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Esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports

BACKGROUND: Blocking the programmed death 1 pathway by immune checkpoint inhibitors induces dramatic antitumor activity in patients with malignant tumors. However, the clinical response to immune checkpoint inhibitors remains limited owing to the patients’ immunological status, such as the number of...

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Autores principales: Takimoto, Rishu, Kamigaki, Takashi, Gotoda, Takuji, Takahashi, Toshimi, Okada, Sachiko, Ibe, Hiroshi, Oguma, Eri, Goto, Shigenori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028114/
https://www.ncbi.nlm.nih.gov/pubmed/33827668
http://dx.doi.org/10.1186/s13256-020-02634-z
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author Takimoto, Rishu
Kamigaki, Takashi
Gotoda, Takuji
Takahashi, Toshimi
Okada, Sachiko
Ibe, Hiroshi
Oguma, Eri
Goto, Shigenori
author_facet Takimoto, Rishu
Kamigaki, Takashi
Gotoda, Takuji
Takahashi, Toshimi
Okada, Sachiko
Ibe, Hiroshi
Oguma, Eri
Goto, Shigenori
author_sort Takimoto, Rishu
collection PubMed
description BACKGROUND: Blocking the programmed death 1 pathway by immune checkpoint inhibitors induces dramatic antitumor activity in patients with malignant tumors. However, the clinical response to immune checkpoint inhibitors remains limited owing to the patients’ immunological status, such as the number of lymphocytes, programmed death ligand 1 expression, and tumor mutation burden. In this study, we successfully treated two patients with advanced esophageal cancer who responded to the combination of adoptive immune cell therapy and a low-dose immune checkpoint inhibitor, nivolumab. CASE PRESENTATION: Two Asian (Japanese) patients with advanced esophageal cancer who were resistant to conventional chemoradiation therapy were referred to our hospital for immune therapy. Case 1 was a 66-year-old woman who was diagnosed as having esophageal cancer. She received concurrent chemoradiation therapy and then underwent subtotal esophagectomy, after which she became cancer free. However, she relapsed, and cancer cells were found in the lung and lymph nodes 6 months later. She enrolled in a clinical trial at our institution (clinical trial number UMIN000028756). She received adoptive immune cell therapy twice at a 2-week interval followed by low-dose nivolumab with adoptive immune cell therapy four times at 2-week intervals. A follow-up computed tomography scan showed partial response, with mass reduction of the metastatic lung and mediastinal lesions. Case 2 was a 77-year-old man. He received concurrent chemoradiation therapy with fluoropyrimidine/platinum, and gastroscopy revealed complete remission of esophageal cancer. He was disease free for 5 months, but routine computed tomography revealed multiple metastases in his lungs and lymph nodes. He visited our clinic to receive adoptive immune cell therapy and immune checkpoint inhibitor combination therapy. Radiographic evidence showed continuous improvement of lesions. There was no evidence of severe adverse events during the combination therapy. CONCLUSION: The combination of adoptive immune cell therapy and an immune checkpoint inhibitor might be a possible treatment strategy for advanced esophageal cancer. Trial registration UMIN000028756. Registered 14 September 2017
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spelling pubmed-80281142021-04-08 Esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports Takimoto, Rishu Kamigaki, Takashi Gotoda, Takuji Takahashi, Toshimi Okada, Sachiko Ibe, Hiroshi Oguma, Eri Goto, Shigenori J Med Case Rep Case Report BACKGROUND: Blocking the programmed death 1 pathway by immune checkpoint inhibitors induces dramatic antitumor activity in patients with malignant tumors. However, the clinical response to immune checkpoint inhibitors remains limited owing to the patients’ immunological status, such as the number of lymphocytes, programmed death ligand 1 expression, and tumor mutation burden. In this study, we successfully treated two patients with advanced esophageal cancer who responded to the combination of adoptive immune cell therapy and a low-dose immune checkpoint inhibitor, nivolumab. CASE PRESENTATION: Two Asian (Japanese) patients with advanced esophageal cancer who were resistant to conventional chemoradiation therapy were referred to our hospital for immune therapy. Case 1 was a 66-year-old woman who was diagnosed as having esophageal cancer. She received concurrent chemoradiation therapy and then underwent subtotal esophagectomy, after which she became cancer free. However, she relapsed, and cancer cells were found in the lung and lymph nodes 6 months later. She enrolled in a clinical trial at our institution (clinical trial number UMIN000028756). She received adoptive immune cell therapy twice at a 2-week interval followed by low-dose nivolumab with adoptive immune cell therapy four times at 2-week intervals. A follow-up computed tomography scan showed partial response, with mass reduction of the metastatic lung and mediastinal lesions. Case 2 was a 77-year-old man. He received concurrent chemoradiation therapy with fluoropyrimidine/platinum, and gastroscopy revealed complete remission of esophageal cancer. He was disease free for 5 months, but routine computed tomography revealed multiple metastases in his lungs and lymph nodes. He visited our clinic to receive adoptive immune cell therapy and immune checkpoint inhibitor combination therapy. Radiographic evidence showed continuous improvement of lesions. There was no evidence of severe adverse events during the combination therapy. CONCLUSION: The combination of adoptive immune cell therapy and an immune checkpoint inhibitor might be a possible treatment strategy for advanced esophageal cancer. Trial registration UMIN000028756. Registered 14 September 2017 BioMed Central 2021-04-08 /pmc/articles/PMC8028114/ /pubmed/33827668 http://dx.doi.org/10.1186/s13256-020-02634-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Takimoto, Rishu
Kamigaki, Takashi
Gotoda, Takuji
Takahashi, Toshimi
Okada, Sachiko
Ibe, Hiroshi
Oguma, Eri
Goto, Shigenori
Esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports
title Esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports
title_full Esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports
title_fullStr Esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports
title_full_unstemmed Esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports
title_short Esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports
title_sort esophageal cancer responsive to the combination of immune cell therapy and low-dose nivolumab: two case reports
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028114/
https://www.ncbi.nlm.nih.gov/pubmed/33827668
http://dx.doi.org/10.1186/s13256-020-02634-z
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