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| Main Authors: | , , , , , , , , , , , |
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| Format: | Artículo Open Access |
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Wiley
2024
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| Online Access: | https://pathsocjournals.onlinelibrary.wiley.com/doi/10.1002/path.6334 |
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| author | Zakhia El Beaino Célia Dupain Grégoire Marret Xavier Paoletti Laëtitia Fuhrmann Charlotte Martinat Yves Allory Maral Halladjian Ivan Bièche Christophe Le Tourneau Maud Kamal Anne Vincent‐Salomon |
| author_facet | Zakhia El Beaino Célia Dupain Grégoire Marret Xavier Paoletti Laëtitia Fuhrmann Charlotte Martinat Yves Allory Maral Halladjian Ivan Bièche Christophe Le Tourneau Maud Kamal Anne Vincent‐Salomon Zakhia El Beaino Célia Dupain Grégoire Marret Xavier Paoletti Laëtitia Fuhrmann Charlotte Martinat Yves Allory Maral Halladjian Ivan Bièche Christophe Le Tourneau Maud Kamal Anne Vincent‐Salomon |
| collection | Wiley Open Access |
| contents | Pan‐cancer evaluation of tumor‐infiltrating lymphocytes and programmed cell death protein ligand‐1 in metastatic biopsies and matched primary tumors Zakhia El Beaino Célia Dupain Grégoire Marret Xavier Paoletti Laëtitia Fuhrmann Charlotte Martinat Yves Allory Maral Halladjian Ivan Bièche Christophe Le Tourneau Maud Kamal Anne Vincent‐Salomon The Journal of Pathology AbstractTumor immunological characterization includes evaluation of tumor‐infiltrating lymphocytes (TILs) and programmed cell death protein ligand‐1 (PD‐L1) expression. This study investigated TIL distribution, its prognostic value, and PD‐L1 expression in metastatic and matched primary tumors (PTs). Specimens from 550 pan‐cancer patients of the SHIVA01 trial (NCT01771458) with available metastatic biopsy and 111 matched PTs were evaluated for TILs and PD‐L1. Combined positive score (CPS), tumor proportion score (TPS), and immune cell (IC) score were determined. TILs and PD‐L1 were assessed according to PT organ of origin, histological subtype, and metastatic biopsy site. We found that TIL distribution in metastases did not vary according to PT organ of origin, histological subtype, or metastatic biopsy site, with a median of 10% (range: 0–70). TILs were decreased in metastases compared to PT (20% [5–60] versus 10% [0–40], p < 0.0001). CPS varied according to histological subtype (p = 0.02) and biopsy site (p < 0.02). TPS varied according to PT organ of origin (p = 0.003), histological subtype (p = 0.0004), and metastatic biopsy site (p = 0.00004). TPS was higher in metastases than in PT (p < 0.0001). TILs in metastases did not correlate with overall survival. In conclusion, metastases harbored fewer TILs than matched PT, regardless of PT organ of origin, histological subtype, and metastatic biopsy site. PD‐L1 expression increased with disease progression. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. 10.1002/path.6334 http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| doi_str_mv | 10.1002/path.6334 |
| format | Artículo Open Access |
| id | wiley_oa_10_1002_path_6334 |
| institution | Wiley Open Access |
| license_str_mv | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| publishDate | 2024 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | Pan‐cancer evaluation of tumor‐infiltrating lymphocytes and programmed cell death protein ligand‐1 in metastatic biopsies and matched primary tumors Zakhia El Beaino Célia Dupain Grégoire Marret Xavier Paoletti Laëtitia Fuhrmann Charlotte Martinat Yves Allory Maral Halladjian Ivan Bièche Christophe Le Tourneau Maud Kamal Anne Vincent‐Salomon The Journal of Pathology Pan‐cancer evaluation of tumor‐infiltrating lymphocytes and programmed cell death protein ligand‐1 in metastatic biopsies and matched primary tumors Zakhia El Beaino Célia Dupain Grégoire Marret Xavier Paoletti Laëtitia Fuhrmann Charlotte Martinat Yves Allory Maral Halladjian Ivan Bièche Christophe Le Tourneau Maud Kamal Anne Vincent‐Salomon The Journal of Pathology AbstractTumor immunological characterization includes evaluation of tumor‐infiltrating lymphocytes (TILs) and programmed cell death protein ligand‐1 (PD‐L1) expression. This study investigated TIL distribution, its prognostic value, and PD‐L1 expression in metastatic and matched primary tumors (PTs). Specimens from 550 pan‐cancer patients of the SHIVA01 trial (NCT01771458) with available metastatic biopsy and 111 matched PTs were evaluated for TILs and PD‐L1. Combined positive score (CPS), tumor proportion score (TPS), and immune cell (IC) score were determined. TILs and PD‐L1 were assessed according to PT organ of origin, histological subtype, and metastatic biopsy site. We found that TIL distribution in metastases did not vary according to PT organ of origin, histological subtype, or metastatic biopsy site, with a median of 10% (range: 0–70). TILs were decreased in metastases compared to PT (20% [5–60] versus 10% [0–40], p < 0.0001). CPS varied according to histological subtype (p = 0.02) and biopsy site (p < 0.02). TPS varied according to PT organ of origin (p = 0.003), histological subtype (p = 0.0004), and metastatic biopsy site (p = 0.00004). TPS was higher in metastases than in PT (p < 0.0001). TILs in metastases did not correlate with overall survival. In conclusion, metastases harbored fewer TILs than matched PT, regardless of PT organ of origin, histological subtype, and metastatic biopsy site. PD‐L1 expression increased with disease progression. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. 10.1002/path.6334 http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| title | Pan‐cancer evaluation of tumor‐infiltrating lymphocytes and programmed cell death protein ligand‐1 in metastatic biopsies and matched primary tumors |
| topic | The Journal of Pathology |
| url | https://pathsocjournals.onlinelibrary.wiley.com/doi/10.1002/path.6334 |