Evaluating abbreviated induction with fludarabine, cyclophosphamide, and dose-dense rituximab in elderly patients with chronic lymphocytic leukemia. Issue 2 (1st February 2016)

• Record Type: Journal Article
• Authors: Dartigeas, Caroline; Van Den Neste, Eric; Berthou, Christian; Maisonneuve, Hervé; Leprêtre, Stéphane; Dilhuydy, Marie-Sarah; Béné, Marie-Christine; Nguyen-Khac, Florence; Letestu, Rémi; Cymbalista, Florence; De Guibert, Sophie; Aurran, Thérèse; Laribi, Kamel; Vilque, Jean-Pierre; Tournilhac, Olivier; Delmer, Alain; Feugier, Pierre; Cazin, Bruno; Michallet, Anne-Sophie; Lévy, Vincent; Troussard, Xavier; Delepine, Roselyne; Tavernier, Elsa; Colombat, Philippe; Leblond, Véronique
• Is Part Of: Leukemia & lymphoma. Volume 57:Issue 2(2016:Feb.)
• Page Start: 328
• Page End: 334
• Publication Date: 2016-02-01
• Subjects: Chemotherapeutic approaches -- chronic lymphocytic leukemia -- immunotherapeutic approaches -- lymphoid leukemias -- purine analogues; Leukemia -- Periodicals; Lymphomas -- Periodicals; 616.99419
• DOI: 10.3109/10428194.2015.1063139
• Languages: English
• ISSNs: 1042-8194

Abstract

Abstract : Elderly patients with chronic lymphocytic leukemia (CLL) are underrepresented in trials evaluating fludarabine, cyclophosphamide, and rituximab (FCR). We assessed four cycles of FCR with two additional rituximab doses on day 14 of cycles 1 and 2 in 194 untreated CLL patients > 65 years (median age 71.2) without del17p. Four FCR cycles were administered to 90.7% (176/194), with ( n = 74) or without ( n = 102) dose-delay and/or dose-reduction. A total of 50% grade 3/4 neutropenia occurred after each cycle. Only 6.2% cycles were associated with severe infection. Complete remission (CR) was achieved in 19.7%, and partial remission (PR) in 73.9% of patients. Minimal residual disease (MRD) was negative in 36.7%. Overall survival at 36 months was estimated at 87.4%. Oral FC and dose-dense rituximab is feasible and active in fit elderly CLL patients. However, myelosuppression is significant and frequent dose adaptations are required implying that these results cannot be generalized to unfit or frail elderly CLL.