Prognostic Value of Stromal Tumor-Infiltrating Lymphocytes in Young, Node-Negative, Triple-Negative Breast Cancer Patients Who Did Not Receive (neo)Adjuvant Systemic Therapy.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 07 2022
Historique:
pubmed: 31 3 2022
medline: 20 7 2022
entrez: 30 3 2022
Statut: ppublish

Résumé

Triple-negative breast cancer (TNBC) is considered aggressive, and therefore, virtually all young patients with TNBC receive (neo)adjuvant chemotherapy. Increased stromal tumor-infiltrating lymphocytes (sTILs) have been associated with a favorable prognosis in TNBC. However, whether this association holds for patients who are node-negative (N0), young (< 40 years), and chemotherapy-naïve, and thus can be used for chemotherapy de-escalation strategies, is unknown. We selected all patients with N0 TNBC diagnosed between 1989 and 2000 from a Dutch population-based registry. Patients were age < 40 years at diagnosis and had not received (neo)adjuvant systemic therapy, as was standard practice at the time. Formalin-fixed paraffin-embedded blocks were retrieved (PALGA: Dutch Pathology Registry), and a pathology review including sTILs was performed. Patients were categorized according to sTILs (< 30%, 30%-75%, and ≥ 75%). Multivariable Cox regression was performed for overall survival, with or without sTILs as a covariate. Cumulative incidence of distant metastasis or death was analyzed in a competing risk model, with second primary tumors as competing risk. sTILs were scored for 441 patients. High sTILs (≥ 75%; 21%) translated into an excellent prognosis with a 15-year cumulative incidence of a distant metastasis or death of only 2.1% (95% CI, 0 to 5.0), whereas low sTILs (< 30%; 52%) had an unfavorable prognosis with a 15-year cumulative incidence of a distant metastasis or death of 38.4% (32.1 to 44.6). In addition, every 10% increment of sTILs decreased the risk of death by 19% (adjusted hazard ratio: 0.81; 95% CI, 0.76 to 0.87), which are an independent predictor adding prognostic information to standard clinicopathologic variables (χ Chemotherapy-naïve, young patients with N0 TNBC with high sTILs (≥ 75%) have an excellent long-term prognosis. Therefore, sTILs should be considered for prospective clinical trials investigating (neo)adjuvant chemotherapy de-escalation strategies.

Identifiants

pubmed: 35353548
doi: 10.1200/JCO.21.01536
pmc: PMC9287283
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2361-2374

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Auteurs

Vincent M T de Jong (VMT)

Department of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Yuwei Wang (Y)

Department of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Natalie D Ter Hoeve (ND)

Division of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.

Mark Opdam (M)

Department of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Nikolas Stathonikos (N)

Division of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.

Katarzyna Jóźwiak (K)

Institute of Biostatistics and Registry Research, Brandenburg Medical School Theodor Fontane, Neuruppin, Germany.

Michael Hauptmann (M)

Institute of Biostatistics and Registry Research, Brandenburg Medical School Theodor Fontane, Neuruppin, Germany.

Sten Cornelissen (S)

Core Facility Molecular Pathology and Biobanking, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Willem Vreuls (W)

Department of Pathology, Canisius Wilhelmina Ziekenhuis, Nijmegen, the Netherlands.

Efraim H Rosenberg (EH)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Esther A Koop (EA)

Department of Pathology, Gelre Ziekenhuizen, Apeldoorn, the Netherlands.

Zsuzsanna Varga (Z)

Departement of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.

Carolien H M van Deurzen (CHM)

Department of Pathology, Erasmus University Medical Center Rotterdam, Rotterdam, the Netherlands.

Antien L Mooyaart (AL)

Department of Pathology, Erasmus University Medical Center Rotterdam, Rotterdam, the Netherlands.

Alicia Córdoba (A)

Department of Pathology, Complejo Hospitalario de Navarra, Pamplona, Spain.

Emma J Groen (EJ)

Department of Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Joost Bart (J)

University of Groningen, University Medical Center Groningen, Department of Pathology and Medical Biology, Groningen, the Netherlands.

Stefan M Willems (SM)

University of Groningen, University Medical Center Groningen, Department of Pathology and Medical Biology, Groningen, the Netherlands.

Vasiliki Zolota (V)

Department of Pathology, Rion University Hospital, Patras, Greece.

Jelle Wesseling (J)

Department of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Department of Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.

Anna Sapino (A)

Department of Medical Sciences, University of Torino, Torino, Italy.
Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.

Ewa Chmielik (E)

Tumor Pathology Department, Maria Sklodowska-Curie Memorial National Research Institute of Oncology, Gliwice, Poland.

Ales Ryska (A)

Charles University Medical Faculty and University Hospital, Hradec Kralove, Czech Republic.

Annegien Broeks (A)

Core Facility Molecular Pathology and Biobanking, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Adri C Voogd (AC)

Department of Epidemiology, Maastricht University, Maastricht, the Netherlands.
Department of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, the Netherlands.

Sherene Loi (S)

Division of Clinical Medicine and Research, Peter MacCallum Cancer Centre, Melbourne, Australia.

Stefan Michiels (S)

Service de Biostatistique et d'Epidémiologie, Gustave Roussy, Oncostat U1018, Inserm, Paris-Saclay University, labeled Ligue Contre le Cancer, Villejuif, France.

Gabe S Sonke (GS)

Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Elsken van der Wall (E)

Cancer Center, University Medical Center Utrecht, Utrecht, the Netherlands.

Sabine Siesling (S)

Division of Clinical Medicine and Research, Peter MacCallum Cancer Centre, Melbourne, Australia.
Department of Health Technology and Services Research, Technical Medical Centre, University of Twente, Enschede, the Netherlands.

Paul J van Diest (PJ)

Division of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.

Marjanka K Schmidt (MK)

Department of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Department of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands.

Marleen Kok (M)

Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

Gwen M H E Dackus (GMHE)

Department of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Division of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.

Roberto Salgado (R)

Division of Clinical Medicine and Research, Peter MacCallum Cancer Centre, Melbourne, Australia.
Department of Pathology, GZA-ZNA Hospitals, Antwerp, Belgium.

Sabine C Linn (SC)

Department of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Division of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.
Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.

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