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Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis
BACKGROUND: Pulmonary Langerhans cell histiocytosis (PLCH) is a rare disorder characterised by granulomatous proliferation of CD1a-positive histiocytes forming granulomas within lung parenchyma, in strong association with tobacco smoking, and which may result in chronic respiratory failure. Smoking...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268858/ https://www.ncbi.nlm.nih.gov/pubmed/25433492 http://dx.doi.org/10.1186/s13023-014-0191-8 |
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author | Grobost, Vincent Khouatra, Chahera Lazor, Romain Cordier, Jean-François Cottin, Vincent |
author_facet | Grobost, Vincent Khouatra, Chahera Lazor, Romain Cordier, Jean-François Cottin, Vincent |
author_sort | Grobost, Vincent |
collection | PubMed |
description | BACKGROUND: Pulmonary Langerhans cell histiocytosis (PLCH) is a rare disorder characterised by granulomatous proliferation of CD1a-positive histiocytes forming granulomas within lung parenchyma, in strong association with tobacco smoking, and which may result in chronic respiratory failure. Smoking cessation is considered to be critical in management, but has variable effects on outcome. No drug therapy has been validated. Cladribine (chlorodeoxyadenosine, 2-CDA) down-regulates histiocyte proliferation and has been successful in curbing multi-system Langerhans cell histiocytosis and isolated PLCH. METHODS AND PATIENTS: We retrospectively studied 5 patients (aged 37–55 years, 3 females) with PLCH who received 3 to 4 courses of cladribine therapy as a single agent (0.1 mg/kg per day for 5 consecutive days at monthly intervals). One patient was treated twice because of relapse at 1 year. Progressive pulmonary disease with obstructive ventilatory pattern despite smoking cessation and/or corticosteroid therapy were indications for treatment. Patients were administered oral trimethoprim/sulfamethoxazole and valaciclovir to prevent opportunistic infections. They gave written consent to receive off-label cladribine in the absence of validated treatment. RESULTS: Functional class dyspnea improved with cladribine therapy in 4 out of 5 cases, and forced expiratory volume in 1 second (FEV1) increased in all cases by a mean of 387 ml (100–920 ml), contrasting with a steady decline prior to treatment. Chest high-resolution computed tomography (HRCT) features improved with cladribine therapy in 4 patients. Hemodynamic improvement was observed in 1 patient with pre-capillary pulmonary hypertension. The results suggested a greater treatment effect in subjects with nodular lung lesions and/or thick-walled cysts on chest HRCT, with diffuse hypermetabolism of lung lesions on positron emission tomography (PET)-scan, and with progressive disease despite smoking cessation. Infectious pneumonia developed in 1 patient, with later grade 4 neutrocytopenia but without infection. DISCUSSION: Data interpretation was limited by the retrospective, uncontrolled study design and small sample size. CONCLUSION: Cladribine as a single agent may be effective therapy in patients with progressive PLCH. |
format | Online Article Text |
id | pubmed-4268858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42688582014-12-17 Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis Grobost, Vincent Khouatra, Chahera Lazor, Romain Cordier, Jean-François Cottin, Vincent Orphanet J Rare Dis Research BACKGROUND: Pulmonary Langerhans cell histiocytosis (PLCH) is a rare disorder characterised by granulomatous proliferation of CD1a-positive histiocytes forming granulomas within lung parenchyma, in strong association with tobacco smoking, and which may result in chronic respiratory failure. Smoking cessation is considered to be critical in management, but has variable effects on outcome. No drug therapy has been validated. Cladribine (chlorodeoxyadenosine, 2-CDA) down-regulates histiocyte proliferation and has been successful in curbing multi-system Langerhans cell histiocytosis and isolated PLCH. METHODS AND PATIENTS: We retrospectively studied 5 patients (aged 37–55 years, 3 females) with PLCH who received 3 to 4 courses of cladribine therapy as a single agent (0.1 mg/kg per day for 5 consecutive days at monthly intervals). One patient was treated twice because of relapse at 1 year. Progressive pulmonary disease with obstructive ventilatory pattern despite smoking cessation and/or corticosteroid therapy were indications for treatment. Patients were administered oral trimethoprim/sulfamethoxazole and valaciclovir to prevent opportunistic infections. They gave written consent to receive off-label cladribine in the absence of validated treatment. RESULTS: Functional class dyspnea improved with cladribine therapy in 4 out of 5 cases, and forced expiratory volume in 1 second (FEV1) increased in all cases by a mean of 387 ml (100–920 ml), contrasting with a steady decline prior to treatment. Chest high-resolution computed tomography (HRCT) features improved with cladribine therapy in 4 patients. Hemodynamic improvement was observed in 1 patient with pre-capillary pulmonary hypertension. The results suggested a greater treatment effect in subjects with nodular lung lesions and/or thick-walled cysts on chest HRCT, with diffuse hypermetabolism of lung lesions on positron emission tomography (PET)-scan, and with progressive disease despite smoking cessation. Infectious pneumonia developed in 1 patient, with later grade 4 neutrocytopenia but without infection. DISCUSSION: Data interpretation was limited by the retrospective, uncontrolled study design and small sample size. CONCLUSION: Cladribine as a single agent may be effective therapy in patients with progressive PLCH. BioMed Central 2014-11-30 /pmc/articles/PMC4268858/ /pubmed/25433492 http://dx.doi.org/10.1186/s13023-014-0191-8 Text en © Grobost et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Grobost, Vincent Khouatra, Chahera Lazor, Romain Cordier, Jean-François Cottin, Vincent Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis |
title | Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis |
title_full | Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis |
title_fullStr | Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis |
title_full_unstemmed | Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis |
title_short | Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis |
title_sort | effectiveness of cladribine therapy in patients with pulmonary langerhans cell histiocytosis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268858/ https://www.ncbi.nlm.nih.gov/pubmed/25433492 http://dx.doi.org/10.1186/s13023-014-0191-8 |
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