Abstract |
Castleman disease is a rare lymphoproliferative disorder, which presents in a unicentric or multicentric fashion. Multicentric Castleman disease (MCD) is associated with significant systemic symptoms, in part related to the underlying role of interleukin-6 in disease pathogenesis. Treatment for MCD has not been well established and prognosis has historically been poor. We present a case of severe MCD in a pediatric patient who has shown sustained remission following multi-agent chemotherapy and targeted maintenance therapy with the interleukin-6 receptor inhibitor, tocilizumab. This represents the first case report of sustained remission of MCD in a pediatric patient following discontinuation of tocilizumab therapy.
|
Authors | Lucie M Turcotte, Colleen K Correll, Robyn C Reed, Christopher L Moertel |
Journal | Pediatric blood & cancer
(Pediatr Blood Cancer)
Vol. 61
Issue 4
Pg. 737-9
(Apr 2014)
ISSN: 1545-5017 [Electronic] United States |
PMID | 24019247
(Publication Type: Case Reports, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
|
Copyright | © 2013 Wiley Periodicals, Inc. |
Chemical References |
- Antibodies, Monoclonal, Humanized
- Receptors, Interleukin-6
- tocilizumab
|
Topics |
- Adolescent
- Antibodies, Monoclonal, Humanized
(therapeutic use)
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Castleman Disease
(drug therapy)
- Drug Therapy, Combination
- Humans
- Male
- Prognosis
- Receptors, Interleukin-6
(antagonists & inhibitors)
- Remission Induction
|