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. 2012 May 3;119(18):4101-7.
doi: 10.1182/blood-2011-11-312421. Epub 2012 Mar 6.

Risk categories and refractory CLL in the era of chemoimmunotherapy

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Risk categories and refractory CLL in the era of chemoimmunotherapy

Thorsten Zenz et al. Blood. .

Abstract

Standardized criteria for diagnosis and response evaluation in chronic lymphocytic leukemia (CLL) are essential to achieve comparability of results and improvement of clinical care. With the increasing range of therapeutic options, the treatment context is important when defining refractory CLL. Refractory CLL has been defined as no response or response lasting ≤ 6 months from last therapy. This subgroup has a very poor outcome, and many trials use this group as an entry point for early drug development. With the intensification of first-line regimens, the proportion of patients with refractory CLL using these criteria decreases. This has immediate consequences for recruitment of patients into trials as well as salvage strategies. Conversely, patients who are not refractory according to the traditional definition but who have suboptimal or short response to intense therapy also have a very poor outcome. In this Perspective, we discuss recent results that may lead to a reassessment of risk categories in CLL focusing on fit patients who are eligible for all treatment options. We cover aspects of the history and biologic basis for refractory CLL and will focus on how emerging data on treatment failure from large trials using chemoimmunotherapy may help to define risk groups in CLL.

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Figures

Figure 1
Figure 1
Treatment algorithm in different “highest-risk” scenarios of CLL. Patients with 17p deletion or TP53 mutation, refractory CLL (refractory to fludarabine, fludarabine combination, and similar regimens) as well as patients with short PFS after FCR (or similar regimens, PCR, BR) have a very high risk of death within 2 years from treatment indication.,, *The recommendations are not based on comparative trial data.

References

    1. Hallek M, Cheson BD, Catovsky D, et al. Guidelines for the diagnosis and treatment of chronic lymphocytic leukemia: a report from the International Workshop on Chronic Lymphocytic Leukemia updating the National Cancer Institute-Working Group 1996 guidelines. Blood. 2008;111(12):5446–5456. - PMC - PubMed
    1. Gribben JG. How I treat CLL up front. Blood. 2010;115(2):187–197. - PMC - PubMed
    1. Montserrat E, Moreno C, Esteve J, Urbano-Ispizua A, Gine E, Bosch F. How I treat refractory CLL. Blood. 2006;107(4):1276–1283. - PubMed
    1. Zenz T, Mertens D, Küppers R, Döhner H, Stilgenbauer S. From pathogenesis to treatment of chronic lymphocytic leukaemia. Nat Rev Cancer. 2010;10(1):37–50. - PubMed
    1. Hallek M, Fischer K, Fingerle-Rowson G, et al. Addition of rituximab to fludarabine and cyclophosphamide in patients with chronic lymphocytic leukaemia: a randomised, open-label, phase 3 trial. Lancet. 2010;376(9747):1164–1174. - PubMed

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