Abstract
As front line therapy has improved, the treatment of relapsed chronic lymphocytic leukaemia has become more difficult as the disease becomes resistant and the patient accumulates comorbidities. The outcome for those who relapse after immunochemotherapy with fludarabine, cyclophosphamide and rituximab is strongly influenced by the duration of initial response. Patients who relapse within the first year or with a TP53 abnormality have very high-risk disease and will not respond to chemotherapy. High dose glucocorticoid and alemtuzumab followed by an allogeneic stem cell transplant is probably the best approach for younger, fitter patients in this category. Those who relapse after 2-3years without TP53 abnormality will probably respond to their initial therapy again. Relapse within 12-24months carries an intermediate outlook. Additional options include bendamustine and rituximab, ofatumumab and lenalidomide. New therapies are on the horizon and patients should be discussed with a specialist centre and entered into a clinical trial whenever possible.
Original language | English |
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Pages (from-to) | 423-435 |
Number of pages | 13 |
Journal | British Journal of Haematology |
Volume | 163 |
Issue number | 4 |
DOIs | |
Publication status | Published - Nov 2013 |
Keywords
- chronic lymphocytic leukaemia
- leukaemia therapy
- relapsed CLL
- refractory CLL
- HIGH-DOSE METHYLPREDNISOLONE
- STEM-CELL TRANSPLANTATION
- FLUDARABINE PLUS CYCLOPHOSPHAMIDE
- CLL STUDY-GROUP
- PHASE-III TRIAL
- TERM-FOLLOW-UP
- SUBCUTANEOUS ALEMTUZUMAB
- RICHTERS-SYNDROME
- ANTIBODY THERAPY
- CLONAL EVOLUTION