Phase I study of magnesium pidolate in combination with hydroxycarbamide for children with sickle cell anaemia

Authors: Hankins, Jane S.1; Wynn, Lynn W.1; Brugnara, Carlo2; Hillery, Cheryl A.3; Li, Chin-Shang1; Wang, Winfred C.1

Source: British Journal of Haematology, Volume 140, Number 1, January 2008 , pp. 80-85(6)

Publisher: Blackwell Publishing

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content

Abstract:

Summary

In sickle cell anaemia, red cell dehydration increases intracellular HbS concentration and promotes sickling. Higher erythrocyte magnesium reduces water loss through negative regulation of membrane transporters. Hydroxycarbamide (also known as hydroxyurea) reduces sickling partly by increasing intracellular HbF. Combining drugs with distinct mechanisms could offer additive effects. A phase I trial combining oral magnesium pidolate and hydroxycarbamide was performed to estimate the maximum tolerated dose (MTD) and toxicity of magnesium. Cohorts of three children with HbSS, who were on a stable dose of hydroxycarbamide (median 28·5 mg/kg/d), received magnesium pidolate for 6 months beginning at 83 mg/kg/d. The dose was escalated by 50% for subsequent cohorts. Laboratory evaluations were performed at 0, 3, 6 and 9 months. Sixteen children (aged 4-12 years) participated. All four dose-limiting toxicities (grade III diarrhoea and abdominal pain) occurred within the first month of starting magnesium. Additionally, diarrhoea grades I (n =1) and II (n =3), and abdominal pain grade II (n =3) occurred. Hydroxycarbamide dose reduction or interruption was not required. The MTD for magnesium pidolate used in combination with hydroxycarbamide was 125 mg/kg/d. KCl co-transporter activity declined after 3 months of magnesium pidolate (P =0·02). A phase II study is needed to investigate the efficacy of this drug combination.

Keywords: magnesium pidolate; hydroxycarbamide; sickle cell anaemia; red cell dehydration

Document Type: Research article

DOI: 10.1111/j.1365-2141.2007.06884.x

Affiliations: 1: Comprehensive Sickle Cell Center, St Jude Children's Research Hospital, Memphis, TN 2: Children's Hospital, Boston, MA 3: Medical College of Wisconsin and Blood Research Institute, Milwaukee, WI, USA

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$50.39 plus tax      Refund Policy

 

OR

Back to top

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages.
Page Help Click here for Page Help
Shopping cart
Tools
Sign in






Need to register?
Sign up here
Text size: A | A | A | A