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神经母细胞瘤免疫治疗的靶点和抗体形式。

Targets and Antibody Formats for Immunotherapy of Neuroblastoma.

机构信息

Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, NY.

出版信息

J Clin Oncol. 2020 Jun 1;38(16):1836-1848. doi: 10.1200/JCO.19.01410. Epub 2020 Mar 13.

Abstract

Neuroblastoma (NB) is a malignant embryonal tumor of the sympathetic nervous system that is most commonly diagnosed in the abdomen, often presenting with signs and symptoms of metastatic spread. Three decades ago, high-risk NB metastatic to bone and bone marrow in children was not curable. Today, with multimodality treatment, 50% of these patients will survive, but most suffer from debilitating treatment-related complications. Novel targeted therapies to improve cure rates while minimizing toxicities are urgently needed. Recent molecular discoveries in oncology have spawned the development of an impressive array of targeted therapies for adult cancers, yet the paucity of recurrent somatic mutations or activated oncogenes in pediatric cancers poses a major challenge to the evolving paradigm of personalized medicine. Although low tumor mutational burden is a major hurdle for immune checkpoint inhibitors, an immature or impaired immune system and inhibitory tumor microenvironment can further complicate the prospects for successful immunotherapy. In this regard, despite the poor immunogenic properties of NB, the success of antibody-based immunotherapy and radioimmunotherapy directed at single targets (eg, GD2 and B7-H3) is both encouraging and surprising, given that most solid tumor antibodies that use Fc-dependent mechanisms or radioimmunotargeting have largely failed. Here, we summarize the current information on the immunologic properties of this tumor, its potential immunotherapeutic targets, and novel antibody-based strategies on the horizon.

摘要

神经母细胞瘤(NB)是交感神经系统的恶性胚胎肿瘤,最常发生在腹部,常伴有转移扩散的迹象和症状。三十年前,儿童高危 NB 转移至骨骼和骨髓是无法治愈的。如今,采用多模式治疗,这些患者中有 50%可以存活,但大多数患者都遭受着使人衰弱的治疗相关并发症的折磨。迫切需要新型靶向疗法来提高治愈率,同时最大限度地减少毒性。最近肿瘤学中的分子发现催生了一系列针对成人癌症的令人印象深刻的靶向疗法,但儿科癌症中复发性体细胞突变或激活的致癌基因的缺乏,对个性化医学这一不断发展的范式构成了重大挑战。尽管低肿瘤突变负担是免疫检查点抑制剂的主要障碍,但不成熟或受损的免疫系统和抑制性肿瘤微环境可能会使成功免疫治疗的前景更加复杂。在这方面,尽管 NB 的免疫原性较差,但针对单一靶点(例如 GD2 和 B7-H3)的基于抗体的免疫疗法和放射免疫疗法的成功,既令人鼓舞,又令人惊讶,因为大多数使用 Fc 依赖性机制或放射免疫靶向的实体瘤抗体在很大程度上都失败了。在这里,我们总结了关于该肿瘤免疫特性、潜在免疫治疗靶点以及新型基于抗体的策略的最新信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89f/7255979/380e8c857913/JCO.19.01410f1.jpg

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