Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancer

Adoptive transfer of autologous tumor-specific lymphocytes represents a viable treatment method for patients with advanced malignancies. Here, we report a patient’s case with metastatic hormone-refractory New York esophageal squamous cell carcinoma 1 (NY-ESO-1) expressing prostate cancer treated wit...

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Main Authors: Elke Jäger, Julia Karbach, Claudia Wahle, Dragan Kiselicki, Kathrin Brand, Evgueni Sinelnikov, Dirk Gustavus, Hans Hoffmeister, Hans-Bernd Prisack, Akin Atmaca
Format: Article
Language:English
Published: BMJ Publishing Group 2023-01-01
Series:Journal for ImmunoTherapy of Cancer
Online Access:https://jitc.bmj.com/content/11/1/e005847.full
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author Elke Jäger
Julia Karbach
Claudia Wahle
Dragan Kiselicki
Kathrin Brand
Evgueni Sinelnikov
Dirk Gustavus
Hans Hoffmeister
Hans-Bernd Prisack
Akin Atmaca
author_facet Elke Jäger
Julia Karbach
Claudia Wahle
Dragan Kiselicki
Kathrin Brand
Evgueni Sinelnikov
Dirk Gustavus
Hans Hoffmeister
Hans-Bernd Prisack
Akin Atmaca
author_sort Elke Jäger
collection DOAJ
description Adoptive transfer of autologous tumor-specific lymphocytes represents a viable treatment method for patients with advanced malignancies. Here, we report a patient’s case with metastatic hormone-refractory New York esophageal squamous cell carcinoma 1 (NY-ESO-1) expressing prostate cancer treated with in vitro expanded tumor-infiltrating lymphocytes (TILs) in conjunction with IL-2 and immune-checkpoint blockade. Complete and durable tumor remission was observed after three TIL infusions consisting of 1.4×109, 2.0×109, and 8.0×109 T cells, respectively, lasting now for more than 3.5 years. Immunological correlates to the clinical development were the decrease of tumor-driven NY-ESO-1 serum antibody and the drop of prostate-specific antigen to <0.01 µg/L. TILs were reactive against cancer-testis antigen NY-ESO-1, individual tumor mutational proteins (eg, PRPF8, TRPS1), and the androgen receptor splice variant 12.
format Article
id doaj-art-59a10633aff74d6bb16b5bc67cc12c34
institution Kabale University
issn 2051-1426
language English
publishDate 2023-01-01
publisher BMJ Publishing Group
record_format Article
series Journal for ImmunoTherapy of Cancer
spelling doaj-art-59a10633aff74d6bb16b5bc67cc12c342025-01-29T11:05:09ZengBMJ Publishing GroupJournal for ImmunoTherapy of Cancer2051-14262023-01-0111110.1136/jitc-2022-005847Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancerElke Jäger0Julia Karbach1Claudia Wahle2Dragan Kiselicki3Kathrin Brand4Evgueni Sinelnikov5Dirk Gustavus6Hans Hoffmeister7Hans-Bernd Prisack8Akin Atmaca91 Oncology and Hematology, Krankenhaus Nordwest, Frankfurt, Germany1 Oncology and Hematology, Krankenhaus Nordwest, Frankfurt, Germany1 Oncology and Hematology, Krankenhaus Nordwest, Frankfurt, Germany1 Oncology and Hematology, Krankenhaus Nordwest, Frankfurt, Germany1 Oncology and Hematology, Krankenhaus Nordwest, Frankfurt, Germany2 Zellwerk GmbH, Oberkrämer, Germany2 Zellwerk GmbH, Oberkrämer, Germany2 Zellwerk GmbH, Oberkrämer, Germany3 NextGen Oncology, Düsseldorf, Germany1Krankenhaus Nordwest, UCT-University Cancer Center, Frankfurt, GermanyAdoptive transfer of autologous tumor-specific lymphocytes represents a viable treatment method for patients with advanced malignancies. Here, we report a patient’s case with metastatic hormone-refractory New York esophageal squamous cell carcinoma 1 (NY-ESO-1) expressing prostate cancer treated with in vitro expanded tumor-infiltrating lymphocytes (TILs) in conjunction with IL-2 and immune-checkpoint blockade. Complete and durable tumor remission was observed after three TIL infusions consisting of 1.4×109, 2.0×109, and 8.0×109 T cells, respectively, lasting now for more than 3.5 years. Immunological correlates to the clinical development were the decrease of tumor-driven NY-ESO-1 serum antibody and the drop of prostate-specific antigen to <0.01 µg/L. TILs were reactive against cancer-testis antigen NY-ESO-1, individual tumor mutational proteins (eg, PRPF8, TRPS1), and the androgen receptor splice variant 12.https://jitc.bmj.com/content/11/1/e005847.full
spellingShingle Elke Jäger
Julia Karbach
Claudia Wahle
Dragan Kiselicki
Kathrin Brand
Evgueni Sinelnikov
Dirk Gustavus
Hans Hoffmeister
Hans-Bernd Prisack
Akin Atmaca
Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancer
Journal for ImmunoTherapy of Cancer
title Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancer
title_full Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancer
title_fullStr Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancer
title_full_unstemmed Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancer
title_short Tumor-infiltrating lymphocytes mediate complete and durable remission in a patient with NY-ESO-1 expressing prostate cancer
title_sort tumor infiltrating lymphocytes mediate complete and durable remission in a patient with ny eso 1 expressing prostate cancer
url https://jitc.bmj.com/content/11/1/e005847.full
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