Literature DB >> 28833354

Immunohistochemical expression of cereblon and MUM1 as potential predictive markers of response to lenalidomide in extranodal marginal zone B-cell lymphoma of the mucosa-associated lymphoid tissue (MALT lymphoma).

Barbara Kiesewetter1, Ingrid Simonitsch-Klupp2, Christoph Kornauth2, Werner Dolak3, Julius Lukas4, Marius E Mayerhoefer5, Markus Raderer1.   

Abstract

Lenalidomide is an active agent for the treatment of MALT lymphoma. Recently, high expression levels of cereblon (CRBN) and MUM1 have been associated with better response rates in multiple myeloma treated with lenalidomide. However, there are no data on CRBN and MUM1 expression in MALT lymphoma. In the current study, we have systematically investigated a potential correlation of CRBN/MUM1 immunohistochemical expression and response to lenalidomide-based therapy in a series of 46 patients with MALT lymphoma treated at the Medical University Vienna 2009 to 2014. In total, 28% (13/46) of biopsy specimens derived from gastric tissues, while 72% (33/46) originated from extragastric MALT lymphoma. In terms of CRBN, 54% showed high expression (CRBN+, ≥50% positive cells); the remaining 46% were classified as low expression (CRBN-). In contrast to other reports, there was a non-significant trend towards worse response rates in CRBN+ (68% versus 86%, P = 0.161). Relapse rates (P = 0.592) and PFS (P = 0.306) did not differ between CRBN+/CRBN-, but all 3 patients progressing on lenalidomide were CRBN+ and both patients completely lacking CRBN expression responded to treatment. Concerning MUM1, 62% were MUM1-negative (MUM1-) and 38% positive (MUM1+). There was no difference in response to lenalidomide by MUM1-status (MUM1+ 71% versus MUM1- 79%, P = 0.546) and also relapse rates (P = 0.828) and PFS (P = 0.681) did not differ. Interestingly, a subgroup analysis of gastric lymphoma revealed a significantly better PFS for CRBN- and MUM1- patients, respectively (both P < 0.05). To conclude, there was no significant difference in response to lenalidomide between patients with low or high expression of CRBN/MUM1 in a general population of MALT lymphoma, and immunohistochemical CRBN/MUM1 assessment cannot be recommended in the clinical routine.
Copyright © 2017 John Wiley & Sons, Ltd.

Entities:  

Keywords:  MALT lymphoma; MUM1; cereblon; lenalidomide; predictive markers

Mesh:

Substances:

Year:  2017        PMID: 28833354     DOI: 10.1002/hon.2472

Source DB:  PubMed          Journal:  Hematol Oncol        ISSN: 0278-0232            Impact factor:   5.271


  4 in total

Review 1.  New developments in the pathology of malignant lymphoma. A review of the literature published from September-August 2017.

Authors:  J H van Krieken
Journal:  J Hematop       Date:  2017-11-29       Impact factor: 0.196

2.  Prolonged follow-up on lenalidomide-based treatment for mucosa-associated lymphoid tissue lymphoma (MALT lymphoma)-Real-world data from the Medical University of Vienna.

Authors:  Barbara Kiesewetter; Wolfgang Lamm; Ortrun Neuper; Marius E Mayerhoefer; Ingrid Simonitsch-Klupp; Markus Raderer
Journal:  Hematol Oncol       Date:  2019-07-28       Impact factor: 5.271

3.  Effects of lenalidomide on the bone marrow microenvironment in acute myeloid leukemia: Translational analysis of the HOVON103 AML/SAKK30/10 Swiss trial cohort.

Authors:  Michael Medinger; Alexandar Tzankov; Magdalena M Brune; Georg Stüssi; Pontus Lundberg; Visar Vela; Dominik Heim; Markus G Manz; Eugenia Haralambieva; Thomas Pabst; Yara Banz; Mario Bargetzi; Rainer Grobholz; Martin Fehr; Sergio Cogliatti; Gert J Ossenkoppele; Bob Löwenberg; Christina Biaggi Rudolf; Qiyu Li; Jakob Passweg; Luca Mazzuchelli
Journal:  Ann Hematol       Date:  2021-03-02       Impact factor: 3.673

4.  A novel prognostic nomogram for patients with extragastric mucosa-associated lymphoid tissue lymphoma: A multicenter study.

Authors:  Xiaoqian Li; Huangming Hong; He Huang; Liqun Zou; Zegeng Chen; Zhihui Zhang; Liling Zhang; Xiaojie Fang; Hongqiang Guo; Ke Xie; Ying Tian; Suxia Lin; Yungchang Chen; Wei Zhang; Yuyi Yao; Fei Pan; Huawei Weng; Tongyu Lin
Journal:  Cancer Med       Date:  2022-04-29       Impact factor: 4.711

  4 in total

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