Rituximab plus gemcitabine and oxaliplatin (R-GemOx) in refractory/relapsed diffuse large B-cell lymphoma: a real-life study in patients ineligible for autologous stem-cell transplantation - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Leukemia & lymphoma Année : 2021

Rituximab plus gemcitabine and oxaliplatin (R-GemOx) in refractory/relapsed diffuse large B-cell lymphoma: a real-life study in patients ineligible for autologous stem-cell transplantation

Clarisse Cazelles
  • Fonction : Auteur
Karim Belhadj
  • Fonction : Auteur
Hélène Vellemans
  • Fonction : Auteur
Elsa Poullot
  • Fonction : Auteur
Philippe Gaulard
  • Fonction : Auteur
Liana Veresezan
  • Fonction : Auteur
Emmanuel Itti
  • Fonction : Auteur
Muriel Carvalho
  • Fonction : Auteur
Jehan Dupuis
  • Fonction : Auteur
Fabien Le Bras
  • Fonction : Auteur
François Lemonnier
Louise Roulin
  • Fonction : Auteur
Taoufik El Gnaoui
  • Fonction : Auteur
Nicolas Mounier
  • Fonction : Auteur
Corinne Haioun
  • Fonction : Auteur

Résumé

There is no established standard treatment for relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) in patients who are not eligible to receive an intensive treatment. The combination of rituximab gemcitabine and oxaliplatin (R-GemOx) is widely used in this population but data are scarce. We retrospectively collected the data of 196 patients with R/R DLBCL treated with R-GemOx in two French centers over a period of 15 years. The median age of the population was 72 years (range, 24-89), 63% of the patients had an international prognostic index of 3 or higher and 57% were refractory to the last treatment. At the end of R-GemOx treatment, 33% of the patients obtained a complete response. The median progression-free survival (PFS) of the population was 5 months and the median overall survival (OS) was 10 months. Several factors were predictors of unfavorable survival: age over 75 years, international prognostic index of 2 or higher, refractory disease and de novo DLBCL. The median PFS and OS of the patients who obtained a complete response were 22 months and 40 months, respectively. The most significant toxicities were grade 3-4 hematological toxicities (31% of patients). Given its efficacy and tolerability, R-GemOx can be used in patients ineligible for intensive treatment and serve as a basis for new regimen combinations.

Dates et versions

hal-03226290 , version 1 (14-05-2021)

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Citer

Clarisse Cazelles, Karim Belhadj, Hélène Vellemans, Vincent Camus, Elsa Poullot, et al.. Rituximab plus gemcitabine and oxaliplatin (R-GemOx) in refractory/relapsed diffuse large B-cell lymphoma: a real-life study in patients ineligible for autologous stem-cell transplantation. Leukemia & lymphoma, 2021, pp.1-8. ⟨10.1080/10428194.2021.1901090⟩. ⟨hal-03226290⟩
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