| Literature DB >> 25749825 |
Renato Bassan1, Arianna Masciulli2, Tamara Intermesoli3, Ernesta Audisio4, Giuseppe Rossi5, Enrico Maria Pogliani6, Vincenzo Cassibba7, Daniele Mattei8, Claudio Romani9, Agostino Cortelezzi10, Consuelo Corti11, Anna Maria Scattolin12, Orietta Spinelli3, Manuela Tosi3, Margherita Parolini3, Filippo Marmont4, Erika Borlenghi5, Monica Fumagalli6, Sergio Cortelazzo7, Andrea Gallamini8, Rosa Maria Marfisi2, Elena Oldani3, Alessandro Rambaldi3.
Abstract
Developing optimal radiation-free central nervous system prophylaxis is a desirable goal in acute lymphoblastic leukemia, to avoid the long-term toxicity associated with cranial irradiation. In a randomized, phase II trial enrolling 145 adult patients, we compared intrathecal liposomal cytarabine (50 mg: 6/8 injections in B-/T-cell subsets, respectively) with intrathecal triple therapy (methotrexate/cytarabine/prednisone: 12 injections). Systemic therapy included methotrexate plus cytarabine or L-asparaginase courses, with methotrexate augmented to 2.5 and 5 g/m(2) in Philadelphia-negative B- and T-cell disease, respectively. The primary study objective was the comparative assessment of the risk/benefit ratio, combining the analysis of feasibility, toxicity and efficacy. In the liposomal cytarabine arm 17/71 patients (24%) developed grade 3-4 neurotoxicity compared to 2/74 (3%) in the triple therapy arm (P=0.0002), the median number of episodes of neurotoxicity of any grade was one per patient compared to zero, respectively (P=0.0001), and even though no permanent disabilities or deaths were registered, four patients (6%) discontinued intrathecal prophylaxis on account of these toxic side effects (P=0.06). Neurotoxicity worsened with liposomal cytarabine every 14 days (T-cell disease), and was improved by the adjunct of intrathecal dexamethasone. Two patients in the liposomal cytarabine arm suffered from a meningeal relapse (none with T-cell disease, only one after high-dose chemotherapy) compared to four in the triple therapy arm (1 with T-cell disease). While intrathecal liposomal cytarabine could contribute to improved, radiation-free central nervous system prophylaxis, the toxicity reported in this trial does not support its use at 50 mg and prompts the investigation of a lower dosage. (clinicaltrials.gov identifier: NCT-00795756). Copyright© Ferrata Storti Foundation.Entities:
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Year: 2015 PMID: 25749825 PMCID: PMC4450624 DOI: 10.3324/haematol.2014.123273
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941