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Prognostic value of histopathologic traits independent of stromal tumor-infiltrating lymphocyte levels in chemotherapy-naïve patients with triple-negative breast cancer.
de Boo, L W; Józwiak, K; Ter Hoeve, N D; van Diest, P J; Opdam, M; Wang, Y; Schmidt, M K; de Jong, V; Kleiterp, S; Cornelissen, S; Baars, D; Koornstra, R H T; Kerver, E D; van Dalen, T; Bins, A D; Beeker, A; van den Heiligenberg, S M; de Jong, P C; Bakker, S D; Rietbroek, R C; Konings, I R; Blankenburgh, R; Bijlsma, R M; Imholz, A L T; Stathonikos, N; Vreuls, W; Sanders, J; Rosenberg, E H; Koop, E A; Varga, Z; van Deurzen, C H M; Mooyaart, A L; Córdoba, A; Groen, E; Bart, J; Willems, S M; Zolota, V; Wesseling, J; Sapino, A; Chmielik, E; Ryska, A; Broeks, A; Voogd, A C; van der Wall, E; Siesling, S; Salgado, R; Dackus, G M H E; Hauptmann, M; Kok, M; Linn, S C.
Afiliação
  • de Boo LW; Department of Molecular Pathology, the Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Józwiak K; Institute of Biostatistics and Registry Research, Brandenburg Medical School Theodor Fontane, Neuruppin, Germany.
  • Ter Hoeve ND; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van Diest PJ; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Opdam M; Department of Molecular Pathology, the Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Wang Y; Department of Molecular Pathology, the Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Schmidt MK; Department of Molecular Pathology, the Netherlands Cancer Institute, Amsterdam, The Netherlands; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • de Jong V; Department of Molecular Pathology, the Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Kleiterp S; Department of Molecular Pathology, the Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Cornelissen S; Core Facility Molecular Pathology and Biobanking, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Baars D; Department of Biometrics, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Koornstra RHT; Department of Medical Oncology, Rijnstate Medical center, Arnhem, The Netherlands.
  • Kerver ED; Department of Medical Oncology, OLVG, Amsterdam, The Netherlands.
  • van Dalen T; Department of Surgery, Diakonessenhuis Utrecht, Utrecht, The Netherlands.
  • Bins AD; Department of Medical Oncology, Amsterdam UMC, Amsterdam, The Netherlands.
  • Beeker A; Department of Medical Oncology, Spaarne Gasthuis, Hoofddorp, The Netherlands.
  • van den Heiligenberg SM; Department of Medical Oncology, Dijklander Ziekenhuis, Hoorn, The Netherlands.
  • de Jong PC; Department of Medical Oncology, Sint Antonius Hospital, Utrecht, The Netherlands.
  • Bakker SD; Department of Internal Medicine, Zaans Medical Centre, Zaandam, The Netherlands.
  • Rietbroek RC; Department of Medical Oncology, Rode Kruis Hospital, Beverwijk, The Netherlands.
  • Konings IR; Department of Medical Oncology, Amsterdam UMC, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Blankenburgh R; Department of Medical Oncology, Saxenburgh Medical Center, Hardenberg, The Netherlands.
  • Bijlsma RM; Department of Medical Oncology, UMC Utrecht Cancer Center, Utrecht, The Netherlands.
  • Imholz ALT; Department of Internal Medicine, Deventer Hospital, Deventer, The Netherlands.
  • Stathonikos N; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Vreuls W; Department of Pathology, Canisius Wilhelmina Ziekenhuis, Nijmegen, The Netherlands.
  • Sanders J; Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Rosenberg EH; Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Koop EA; Department of Pathology, Gelre Ziekenhuizen, Apeldoorn, The Netherlands.
  • Varga Z; Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
  • van Deurzen CHM; Department of Pathology, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Mooyaart AL; Department of Pathology, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Córdoba A; Department of Pathology, Complejo Hospitalaria de Navarra, Pamplona, Spain.
  • Groen E; Department of Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Bart J; Department of Pathology and Medical Biology, University Medical Center Groningen, Groningen, The Netherlands.
  • Willems SM; Department of Pathology and Medical Biology, University Medical Center Groningen, Groningen, The Netherlands.
  • Zolota V; Department of Pathology, Rion University Hospital, Patras, Greece.
  • Wesseling J; Department of Molecular Pathology, the 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.
  • Sapino A; Department of Medical Sciences, University of Torino, Torino, Italy; Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
  • Chmielik E; Tumor Pathology Department, Maria Sklodowska-Curie Memorial National Research Institute of Oncology, Gliwice, Poland.
  • Ryska A; Charles University Medical Faculty and University Hospital, Hradec Kralove, Czech Republic.
  • Broeks A; Core Facility Molecular Pathology and Biobanking, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Voogd AC; Department of Epidemiology, Maastricht University, Maastricht, The Netherlands; Department of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands.
  • van der Wall E; Cancer Center, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Siesling S; Department of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands; Department of Health Technology and Services Research, Technical Medical Centre, University of Twente, Enschede, The Netherlands.
  • Salgado R; Division of Clinical Medicine and Research, Peter MacCallum Cancer Centre, Melbourne, Australia; Department of Pathology, GZA-ZNA Hospitals, Antwerp, Belgium.
  • Dackus GMHE; Department of Molecular Pathology, the Netherlands Cancer Institute, Amsterdam, The Netherlands; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Hauptmann M; Institute of Biostatistics and Registry Research, Brandenburg Medical School Theodor Fontane, Neuruppin, Germany.
  • Kok M; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands; Department of Tumorbiology & Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Linn SC; Department of Molecular Pathology, the Netherlands Cancer Institute, Amsterdam, The Netherlands; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands. Electronic address: s.l
ESMO Open ; 9(3): 102923, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38452438
ABSTRACT

BACKGROUND:

In the absence of prognostic biomarkers, most patients with early-stage triple-negative breast cancer (eTNBC) are treated with combination chemotherapy. The identification of biomarkers to select patients for whom treatment de-escalation or escalation could be considered remains an unmet need. We evaluated the prognostic value of histopathologic traits in a unique cohort of young, (neo)adjuvant chemotherapy-naïve patients with early-stage (stage I or II), node-negative TNBC and long-term follow-up, in relation to stromal tumor-infiltrating lymphocytes (sTILs) for which the prognostic value was recently reported. MATERIALS AND

METHODS:

We studied all 485 patients with node-negative eTNBC from the population-based PARADIGM cohort which selected women aged <40 years diagnosed between 1989 and 2000. None of the patients had received (neo)adjuvant chemotherapy according to standard practice at the time. Associations between histopathologic traits and breast cancer-specific survival (BCSS) were analyzed with Cox proportional hazard models.

RESULTS:

With a median follow-up of 20.0 years, an independent prognostic value for BCSS was observed for lymphovascular invasion (LVI) [adjusted (adj.) hazard ratio (HR) 2.35, 95% confidence interval (CI) 1.49-3.69], fibrotic focus (adj. HR 1.61, 95% CI 1.09-2.37) and sTILs (per 10% increment adj. HR 0.75, 95% CI 0.69-0.82). In the sTILs <30% subgroup, the presence of LVI resulted in a higher cumulative incidence of breast cancer death (at 20 years, 58%; 95% CI 41% to 72%) compared with when LVI was absent (at 20 years, 32%; 95% CI 26% to 39%). In the ≥75% sTILs subgroup, the presence of LVI might be associated with poor survival (HR 11.45, 95% CI 0.71-182.36, two deaths). We confirm the lack of prognostic value of androgen receptor expression and human epidermal growth factor receptor 2 -low status.

CONCLUSIONS:

sTILs, LVI and fibrotic focus provide independent prognostic information in young women with node-negative eTNBC. Our results are of importance for the selection of patients for de-escalation and escalation trials.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias de Mama Triplo Negativas Limite: Female / Humans Idioma: En Revista: ESMO Open Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias de Mama Triplo Negativas Limite: Female / Humans Idioma: En Revista: ESMO Open Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda