Advances in Transplantation - Your concise update to the latest transplant research
Vol. 8, No. 5: September/October 2008
Cord blood transplants co-infused with peripheral blood stem cells

Adults with high-risk disease transplanted with cord blood co-infused with third-party stem cells had a 5-year overall survival (OS) of 56%, according to a study to appear in Bone Marrow Transplantation. The 55 adults in the study had a median age of 34 years and received a median cord blood cell dose of 2.39 x 107 cells/kg, just under the consensus minimum cell dose of 2.5 x 107 cells/kg. Grafts were supplemented with mobilized hematopoietic stem cells from haploidentical donors (n=38) or related or unrelated donors (n=17). Patients <40 years had a 5-year OS and disease-free survival of 63% and 54%, respectively. The researchers state that their technique will permit lower-dose single cord blood units to be a first option for adult patients lacking an adult donor.

Bautista G, et al. Bone Marrow Transplant 2008; E-pub ahead of print, Oct. 13. (More)
Comparing cord blood to mismatched unrelated donors

Despite more than 12 million volunteers listed on worldwide registries, some patients with rare HLA types may still not find a suitably matched donor. Although some receive haploidentical transplants, often the choice is between a mismatched unrelated donor and a cord blood graft. Results from a study comparing 27 cord blood transplants with 14 mismatched unrelated donor transplants show that cord blood may be the better choice. The study found that 3-year overall survival in cord blood recipients was 66% compared to 14% in the mismatched unrelated donor group (p=0.006).

Ringdén O, et al. Bone Marrow Transplant 2008; E-pub ahead of print, Sept. 1. (More)
Related, unrelated HCT comparable for older adult AML

A multi-center study of 368 transplants found no significant difference in survival after unrelated and related donor transplants in adults >50 transplanted for acute myeloid leukemia (AML). Patients with normal cytogenetics in first complete remission (CR1) had 2-year event-free survival (EFS) of 64% (matched sibling donor) and 53% (unrelated donor). A multivariate analysis showed that both disease status and cytogenetic risk were highly significantly predictors of EFS and overall survival (p<0.001). Delaying transplant reduced survival: patients with normal cytogenetics beyond CR1 had 2-year EFS of 24% (matched sibling) and 33% (unrelated).

Schetelig J, et al. J Clin Oncol 2008; E-pub ahead of print, Sept. 2. (More)
Comparable outcomes in related, alternative donor HCT for pediatric ALL

A study of 83 children with acute lymphoblastic leukemia (ALL) undergoing myeloablative hematopoietic cell transplantation (HCT) in first or second complete remission. Forty-one patients had matched sibling donors and 42 had alternate donors (31 matched unrelated, 9 mismatched, and 2 mismatched related donors). Conditioning was similar in the two groups, but the alternate donor group also received alemtuzumab. Three-year disease-free survival in the matched sibling group was 72% vs. 62% in the alternate donor group (p=0.232). The researchers conclude that myeloablative transplantation using alemtuzumab with alternative donors can result in survival comparable to transplant using matched sibling donors.

Kennedy-Nasser AA, et al. Biol Blood Marrow Transplant November 2008; 14(11): 1245-1252. (More)
Sirolimus for GVHD associated with VOD after myeloablative transplantation

Sirolimus can effectively treat GVHD, but according to a new report it may also raise the incidence of veno-occlusive disease (VOD) when combined with other drugs used in transplantation. In a retrospective study of 488 myeloablative transplants, researchers found that sirolimus used with cyclophosphamide and total body irradiation significantly raises the incidence of VOD (OR 2.35, p=0.005). The incidence of VOD was also significantly increased when sirolimus was used with methotrexate (OR 3.23, p<0.001) and when used with busulfan-based conditioning (OR 8.8, P=0.008). However, sirolimus without methotrexate was not associated with an increased risk of VOD (OR 1.55, p=0.33).

Cutler C, et al. Blood 2008; E-pub ahead of print, Sept. 5. (More)
Lower infection-related mortality after non-myeloablative HCT than after myeloablative HCT

In a retrospective single-center study of 141 consecutive transplants, there were fewer early post-transplant infections in lymphoma patients undergoing non-myeloablative transplantation (n=76) compared to patients transplanted after myeloablative conditioning (n=65). Before neutrophil engraftment, the non-myeloablative group had a 53% lower rate of bacterial infection (RR=0.47; p=0.06). After engraftment, the density of bacterial infections was similar in the two groups. The 1-year infection-related mortality was significantly lower in the non-myeloablative group than in the myeloablative group (9% vs. 22%, respectively; p=0.03).

Bachanova V, et al. Bone Marrow Transplant 2008; E-pub ahead of print, Sept. 22. (More)
Non-myeloablative HCT can be effective in refractory CLL

This is a 5-year follow-up to an earlier 2-year report on non-myeloablative hematopoietic cell transplantation (HCT) in adults with fludarabine-refractory chronic lymphocytic leukemia (CLL). The 82 patients in this update had a median age of 56 years (range 42-72), and were transplanted using related (n=52) or unrelated (n=30) donors. At a median of 5 years post-transplant, overall survival was 50%. As noted in an accompanying editorial by Dr. J.G. Gribben, this 5-year median survival is notably better than the median survival time of less than 1 year experienced by fludarabine-refractory CLL patients not undergoing HCT.

Sorror ML, et al. J Clin Oncol 2008; 26(30): 4912-4920. (More)
Review: Donor lymphocyte infusions

A review of the use of donor lymphocyte infusion (DLI) in allogeneic transplant recipients to: enhance the graft-versus-tumor effect, treat tumor recurrence, prevent disease relapse, or convert recipients from mixed- to full-donor chimerism. The authors make a distinction between therapeutic DLI and pre-emptive DLI, and review the medical literature on the use of DLI in specific diseases.

Tomblyn M, et al. Bone Marrow Transplant 2008; E-pub ahead of print, Aug. 18. (More)
Review: Allogeneic HCT for Hodgkin lymphoma

This review examines recent data on using reduced-intensity allogeneic transplantation to treat the subset of Hodgkin lymphoma (HL) patients not cured by conventional therapy or who relapse after autologous transplantation. The authors evaluate the clinical evidence for a graft-versus-tumor response in HL and discuss prognostic factors to identify HL patients who could benefit most from allogeneic transplantation.

Peggs KS, et al. Br J Haematol 2008; 143(4): 468-480. (More)
Other journal articles of note:

Advances in Transplantation is an electronic newsletter published six times a year by the Medical Education Team of the National Marrow Donor Program (NMDP).

This newsletter is sent only to those
individuals who have requested it.

To unsubscribe or change your subscription options,
see link at the bottom of this newsletter.

E-mail your comments or suggestions
Supported by an unrestricted educational grant from Otsuka America Pharmaceutical, Inc., provided to the National Marrow Donor Program through The Marrow Foundation, the funding partner of the NMDP.

Otsuka America Pharmaceutical, Inc.
IN THIS ISSUE
Cord blood co-infused with stem cells

Comparing cord blood, mismatched donors

Related, unrelated HCT comparable

Pediatric ALL transplant outcomes

Sirolimus associated with VOD

Reduced conditioning, fewer infections

Transplants in advanced CLL

Donor lymphocyte infusions

Allo-HCT for Hodgkin lymphoma

Other journal articles of note

NMDP NEWS
BBMT supplement marks 20th anniversary of NMDP
Order a free printed copy of the September supplement to BBMT, which highlights major advances and trends in unrelated transplants through the work of the NMDP.
Order supplement
Allogeneic Transplantation: Applying New Research for Improved Outcomes
Discover the latest clinical advances in allogeneic transplantation that have expanded patient eligibility, improved outcomes, and stimulated a dramatic growth in transplantation.
NMDP ASH Symposium: Friday, Dec. 5, 2008, 7:00 a.m.
San Francisco, California
More information
Access the latest data and tools on transplantation
Visit the NMDP booth #700 at ASH and get a 2GB USB drive that will plug you in to the latest transplant tools and data, including:
  • Improved transplant outcomes
  • Post-transplant guidelines
  • Free patient materials
  • Medical education programs
ASH Annual Meeting
San Francisco, Calif.
December 6-8
NMDP LINKS
Physicians' Resource Center

Patient Resource Center

Transplant outcomes data

Available CME programs

Office of Patient Advocacy

NMDP Research Program

THANK YOU FOR SIGNING UP!
Thank you for subscribing to Advances in Transplantation.
To unsubscribe or change your subscription options, see link at the bottom of this newsletter.

Privacy Policy | Copyright © 2001-2008 | National Marrow Donor Program
3001 Broadway St. N.E. Suite 100 | Minneapolis, MN 55413-1753
1 (612) 627-5800 | 1 (800) 526-7809 | www.marrow.org