Refractory diffuse large B-cell lymphoma after first-line immuno-CT: Treatment options and outcomes.
Lauriane Filliatre-ClementDelphine Maucort-BoulchEstelle BourbonLionel KarlinViolaine SafarEmmanuel BachyPierre SesquesEmmanuelle FerrantFadela BouafiaAnne LazarethDana GhergusBertrand CoiffierAlexandra Traverse GlehenGilles SallesHervé GhesquieresClémentine SarkozyPublished in: Hematological oncology (2018)
In the rituximab era, one-third of diffuse large B-cell lymphoma patients experience relapse/refractory disease after first-line anthracycline-based immunochemotherapy. Optimal management remains an unmet medical need. The aim of this study was to report the outcomes of a cohort of refractory patients according to their patterns of refractoriness and the type of salvage option. We performed a retrospective analysis, which included 104 diffuse large B-cell lymphoma patients treated at Lyon Sud University Hospital (2002-2017) who presented with refractory disease. Refractoriness was defined as progressive/stable disease during first-line treatment (primary refractory, N = 47), a partial response after the end of first-line treatment that required subsequent treatment (residual disease, N = 19), or relapse within 1 year of diagnosis after an initial complete response (CR) (early relapse, N = 38). The 2-year overall survival (OS) rates for primary refractory, early relapse, and residual disease patients were 27%, 25%, and 52%, respectively, while the event-free survival rates for those groups were 13%, 13%, and 42%, respectively. In a univariate analysis, lactate dehydrogenase level, Ann Arbor stage, poor performance status, high age-adjusted International Prognostic Index score, and age > 65 years were associated with shorter OS. The use of rituximab and platinum-based chemo during the first salvage treatment was associated with prolonged OS. In a multivariate analysis, age (HR:2.06) and rituximab use (HR:0.54) were associated with OS. Among patients <65 years who achieved a CR, autologous stem-cell transplant was associated with higher 2-year OS (90% vs 74%, P = 0.10). Patients who were treated with a targeted therapy in the context of a clinical trial after second-line treatment had a higher 2-year OS (34% vs 19%, P = 0.06). In conclusion, patients with primary refractory disease or early relapse have very poor outcomes but may benefit from rituximab retreatment during the first salvage treatment.
Keyphrases
- diffuse large b cell lymphoma
- free survival
- epstein barr virus
- end stage renal disease
- newly diagnosed
- clinical trial
- stem cells
- ejection fraction
- chronic kidney disease
- multiple sclerosis
- healthcare
- peritoneal dialysis
- metabolic syndrome
- photodynamic therapy
- magnetic resonance
- hodgkin lymphoma
- chronic lymphocytic leukemia
- locally advanced
- magnetic resonance imaging
- bone marrow
- replacement therapy
- weight loss
- cell therapy
- smoking cessation