Marinoff Amanda E, Thrall Allyson, Aaronson Kathryn, Braun Benjamin S, Castellanos Maria, Chu Julia, Hermiston Michelle, Huang Benjamin J, Levinson Anya, Southworth Erica, Winger Beth Apsel, Olshen Adam, Stieglitz Elliot
Department of Pediatrics, Benioff Children's Hospitals, University of California, San Francisco, California, USA.
VinUniversity (Trường Đại học VinUni), Vinhomes Ocean Park, Gia Lâm, Vietnam.
Pediatr Blood Cancer. 2025 Mar;72(3):e31528. doi: 10.1002/pbc.31528. Epub 2025 Jan 8.
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.
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.
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 × 10/L at baseline to 54 × 10/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.
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.
血小板生成素受体激动剂(TPO-RAs)已被证明在治疗临床上显著的血小板减少症方面有效,包括成人化疗引起的血小板减少症。然而,关于其在患有血液系统恶性肿瘤的儿科、青少年和年轻成人(AYA)患者中的安全性和有效性的数据有限。
我们回顾性确定了2015年至2023年间在加州大学旧金山分校贝尼奥夫儿童医院接受TPO-RA治疗的15名25岁及以下患有血液系统恶性肿瘤的儿科和AYA患者。比较了TPO-RA治疗前后的血小板计数和输血需求。
开始使用TPO-RA时的中位年龄为16岁(范围:7 - 25岁)。9名患者(60%)有出血史或合并症,这些因素使他们有严重出血风险。11名患者接受了罗米司亭治疗,4名患者接受了艾曲泊帕治疗。在接受任何TPO-RA治疗3周后,中位血小板计数从基线时的24×10⁹/L显著增加至54×10⁹/L(p = 0.029)。TPO-RA治疗后每月血小板输注需求从中位数15单位显著降至2单位(p = 0.007)。15名患者中有14名(93%)在8周内血小板计数持续>50,000/µL,中位反应时间为3周。未观察到与TPO-RA相关的不良事件。
TPO-RAs在治疗患有血液系统恶性肿瘤的儿科和年轻成人患者的难治性血小板减少症方面有效,安全性良好,即使在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研究,以确认疗效并为该人群建立临床指南。