| Literature DB >> 25161267 |
Adam M Petrich1, Mitul Gandhi1, Borko Jovanovic1, Jorge J Castillo2, Saurabh Rajguru3, David T Yang4, Khushboo A Shah5, Jeremy D Whyman5, Frederick Lansigan5, Francisco J Hernandez-Ilizaliturri6, Lisa X Lee7, Stefan K Barta7, Shruthi Melinamani8, Reem Karmali8, Camille Adeimy9, Scott Smith9, Neil Dalal10, Chadi Nabhan11, David Peace12, Julie Vose13, Andrew M Evens14, Namrata Shah15, Timothy S Fenske15, Andrew D Zelenetz16, Daniel J Landsburg17, Christina Howlett18, Anthony Mato19, Michael Jaglal20, Julio C Chavez20, Judy P Tsai3, Nishitha Reddy3, Shaoying Li21, Caitlin Handler22, Christopher R Flowers22, Jonathon B Cohen23, Kristie A Blum24, Kevin Song25, Haowei Linda Sun25, Oliver Press26, Ryan Cassaday26, Jesse Jaso27, L Jeffrey Medeiros27, Aliyah R Sohani28, Jeremy S Abramson29.
Abstract
Patients with double-hit lymphoma (DHL), which is characterized by rearrangements of MYC and either BCL2 or BCL6, face poor prognoses. We conducted a retrospective multicenter study of the impact of baseline clinical factors, induction therapy, and stem cell transplant (SCT) on the outcomes of 311 patients with previously untreated DHL. At median follow-up of 23 months, the median progression-free survival (PFS) and overall survival (OS) rates among all patients were 10.9 and 21.9 months, respectively. Forty percent of patients remain disease-free and 49% remain alive at 2 years. Intensive induction was associated with improved PFS, but not OS, and SCT was not associated with improved OS among patients achieving first complete remission (P = .14). By multivariate analysis, advanced stage, central nervous system involvement, leukocytosis, and LDH >3 times the upper limit of normal were associated with higher risk of death. Correcting for these, intensive induction was associated with improved OS. We developed a novel risk score for DHL, which divides patients into high-, intermediate-, and low-risk groups. In conclusion, a subset of DHL patients may be cured, and some patients may benefit from intensive induction. Further investigations into the roles of SCT and novel agents are needed.Entities:
Mesh:
Year: 2014 PMID: 25161267 DOI: 10.1182/blood-2014-05-578963
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113