Cargando…
Exceptionally rapid response to pembrolizumab in a SMARCA4‐deficient thoracic sarcoma overexpressing PD‐L1: A case report
SMARCA4‐deficient thoracic sarcoma (SMARCA4‐DTS) is a new clinical entity characterized by SMARCA4 inactivation and has a dismal prognosis because of rapid growth. Effective treatments for SMARCA4‐DTS have not yet been developed. Most recently, anti‐programmed cell death 1 receptor (PD‐1) blockade h...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885443/ https://www.ncbi.nlm.nih.gov/pubmed/31617320 http://dx.doi.org/10.1111/1759-7714.13215 |
_version_ | 1783474739306561536 |
---|---|
author | Takada, Kohichi Sugita, Shintaro Murase, Kazuyuki Kikuchi, Tomoki Oomori, Ginji Ito, Ryo Hayasaka, Naotaka Miyanishi, Koji Iyama, Satoshi Ikeda, Hiroshi Kobune, Masayoshi Emori, Makoto Kato, Junji Hasegawa, Tadashi |
author_facet | Takada, Kohichi Sugita, Shintaro Murase, Kazuyuki Kikuchi, Tomoki Oomori, Ginji Ito, Ryo Hayasaka, Naotaka Miyanishi, Koji Iyama, Satoshi Ikeda, Hiroshi Kobune, Masayoshi Emori, Makoto Kato, Junji Hasegawa, Tadashi |
author_sort | Takada, Kohichi |
collection | PubMed |
description | SMARCA4‐deficient thoracic sarcoma (SMARCA4‐DTS) is a new clinical entity characterized by SMARCA4 inactivation and has a dismal prognosis because of rapid growth. Effective treatments for SMARCA4‐DTS have not yet been developed. Most recently, anti‐programmed cell death 1 receptor (PD‐1) blockade has been effective for SMARCA4‐deficient lung cancer and malignant rhabdoid tumor‐like tumors. Here, we describe a patient with SMARCA4‐DTC who experienced a marked response to the administration of pembrolizumab. A 70‐year‐old female was referred to our department for treatment of SMARCA4‐DTC. Positron emission tomography‐computed tomography had revealed a left mediastinal tumor, peritoneal dissemination and multiple cutaneous metastases at diagnosis. Immunohistochemical analyses revealed 60% of tumor cells expressed programmed cell death ligand 1 (PD‐L1). The patient was given pembrolizumab as first‐line treatment. Pembrolizumab suppressed tumor growth dramatically, with only one dose leading to a partial response. Our case suggests the immunohistochemical analysis of PD‐L1 expression be undertaken for patients with SMARCA4‐DTS and that pembrolizumab treatment may be a promising strategy for PD‐L1‐positive SMARCA4‐DTS. |
format | Online Article Text |
id | pubmed-6885443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68854432019-12-09 Exceptionally rapid response to pembrolizumab in a SMARCA4‐deficient thoracic sarcoma overexpressing PD‐L1: A case report Takada, Kohichi Sugita, Shintaro Murase, Kazuyuki Kikuchi, Tomoki Oomori, Ginji Ito, Ryo Hayasaka, Naotaka Miyanishi, Koji Iyama, Satoshi Ikeda, Hiroshi Kobune, Masayoshi Emori, Makoto Kato, Junji Hasegawa, Tadashi Thorac Cancer Case Reports SMARCA4‐deficient thoracic sarcoma (SMARCA4‐DTS) is a new clinical entity characterized by SMARCA4 inactivation and has a dismal prognosis because of rapid growth. Effective treatments for SMARCA4‐DTS have not yet been developed. Most recently, anti‐programmed cell death 1 receptor (PD‐1) blockade has been effective for SMARCA4‐deficient lung cancer and malignant rhabdoid tumor‐like tumors. Here, we describe a patient with SMARCA4‐DTC who experienced a marked response to the administration of pembrolizumab. A 70‐year‐old female was referred to our department for treatment of SMARCA4‐DTC. Positron emission tomography‐computed tomography had revealed a left mediastinal tumor, peritoneal dissemination and multiple cutaneous metastases at diagnosis. Immunohistochemical analyses revealed 60% of tumor cells expressed programmed cell death ligand 1 (PD‐L1). The patient was given pembrolizumab as first‐line treatment. Pembrolizumab suppressed tumor growth dramatically, with only one dose leading to a partial response. Our case suggests the immunohistochemical analysis of PD‐L1 expression be undertaken for patients with SMARCA4‐DTS and that pembrolizumab treatment may be a promising strategy for PD‐L1‐positive SMARCA4‐DTS. John Wiley & Sons Australia, Ltd 2019-10-16 2019-12 /pmc/articles/PMC6885443/ /pubmed/31617320 http://dx.doi.org/10.1111/1759-7714.13215 Text en © 2019 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Takada, Kohichi Sugita, Shintaro Murase, Kazuyuki Kikuchi, Tomoki Oomori, Ginji Ito, Ryo Hayasaka, Naotaka Miyanishi, Koji Iyama, Satoshi Ikeda, Hiroshi Kobune, Masayoshi Emori, Makoto Kato, Junji Hasegawa, Tadashi Exceptionally rapid response to pembrolizumab in a SMARCA4‐deficient thoracic sarcoma overexpressing PD‐L1: A case report |
title | Exceptionally rapid response to pembrolizumab in a SMARCA4‐deficient thoracic sarcoma overexpressing PD‐L1: A case report |
title_full | Exceptionally rapid response to pembrolizumab in a SMARCA4‐deficient thoracic sarcoma overexpressing PD‐L1: A case report |
title_fullStr | Exceptionally rapid response to pembrolizumab in a SMARCA4‐deficient thoracic sarcoma overexpressing PD‐L1: A case report |
title_full_unstemmed | Exceptionally rapid response to pembrolizumab in a SMARCA4‐deficient thoracic sarcoma overexpressing PD‐L1: A case report |
title_short | Exceptionally rapid response to pembrolizumab in a SMARCA4‐deficient thoracic sarcoma overexpressing PD‐L1: A case report |
title_sort | exceptionally rapid response to pembrolizumab in a smarca4‐deficient thoracic sarcoma overexpressing pd‐l1: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885443/ https://www.ncbi.nlm.nih.gov/pubmed/31617320 http://dx.doi.org/10.1111/1759-7714.13215 |
work_keys_str_mv | AT takadakohichi exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT sugitashintaro exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT murasekazuyuki exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT kikuchitomoki exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT oomoriginji exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT itoryo exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT hayasakanaotaka exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT miyanishikoji exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT iyamasatoshi exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT ikedahiroshi exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT kobunemasayoshi exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT emorimakoto exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT katojunji exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport AT hasegawatadashi exceptionallyrapidresponsetopembrolizumabinasmarca4deficientthoracicsarcomaoverexpressingpdl1acasereport |