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Comorbidity is an independent prognostic factor in patients with advanced‐stage diffuse large B‐cell lymphoma treated with R‐CHOP: a population‐based cohort study
Authors:Mels Hoogendoorn  Peter Joosten  Tim Beerden  Huib Storm  Robby E Kibbelaar  Gerrit J Veldhuis  Harmen van Kamp  Bastiaan van Rees  Hanneke C Kluin‐Nelemans  Nic J G M Veeger  Eric N van Roon
Institution:1. Department of Haematology, Medical Centre Leeuwarden, , Leeuwarden, The Netherlands;2. Department of Pharmacotherapy & Pharmaceutical Care, University Centre for Pharmacy, University of Groningen, , Groningen, The Netherlands;3. Department of Clinical Chemistry, Medical Centre Leeuwarden KCL, , Leeuwarden, The Netherlands;4. Department of Pathology, Pathology Friesland, , Leeuwarden, The Netherlands;5. Department of Haematology, Antonius Hospital, , Sneek, The Netherlands;6. Department of Haematology, Nij Smellinghe Hospital, , Drachten, The Netherlands;7. Department of Haematology, Tjongerschans Hospital, , Heerenveen, The Netherlands;8. Department of Haematology, University Medical Centre Groningen, University of Groningen, , Groningen, The Netherlands;9. Department of Epidemiology, MCL Academy, , Leeuwarden, The Netherlands;10. Department of Clinical Pharmacy & Pharmacology, Medical Centre Leeuwarden, , Leeuwarden, The Netherlands
Abstract:An observational population‐based cohort study was performed to investigate the role of comorbidity on outcome and treatment‐related toxicity in patients with newly diagnosed advanced‐stage diffuse large B‐cell lymphoma (DLBCL) treated with R‐CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone). Data for the clinical characteristics of 154 patients (median age 69 years), including Charlson Comorbidity Index (CCI), treatment, toxicity and outcome were evaluated. Forty‐five percent of the patients had an International Prognistic index ≥3 and 16% had a CCI ≥2. The planned R‐CHOP schedule was completed by 84% and 75% reached complete remission (CR). In those with CCI ≥2, 67% completed treatment with 46% CR. In patients with a CCI <2, overall survival (OS) after 1, 2 and 5 years was 84%, 79% and 65% respectively and it was 64%, 48% and 48% for those with CCI ≥2. Grade III/IV toxicity was documented in 53%, most frequently febrile neutropenia (27%) and infections (23%). In multivariate analysis CCI ≥2 and IPI ≥3 were independent risk indicators for OS and grade III/IV toxicity. In conclusion, comorbidity is an independent risk indicator for worse OS in patients with advanced DLBCL treated with R‐CHOP by interference with intensive treatment schedules and more grade III/IV toxicity. Future studies are warranted to determine the optimal treatment approach in patients with significant comorbidities.
Keywords:diffuse large B‐cell lymphoma  comorbidity  population‐based  toxicity  R‐CHOP
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