Best Practice & Research Clinical Haematology
Volume 20, Issue 3 , Pages 499-512, September 2007

Minimal residual disease assessment in chronic lymphocytic leukaemia

  • Hazem A. Sayala, MRCP(UK) (Clinical Reasearch Fellow)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +44 113 3926285; Fax: +44 113 3926286.
  • ,
  • Andy C. Rawstron, PhD (Principal Clinical Scientist)
  • ,
  • Peter Hillmen, MD, PhD (Consultant Haematologist)

Haematological Malignancy Diagnostic Service, Leeds General Infirmary, Great George Street, Leeds LS1 3EX, UK

The concept of minimal residual disease (MRD) eradication in chronic lymphocytic leukaemia (CLL) is a relatively new one, as conventional therapy with alkylating agents is relatively ineffective and responding patients almost always have a significant tumour burden remaining at the end of treatment. However, a variety of novel therapies is now yielding higher response rates, and responses of better quality are now routinely achieved. This progress in therapy has been paralleled by an improvement in laboratory assays, allowing detection of CLL cells to levels as low as ten CLL cells in a million leukocytes. In this chapter we briefly review the existing methods for MRD assessment, the clinical relevance of MRD eradication in CLL, and the therapies available to attain this endpoint.

Key words: chronic lymphocytic leukaemia, minimal residual disease

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1521-6926(07)00041-2

doi:10.1016/j.beha.2007.03.004

Best Practice & Research Clinical Haematology
Volume 20, Issue 3 , Pages 499-512, September 2007