4.4 Article

Severe Neurologic Side Effects in Patients Being Treated for Hemophagocytic Lymphohistiocytosis

Journal

PEDIATRIC BLOOD & CANCER
Volume 52, Issue 5, Pages 621-625

Publisher

WILEY
DOI: 10.1002/pbc.21838

Keywords

hemophagocytic lymphohystiocytosis; neurotoxicity; PRES

Funding

  1. NICHD NIH HHS [U10 HD037249, U10 HD037249-10] Funding Source: Medline

Ask authors/readers for more resources

Background. Hemophagocytic Lymphohistiocytosis (HLH) is characterized by uncontrolled inflammation that is generally fatal Without immune Modulating chemotherapy. At Texas Children's Hospital, we have observed significant central nervous system (CNS) toxicity in several patients treated for HLH according to the Histiocyte Society protocol HLH 2004 in which cyclosporine is given early in the treatment regimen, Methods. Patients diagnosed with HLH at Texas Children's Hospital between April 2004 and October 2007 were identified and (harts were reviewed. A reference group of patients treated between August 2001 and Marc It 2004, prior to the introduction of HLH-2004, was also evaluated, Results, Five of 17 patients in the study group developed Severe neurotoxicity. Four had new onset seizures associated with significant MRI abnormalities, while the fifth died of intracerebral hemorrhage. Timing Of the development of neurologic side effects ranged from day 5 to week 6 of therapy. Cyclosporine levels were outside the therapeutic range (200-300 ng/ml) prior to the onset of symptoms in two of the five patients. Systolic blood pressures for all five patients were greater than the 95th percentile for age on at least One Measurement within 24 hr of the onset Of neurologic symptoms. MRI scans obtained within 24 hr of seizure activity ill four patients were consistent with posterior reversible encephalopathy syndrome (PRES), By comparison only one patient in the reference group (n = 15) had neurotoxicity (PRES). Conclusions, Patients being treated for HI-H appear to he at risk for neurotoxicity, particularly PRES. Elevated blood pressure, worsening renal and liver function, increased cyclosporine levels, and CNS involvement of HLH may be triggers for the neurotoxic side effects of treatment. Patients being treated on HLH-2004 require close monitoring of their neurologic status and modifiable risk factors such as hypertension should managed aggressively. If larger Studies validate Our observations, it will be important to determine if up-front cyclosporine in HLH protocols confers a survival benefit that Outweighs the potential risk of increased neurotoxicity. Pediatr Blood Cancer 2009;52:621-625. (C) 2009 Wiley-Liss, Inc.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available