| Literature DB >> 26811013 |
Pier Luigi Zinzani1, Vijayveer Bonthapally2, Dirk Huebner3, Richard Lutes3, Andy Chi4, Stefano Pileri5.
Abstract
Peripheral T-cell lymphomas (PTCLs) tend to be aggressive and chemorefractory, with about 70% of patients developing relapsed/refractory disease. Prior to 2009, chemotherapies were the only options for relapsed/refractory PTCL, other than hematopoietic transplants. However, chemotherapy only improves survival by about 1 month compared with palliation. Four drugs are now approved in the US to treat relapsed/refractory PTCL: pralatrexate, romidepsin, belinostat, and brentuximab vedotin (for systemic anaplastic large cell lymphoma [sALCL]). Response rates with pralatrexate, romidepsin, and belinostat range from 25 to 54% in mixed relapsed/refractory PTCL populations, while 86% of sALCL patients respond to brentuximab vedotin. Here, we critically evaluate the evidence supporting the current drug treatment of relapsed/refractory PTCL, and look to the future to see how the treatment panorama may change with the advent of new targeted therapies, some of which (e.g., alisertib in PTCL and mogamulizumab in CCR4-positive adult T-cell leukemia/lymphoma) are already in phase 3 trials.Entities:
Keywords: Adult T-cell leukemia/lymphoma; Anaplastic large cell lymphoma; Angioimmunoblastic T-cell lymphoma; Belinostat; Brentuximab vedotin; Peripheral T-cell lymphoma; Pralatrexate; Romidepsin
Mesh:
Year: 2016 PMID: 26811013 DOI: 10.1016/j.critrevonc.2015.12.016
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312