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

Author:

de Jong Vincent M.T.1ORCID,Wang Yuwei1ORCID,ter Hoeve Natalie D.2ORCID,Opdam Mark1ORCID,Stathonikos Nikolas2ORCID,Jóźwiak Katarzyna3,Hauptmann Michael3ORCID,Cornelissen Sten4,Vreuls Willem5,Rosenberg Efraim H.6ORCID,Koop Esther A.7,Varga Zsuzsanna8,van Deurzen Carolien H.M.9,Mooyaart Antien L.9,Córdoba Alicia10ORCID,Groen Emma J.6,Bart Joost11ORCID,Willems Stefan M.11,Zolota Vasiliki12,Wesseling Jelle1613,Sapino Anna1415ORCID,Chmielik Ewa16ORCID,Ryska Ales17ORCID,Broeks Annegien4,Voogd Adri C.1819ORCID,Loi Sherene20ORCID,Michiels Stefan21ORCID,Sonke Gabe S.22ORCID,van der Wall Elsken23ORCID,Siesling Sabine2024ORCID,van Diest Paul J.2ORCID,Schmidt Marjanka K.125ORCID,Kok Marleen22ORCID,Dackus Gwen M.H.E.12ORCID,Salgado Roberto2026ORCID,Linn Sabine C.1222ORCID

Affiliation:

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

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

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

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

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

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

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

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

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

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

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

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

13. Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands

14. Department of Medical Sciences, University of Torino, Torino, Italy

15. Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy

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

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

18. Department of Epidemiology, Maastricht University, Maastricht, the Netherlands

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

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

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

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

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

24. Department of Health Technology and Services Research, Technical Medical Centre, University of Twente, Enschede, the Netherlands

25. Department of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands

26. Department of Pathology, GZA-ZNA Hospitals, Antwerp, Belgium

Abstract

PURPOSE 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. METHODS 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. RESULTS 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 (χ2 = 46.7, P < .001). CONCLUSION 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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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