < 3 cm in axial diameter
  • Received ≤ 3 prior chemotherapy regimens (monoclonal antibody therapy and involved-field radiotherapy are not considered a prior regimen)
  • No bulky tumor masses, elevated LDH, B symptoms, or progressive disease prior to transplant

• Mantle cell lymphoma, with the following:

  • Failed to achieve remission or recurred after either conventional chemotherapy or ASCT
  • Responsive or stable disease to most recent prior therapy
  • No bulky tumor masses, elevated LDH, B symptoms, or progressive disease prior to transplant

• Intermediate-grade NHL (i.e., follicular center lymphoma [grade 3] or diffuse large cell lymphoma), meeting the following criteria:

  • Failed to achieve remission or recurred after either conventional chemotherapy or ASCT
  • Documented chemosensitive, non-bulky disease prior to transplant, defined as at least a partial remission to salvage chemotherapy (≥ 50% reduction in diameter of all disease sites)
  • No bulky tumor masses, elevated LDH, B symptoms, or progressive disease prior to transplant

• Hodgkin lymphoma, with the following:

  • Relapsed after prior ASCT OR after ≥ 2 combination chemotherapy regimens and ineligible for ASCT
  • Documented chemosensitive, non-bulky disease prior to transplant, defined as at least a partial remission to salvage chemotherapy (≥ 50% reduction in diameter of all disease sites)
  • No bulky tumor masses, elevated LDH, B symptoms, or progressive disease prior to transplant

• Peripheral T-cell NHL, with the following:

  • Failed to achieve remission or recurred after either conventional chemotherapy or ASCT
  • Documented chemosensitive, non-bulky disease prior to transplant, defined as at least a partial remission to salvage chemotherapy (≥ 50% reduction in diameter of all disease sites)
  • No bulky tumor masses, elevated LDH, B symptoms, or progressive disease prior to transplant

Myeloproliferative syndrome with poor risk features, meeting 1 of the following criteria:

• < 55 years old AND Lille score of 1
• Lille score of 2
• HgB < 10 g/dL AND abnormal karyotype

High-risk disease, with 1 of the following:

• Age 40-72 years
• Any age AND deemed to be at significantly increased risk of morbidity and death following a standard, myeloablative unrelated donor stem cell transplant (e.g., received extensive prior therapy, including ASCT)

HLA-matched unrelated donor available, with 1 of the following:

• 8/8 match at HLA-A, B, C, or DR loci by high-resolution genotyping

• Single allelic mismatch at either the HLA-B or HLA-C loci donor by high-resolution molecular typing

  • No single allelic mismatch at HLA-A or HLA-DR loci