Tocilizumab Controls Paraneoplastic Inflammatory Syndrome but Does Not Suppress Tumor Growth of Angiomatoid Fibrous Histiocytoma.

IF 0.6 Q4 ONCOLOGY Case Reports in Oncological Medicine Pub Date : 2021-06-16 eCollection Date: 2021-01-01 DOI:10.1155/2021/5532258
Hideaki Sabe, Akitomo Inoue, Shigenori Nagata, Yoshinori Imura, Toru Wakamatsu, Satoshi Takenaka, Hironari Tamiya
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引用次数: 2

Abstract

Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor that rarely metastasizes but lacks effective systemic therapy once it propagates. In some reports, high interleukin-6 (IL-6) production promotes tumor growth by autocrine stimulation and tocilizumab, an IL-6 receptor antagonist, can control AFH growth. Here, we present a case report on a patient with local recurrence and distant lymph node metastasis of AFH treated with tocilizumab. As a result, the inhibition of the IL-6 signaling pathway controlled paraneoplastic inflammatory syndrome (PIS); however, the local recurrent tumor progressed. This case implied that IL-6 is not necessarily the cause of tumor growth in AFH. Therefore, physicians should bear in mind that watchful observation is needed whether tocilizumab can control tumor progression despite the amelioration of PIS associated with the attenuated effect of IL-6 on AFH.

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Tocilizumab控制副肿瘤炎症综合征,但不抑制血管瘤样纤维组织细胞瘤的肿瘤生长。
血管瘤样纤维组织细胞瘤(AFH)是一种罕见的软组织肿瘤,很少转移,但一旦扩散缺乏有效的全身治疗。在一些报道中,高水平的白细胞介素-6 (IL-6)产生通过自分泌刺激促进肿瘤生长,而IL-6受体拮抗剂tocilizumab可以控制AFH的生长。在这里,我们提出了一个病例报告的病人局部复发和远处淋巴结转移的AFH治疗托珠单抗。因此,抑制IL-6信号通路控制副肿瘤炎症综合征(PIS);然而,局部复发肿瘤进展。本病例提示IL-6不一定是AFH中肿瘤生长的原因。因此,尽管PIS的改善与IL-6对AFH的减弱作用相关,但托珠单抗是否能控制肿瘤进展仍需密切观察。
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来源期刊
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发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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