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Published on: June 14, 2015
Relationship between response to lusutrombopag and splenic volume
Haruki Uojima1, Yoshitaka Arase2, Norio Itokawa3
1Department of Gastroenterology, Shonan Kamakura General Hospital, Kamakura 247-8533, Japan.
Insights
Splenic volume impacts lusutrombopag efficacy in chronic liver disease patients. Lower splenic volume correlated with increased platelet counts, suggesting it
Area of Science:
- Hepatology
- Hematology
- Pharmacology
Background:
- Chronic liver disease (CLD) frequently leads to thrombocytopenia, increasing bleeding risk.
- Lusutrombopag is a thrombopoietin receptor agonist used to increase platelet counts.
- Predictors of lusutrombopag response in CLD patients require further investigation.
Purpose of the Study:
- To evaluate the correlation between lusutrombopag efficacy and patient clinical characteristics.
- To identify factors influencing treatment response in thrombocytopenic CLD patients.
Main Methods:
- Retrospective, multicenter study of 50 thrombocytopenic CLD patients in Japan.
- Patients received oral lusutrombopag (3.0 mg/day for 7 days).
- Treatment response defined by specific platelet count increases post-administration.
Main Results:
- 80% of patients responded to lusutrombopag.
- Responders had significantly lower splenic volume and body weight compared to non-responders.
- Higher white blood cell count and hemoglobin levels were observed in responders.
- Multivariate analysis identified splenic volume as an independent predictor of response (OR=11.2, P=0.025).
- Splenic volume negatively correlated with changes in platelet count (r=-0.524, P=0.001).
Conclusions:
- Splenic volume is a key factor influencing platelet count changes after lusutrombopag administration in CLD patients.
- This finding may aid in predicting treatment outcomes and optimizing therapy.
Aim:
To assess the correlation between the efficacy of lusutrombopag and clinical characteristics in patients with chronic liver disease.
Methods:
In this retrospective, multicenter study, which conducted at four locations in Japan, 50 thrombocytopenic patients with chronic liver disease were enrolled. All patients received oral lusutrombopag (3.0 mg/d for 7 d) for chronic liver disease. We assessed the increase in platelet count after the trial drug administration. A treatment response was defined as a platelet count ≥ 5 × 104/μL and an increased platelet count ≥ 2 × 104/μL from baseline after drug administration. We evaluated the response to lusutrombopag compared to baseline clinical characteristics in patients with chronic liver disease.
Results:
The numbers of responders and non-responders were 40 (80.0%) and 10 (20.0%), respectively. The patients were divided into a responder and non-responder group, and we added factors that may correspond to successful treatment with lusutrombopag. Splenic volume and body weight were lower in the responder group than in the non-responder group. White blood cell count and hemoglobin level were higher in responders compared with non-responders. Using a logistic regression model to assess the relationship between response to lusutrombopag and clinical characteristics, multivariate analysis confirmed that splenic volume was an independent factor that predicted the response of platelet counts (P = 0.025; odds ratio = 11.2; 95% confidence interval: 1.354-103.0). Splenic volume negatively correlated to changes in platelet count (r = -0.524, P = 0.001).
Conclusion:
Splenic volume influences the change in platelet counts after administration of lusutrombopag in patients with chronic liver disease.
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