Literature DB >> 22070019

[Partial regression of CNS lesions of Erdheim-Chester disease after treatment with 2-chlorodeoxadenosine and their full remission following treatment with lenalidomide].

Z Adam1, A Sprláková, Z Rehák, R Koukalová, P Szturz, M Krejcí, L Pour, L Zahradová, L Cervinek, L Kren, M Moulis, M Hermanová, M Mechl, J Prásek, R Hájek, Z Král, J Mayer.   

Abstract

INTRODUCTION: Erdheim-Chester disease is a very rare syndrome affecting adult population. It typically causes hyperostosis of long bones, retroperitoneal fibrosis and widening of the aortic wall. Patients frequently suffer from disease-associated fevers and pain in the lower limbs. No guidelines are available for the treatment of this rare ailment. Therefore, we describe our experience with lenalidomide in a patient with poor treatment response to 2-chlorodeoxyadenosine. CASE: Diabetes insipidus and neurological problems developing over 4 years were the first signs of the disease. The disease was diagnosed from histology of the bone marrow extracted from the ilium. At diagnosis, the patient had multiple infiltrates in the brain, widened wall of the thoracic and abdominal aorta, fibrotic changes to retroperitoneum and typical hyperostosis of the long bones of lower limbs with high accumulation of technetium pyrophosphate as well as fluorodeoxyglucose. First line treatment involved 2-chlorodeoxyadenosine 5 mg/m2 s.c. for 5 consecutive days every 28 days. There was no clear treatment response identifiable on the MR scan of the brain following the third cycle and thus 4th-6th cycle consisted of 2-chlorodexyadenosine 5 mg/m2 + cyclophosphamide 150 mg/m2 + dexamethasone 24 mg day 1-5 every 28 days. After the 6th cycle, MR showed partial regression of the brain lesions. PET-CT showed an increased accumulation of fluorodeoxyglucose in bone lesions. Second line treatment involved lenalidomide 25 mg/day days 1-21 every 28 days. Lenalidomide tolerance was excellent; the number of neutrophils and thrombocytes was within the physiological range throughout the treatment period. Follow-up MR showed complete remission of the brain lesions, while follow-up PET-CT showed further increase in fluorodeoxyglucose accumulation in the bones of lower limbs.
CONCLUSION: Treatment with 2-chlorodeoxyadenosine-based regimen provided partial remission of Erdheim-Chester disease lesions in the brain, while treatment with lenalidomide resulted in complete remission of these lesions. Fluorodeoxyglucose continues to accumulate in the long bones of lower limbs. We are unable to elucidate the reasons for complete remission of the disease in the brain as per the MR and its progression in the long bones according to PET-CT. Further testing of lenalidomide in the treatment of this disease is required to support further use of this perspective treatment option.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22070019

Source DB:  PubMed          Journal:  Klin Onkol        ISSN: 0862-495X


  9 in total

Review 1.  Erdheim-Chester Disease: a comprehensive review of the literature.

Authors:  Roei D Mazor; Mirra Manevich-Mazor; Yehuda Shoenfeld
Journal:  Orphanet J Rare Dis       Date:  2013-09-08       Impact factor: 4.123

2.  Consensus guidelines for the diagnosis and clinical management of Erdheim-Chester disease.

Authors:  Eli L Diamond; Lorenzo Dagna; David M Hyman; Giulio Cavalli; Filip Janku; Juvianee Estrada-Veras; Marina Ferrarini; Omar Abdel-Wahab; Mark L Heaney; Paul J Scheel; Nancy K Feeley; Elisabetta Ferrero; Kenneth L McClain; Augusto Vaglio; Thomas Colby; Laurent Arnaud; Julien Haroche
Journal:  Blood       Date:  2014-05-21       Impact factor: 22.113

3.  The clinical spectrum of Erdheim-Chester disease: an observational cohort study.

Authors:  Juvianee I Estrada-Veras; Kevin J O'Brien; Louisa C Boyd; Rahul H Dave; Benjamin Durham; Liqiang Xi; Ashkan A Malayeri; Marcus Y Chen; Pamela J Gardner; Jhonell R Alvarado-Enriquez; Nikeith Shah; Omar Abdel-Wahab; Bernadette R Gochuico; Mark Raffeld; Elaine S Jaffe; William A Gahl
Journal:  Blood Adv       Date:  2017-02-14

4.  Erdheim Chester disease with appendicular skeletal, renal and pleural involvement responding to Zelboraf (BRAF inhibitor) treatment: case report.

Authors:  Dariusz Borys; Lucas Nystrom; Albert Song; Laurie M Lomasney
Journal:  Skeletal Radiol       Date:  2016-07-16       Impact factor: 2.199

5.  Clinical and Radiologic Responses to Cladribine for the Treatment of Erdheim-Chester Disease.

Authors:  Gaurav Goyal; Mithun V Shah; Timothy G Call; Mark R Litzow; William J Hogan; Ronald S Go
Journal:  JAMA Oncol       Date:  2017-09-01       Impact factor: 31.777

6.  Erdheim-Chester disease: from palliative care to targeted treatment.

Authors:  Giorgio Graziani; Manuel A Podestà; David Cucchiari; Francesco Reggiani; Claudio Ponticelli
Journal:  Clin Kidney J       Date:  2014-07-15

Review 7.  Oncogene-induced senescence as a new mechanism of disease: the paradigm of erdheim-chester disease.

Authors:  Giulio Cavalli; Riccardo Biavasco; Bruno Borgiani; Lorenzo Dagna
Journal:  Front Immunol       Date:  2014-06-13       Impact factor: 7.561

8.  Clinical considerations and key issues in the management of patients with Erdheim-Chester Disease: a seven case series.

Authors:  Roei D Mazor; Mirra Manevich-Mazor; Anat Kesler; Orna Aizenstein; Iris Eshed; Ronald Jaffe; Yakov Pessach; Ilan Goldberg; Eli Sprecher; Iris Yaish; Alexander Gural; Chezi Ganzel; Yehuda Shoenfeld
Journal:  BMC Med       Date:  2014-12-01       Impact factor: 8.775

9.  Resolved heart tamponade and controlled exophthalmos, facial pain and diabetes insipidus due to Erdheim-Chester disease.

Authors:  Jaume Monmany; Esther Granell; Laura López; Pere Domingo
Journal:  BMJ Case Rep       Date:  2018-10-17
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.