Abstract
The intensity of the conditioning regimen in hematopoietic stem cell transplantation (HSCT) correlates with the risk of relapse, however its potential benefit may be outweighed by the associated risk of toxicity. The addition of total marrow irradiation (TMI) to myeloablative conditioning provides an opportunity to increase intensity with minimal additional toxicity. In this phase II clinical trial, 30 patients with high-risk myeloid malignancies underwent allogeneic HSCT using myeloablative TMI at 9 Gy in combination with standard myeloablative fludarabine/intravenous busulfan (FluBu4) chemotherapy. The study included patients with matched related donors (N=10) receiving TMI/FluBu4 and patients with matched unrelated (N=14) or one-antigen mismatched unrelated (N=6) donors receiving TMI/FluBu4 and rabbit anti-thymocyte globulin. All patients achieved sustained engraftment. Grade 3-4 extramedullary toxicities were mucositis in 59% (N=17), nausea/vomiting in 10% (N=3) and diarrhea in 7% (N=2) of the patients. Acute graft-versus-host disease (GvHD) grade 3 or 4 was seen in four patients (13.3%). Moderate/severe chronic GvHD was observed in 11 patients (36.7%). With a median follow-up of 1,483 days (range, 63-2,260 days) for patients alive, the overall survival and disease-free survival at 1 year were 72.4% and 65.5%, respectively. GvHD-free relapse-free survival at 1 year was 41.4%. Of 30 patients in the study, six relapsed/progressed (20%) and five of them died of the disease (16.7%), whereas six patients (20%) died of transplant-related causes. We conclude that a myeloablative regimen with TMI at 9 Gy and FluBu4 was well tolerated and achieved encouraging results in patients with myeloid malignancies at high risk of relapse (clinicaltrials.gov identifier: NCT03121014).