| Literature DB >> 28774879 |
Michael Crump1, Sattva S Neelapu2, Umar Farooq3, Eric Van Den Neste4, John Kuruvilla1, Jason Westin2, Brian K Link3, Annette Hay1, James R Cerhan5, Liting Zhu1, Sami Boussetta4, Lei Feng2, Matthew J Maurer5, Lynn Navale6, Jeff Wiezorek6, William Y Go6, Christian Gisselbrecht4.
Abstract
Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of non-Hodgkin lymphoma. Although 5-year survival rates in the first-line setting range from 60% to 70%, up to 50% of patients become refractory to or relapse after treatment. Published analyses of large-scale outcome data from patients with refractory DLBCL are limited. SCHOLAR-1, an international, multicohort retrospective non-Hodgkin lymphoma research study, retrospectively evaluated outcomes in patients with refractory DLBCL which, for this study, was defined as progressive disease or stable disease as best response at any point during chemotherapy (>4 cycles of first-line or 2 cycles of later-line therapy) or relapsed at ≤12 months from autologous stem cell transplantation. SCHOLAR-1 pooled data from 2 phase 3 clinical trials (Lymphoma Academic Research Organization-CORAL and Canadian Cancer Trials Group LY.12) and 2 observational cohorts (MD Anderson Cancer Center and University of Iowa/Mayo Clinic Lymphoma Specialized Program of Research Excellence). Response rates and overall survival were estimated from the time of initiation of salvage therapy for refractory disease. Among 861 patients, 636 were included on the basis of refractory disease inclusion criteria. For patients with refractory DLBCL, the objective response rate was 26% (complete response rate, 7%) to the next line of therapy, and the median overall survival was 6.3 months. Twenty percent of patients were alive at 2 years. Outcomes were consistently poor across patient subgroups and study cohorts. SCHOLAR-1 is the largest patient-level pooled retrospective analysis to characterize response rates and survival for a population of patients with refractory DLBCL.Entities:
Mesh:
Year: 2017 PMID: 28774879 PMCID: PMC5649550 DOI: 10.1182/blood-2017-03-769620
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113