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尼伏单抗和丁酸钠在两名难治性神经母细胞瘤患者中的应用。

Nivolumab and dinutuximab beta in two patients with refractory neuroblastoma.

机构信息

Department of Pediatric Hematology and Oncology, Greifswald University Medicine, Greifswald, Germany

Department of Pediatric Hematology and Oncology, Greifswald University Medicine, Greifswald, Germany.

出版信息

J Immunother Cancer. 2020 May;8(1). doi: 10.1136/jitc-2020-000540.

Abstract

BACKGROUND

Neuroblastoma (NB) is the most frequent extracranial solid tumor in children. More than 50% of patients present with widespread (stage M) or refractory disease. In these patients, event-free and overall survival was improved by the addition of the anti-disialoganglioside antibody dinutuximab beta (DB) following multimodal conventional therapy. However, the prognosis of patients with refractory/relapsed NB remains poor. In the past decade, immunotherapy approaches with checkpoint inhibitors were approved for patients with certain malignant diseases such as melanoma or Hodgkin lymphoma. In preclinical models, DB resulted in an upregulation of the programmed cell death protein 1 (PD-1) checkpoint in NB cell lines and a combined treatment of DB with a murine anti-PD-1 checkpoint inhibitor showed a synergistic effect in a NB mouse model.

CASE PRESENTATIONS

Two patients were admitted with refractory metastatic NB. In the 4-year-old girl, NB was diagnosed in 2013. She completed her first-line therapy with a first remission in 2015, but suffered a relapse in 2017. Treatment with chemotherapy and DB resulted in progressive disease after transient improvement. In the 17-year-old young man, NB was first diagnosed in April 2010. After two local relapses in 2011 and 2014, a metastatic relapse and a large abdominal tumor bulk were found in 2018. Despite transient improvement with multimodal therapy, progressive metastatic disease was observed in May 2019. Both patients had a satisfactory quality of life. Therefore, treatment with DB and nivolumab was performed-in the girl from October 2018 until August 2019, in the young man since June 2019. Tolerance to treatment was excellent. The girl continues to be in complete remission 6 months after therapy was stopped. In the young man, the soft tissue lesions disappeared completely, the skeletal lesions regressed substantially after 9 months of his still ongoing treatment.

CONCLUSIONS

The combination of DB with the checkpoint inhibitor nivolumab led to complete and a very good partial remission in two patients with relapsed/refractory NB. Prospective trials are warranted to clarify the role of this novel approach in a larger number of patients.

摘要

背景

神经母细胞瘤(NB)是儿童最常见的颅外实体瘤。超过 50%的患者存在广泛(M 期)或难治性疾病。在这些患者中,在多模式常规治疗的基础上,添加抗二唾液酸神经节苷脂抗体丁酸钠(DB)可改善无事件生存和总生存。然而,难治性/复发性 NB 患者的预后仍然较差。在过去的十年中,免疫检查点抑制剂的免疫治疗方法已被批准用于某些恶性疾病,如黑色素瘤或霍奇金淋巴瘤。在临床前模型中,DB 导致 NB 细胞系中程序性死亡蛋白 1(PD-1)检查点上调,DB 与鼠抗 PD-1 检查点抑制剂联合治疗在 NB 小鼠模型中显示协同作用。

病例介绍

两名患者因难治性转移性 NB 入院。在 4 岁女孩中,2013 年诊断为 NB。她于 2015 年首次缓解,首次接受一线治疗,但于 2017 年复发。化疗和 DB 治疗导致疾病进展,短暂缓解后病情恶化。在 17 岁的年轻男性中,2010 年 4 月首次诊断为 NB。2011 年和 2014 年两次局部复发后,2018 年发现转移性复发和巨大腹部肿瘤。尽管采用多模式治疗后短暂缓解,但 2019 年 5 月观察到转移性疾病进展。两名患者的生活质量均满意。因此,从 2018 年 10 月至 2019 年 8 月对女孩,自 2019 年 6 月对男孩,给予 DB 和纳武单抗治疗。治疗耐受性良好。治疗停止后 6 个月,女孩持续完全缓解。在男孩中,软组织病变完全消失,骨骼病变在 9 个月的治疗后显著消退,仍在持续。

结论

DB 与检查点抑制剂纳武单抗联合应用于两名复发性/难治性 NB 患者,导致完全缓解和非常好的部分缓解。需要前瞻性试验来明确这种新方法在更多患者中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca2b/7239695/7176b9e46570/jitc-2020-000540f01.jpg

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