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

Author:

Huff Daniel1,Fortin Ensign Shannon2,Ryan Margaret S.3,Palmer Jeanne2,Munoz Javier2

Affiliation:

1. 1 Department of Internal Medicine, Mayo Clinic, Phoenix, AZ, USA

2. 2 Department of Hematology and Oncology, Mayo Clinic, Phoenix, AZ, USA

3. 3 Department of Pathology, Mayo Clinic, Phoenix, AZ, USA

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, the 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.

Publisher

Innovative Healthcare Institute

Subject

Cancer Research,Oncology,Immunology,Immunology and Allergy

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