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Personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report
BACKGROUND: Collecting duct carcinoma (CDC) of the kidney is a rare and highly aggressive malignant tumor with the worst prognosis among all renal cancers. Nevertheless, the first-line treatments, including chemotherapy and target therapy, usually show poor response to CDC. Recent studies have sugge...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247377/ https://www.ncbi.nlm.nih.gov/pubmed/32439798 http://dx.doi.org/10.1136/jitc-2019-000217 |
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author | Zeng, Yongyi Zhang, Wei Li, Zhenli Zheng, Youshi Wang, Yingchao Chen, Geng Qiu, Liman Ke, Kun Su, Xiaoping Cai, Zhixiong Liu, Jingfeng Liu, Xiaolong |
author_facet | Zeng, Yongyi Zhang, Wei Li, Zhenli Zheng, Youshi Wang, Yingchao Chen, Geng Qiu, Liman Ke, Kun Su, Xiaoping Cai, Zhixiong Liu, Jingfeng Liu, Xiaolong |
author_sort | Zeng, Yongyi |
collection | PubMed |
description | BACKGROUND: Collecting duct carcinoma (CDC) of the kidney is a rare and highly aggressive malignant tumor with the worst prognosis among all renal cancers. Nevertheless, the first-line treatments, including chemotherapy and target therapy, usually show poor response to CDC. Recent studies have suggested that immunotherapy targeting personal tumor-specific neoantigens could be a promising strategy for several solid cancers. However, whether it has therapeutic potential in CDC remains unclear. CASE PRESENTATION: Here, we report a case of an Asian patient who underwent personalized neoantigen-based immunotherapy. The patient was diagnosed with metastatic CDC and suffered extensive tumor progression following sorafenib treatment. Based on the patient’s own somatic mutational profile, a total of 13 neoantigens were identified and corresponding long-peptide vaccine and neoantigen-reactive T cells (NRTs) were prepared. After six cycles of neoantigen-based vaccination and T-cell immunotherapy, the patient was reported with stable disease status in tumor burden and significant alleviation of bone pain. Ex vivo interferon-γ enzyme-linked immunospot assay proved the reactivity to 12 of 13 neoantigens in peripheral blood mononuclear cells collected after immunotherapy, and the preferential reactivity to mutant peptides compared with corresponding wild-type peptides was also observed for 3 of the neoantigens. Surprisingly, biopsy sample collected from CDC sites after 3 months of immunotherapy showed decreased mutant allele frequency corresponding to 92% (12/13) of the neoantigens, indicating the elimination of tumor cells carrying these neoantigens. CONCLUSIONS: Our case report demonstrated that the combined therapy of neoantigen peptide vaccination and NRT cell infusion showed certain efficacy in this CDC case, even when the patient carried only a relatively low tumor mutation burden. These results indicated that the personalized neoantigen-based immunotherapy was a promising new strategy for advanced CDC. TRIAL REGISTRATION NUMBER: ChiCTR1800017836. |
format | Online Article Text |
id | pubmed-7247377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-72473772020-06-03 Personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report Zeng, Yongyi Zhang, Wei Li, Zhenli Zheng, Youshi Wang, Yingchao Chen, Geng Qiu, Liman Ke, Kun Su, Xiaoping Cai, Zhixiong Liu, Jingfeng Liu, Xiaolong J Immunother Cancer Case Report BACKGROUND: Collecting duct carcinoma (CDC) of the kidney is a rare and highly aggressive malignant tumor with the worst prognosis among all renal cancers. Nevertheless, the first-line treatments, including chemotherapy and target therapy, usually show poor response to CDC. Recent studies have suggested that immunotherapy targeting personal tumor-specific neoantigens could be a promising strategy for several solid cancers. However, whether it has therapeutic potential in CDC remains unclear. CASE PRESENTATION: Here, we report a case of an Asian patient who underwent personalized neoantigen-based immunotherapy. The patient was diagnosed with metastatic CDC and suffered extensive tumor progression following sorafenib treatment. Based on the patient’s own somatic mutational profile, a total of 13 neoantigens were identified and corresponding long-peptide vaccine and neoantigen-reactive T cells (NRTs) were prepared. After six cycles of neoantigen-based vaccination and T-cell immunotherapy, the patient was reported with stable disease status in tumor burden and significant alleviation of bone pain. Ex vivo interferon-γ enzyme-linked immunospot assay proved the reactivity to 12 of 13 neoantigens in peripheral blood mononuclear cells collected after immunotherapy, and the preferential reactivity to mutant peptides compared with corresponding wild-type peptides was also observed for 3 of the neoantigens. Surprisingly, biopsy sample collected from CDC sites after 3 months of immunotherapy showed decreased mutant allele frequency corresponding to 92% (12/13) of the neoantigens, indicating the elimination of tumor cells carrying these neoantigens. CONCLUSIONS: Our case report demonstrated that the combined therapy of neoantigen peptide vaccination and NRT cell infusion showed certain efficacy in this CDC case, even when the patient carried only a relatively low tumor mutation burden. These results indicated that the personalized neoantigen-based immunotherapy was a promising new strategy for advanced CDC. TRIAL REGISTRATION NUMBER: ChiCTR1800017836. BMJ Publishing Group 2020-05-20 /pmc/articles/PMC7247377/ /pubmed/32439798 http://dx.doi.org/10.1136/jitc-2019-000217 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Case Report Zeng, Yongyi Zhang, Wei Li, Zhenli Zheng, Youshi Wang, Yingchao Chen, Geng Qiu, Liman Ke, Kun Su, Xiaoping Cai, Zhixiong Liu, Jingfeng Liu, Xiaolong Personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report |
title | Personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report |
title_full | Personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report |
title_fullStr | Personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report |
title_full_unstemmed | Personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report |
title_short | Personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report |
title_sort | personalized neoantigen-based immunotherapy for advanced collecting duct carcinoma: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247377/ https://www.ncbi.nlm.nih.gov/pubmed/32439798 http://dx.doi.org/10.1136/jitc-2019-000217 |
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