Histiocytic Sarcoma Treated with Pembrolizumab: A Case Report and Literature Review

Daniel Huff, Shannon Fortin Ensign, Margaret S. Ryan, Jeanne Palmer, Javier Munoz
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Abstract

ABSTRACT Histiocytic sarcoma (HS) is a rare hematologic malignancy that has historically been treated with lymphoma-based regimens with a median survival of 6 months. We describe a case of a 51-year-old woman who presented with acute back pain and cord compression. She was diagnosed with HS with diffuse skeletal lesions and high expression of programmed death ligand 1 (PD-L1). She was subsequently treated with chemotherapy plus off-label use of pembrolizumab followed by allogeneic stem cell transplantation. Ultimately, patient died in the setting of progression of disease 17 months after her stem cell transplantation and 26 months after her diagnosis. This article also presents a literature review of cases of HS treated with programmed death ligand inhibition.
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派姆单抗治疗组织细胞肉瘤1例报告及文献回顾
组织细胞肉瘤(HS)是一种罕见的血液恶性肿瘤,历来以淋巴瘤为基础的治疗方案,中位生存期为6个月。我们描述了一个51岁的妇女谁提出了急性背痛和脊髓压迫的情况。她被诊断为HS,伴有弥漫性骨骼病变和程序性死亡配体1 (PD-L1)高表达。随后,她接受了化疗和超说明书使用派姆单抗的治疗,随后进行了异体干细胞移植。最终,患者在干细胞移植后17个月和诊断后26个月因疾病进展而死亡。本文还介绍了用程序死亡配体抑制治疗HS病例的文献综述。
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CiteScore
2.40
自引率
0.00%
发文量
17
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