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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.

Authors :
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service d'hématologie
Cazelles, Clarisse
Belhadj, Karim
Vellemans, Hélène
Camus, Vincent
Poullot, Elsa
Gaulard, Philippe
Veresezan, Liana
Itti, Emmanuel
Becker, Stéphanie
Carvalho, Muriel
Dupuis, Jehan
Le Bras, Fabien
Lemonnier, François
Roulin, Louise
El Gnaoui, Taoufik
Jardin, Fabrice
Mounier, Nicolas
Tilly, Hervé
Haioun, Corinne
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service d'hématologie
Cazelles, Clarisse
Belhadj, Karim
Vellemans, Hélène
Camus, Vincent
Poullot, Elsa
Gaulard, Philippe
Veresezan, Liana
Itti, Emmanuel
Becker, Stéphanie
Carvalho, Muriel
Dupuis, Jehan
Le Bras, Fabien
Lemonnier, François
Roulin, Louise
El Gnaoui, Taoufik
Jardin, Fabrice
Mounier, Nicolas
Tilly, Hervé
Haioun, Corinne
Source :
Leukemia & lymphoma, Vol. 62, no. 9, p. 2161-2168 (2021)
Publication Year :
2021

Abstract

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.

Details

Database :
OAIster
Journal :
Leukemia & lymphoma, Vol. 62, no. 9, p. 2161-2168 (2021)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1288281573
Document Type :
Electronic Resource