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Acta Haematol ; 144(3): 259-263, 2021.
Article in English | MEDLINE | ID: mdl-33040061

ABSTRACT

INTRODUCTION: Treatment of relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) represents a challenge for clinicians due to the lack of therapeutic options. DLBCL is not a rare disease in Italy. Pixantrone is an aza-anthracenedione, which, when compared to anthracyclines and anthracenediones, has a significantly reduced cardiotoxicity while maintaining good anti-tumor activity. However, the evidence on the use of pixantrone in the context of daily clinical practice is scarce. METHODS: We focused on the Italian patient subset of a larger European retrospective study (the PIXA Registry) to assess the efficacy and safety of pixantrone in a real-life DLBCL population. The molecular profile of the disease and its impact on drug efficacy were also assessed. RESULTS: Fifteen heavily pretreated DLBCL patients (13 males and 2 females) underwent treatment with pixantrone for a median of 2 cycles (range 1-6). Eight patients were bcl2 positive, 7 bcl6 positive, and 4 myc positive; 4 patients were diagnosed as double-hit, and 2 as triple-hit DLBCL. The overall response rate was 26.7% with a best response rate of 46.7%. Three patients had grade IV adverse events, which caused drug discontinuation. Four patients had 5 cases of grade III toxicities (1 thrombocytopenia, 1 stomatitis, and 3 neutropenia). One mild cardiac toxicity (sinus tachycardia for which no action was required) was possibly related to the study drug. CONCLUSION: Our data documented drug efficacy that is satisfactory for this high-risk subset of patients with an acceptable toxicity profile. Results indicate that pixantrone could be a significant treatment option in patients with R/R aggressive DLBCL treated in everyday clinical practice.


Subject(s)
Isoquinolines/therapeutic use , Lymphoma, Large B-Cell, Diffuse/drug therapy , Topoisomerase II Inhibitors/therapeutic use , Adult , Aged , Aged, 80 and over , Cohort Studies , Drug Administration Schedule , Female , Genetic Diseases, X-Linked/etiology , Humans , Isoquinolines/adverse effects , Italy , Male , Middle Aged , Neutropenia/etiology , Registries , Retrospective Studies , Thrombocytopenia/etiology , Topoisomerase II Inhibitors/adverse effects , Treatment Outcome
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