Title |
Update and new approaches in the treatment of Castleman disease
|
---|---|
Published in |
Journal of Blood Medicine, August 2016
|
DOI | 10.2147/jbm.s60514 |
Pubmed ID | |
Authors |
Kah-Lok Chan, Stephen Lade, H Miles Prince, Simon J Harrison |
Abstract |
First described 60 years ago, Castleman disease comprises a rare and heterogeneous cluster of disorders, characterized by lymphadenopathy with unique histological features and associated with cytokine-driven constitutional symptoms and biochemical disturbances. Although unicentric Castleman disease is curable with complete surgical excision, its multicentric counterpart is a considerable therapeutic challenge. The recent development of biological agents, particularly monoclonal antibodies to interleukin-6 and its receptor, allow for more targeted disease-specific intervention that promises improved response rates and more durable disease control; however, further work is required to fill knowledge gaps in terms of underlying pathophysiology and to facilitate alternative treatment options for refractory cases. |
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Unknown | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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Unknown | 77 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Postgraduate | 17 | 22% |
Other | 12 | 16% |
Researcher | 11 | 14% |
Student > Doctoral Student | 7 | 9% |
Student > Bachelor | 6 | 8% |
Other | 15 | 19% |
Unknown | 9 | 12% |
Readers by discipline | Count | As % |
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Medicine and Dentistry | 56 | 73% |
Biochemistry, Genetics and Molecular Biology | 2 | 3% |
Neuroscience | 2 | 3% |
Linguistics | 1 | 1% |
Agricultural and Biological Sciences | 1 | 1% |
Other | 5 | 6% |
Unknown | 10 | 13% |