Among the primary objectives of the American Society for Blood and Marrow Transplantation are to:
Toward this end, in 1999, the Society began sponsoring evidence-based reviews of the scientific and medical literature to document when blood and marrow transplantation is indicated in the treatment of selected diseases.
The goals of the evidence-based reviews are to:
The following treatment recommendations are offered for the role of SCT as treatment for follicular lymphoma (FL), and are based on consensus reached by an expert panel 1 following a systematic review of the literature. 2
1. Based on prerituximab data, there is a statistically significant improvement in overall survival (OS) and progression-free survival (PFS) using autologous SCT as salvage therapy.
2. With only one retrospective study, there are insufficient data to make a recommendation on the use of autologous SCT versus nontransplantation therapy as salvage treatment for patients who have had rituximab as part of their salvage therapy.
3. Autologous SCT is recommended for transformed FL based on expert opinion and accepted clinical practice.
4. Although there is consistent improvement in PFS and event-free survival (EFS) with autologous SCT, it is not recommended as first-line treatment for most patients because of no significant improvement in OS, a higher incidence of secondary myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML), and a lack of comparative data with rituximab-containing regimens. Longer follow-up may be needed to identify differences in OS.
1. There are insufficient data to make a recommendation on the efficacy of autologous SCT as first-line versus salvage therapy.
2. Because of conflicting data, a recommendation cannot be made on the use of rituximab as part of firstline or salvage regimens prior to autologous SCT.
3. There are insufficient data to make a recommendation regarding purging of autologous SCT.
4. There are insufficient data to recommend one highdose regimen over another. Total-body irradiation (TBI)-containing regimens are usually avoided because of a concern for the risk of secondary MDS or AML.
1. There are insufficient data comparing autologous SCT and myeloablative allogeneic SCT to recommend one option over the other; both appear to have a survival benefit, but have competing risks. Comparison of these two techniques is biased by different patient selection criteria.
2. There are currently no data available to make a recommendation regarding the use of reduced intensity/nonmyeloablative allogeneic SCT versus autologous SCT. Comparison of these two techniques is biased by different patient selection criteria.
1. Reduced intensity conditioning (RIC) appears to be an acceptable alternative approach in allogeneic SCT based on one study and expert opinion.
2. There are insufficient data to recommend one conditioning regimen over another for allogeneic SCT.
3. In allogeneic SCT, an HLA-matched unrelated donor appears to be as effective as an HLA-matched related donor using RIC based on expert opinion.