Tumour-infiltrating lymphocyte density is associated with favourable outcome in patients with advanced non-small cell lung cancer treated with immunotherapy.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
03 2021
Historique:
received: 12 06 2020
revised: 01 10 2020
accepted: 08 10 2020
pubmed: 31 1 2021
medline: 21 9 2021
entrez: 30 1 2021
Statut: ppublish

Résumé

The established role of morphological evaluation of tumour-infiltrating lymphocytes (TILs) with immune checkpoint inhibitors (ICIs) in non-small cell lung cancer (NSCLC) is unknown. We aimed to determine TIL association with the outcome for ICIs and for chemotherapy in advanced NSCLC. This is a multicenter retrospective study of a nivolumab cohort of 221 patients treated between November 2012 and February 2017 and a chemotherapy cohort of 189 patients treated between June 2009 and October 2016. Patients with available tissue for stromal TIL evaluation were analysed. The presence of a high TIL count (high-TIL) was defined as ≥10% density. The primary end-point was overall survival (OS). Among the nivolumab cohort, 64% were male, with median age of 63 years, 82.3% were smokers, 77% had performance status ≤1 and 63% had adenocarcinoma histology. High-TIL was observed in 22% patients and associated with OS (hazard ratio [HR] 0.48; 95% confidence interval [95% CI]: 0.28-0.81) and progression-free survival [PFS] (HR = 0.40; 95% CI: 0.25-0.64). Median PFS was 13.0 months (95% CI: 5.0-not reached) with high-TIL versus 2.2 months (95% CI: 1.7-3.0) with the presence of a low TIL count (low-TIL). Median OS for high-TIL was not reached (95% CI: 12.2-not reached) versus 8.4 months (95% CI: 5.0-11.6) in the low-TIL group. High-TIL was associated with the overall response rate (ORR) and disease control rate (DCR) (both, P < .0001). Among the chemotherapy cohort, 69% were male, 89% were smokers, 86% had performance status ≤1 and 90% had adenocarcinoma histology. High-TIL was seen in 37%. Median PFS and OS were 5.7 months (95% CI: 4.9-6.7) and 11.7 months (95% CI: 9.3-13.0), respectively, with no association with TILs. High-TIL was associated with favourable outcomes in a real-world immunotherapy cohort of patients with NSCLC, but not with chemotherapy, suggesting that TILs may be useful in selecting patients for immunotherapy.

Sections du résumé

BACKGROUND
The established role of morphological evaluation of tumour-infiltrating lymphocytes (TILs) with immune checkpoint inhibitors (ICIs) in non-small cell lung cancer (NSCLC) is unknown. We aimed to determine TIL association with the outcome for ICIs and for chemotherapy in advanced NSCLC.
METHODS
This is a multicenter retrospective study of a nivolumab cohort of 221 patients treated between November 2012 and February 2017 and a chemotherapy cohort of 189 patients treated between June 2009 and October 2016. Patients with available tissue for stromal TIL evaluation were analysed. The presence of a high TIL count (high-TIL) was defined as ≥10% density. The primary end-point was overall survival (OS).
RESULTS
Among the nivolumab cohort, 64% were male, with median age of 63 years, 82.3% were smokers, 77% had performance status ≤1 and 63% had adenocarcinoma histology. High-TIL was observed in 22% patients and associated with OS (hazard ratio [HR] 0.48; 95% confidence interval [95% CI]: 0.28-0.81) and progression-free survival [PFS] (HR = 0.40; 95% CI: 0.25-0.64). Median PFS was 13.0 months (95% CI: 5.0-not reached) with high-TIL versus 2.2 months (95% CI: 1.7-3.0) with the presence of a low TIL count (low-TIL). Median OS for high-TIL was not reached (95% CI: 12.2-not reached) versus 8.4 months (95% CI: 5.0-11.6) in the low-TIL group. High-TIL was associated with the overall response rate (ORR) and disease control rate (DCR) (both, P < .0001). Among the chemotherapy cohort, 69% were male, 89% were smokers, 86% had performance status ≤1 and 90% had adenocarcinoma histology. High-TIL was seen in 37%. Median PFS and OS were 5.7 months (95% CI: 4.9-6.7) and 11.7 months (95% CI: 9.3-13.0), respectively, with no association with TILs.
CONCLUSIONS
High-TIL was associated with favourable outcomes in a real-world immunotherapy cohort of patients with NSCLC, but not with chemotherapy, suggesting that TILs may be useful in selecting patients for immunotherapy.

Identifiants

pubmed: 33516050
pii: S0959-8049(20)31276-4
doi: 10.1016/j.ejca.2020.10.017
pii:
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Immune Checkpoint Inhibitors 0
Nivolumab 31YO63LBSN

Types de publication

Comparative Study Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

221-229

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest statement The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Laura Mezquita reports receiving research sponsorship from Bristol-Myers Squibb and Boehringer Ingelheim; consulting and advisory roles in Roche Diagnostics and Takeda; lectures and educational activities in Bristol-Myers Squibb, Tecnofarma and Roche; receiving travel, accommodations and expenses from Roche; and participation in the mentorship program with key opinion leaders, funded by AstraZeneca. Edouard Auclin reports receiving travel expenses from Mundipharma and lectures and educational activities in Sanofi Genzymes. Lizza Hendriks reports no conflicts related to the current manuscript; however, outside of current manuscript LH reports receiving research funding from Roche, Boehringer Ingelheim and AstraZeneca (all institution); advisory board roles in Boehringer, BMS, Lilly, Roche, Pfizer, Takeda, MSD and Boehringer Ingelheim (all institution); and speaker roles in MSD; receiving travel/conference reimbursements from Roche and BMS (self); participation in the mentorship program with key opinion leaders, funded by AstraZeneca; receiving fees for educational webinars from Quadia (self); and participation in interview sessions funded by Roche (institution). Anas Gazzah reports receiving travel, accommodation and congress registration expenses from Boehringer Ingelheim, Novartis, Pfizer and Roche; consultant/expert roles in Novartis; roles principal/sub-investigator of clinical trials for Aduro Biotech, Agios Pharmaceuticals, Amgen, Argen-X Bvba, Arno Therapeutics, Astex Pharmaceuticals, Astra Zeneca, Aveo, Bayer Healthcare Ag, Bbb Technologies Bv, Beigene, Bioalliance Pharma, Biontech Ag, Blueprint Medicines, Boehringer Ingelheim, Bristol-Myers Squibb, Ca, Celgene Corporation, Chugai Pharmaceutical Co., Clovis Oncology, Daiichi Sankyo, Debiopharm S.A., Eisai, Exelixis, Forma, Gamamabs, Genentech, Inc., Gilead Sciences, Inc, Glaxosmithkline, Glenmark Pharmaceuticals, H3 Biomedicine, Inc, Hoffmann La Roche Ag, Incyte Corporation, Innate Pharma, Iris Servier, Janssen, Kura Oncology, Kyowa Kirin Pharm, Lilly, Loxo Oncology, Lytix Biopharma As, Medimmune, Menarini Ricerche, Merck Sharp & Dohme Chibret, Merrimack Pharmaceuticals, Merus, Millennium Pharmaceuticals, Nanobiotix, Nektar Therapeutics, Novartis Pharma, Octimet Oncology Nv, Oncoethix, Oncomed, Oncopeptides, Onyx Therapeutics, Orion Pharma, Oryzon Genomics, Pfizer, Pharma Mar, Pierre Fabre, Rigontec Gmbh, Roche, Sanofi-Aventis, Sierra Oncology, Taiho Pharma, Tesaro Inc., Tioma Therapeutics Inc. and Xencor; receiving research grants from Astrazeneca, BMS, Boehringer Ingelheim, Janssen Cilag, Merck, Novartis, Pfizer, Roche and Sanofi; receiving on-financial support (drug supplied) from Astrazeneca, Bayer, BMS, Boringher Ingelheim, Johnson & Johnson, Lilly, Medimmune, Merck, NH TherAGuiX, Pfizer and Roche. David Planchard reports consulting, advisory roles or lectures in AstraZeneca, Bristol-Myers Squibb, Boehringer Ingelheim, Celgene, Daiichi Sankyo, Eli Lilly, Merck, Novartis, Pfizer, prIME Oncology, Peer CME, Roche; Honoraria from AstraZeneca, Bristol-Myers Squibb, Boehringer Ingelheim, Celgene, Eli Lilly, Merck, Novartis, Pfizer, prIME Oncology, Peer CME, Roche; roles in clinical trials research: AstraZeneca, Bristol-Myers Squibb, Boehringer Ingelheim, Eli Lilly, Merck, Novartis, Pfizer, Roche, Medimmune, Sanofi-Aventis, Taiho Pharma, Novocure and Daiichi Sankyo; receiving travel and accommodation expenses from AstraZeneca, Roche, Novartis, prIME Oncology and Pfizer. Benjamin Besse reports Sponsored research sponsorship from Gustave Roussy Cancer Center Abbvie, Amgen, AstraZeneca, Biogen, Blueprint Medicines, BMS, Celgene, Eli Lilly, GSK, Ignyta, IPSEN, Merck KGaA, MSD, Nektar, Onxeo, Pfizer, Pharma Mar, Sanofi, Spectrum Pharmaceuticals, Takeda and Tiziana Pharma. Julien Adam reports advisory board roles in AstraZeneca and Bayer and honoraria from MSD and BMS. Remaining authors nothing to disclose.

Auteurs

Ithar Gataa (I)

Cancer Medicine Department, Gustave Roussy, Villejuif, France; Medical Oncology Department, Cochin Hospital, Paris, France. Electronic address: Ithar.gataa@aphp.fr.

Laura Mezquita (L)

Cancer Medicine Department, Gustave Roussy, Villejuif, France; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Medical Oncology Department, Hospital Clínic, Barcelona, Spain. Electronic address: lmezquita@clinic.cat.

Caroline Rossoni (C)

Department of Biostatistics and Epidemiology, Gustave Roussy, University Paris-Saclay, Villejuif, France; Inserm, University Paris-Saclay, Labeled Ligue Contre le Cancer, Oncostat, U1018, Villejuif, France. Electronic address: caroline.rossoni@outlook.fr.

Edouard Auclin (E)

Medical and Thoracic Oncology Department, Hôpital Européen Georges Pompidou AP-HP, Paris, France. Electronic address: ed.auclin@gmail.com.

Myriam Kossai (M)

Pathology Department, Gustave Roussy, Villejuif, France. Electronic address: myriamkossai@gmail.com.

Frank Aboubakar (F)

Cancer Medicine Department, Gustave Roussy, Villejuif, France. Electronic address: frank.aboubakar@uclouvain.be.

Sylvestre Le Moulec (S)

Medical Oncology Department, Institut Bergonié, Bordeaux, France. Electronic address: sylvestre.lemoulec@gmail.com.

Julie Massé (J)

Pathology Department, Institut Bergonié, Bordeaux, France. Electronic address: julie.masse@cjp.fr.

Morgane Masson (M)

Medical Oncology Department, Centre Jean Perrin, Clermont-Ferrand, France. Electronic address: morganemasson1@hotmail.fr.

Nina Radosevic-Robin (N)

Pathology Department, Centre Jean Perrin, Clermont-Ferrand, France. Electronic address: nina.radosevic.robin@gmail.com.

Pierre Alemany (P)

Pathology Department, Gustave Roussy, Villejuif, France. Electronic address: pierre.alemany@yahoo.fr.

Mathieu Rouanne (M)

INSERM U1015, Gustave Roussy, Villejuif, France; Hôpital Foch, UVSQ-Université Paris-Saclay, Suresnes, France. Electronic address: mathieu.rouanne@gustaveroussy.fr.

Virginia Bluthgen (V)

Cancer Medicine Department, Gustave Roussy, Villejuif, France. Electronic address: mvbluthgen@gmail.com.

Lizza Hendriks (L)

Cancer Medicine Department, Gustave Roussy, Villejuif, France; Department of Pulmonary Diseases, GROW - School for Oncology and Developmental Biology, Maastricht UMC+, Maastricht, the Netherlands. Electronic address: lizza.hendriks@mumc.nl.

Caroline Caramella (C)

Radiology Department, Gustave Roussy, Villejuif, France. Electronic address: Caroline.caramella@gmail.com.

Anas Gazzah (A)

Early Drug Development Department, Gustave Roussy, Villejuif, France. Electronic address: anas.gazzah@gustaveroussy.fr.

David Planchard (D)

Cancer Medicine Department, Gustave Roussy, Villejuif, France. Electronic address: david.planchard@gustaveroussy.fr.

Jean-Pierre Pignon (JP)

Department of Biostatistics and Epidemiology, Gustave Roussy, University Paris-Saclay, Villejuif, France; Inserm, University Paris-Saclay, Labeled Ligue Contre le Cancer, Oncostat, U1018, Villejuif, France. Electronic address: Jean-pierre.PIGNON@gustaveroussy.fr.

Benjamin Besse (B)

Cancer Medicine Department, Gustave Roussy, Villejuif, France; Paris-Saclay University, Faculty of Medicine, Le Kremlin, Bicêtre, France. Electronic address: benjamin.besse@gustaveroussy.fr.

Julien Adam (J)

Pathology Department, Gustave Roussy, Villejuif, France. Electronic address: julien.adam@gustaveroussy.fr.

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