| Literature DB >> 25596264 |
Carol Moreno1, Marco Montillo2, Panayiotis Panayiotidis3, Maria Dimou3, Adrian Bloor4, Jehan Dupuis5, Anna Schuh6, Stefan Norin7, Christian Geisler8, Peter Hillmen9, Michael Doubek10, Marek Trněný11, Petra Obrtlikova11, Luca Laurenti12, Stephan Stilgenbauer13, Lukas Smolej14, Paolo Ghia15, Florence Cymbalista16, Ulrich Jaeger17, Kostas Stamatopoulos18, Niki Stavroyianni18, Patrick Carrington19, Hamadi Zouabi20, Veronique Leblond20, Juan C Gomez-Garcia21, Martin Rubio21, Roberto Marasca22, Gerardo Musuraca23, Luigi Rigacci24, Lucia Farina25, Rossella Paolini26, Sarka Pospisilova10, Eva Kimby7, Colm Bradley27, Emili Montserrat28.
Abstract
We report the largest retrospective, phase IV non-interventional, observational study of ofatumumab therapy in heavily pre-treated patients with poor-prognosis chronic lymphocytic leukemia. Total number of patients was 103; median age was 65 years (range 39-85). Median number of prior lines of therapy was 4 (range 1-13), including, in most cases, rituximab-, fludarabine- and alemtuzumab-based regimens; 13 patients had been allografted. Of 113 adverse events, 28 (29%) were considered to be directly related to ofatumumab. Grade 3-4 toxicities included neutropenia (10%), thrombocytopenia (5%), anemia (3%), pneumonia (17%), and fever (3%). Two heavily pre-treated patients developed progressive multifocal leukoencephalopathy. On an intention-to-treat analysis, the overall response rate was 22% (3 complete response, 1 incomplete complete response). Median progression-free and overall survival times were 5 and 11 months, respectively. This study confirms in a daily-life setting the feasibility and acceptable toxicity of ofatumumab treatment in advanced chronic lymphocytic leukemia. The complete response rate, however, was low. Therefore, treatment with ofatumumab should be moved to earlier phases of the disease. Ideally, this should be done in combination with other agents, as recently approved for ofatumumab plus chlorambucil as front-line treatment for patients unfit for fludarabine. This study is registered at clinicaltrials.gov identifier:01453062. Copyright© Ferrata Storti Foundation.Entities:
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Year: 2015 PMID: 25596264 PMCID: PMC4380724 DOI: 10.3324/haematol.2014.118158
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941