ASH Clinical News December 2015 | Page 47

CLINICAL NEWS the mutated IGHV gene. After a median follow-up of 12.8 years, PFS was 30.9 percent among all patients (median PFS=6.4 years); for patients with the IGHV mutation, though, PFS was 53.9 percent and those with unmutated IGHV had a PFS of 8.7 percent. Half (50.7%) of the patients who achieved MRDnegativity post-treatment had the IGHV mutation, with a PFS of 70.9 percent. IGHV-mutated patients with MRD-negativity also had superior long-term survival (87.2% vs. 56.5%; p=0.003). “The high rate of very long-term PFS in patients with mutated IGHV after FCR argues for the continued use of chemoimmunotherapy in this patient subgroup,” the researchers concluded. Dr. Thompson and colleagues also identified a plateau for patients with mutated IGHV, finding no relapses beyond 10.4 years in 42 patients. “The existence of PFS plateaus in mutated IGHV patients treated with FCR raises the prospect that many of these patients may be cured of their CLL,” the authors wrote. “Further follow-up of the patients in this plateau in the coming years, as well as systematic testing of all patients for MRD, is planned to determine whether this prospect is indeed a reality.” The researchers noted two limitations of the study: Standard response assessment was based on clinical criteria rather than the results of computed tomography scans, and the patient population was younger and, therefore, more likely to have earlystage CLL. ● REFERENCES Fischer K, Bahlo J, Fink AM, et al. Long term remissions after FCR chemoimmunotherapy in previously untreated patients with CLL: updated results of the CLL8 trial. Blood. 2015 October 20. [Epub ahead of print] Thompson PA, Tam CS, O’Brien SM, et al. Fludarabine, cyclophosphamide and rituximab achieves long-term disease-free survival in IGHVmutated chronic lymphocytic leukemia. Blood. 2015 October 22. [Epub ahead of print] Prioritizing Unrelated Donor Characteristics in Allogeneic Transplants How Do Age, HLA Disparity Affect Survival? The number of adults registered as unrelated donors for hematopoietic stem cell transplantation has topped 24 million worldwide, and that number is still increasing. Given the large number of unrelated-donor transplantations, it is important to understand which donor characteristics are associated with better survival in patients with hematologic malignancies. “While there is agreement that donor–recipient HLA-match is an important criterion and that HLA-matching should consider allele-level HLA-match, strategies vary when prioritizing among comparably HLA-matched potential donors,” Craig Kollman, PhD, from the Jaeb Center for Health Research in Tampa, Florida, and colleagues wrote in a study recently published in Blood. “With increasing numbers of transplantations being performed with grafts from adult unrelated donors, it is critical to identify donor characteristics associated with survival after transplantation after adjusting for relevant patient, disease, and transplantation characteristics.” Characteristics of Patients, Their Donors, and Transplantation Dr. Kollman and co-authors analyzed the following donor characteristics on survival, hematopoietic recovery, and graft-versus-host disease (GVHD) in donors and recipients with allele-level HLA typing at HLA-A, -B, -C, and -DBR1: • Age • Sex • Parity • Cytomegalovirus serostatus • HLA-match • ABO blood group match Data were collected from the Center for International Blood and Marrow Transplant Research, a network of more than 450 transplant centers worldwide, including information on patient, disease, and transplantation characteristics. Patients who had previously received autologous or allogeneic transplantation, had ex vivo T-cell depletion, or CD34-selected grafts were excluded from the study. Patients inc