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首例 SL-401(一种靶向 CD123 的疗法)治疗原始浆细胞样树突状细胞瘤患儿的临床经验:三例报告。

First pediatric experience of SL-401, a CD123-targeted therapy, in patients with blastic plasmacytoid dendritic cell neoplasm: report of three cases.

机构信息

Department of Pediatrics, City of Hope National Medical Center, 1500 E. Duarte Road, Duarte, CA, 91010, USA.

Department of Pediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

J Hematol Oncol. 2018 May 2;11(1):61. doi: 10.1186/s13045-018-0604-6.

Abstract

BACKGROUND

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a highly aggressive hematological malignancy with extremely poor outcome. The median overall survival for adult patients is 9-13 months. Pediatric patients are exceedingly rare with an unclear clinical course. Currently, no standardized therapy has been established, although an acute lymphoblastic leukemia type of treatment appears to be more effective in those patients who are able to tolerate aggressive chemotherapy. SL-401 is a targeted therapy directed to CD123, a protein ubiquitously expressed at high level on the surface of BPDCN blasts. In adult phase 2 trials, it has demonstrated efficacy with 90% overall response rate. No pediatric patients with BPDCN using SL-401 have been reported.

CASE PRESENTATION

Here, we report the first pediatric experience of three children with BPDCN treated with SL-401 at our institution. All patients tolerated SL-401 without significant toxicities. One patient with multiply relapsed and refractory disease had no response. The other two cases had significant and rapid clinical improvement after the two courses of treatment. However, the response was transient, and growth of soft tissue mass was observed in-between cycles in both patients with large tumor burden.

CONCLUSIONS

This is the first report of SL-401 in pediatric patients with BPDCN. Sl-401 was well tolerated and can produce a promising response. Further testing this agent in children is warranted.

摘要

背景

原始血液细胞瘤样树突细胞肿瘤(BPDCN)是一种高度侵袭性的血液恶性肿瘤,预后极差。成年患者的中位总生存期为 9-13 个月。儿科患者极为罕见,临床过程尚不清楚。目前,尚未确立标准化的治疗方法,尽管对于能够耐受强化化疗的患者,急性淋巴细胞白血病样治疗似乎更有效。SL-401 是一种针对 CD123 的靶向治疗药物,CD123 是一种在 BPDCN 原始细胞表面高水平广泛表达的蛋白。在成人阶段 2 试验中,它显示出 90%的总缓解率的疗效。尚未有使用 SL-401 治疗 BPDCN 的儿科患者的报道。

病例介绍

在这里,我们报告了在我们机构中使用 SL-401 治疗的三例 BPDCN 儿科患者的首次儿科经验。所有患者均耐受 SL-401,无明显毒性。一名患有多发复发和难治性疾病的患者没有反应。另外两例患者在接受两个疗程的治疗后,有显著且快速的临床改善。然而,反应是短暂的,并且在两个肿瘤负荷较大的患者中,在治疗周期之间观察到软组织肿块的生长。

结论

这是首例 SL-401 在儿科 BPDCN 患者中的报告。SL-401 耐受性良好,能产生有希望的反应。有必要进一步在儿童中测试该药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fb3/5932872/7692912c0200/13045_2018_604_Fig1_HTML.jpg

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