Evidence map›Paper›PMID 25214542›Full record

GuidelineAnnals of oncology : official journal of the European Society for Medical Oncology2015

The evaluation of tumor-infiltrating lymphocytes (TILs) in breast cancer: recommendations by an International TILs Working Group 2014.

R Salgado, C Denkert, S Demaria, N Sirtaine, F Klauschen, G Pruneri, S Wienert, G Van den Eynden, F L Baehner, F Penault-Llorca and 23 more

4 registry-linked trialsAbstract readPractice Guideline
In one paragraph

Guideline in Annals of oncology : official journal of the European Society for Medical Oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 1,803 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,803citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03515798 phase2active not recruitingnot on this mapstarted 2018, after this paper: background citation

A Prospective Multicenter Open-label, Randomized Phase II Study of Pembrolizumab in Combination With Neoadjuvant EC-Paclitaxel Regimen in HER2-negative Inflammatory Breast Cancer.

TypeinterventionalSponsorInstitut Paoli-CalmettesRan2018 to 2027Enrolled52ConditionsInflammatory Breast CancerArmsPembrolizumab Injection, neoadjuvant EC-paclitaxel chemotherapy
NCT03922776 naterminatednot on this mapstarted 2019, after this paper: background citation

Phenotypic Characterization Tumor-infiltrating Lymphocytes at Diagnosis and After Chemotherapy in Advanced High-grade Serous Ovarian Cancer in Blood, Ascites, Peritoneal Biopsy

TypeinterventionalSponsorCentre Oscar LambretRan2019 to 2024Enrolled36ConditionsOvarian Cancer Stage IIIC, Fallopian Tube Cancer Stage IIIC, Fallopian Tube Cancer Stage IV, Ovarian Cancer Stage IVArmsBlood sample collection
NCT04368468 completednot on this mapstarted 2020, after this paper: background citation

Study of the Modifications of the Immune Microenvironment Induced by Neoadjuvant Chemotherapy in Triple-negative Breast Cancers

TypeobservationalSponsorInstitut Claudius RegaudRan2020 to 2021Enrolled100ConditionsTriple Negative Breast CancerArmsbiomarker evolution
NCT05250336 unknown statusnot on this mapstarted 2019, after this paper: background citation

Prognostic and Predictive Value of Tumor-Infiltrating Lymphocytes and Programmed Cell Death - Ligand 1 in Breast Cancer

TypeobservationalSponsorSanjay Gandhi Postgraduate Institute of Medical SciencesRan2019 to 2022Enrolled1,000ConditionsBreast Cancer, Tumor Infiltrating Lymphocytes, Programmed Cell Death Ligand 1ArmsObservational Study
3 · Its place in the literature

Who cites it

1,803 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Tumor-Infiltrating Lymphocytes as a Predictor of Adjuvant Avelumab Efficacy in Patients with High-risk Triple-Negative Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  8. Computationally Derived Spatial Immune Signature Identifies Trastuzumab Responders in HER2+ Breast Cancer: NSABP B-41 Clinical Trial Validation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  11. Pembrolizumab and Paclitaxel in Patients with HR+/HER2- Breast Cancer with HER2-Enriched or Basal-like Subtypes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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1,743 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors.

R SalgadoBreast Cancer Translational Research Laboratory/Breast International Group, Institut Jules Bordet, Brussels Department of Pathology and TCRU, GZA, Antwerp, Belgium.
C DenkertInstitute of Pathology, Charité -University Hospital, Berlin, Germany.
S DemariaPerlmutter Cancer Center, New York University Medical School, New York, USA.
N SirtaineDepartment of Pathology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
F KlauschenInstitute of Pathology, Charité -University Hospital, Berlin, Germany.
G PruneriEuropean Institute of Oncology (IEO) and University of Milan, Milan, Italy.
S WienertInstitute of Pathology, Charité -University Hospital, Berlin, Germany.
G Van den EyndenDepartment of Pathology GZA, TCRU Hospitals and CORE Antwerp University, Antwerp, Belgium.
F L BaehnerGenomic Health, Inc., Redwood City, USA University of California San Francisco, San Francisco, USA.
F Penault-LlorcaClermont-Ferrand Biopathology, University of Auvergne, Jean Perrin Comprehensive Cancer Centre, Clermont-Ferrand, France.
E A PerezDivision of Haematology/Medical Oncology and.
E A ThompsonDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Mayo Clinic, Jacksonville.
W F SymmansDepartment of Pathology, The UT M.D. Anderson Cancer Center, Boston.
A L RichardsonDepartment of Pathology, Brigham and Women's Hospital, Boston Department of Cancer Biology, Dana Farber Cancer Institute, Boston.
J BrockDepartment of Cancer Biology, Dana Farber Cancer Institute, Boston Department of Cancer Biology, Harvard Medical School, Boston, USA.
C CriscitielloIstituto Europeo di Oncologia, Milan, Italy.
H BaileyGenomic Health, Inc., Redwood City, USA.
M IgnatiadisDepartment of Medical Oncology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels.
G FlorisDepartment of Pathology, University Hospital Leuven, Leuven, Belgium.
J SparanoDepartment of Medicine, Department of Obstetrics and Gynecology and Women's Health, Albert Einstein Medical Center, Bronx, USA.
Z KosLaboratory Medicine Program, University Health Network, University of Toronto, Toronto.
T NielsenDepartment of Pathology and Laboratory Medicine, Genetic Pathology Evaluation Centre, University of British Columbia, Vancouver, Canada.
D L RimmDepartment of Pathology, Yale University School of Medicine, New Haven.
K H AllisonDepartment of Pathology, Stanford University Medical Centre, Stanford.
J S Reis-FilhoDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, USA.
S LoiblGerman Breast Group, Neu-Isenburg, Germany.
C SotiriouDepartment of Medical Oncology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels.
G VialeDepartment of Pathology, Istituto Europeo di Oncologia, University of Milan, Milan, Italy.
S BadveDepartment of Pathology and Laboratory Medicine, Indiana University, Indianapolis, USA.
S AdamsPerlmutter Cancer Center, New York University Medical School, New York, USA.
K Willard-GalloMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
S LoiDivision of Research and Cancer Medicine, Peter MacCallum Cancer Centre, University of Melbourne, Victoria, Australia sherene.loi@petermac.org.
International TILs Working Group 2014

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
6 · The paper itself

Abstract

backgroundThe morphological evaluation of tumor-infiltrating lymphocytes (TILs) in breast cancer (BC) is gaining momentum as evidence strengthens for the clinical relevance of this immunological biomarker. Accumulating evidence suggests that the extent of lymphocytic infiltration in tumor tissue can be assessed as a major parameter by evaluation of hematoxylin and eosin (H&E)-stained tumor sections. TILs have been shown to provide prognostic and potentially predictive value, particularly in triple-negative and human epidermal growth factor receptor 2-overexpressing BC.

designA standardized methodology for evaluating TILs is now needed as a prerequisite for integrating this parameter in standard histopathological practice, in a research setting as well as in clinical trials. This article reviews current data on the clinical validity and utility of TILs in BC in an effort to foster better knowledge and insight in this rapidly evolving field, and to develop a standardized methodology for visual assessment on H&E sections, acknowledging the future potential of molecular/multiplexed approaches.

conclusionsThe methodology provided is sufficiently detailed to offer a uniformly applied, pragmatic starting point and improve consistency and reproducibility in the measurement of TILs for future studies.

Indexed as

Lymphocytes, Tumor-InfiltratingBreast NeoplasmsFemaleHumansbreast cancer (BC)clinical validitypredictionprognosistumor-infiltrating lymphocytes (TILs)

Identifiers

PMID25214542
PMCPMC6267863

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.