» Articles » PMID: 30581275

Relationship Between Response to Lusutrombopag and Splenic Volume

Abstract

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 × 10/μL and an increased platelet count ≥ 2 × 10/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 ( = 0.025; odds ratio = 11.2; 95% confidence interval: 1.354-103.0). Splenic volume negatively correlated to changes in platelet count ( = -0.524, = 0.001).

Conclusion: Splenic volume influences the change in platelet counts after administration of lusutrombopag in patients with chronic liver disease.

Citing Articles

Evaluation of the Efficacy of Lusutrombopag for Chronic Liver Disease Based on Pre-Treatment Platelet Counts: A Retrospective Multicenter Study.

Suga T, Kakizaki S, Naganuma A, Hatanaka T, Takakusagi S, Takizawa D JGH Open. 2025; 9(1):e70081.

PMID: 39742152 PMC: 11686089. DOI: 10.1002/jgh3.70081.


A study on prevention of bleeding complications using lusutrombopag for safe RFA in patients with hepatocellular carcinoma with low platelet counts: prospective observational study.

Yoshida H, Ohki T, Kanezaki M, Teratani T, Sato S, Obi S BMC Gastroenterol. 2023; 23(1):250.

PMID: 37488476 PMC: 10364390. DOI: 10.1186/s12876-023-02879-0.


Thrombocytopenia in chronic liver disease: Physiopathology and new therapeutic strategies before invasive procedures.

Gallo P, Terracciani F, Di Pasquale G, Esposito M, Picardi A, Vespasiani-Gentilucci U World J Gastroenterol. 2022; 28(30):4061-4074.

PMID: 36157107 PMC: 9403422. DOI: 10.3748/wjg.v28.i30.4061.


Assessing the periprocedural magnitude of platelet count change in response to lusutrombopag.

Brown Jr R, Imawari M, Izumi N, Osaki Y, Bentley R, Ochiai T JHEP Rep. 2021; 3(2):100228.

PMID: 33644726 PMC: 7887643. DOI: 10.1016/j.jhepr.2021.100228.


Lusutrombopag is effective and safe in patients with chronic liver disease and severe thrombocytopenia: a multicenter retrospective study.

Nomoto H, Morimoto N, Miura K, Watanabe S, Takaoka Y, Maeda H BMC Gastroenterol. 2020; 20(1):427.

PMID: 33317473 PMC: 7737263. DOI: 10.1186/s12876-020-01573-9.


References
1.
Hayashi H, Beppu T, Okabe K, Masuda T, Okabe H, Baba H . Risk factors for complications after partial splenic embolization for liver cirrhosis. Br J Surg. 2008; 95(6):744-50. DOI: 10.1002/bjs.6081. View

2.
Eichner E . Splenic function: normal, too much and too little. Am J Med. 1979; 66(2):311-20. DOI: 10.1016/0002-9343(79)90554-0. View

3.
Grotzinger K, Younossi Z, Giannini E, Chen P, Rendas-Baum R, Theodore D . Health-related quality of life in thrombocytopenic patients with chronic hepatitis C with or without cirrhosis in the ENABLE-1 and ENABLE-2 studies. Health Qual Life Outcomes. 2016; 14:49. PMC: 4802726. DOI: 10.1186/s12955-016-0447-1. View

4.
Wong R, Saleh M, Khelif A, Salama A, Portella M, Burgess P . Safety and efficacy of long-term treatment of chronic/persistent ITP with eltrombopag: final results of the EXTEND study. Blood. 2017; 130(23):2527-2536. DOI: 10.1182/blood-2017-04-748707. View

5.
Kim E . Lusutrombopag: First Global Approval. Drugs. 2015; 76(1):155-8. DOI: 10.1007/s40265-015-0525-4. View