A Research Study of Bone Marrow Transplantation From Unrelated or Partially Matched Related Donors

The primary rationale for the development of this research study is to find out if the use of
cyclophosphamide after a "blood" stem cell transplant is an effective treatment for patients
with blood cancers who require transplant for long-term survival but are without an available
matched-sibling donor. Historically, survival rates for patients undergoing partially matched
related or unrelated donor transplants (henceforth to be called alternative donor
transplants) have been much lower than those observed after matched sibling stem cell
transplants. Survival post alternative donor stem cell transplant has also been affected by
the requirement to remove or reduce the numbers of donor T cells resulting in higher rates of
infection, graft rejection, and relapse. One significant limitation to conventional donor
transplants with HLA matched siblings has been that over 50% of patients do not have HLA
matched siblings so that increasing the safety of alternative donor transplants could have a
significant influence on the number of patients who could safely receive transplants. Because
of the historically low overall survival (OS) after alternative donor transplants, it has
become a procedure of "last resort" in many centers unwilling to consider it unless all other
options are exhausted. There fore several centers including ours have sought to overcome
problems using various strategies. The strategy the investigators have proposed for this
study (which has been used similarly by other centers) has been to administer
cyclophosphamide post the stem cell infusion (traditionally it is given before the stem cell
infusion) thereby hopefully destroying the activated T-cells causing graft-versus host
disease (GVHD) and allow T cell tolerization and engraftment; but, not the inactivated T
cells thereby hopefully preserving the anti-tumor effects of the donor immune system. Thus,
the major aim of this study will be to measure the engraftment with this regimen and
secondarily to measure incidence of GVHD and day 100 mortality. The goal is to see if in the
first 3 months the use of cyclophosphamide post stem cell infusion with alternative donors is
as safe and as effective as traditional matched transplants.

Inclusion Criteria:

1. Any patient with a hematological or oncological diagnosis in which allogeneic
hematopoietic stem cell transplantation (HSCT) is thought to be beneficial.

1. Patients without morphological or molecular evidence of disease

2. For patients with "indolent diseases," if the patient has evidence of disease the
disease burden must be minimal (at least PR) and the disease must be
chemoresponsive. Thus for example patients with acute leukemia (not an indolent
disease) must be in a morphological CR or CRp.

2. For patients with MDS the inclusion criteria is specifically as follows:

- For patients with RA or RARS or isolated 5q- they can proceed to transplant
without any treatment.

- For patients with RAEB-1, RCMD+/-RS, or MDS NOS must have stable disease for 6
months (as documented by serial bone marrow examinations) in the absence of any
therapy but growth factors or transfusion support. Patients who require treatment
to "control their disease" must show chemo-responsiveness

- For patients with CMML or RAEB-2 they must demonstrate chemo-responsiveness

- Chemo-responsiveness is defined as a blast percentage decrease by at least 5
percentage points and there must be less than 10% blasts after treatment and at
the time of transplant, if there are more than 10% blasts at any point during the
disease course

- Chemo-responsiveness must also include at least one of the following if
applicable:

- A cytogenetic response

- A well-documented decrease in transfusion requirements.

3. Patients must have a related donor who is zero, one, two, three, or four antigen
mismatched at the HLA-A; B; C; DR loci or an unrelated donor up to a two antigen
mismatch. DNA will be retained by the tissue typing laboratory for possible typing for
DQ and DP. When multiple related donor options are available donor selection will be
determined the same as in the TJU two-step protocols. When multiple unrelated donors
are available care will be made to avoid HLA-A and HLA-B mismatches if possible based
on data from the Japanese Marrow Donor Registry studies. An HLA antibody screen will
be performed on each patient.

4. All patients must have adequate organ function:

1. Patients with related donors must have an LVEF of >35%. Patients with unrelated
donors must have an LVEF >45%. Patients with LVEF ≤50% and all patients with
symptoms or history of heart failure or coronary artery disease must have a
stress echo or equivalent test and a cardiological evaluation.

2. Patients with related donors must have a DLCO >35% of predicted corrected for
hemoglobin. Patients with unrelated donors must have a DLCO >45% of predicted
corrected for hemoglobin. For related donors if the DLCO is less than 45% the EF
must be greater than 45% and vice versa.

3. Patients with related donors must have an adequate liver function as defined by a
serum bilirubin <3.0, AST and ALT <3.0X upper limit of normal. Patients with
unrelated donors must have an adequate liver function as defined by a serum
bilirubin <1.8, AST and ALT < 2.5X upper limit of normal. Exceptions may be
granted for patients with "benign" liver disorders such as Gilbert's disease.

4. Patients with related donors or with unrelated donors must have a creatinine
clearance of > 60 ml/min/1.73 m^2.

5. Patients with related donors must have a performance status > 60% (TJU
Karnofsky14) (Appendix A). Patients with unrelated donors must have a Performance
status > 70% (TJU Karnofsky).

6. Patients with related donors must have a HCT-CI Score < 6 Points (Appendix B).
Patients with unrelated donors must have a HCT-CI Score < 5 Points.

7. Patients must be willing to use contraception if they are of childbearing
potential.

8. Patients must be able to give informed consent or have a care giver who can give
consent.

9. Patients that are HIV positive will be eligible for the study if they have an
undetectable viral load and meet the above criteria for patients with unrelated
donors.

Exclusion Criteria:

1. Patients with related donors who have a combination of Performance status of < 70%
(TJU Karnofsky) and an HCT-CI of 4 points or more. Patients with unrelated donors with
a combination of Performance status of < 80% (TJU Karnofsky) and an HCT-CI of 4 points
or more.

2. Patients with active involvement of the central nervous system with malignancy.
Patients with a disease with potential for CNS involvement should have documentation
of the lack of CNS involvement via lumbar puncture or similar procedure performed
within two months of admission or as per TJU standard practice guidelines.

3. Patients with a psychiatric disorder that would preclude patients from complying with
the protocol even with a caregiver. Patients with a lack of social support that would
interfere with the ability to receive appropriate medical care will also be excluded.

4. Pregnancy

5. Patients with life expectancy of < 6 months for reasons other than their underlying
hematological/oncological disorder.

6. Patients who have received alemtuzumab within 8 weeks of the transplant admission, or
who have recently received horse or rabbit ant-thymocyte globulin and have an ATG
level of > 2 μg/ml. Patients on systemic corticosteroids at a dose equivalent of
prednisone 7.5mg/day or higher.

7. Patients who cannot receive cyclophosphamide.

8. Patients with evidence of another malignancy, exclusive of a skin cancer that requires
only local treatment, should not be enrolled on this protocol.

9. Patients with refractory disease.

10. Patients with preformed antibodies to their donors.

11. Patients who require supplemental oxygen other than for sleep apnea will be excluded.