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Eltrombopag: A Review in Paediatric Chronic Immune Thrombocytopenia
Celeste B Burness1, Gillian M Keating2, Karly P Garnock-Jones2
1Springer, Private Bag 65901, Mairangi Bay, 0754, Auckland, New Zealand. demail@springer.com.
Insights
Eltrombopag significantly improved platelet counts and reduced bleeding in children with chronic immune thrombocytopenia (ITP) refractory to other treatments. This oral therapy offers a valuable new option for managing ITP in pediatric patients.
Area of Science:
- Hematology
- Pediatric Medicine
- Pharmacology
Background:
- Chronic immune thrombocytopenia (ITP) in children presents limited treatment options for those refractory to standard therapies.
- Eltrombopag, a thrombopoietin receptor agonist, offers a novel therapeutic approach.
Purpose of the Study:
- To evaluate the efficacy and safety of oral eltrombopag in pediatric patients with chronic ITP.
- To assess eltrombopag's impact on platelet counts, bleeding events, and need for rescue therapy.
Main Methods:
- Randomized, double-blind, placebo-controlled phase II and III trials (PETIT and PETIT-2) were conducted.
- Eltrombopag (up to 75 mg/day) was administered orally for 7 or 13 weeks to patients aged 1-17 years.
- Longer-term open-label treatment assessed sustained efficacy and safety.
Main Results:
- Eltrombopag demonstrated significantly higher platelet response rates compared to placebo.
- A reduction in rescue therapy and clinically significant bleeding was observed with eltrombopag.
- Long-term treatment maintained platelet counts and allowed for reduction/discontinuation of other ITP medications in approximately half of patients.
Conclusions:
- Eltrombopag is effective in improving platelet counts and clinical outcomes in pediatric patients with chronic ITP.
- The drug is generally well-tolerated, representing a valuable addition to ITP management.
- Eltrombopag provides a new therapeutic avenue for children with inadequate response to first-line ITP treatments.
Abstract:
Eltrombopag (Promacta(®); Revolade(®)) is an orally active thrombopoietin receptor agonist recently approved in the USA and the EU for use in paediatric patients aged ≥1 year with chronic immune thrombocytopenia (ITP) who have had an insufficient response or are refractory to other ITP treatments (e.g. corticosteroids, immunoglobulins or splenectomy). The efficacy of 7 or 13 weeks' therapy with oral eltrombopag (up to 75 mg/day) was compared with that of placebo in patients aged 1-17 years with previously treated chronic ITP in randomized, double-blind, multicentre phase II and III trials (PETIT and PETIT-2). In these trials, the platelet response rate (primary endpoint of PETIT) and the sustained platelet response rate (primary endpoint of PETIT-2) were significantly higher with eltrombopag than with placebo. A clinical benefit was shown by a reduction in the need for rescue therapy with eltrombopag versus placebo in both trials and a reduction of clinically significant bleeding in PETIT. During longer-term therapy (open-label treatment period for ≥24 weeks), eltrombopag maintained platelet counts above 50 × 10(9)/L in the majority of patients and approximately one-half of patients were able to reduce or discontinue concurrent ITP drugs. Eltrombopag was generally well tolerated. Current evidence suggests that eltrombopag is a valuable addition to the limited treatment options available for the management of chronic ITP in paediatric patients with an inadequate response to first-line therapies.
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