Thrombopoietin Receptor Agonists for Thrombocytopenia in Pediatric Hematologic Malignancies

IF 2.4 3区 医学 Q2 HEMATOLOGY Pediatric Blood & Cancer Pub Date : 2025-01-08 DOI:10.1002/pbc.31528
Amanda E. Marinoff, Allyson Thrall, Kathryn Aaronson, Benjamin S. Braun, Maria Castellanos, Julia Chu, Michelle Hermiston, Benjamin J. Huang, Anya Levinson, Erica Southworth, Beth Apsel Winger, Adam Olshen, Elliot Stieglitz
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Abstract

Background

Thrombopoietin receptor agonists (TPO-RAs) have demonstrated efficacy in treating clinically significant thrombocytopenia, including chemotherapy-induced thrombocytopenia in adults. However, data regarding their safety and efficacy in pediatric, adolescents, and young adult (AYA) patients with hematologic malignancies are limited.

Methods

We retrospectively identified 15 pediatric and AYA patients aged 25 years or younger with hematologic malignancies treated with a TPO-RA at UCSF Benioff Children's Hospitals between 2015 and 2023. Platelet counts and transfusion requirements were compared before and after TPO-RA therapy.

Results

The median age at TPO-RA initiation was 16 years (range: 7–25 years). Nine patients (60%) had a history of bleeding or comorbidity that predisposed to severe bleeding risk. Eleven patients received romiplostim and four patients received eltrombopag. The median platelet count significantly increased from 24 × 109/L at baseline to 54 × 109/L after 3 weeks of any TPO-RA therapy (p = 0.029). Monthly platelet transfusion requirements significantly decreased from a median of 15 to two units after TPO-RA therapy (p = 0.007). Fourteen of the 15 patients (93%) achieved a sustained platelet count >50,000/µL within 8 weeks, with a median time to response of 3 weeks. No TPO-RA-related adverse events were observed.

Conclusion

TPO-RAs were effective in managing refractory thrombocytopenia in pediatric and young adult patients being treated for hematologic malignancies, with a favorable safety profile, even among patients with multiple comorbidities. These findings warrant further investigation through prospective clinical trials to confirm efficacy and establish clinical guidelines for this population.

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血小板生成素受体激动剂治疗儿童血液恶性肿瘤中的血小板减少症。
背景:血小板生成素受体激动剂(TPO-RAs)已被证明对治疗临床显著的血小板减少症有效,包括化疗引起的成人血小板减少症。然而,关于其在儿童、青少年和年轻成人(AYA)血液恶性肿瘤患者中的安全性和有效性的数据有限。方法:我们回顾性研究了2015年至2023年在UCSF Benioff儿童医院接受TPO-RA治疗的15例25岁或以下的儿科和AYA血液恶性肿瘤患者。比较TPO-RA治疗前后血小板计数和输血需要量。结果:TPO-RA起始的中位年龄为16岁(范围:7-25岁)。9例患者(60%)有出血史或合并症,易发生严重出血风险。11例患者使用罗米普罗斯汀,4例患者使用伊曲波巴。血小板中位数从基线时的24 × 109/L显著增加到TPO-RA治疗3周后的54 × 109/L (p = 0.029)。TPO-RA治疗后,每月血小板输注需要量从中位数15个单位显著降低至2个单位(p = 0.007)。15例患者中有14例(93%)在8周内达到持续血小板计数bb50万/µL,中位反应时间为3周。未观察到tpo - ra相关不良事件。结论:TPO-RAs对于治疗血液系统恶性肿瘤的儿童和年轻成人患者的难治性血小板减少症是有效的,具有良好的安全性,即使在患有多种合并症的患者中也是如此。这些发现值得通过前瞻性临床试验进一步调查,以确认疗效并为这一人群建立临床指南。
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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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