Association of tumor-infiltrating lymphocytes with recurrence score in hormone receptor-positive/HER2-negative breast cancer : Analysis of four prospective studies
Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved..
BACKGROUND: The clinical value of tumor infiltrating lymphocytes (TILs) in hormone receptor-positive (HR+)/HER2- breast cancer (BC) may be unearthed by focusing on more biologically aggressive tumors. Here we deepen and describe the correlation between RS and TILs, proposing an immuno-genomic model for HR+ /HER2- BC.
METHODS: We enrolled T1-T3, N0-N1 BC patients with available RS® and TILs in the context of four multicenter, prospective studies. RS® and TILs were considered as continuous and categorical variables. RS® was categorized into: 0-10 (low risk), 11-25 (intermediate risk) and 26-100 (high risk); TILs were categorized into: low TILs (0-10%), intermediate TILs (11-59%) and high TILs (60-100%).
RESULTS: 811 patients were included. RS distribution was (n = 810): low risk 22.0%, intermediate risk 61.2%, high risk 16.8%. TIL distribution was (n = 455): low TILs 84.6%, intermediate TILs 13.6% and high TILs 1.8%. A significant, weak positive, linear correlation was found between continuous TILs and RS (Pearson coefficient=0.223, p < 0.001). When considering RS and TILs categories, tumors with intermediate/high TIL levels significantly enriched the high RS subgroup (p = 0.006). This was confirmed both within Luminal A and Luminal B cohorts. Among high-RS patients, 16.7% of Luminal A and 26.7% of Luminal B tumors had intermediate/high TILs.
CONCLUSIONS: We observed that RS® and TILs capture only slightly overlapping information on the biology of HR+ /HER2- tumor microenvironment. We demonstrated the feasibility of combining RS and TILs into a composite immuno-genomic model, which may serve the purpose of guiding and focalizing patient selection in the further development of immunotherapy strategies for Luminal-like disease.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:195 |
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Enthalten in: |
European journal of cancer (Oxford, England : 1990) - 195(2023) vom: 05. Dez., Seite 113399 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Miglietta, Federica [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 27.11.2023 Date Revised 05.12.2023 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1016/j.ejca.2023.113399 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM364426004 |
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100 | 1 | |a Miglietta, Federica |e verfasserin |4 aut | |
245 | 1 | 0 | |a Association of tumor-infiltrating lymphocytes with recurrence score in hormone receptor-positive/HER2-negative breast cancer |b Analysis of four prospective studies |
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500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved. | ||
520 | |a BACKGROUND: The clinical value of tumor infiltrating lymphocytes (TILs) in hormone receptor-positive (HR+)/HER2- breast cancer (BC) may be unearthed by focusing on more biologically aggressive tumors. Here we deepen and describe the correlation between RS and TILs, proposing an immuno-genomic model for HR+ /HER2- BC | ||
520 | |a METHODS: We enrolled T1-T3, N0-N1 BC patients with available RS® and TILs in the context of four multicenter, prospective studies. RS® and TILs were considered as continuous and categorical variables. RS® was categorized into: 0-10 (low risk), 11-25 (intermediate risk) and 26-100 (high risk); TILs were categorized into: low TILs (0-10%), intermediate TILs (11-59%) and high TILs (60-100%) | ||
520 | |a RESULTS: 811 patients were included. RS distribution was (n = 810): low risk 22.0%, intermediate risk 61.2%, high risk 16.8%. TIL distribution was (n = 455): low TILs 84.6%, intermediate TILs 13.6% and high TILs 1.8%. A significant, weak positive, linear correlation was found between continuous TILs and RS (Pearson coefficient=0.223, p < 0.001). When considering RS and TILs categories, tumors with intermediate/high TIL levels significantly enriched the high RS subgroup (p = 0.006). This was confirmed both within Luminal A and Luminal B cohorts. Among high-RS patients, 16.7% of Luminal A and 26.7% of Luminal B tumors had intermediate/high TILs | ||
520 | |a CONCLUSIONS: We observed that RS® and TILs capture only slightly overlapping information on the biology of HR+ /HER2- tumor microenvironment. We demonstrated the feasibility of combining RS and TILs into a composite immuno-genomic model, which may serve the purpose of guiding and focalizing patient selection in the further development of immunotherapy strategies for Luminal-like disease | ||
650 | 4 | |a Multicenter Study | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Breast cancer | |
650 | 4 | |a Hormone receptor-positive/HER2-negative | |
650 | 4 | |a Oncotype Dx | |
650 | 4 | |a Recurrence Score® | |
650 | 4 | |a Tumor infiltrating lymphocytes | |
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700 | 1 | |a Dieci, Maria Vittoria |e verfasserin |4 aut | |
700 | 1 | |a Giarratano, Tommaso |e verfasserin |4 aut | |
700 | 1 | |a Torri, Valter |e verfasserin |4 aut | |
700 | 1 | |a Giuliano, Mario |e verfasserin |4 aut | |
700 | 1 | |a Zustovich, Fable |e verfasserin |4 aut | |
700 | 1 | |a Mion, Marta |e verfasserin |4 aut | |
700 | 1 | |a Tondini, Carlo Alberto |e verfasserin |4 aut | |
700 | 1 | |a De Rossi, Costanza |e verfasserin |4 aut | |
700 | 1 | |a Bria, Emilio |e verfasserin |4 aut | |
700 | 1 | |a Franchi, Michela |e verfasserin |4 aut | |
700 | 1 | |a Merlini, Laura |e verfasserin |4 aut | |
700 | 1 | |a Giannatiempo, Rosa |e verfasserin |4 aut | |
700 | 1 | |a Russo, Daniela |e verfasserin |4 aut | |
700 | 1 | |a Fotia, Vittoria |e verfasserin |4 aut | |
700 | 1 | |a Poletti, Paola |e verfasserin |4 aut | |
700 | 1 | |a Caremoli, Elena Rota |e verfasserin |4 aut | |
700 | 1 | |a Arpino, Maria Grazia |e verfasserin |4 aut | |
700 | 1 | |a De Salvo, Gian Luca |e verfasserin |4 aut | |
700 | 1 | |a Zambelli, Alberto |e verfasserin |4 aut | |
700 | 1 | |a Guarneri, Valentina |e verfasserin |4 aut | |
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