| Literature DB >> 26627450 |
Ranjana H Advani1, Stephen M Ansell2, Mary J Lechowicz3, Anne W Beaven4, Fausto Loberiza5, Kenneth R Carson6, Andrew M Evens7, Francine Foss8, Steven Horwitz9, Barbara Pro10, Lauren C Pinter-Brown11, Sonali M Smith12, Andrei R Shustov13, Kerry J Savage14, Julie M Vose5.
Abstract
Peripheral T-cell lymphomas (PTCL) have suboptimal outcomes using conventional CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) chemotherapy. The anti-folate pralatrexate, the first drug approved for patients with relapsed/refractory PTCL, provided a rationale to incorporate it into the front-line setting. This phase 2 study evaluated a novel front-line combination whereby cyclophosphamide, etoposide, vincristine and prednisone (CEOP) alternated with pralatrexate (CEOP-P) in PTCL. Patients achieving a complete or partial remission (CR/PR) were eligible for consolidative stem cell transplantation (SCT) after 4 cycles. Thirty-three stage II-IV PTCL patients were treated: 21 PTCL-not otherwise specified (64%), 8 angioimmunoblastic T cell lymphoma (24%) and 4 anaplastic large cell lymphoma (12%). The majority (61%) had stage IV disease and 46% were International Prognostic Index high/intermediate or high risk. Grade 3-4 toxicities included anaemia (27%), thrombocytopenia (12%), febrile neutropenia (18%), mucositis (18%), sepsis (15%), increased creatinine (12%) and liver transaminases (12%). Seventeen patients (52%) achieved a CR. The 2-year progression-free survival and overall survival, were 39% (95% confidence interval 21-57) and 60% (95% confidence interval 39-76), respectively. Fifteen patients (45%) (12 CR) received SCT and all remained in CR at a median follow-up of 21·5 months. CEOP-P did not improve outcomes compared to historical data using CHOP. Defining optimal front line therapy in PTCL continues to be a challenge and an unmet need.Entities:
Keywords: T-cell lymphoma; clinical trials; therapy
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Year: 2015 PMID: 26627450 PMCID: PMC5642048 DOI: 10.1111/bjh.13855
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998