The prognostic impact of the tumour stroma fraction: A machine learning-based analysis in 16 human solid tumour types.


Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
Mar 2021
Historique:
received: 13 10 2020
revised: 04 02 2021
accepted: 18 02 2021
pubmed: 12 3 2021
medline: 3 11 2021
entrez: 11 3 2021
Statut: ppublish

Résumé

The development of a reactive tumour stroma is a hallmark of tumour progression and pronounced tumour stroma is generally considered to be associated with clinical aggressiveness. The variability between tumour types regarding stroma fraction, and its prognosis associations, have not been systematically analysed. Using an objective machine-learning method we quantified the tumour stroma in 16 solid cancer types from 2732 patients, representing retrospective tissue collections of surgically resected primary tumours. Image analysis performed tissue segmentation into stromal and epithelial compartment based on pan-cytokeratin staining and autofluorescence patterns. The stroma fraction was highly variable within and across the tumour types, with kidney cancer showing the lowest and pancreato-biliary type periampullary cancer showing the highest stroma proportion (median 19% and 73% respectively). Adjusted Cox regression models revealed both positive (pancreato-biliary type periampullary cancer and oestrogen negative breast cancer, HR(95%CI)=0.56(0.34-0.92) and HR(95%CI)=0.41(0.17-0.98) respectively) and negative (intestinal type periampullary cancer, HR(95%CI)=3.59(1.49-8.62)) associations of the tumour stroma fraction with survival. Our study provides an objective quantification of the tumour stroma fraction across major types of solid cancer. Findings strongly argue against the commonly promoted view of a general associations between high stroma abundance and poor prognosis. The results also suggest that full exploitation of the prognostic potential of tumour stroma requires analyses that go beyond determination of stroma abundance. The Swedish Cancer Society, The Lions Cancer Foundation Uppsala, The Swedish Government Grant for Clinical Research, The Mrs Berta Kamprad Foundation, Sweden, Sellanders foundation, P.O.Zetterling Foundation, and The Sjöberg Foundation, Sweden.

Sections du résumé

BACKGROUND BACKGROUND
The development of a reactive tumour stroma is a hallmark of tumour progression and pronounced tumour stroma is generally considered to be associated with clinical aggressiveness. The variability between tumour types regarding stroma fraction, and its prognosis associations, have not been systematically analysed.
METHODS METHODS
Using an objective machine-learning method we quantified the tumour stroma in 16 solid cancer types from 2732 patients, representing retrospective tissue collections of surgically resected primary tumours. Image analysis performed tissue segmentation into stromal and epithelial compartment based on pan-cytokeratin staining and autofluorescence patterns.
FINDINGS RESULTS
The stroma fraction was highly variable within and across the tumour types, with kidney cancer showing the lowest and pancreato-biliary type periampullary cancer showing the highest stroma proportion (median 19% and 73% respectively). Adjusted Cox regression models revealed both positive (pancreato-biliary type periampullary cancer and oestrogen negative breast cancer, HR(95%CI)=0.56(0.34-0.92) and HR(95%CI)=0.41(0.17-0.98) respectively) and negative (intestinal type periampullary cancer, HR(95%CI)=3.59(1.49-8.62)) associations of the tumour stroma fraction with survival.
INTERPRETATION CONCLUSIONS
Our study provides an objective quantification of the tumour stroma fraction across major types of solid cancer. Findings strongly argue against the commonly promoted view of a general associations between high stroma abundance and poor prognosis. The results also suggest that full exploitation of the prognostic potential of tumour stroma requires analyses that go beyond determination of stroma abundance.
FUNDING BACKGROUND
The Swedish Cancer Society, The Lions Cancer Foundation Uppsala, The Swedish Government Grant for Clinical Research, The Mrs Berta Kamprad Foundation, Sweden, Sellanders foundation, P.O.Zetterling Foundation, and The Sjöberg Foundation, Sweden.

Identifiants

pubmed: 33706249
pii: S2352-3964(21)00062-1
doi: 10.1016/j.ebiom.2021.103269
pmc: PMC7960932
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103269

Informations de copyright

Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Conflict of interest statement: Artur Mezheyeuski, Carina Strell and Patrick Micke own shares in the company HistoOne AB, Uppsala, Sweden, which infrastructure was used for the pathology assessment of tissue samples in the study. The other authors have no conflicts of interest to disclose.

Auteurs

Patrick Micke (P)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Carina Strell (C)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Johanna Mattsson (J)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Alfonso Martín-Bernabé (A)

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.

Hans Brunnström (H)

Department of Clinical Sciences Lund, Division of Pathology, Lund University, Lund, Sweden; Department of Genetics and Pathology, Division of Laboratory Medicine, Region Skåne, Lund, Sweden.

Jutta Huvila (J)

Department of Pathology, University of British Columbia, Vancouver, Canada; Department of Pathology, University of Turku, Turku, Finland.

Malin Sund (M)

Department of Surgical and perioperative sciences/Surgery, Umeå University, Umeå, Sweden.

Fredrik Wärnberg (F)

Department of Surgery at Institute of Clinical Sciences, Sahlgrenska University Hospital Göteborg, Göteborg, Sweden.

Fredrik Ponten (F)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Bengt Glimelius (B)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Ina Hrynchyk (I)

City Clinical Pathologoanatomic Bureau, Minsk, Belarus.

Siarhei Mauchanski (S)

N.N. Alexandrov National Cancer Centre of Belarus, 223040 Minsk, Belarus.

Salome Khelashvili (S)

N.N. Alexandrov National Cancer Centre of Belarus, 223040 Minsk, Belarus.

Gemma Garcia-Vicién (G)

ProCURE, Program Against Cancer therapeutic Resistance, Catalan Institute of Oncology, Molecular Mechanisms and Experimental Therapy in Oncology Program (ONCOBELL), IDIBELL, L'Hospitalet de Llobregat, Barcelona, Catalonia, Spain.

David G Molleví (DG)

ProCURE, Program Against Cancer therapeutic Resistance, Catalan Institute of Oncology, Molecular Mechanisms and Experimental Therapy in Oncology Program (ONCOBELL), IDIBELL, L'Hospitalet de Llobregat, Barcelona, Catalonia, Spain.

Per-Henrik Edqvist (PH)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Aine O Reilly (A)

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.

Sara Corvigno (S)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.

Hanna Dahlstrand (H)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.

Johan Botling (J)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Ulrika Segersten (U)

Department of Surgical Sciences, Uppsala University, Uppsala 751 85, Sweden.

Agnieszka Krzyzanowska (A)

Department of Translational Medicine, Division of Urological Cancers, Lund University, Lund, Sweden.

Anders Bjartell (A)

Department of Translational Medicine, Division of Urological Cancers, Lund University, Lund, Sweden.

Jacob Elebro (J)

Department of Clinical Sciences Lund, Division of Oncology and Therapeutic Pathology, Lund University, SE-221 00 Lund, Sweden.

Margareta Heby (M)

Department of Clinical Sciences Lund, Division of Oncology and Therapeutic Pathology, Lund University, SE-221 00 Lund, Sweden.

Sebastian Lundgren (S)

Department of Clinical Sciences Lund, Division of Oncology and Therapeutic Pathology, Lund University, SE-221 00 Lund, Sweden.

Charlotta Hedner (C)

Department of Clinical Sciences Lund, Division of Oncology and Therapeutic Pathology, Lund University, SE-221 00 Lund, Sweden.

David Borg (D)

Department of Clinical Sciences Lund, Division of Oncology and Therapeutic Pathology, Lund University, SE-221 00 Lund, Sweden.

Jenny Brändstedt (J)

Department of Clinical Sciences Lund, Division of Oncology and Therapeutic Pathology, Lund University, SE-221 00 Lund, Sweden.

Hanna Sartor (H)

Diagnostic Radiology, Department of Translational Medicine, Lund University, Skåne University Hospital, Lund, Sweden.

Per-Uno Malmström (PU)

Department of Surgical Sciences, Uppsala University, Uppsala 751 85, Sweden.

Martin Johansson (M)

Department of Laboratory Medicine at Institute of Biomedicine, Sahlgrenska Universitety Hospital Göteborg, Göteborg, Sweden.

Björn Nodin (B)

Department of Clinical Sciences Lund, Division of Oncology and Therapeutic Pathology, Lund University, SE-221 00 Lund, Sweden.

Max Backman (M)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Cecilia Lindskog (C)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden.

Karin Jirström (K)

Department of Genetics and Pathology, Division of Laboratory Medicine, Region Skåne, Lund, Sweden; Department of Clinical Sciences Lund, Division of Oncology and Therapeutic Pathology, Lund University, SE-221 00 Lund, Sweden.

Artur Mezheyeuski (A)

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala 751 85, Sweden. Electronic address: artur.mezheyeuski@igp.uu.se.

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Classifications MeSH