Literature DB >> 26332019

Advances in first-line treatment of chronic lymphocytic leukemia: current recommendations on management and first-line treatment by the German CLL Study Group (GCLLSG).

Paula Cramer1, Petra Langerbeins1, Barbara Eichhorst1, Michael Hallek1,2.   

Abstract

The management of patients with CLL is undergoing significant changes; during the last decade, the outcome of first-line therapies has been markedly improved with the addition of anti-CD20 antibodies to chemotherapy. Today, chemoimmunotherapy for physically fit patients ≤ 65 years should consist of fludarabine, cyclophosphamide, and rituximab (FCR). The combination of bendamustine and rituximab (BR) should be considered in physically fit patients > 65 years and in patients with a higher risk of infections. Patients with reduced fitness and/or relevant comorbidity should receive chlorambucil with a CD20 antibody, preferably obinutuzumab. Regardless of their fitness, patients with CLL carrying genetic aberrations such as del(17p) and/or TP53 mutation poorly respond to chemoimmunotherapy and therefore require different therapeutic approaches. An increasing understanding of the disease biology has led to the development of targeted drugs for the treatment of CLL, such as the BTK inhibitor ibrutinib and PI3K inhibitor idelalisib. These agents have shown efficacy in high-risk and relapsed/refractory patients and are currently being evaluated in clinical trials for first-line therapy. It is anticipated that these compounds and further other novel agents will profoundly change the therapy of CLL.
© 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  CLL; first-line treatment; high-risk

Mesh:

Substances:

Year:  2015        PMID: 26332019     DOI: 10.1111/ejh.12678

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  9 in total

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4.  The Phospholipase Cγ2 Mutants R665W and L845F Identified in Ibrutinib-resistant Chronic Lymphocytic Leukemia Patients Are Hypersensitive to the Rho GTPase Rac2 Protein.

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Journal:  Nat Commun       Date:  2017-07-28       Impact factor: 14.919

7.  Early treatment with FCR versus watch and wait in patients with stage Binet A high-risk chronic lymphocytic leukemia (CLL): a randomized phase 3 trial.

Authors:  Carmen D Herling; Florence Cymbalista; Carolin Groß-Ophoff-Müller; Jasmin Bahlo; Sandra Robrecht; Petra Langerbeins; Anna-Maria Fink; Othman Al-Sawaf; Raymonde Busch; Raphael Porcher; Bruno Cazin; Brigitte Dreyfus; Stefan Ibach; Stéphane Leprêtre; Kirsten Fischer; Florian Kaiser; Barbara Eichhorst; Clemens-Martin Wentner; Manuela A Hoechstetter; Hartmut Döhner; Veronique Leblond; Michael Kneba; Remi Letestu; Sebastian Böttcher; Stephan Stilgenbauer; Michael Hallek; Vincent Levy
Journal:  Leukemia       Date:  2020-02-18       Impact factor: 11.528

8.  Resistance to complement activation, cell membrane hypersialylation and relapses in chronic lymphocytic leukemia patients treated with rituximab and chemotherapy.

Authors:  Anne Bordron; Cristina Bagacean; Jacques-Olivier Pers; Yves Renaudineau; Audrey Mohr; Adrian Tempescul; Boutahar Bendaoud; Stéphanie Deshayes; Florence Dalbies; Caroline Buors; Hussam Saad; Christian Berthou
Journal:  Oncotarget       Date:  2018-08-03

9.  DAP Kinase-Related Apoptosis-Inducing Protein Kinase 2 (DRAK2) Is a Key Regulator and Molecular Marker in Chronic Lymphocytic Leukemia.

Authors:  Katarzyna Szoltysek; Carmela Ciardullo; Peixun Zhou; Anna Walaszczyk; Elaine Willmore; Vikki Rand; Scott Marshall; Andy Hall; Christine J Harrison; Jeyanthy Eswaran; Meera Soundararajan
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  9 in total

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