Best Practice & Research Clinical Haematology
Volume 23, Issue 1 , Pages 85-96, March 2010

Therapy of chronic lymphocytic leukaemia

  • Michael Hallek, MD (Director and Chair)

      Affiliations

    • Corresponding Author InformationTel.: +49 221 478 4400; Fax: +49 221 478 5455.

Klinik I für Innere Medizin, Center for Integrated Oncology Köln Bonn, Universität zu Köln, Joseph-Stelzmann Str. 9, 50924 Köln, Germany

Rapid progress has been achieved recently in the management of chronic lymphocytic leukaemia (CLL). New insights into the molecular pathology of CLL have generated a plethora of biological markers that predict the prognosis and influence therapeutic decisions. Moreover, fludarabine, bendamustine and two monoclonal antibodies, alemtuzumab and rituximab, have been approved by European and/or American regulatory agencies. Additional monoclonal antibodies targeting CD20, CD23, CD37, CD38 or CD40, as well as drugs designed to interfere with proteins regulating the cell cycle, apoptotic machinery or leukaemic microenvironment (e.g., flavopiridol, oblimersen, ABT-263 or lenalidomide) are investigated in clinical trials. An increased experience with reduced-intensity allogeneic progenitor cell transplantation allows offering this option to physically fit patients. This review attempts to summarise the current use of these different modalities in CLL therapy.

Keywords: therapy, antibody, purin analogue, rituximab, fitness, first-line second-line, allogeneic stem cell transplantation, CLL

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PII: S1521-6926(09)00103-0

doi:10.1016/j.beha.2009.12.002

Best Practice & Research Clinical Haematology
Volume 23, Issue 1 , Pages 85-96, March 2010