| Literature DB >> 25818067 |
Yasuhiro Oki1, Sattva S Neelapu1, Michelle Fanale1, Larry W Kwak1, Luis Fayad1, Maria A Rodriguez1, Michael Wallace2, Mark Klinger3, Victoria Carlton3, Katherine Kong3, Malek Faham3, Anas Younes1.
Abstract
We applied a highly sensitive next-generation sequencing method to identify lymphoma-specific immunoglobulin gene segments in classical Hodgkin lymphoma (CHL) at initial diagnosis or recurrence, and assessed the ability of detecting such lymphoma-specific sequences in peripheral blood (PB). Seventeen CHL cases were tested and lymphoma-specific sequences were identified in 12 of the primary tumour biopsies. In 11 of these patients whose paired PB samples were available, tumour-specific clonotypes were detected in PB in eight patients. This data demonstrates the feasibility of detecting circulating tumour-specific sequences, creating an unprecedented opportunity to optimize the future treatment and monitoring strategies for patients with CHL.Entities:
Keywords: Hodgkin lymphoma; minimal residual disease; sequencing
Mesh:
Year: 2015 PMID: 25818067 PMCID: PMC5279064 DOI: 10.1111/bjh.13349
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998