Literature DB >> 14630811

Early prediction of outcome and response to alemtuzumab therapy in chronic lymphocytic leukemia.

Andy C Rawstron1, Ben Kennedy, Paul Moreton, Anita J Dickinson, Matthew J Cullen, Stephen J Richards, Andrew S Jack, Peter Hillmen.   

Abstract

Alemtuzumab therapy is effective for some refractory chronic lymphocytic leukemia (CLL), but identifying responders requires at least 8 weeks of therapy. Early identification of nonresponders would minimize toxicity and/or facilitate more effective strategies. The aim of this study was to identify a minimally invasive method for early prediction of response and relapse. Flow cytometric monitoring was performed in 887 blood samples and 201 marrow samples from 43 patients undergoing intravenous alemtuzumab therapy. Although the absolute lymphocytosis was resolved in all patients by week 4, significant depletion of bone marrow tumor only occurred if circulating B-lymphocyte counts were persistently less than 0.001 x 10(9)/L, which was rare in nonresponders. The majority of patients (16/28) who did not benefit from a full course of therapy were identified with 100% positive predictive value using the following algorithm: peripheral B-cell count greater than 0.001 x 10(9)/L at week 2 with less than 1 log depletion of circulating B cells between weeks 2 and 4. Monitoring CLL levels after treatment identified patients at risk of early disease progression and could potentially improve patient management. During alemtuzumab therapy, bone marrow CLL depletion only occurs after abrogation of circulating tumor, requiring close monitoring of circulating B-cell levels. If validated in prospective studies, blood monitoring at 2 and 4 weeks may be used to optimize therapy.

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Year:  2003        PMID: 14630811     DOI: 10.1182/blood-2002-10-3270

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  9 in total

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3.  Complement dependent cytotoxicity in chronic lymphocytic leukemia: ofatumumab enhances alemtuzumab complement dependent cytotoxicity and reveals cells resistant to activated complement.

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Review 4.  New agents in chronic lymphocytic leukemia.

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Authors:  Jeremy L Warner; Jon E Arnason
Journal:  Ther Adv Hematol       Date:  2012-12

6.  Current and emerging treatments for chronic lymphocytic leukaemia.

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Review 7.  Therapeutic Value of Single Nucleotide Polymorphisms on the Efficacy of New Therapies in Patients with Multiple Sclerosis.

Authors:  María José Zarzuelo Romero; Cristina Pérez Ramírez; María Isabel Carrasco Campos; Almudena Sánchez Martín; Miguel Ángel Calleja Hernández; María Carmen Ramírez Tortosa; Alberto Jiménez Morales
Journal:  J Pers Med       Date:  2021-04-23

8.  Minimal residual disease quantification using consensus primers and high-throughput IGH sequencing predicts post-transplant relapse in chronic lymphocytic leukemia.

Authors:  A C Logan; B Zhang; B Narasimhan; V Carlton; J Zheng; M Moorhead; M R Krampf; C D Jones; A N Waqar; M Faham; J L Zehnder; D B Miklos
Journal:  Leukemia       Date:  2013-02-19       Impact factor: 11.528

9.  Impact of FcγR variants on the response to alemtuzumab in multiple sclerosis.

Authors:  Christian W Keller; Tobias Ruck; Donal McHugh; Steffen Pfeuffer; Catharina C Gross; Catharina Korsukewitz; Nico Melzer; Luisa Klotz; Sven G Meuth; Christian Münz; Falk Nimmerjahn; Heinz Wiendl; Jan D Lünemann
Journal:  Ann Clin Transl Neurol       Date:  2019-11-04       Impact factor: 4.511

  9 in total

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