Dynamic clonal remodelling in breast cancer metastases is associated with subtype conversion.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
10 2019
Historique:
received: 07 02 2019
revised: 03 07 2019
accepted: 04 07 2019
pubmed: 7 9 2019
medline: 10 6 2020
entrez: 7 9 2019
Statut: ppublish

Résumé

Changes in the clinical subtype (CS) and intrinsic subtype (IS) between breast cancer (BC) metastases and corresponding primary tumours have been reported. However, their relationship with tumour genomic changes remains poorly characterised. Here, we analysed the association between genomic remodelling and subtype conversion in paired primary and metastatic BC samples. A total of 57 paired primary and metastatic tumours from GEICAM/2009-03 (ConvertHER, NCT01377363) study participants with centrally assessed CS (n = 57) and IS (n = 46) were analysed. Targeted capture and next-generation sequencing of 202 genes on formalin-fixed paraffin-embedded samples was performed. The cancer cell fraction (CCF) of mutations in primary and metastatic pairs was estimated as a surrogate of tumour clonal architecture. Changes in mutation CCF between matched primary and metastatic tumours were analysed in the presence or absence of subtype conversion. CS conversion occurred in 24.6% and IS conversion occurred in 36.9% of metastases. Primary tumours and metastases had a median of 11 (range, 3-29) and 9 (range, 1-38) mutations, respectively (P = 0.05). Overall, mutations in metastases showed a higher estimated CCF than in primary tumours (median CCF, 0.51 and 0.47, respectively; P = 0.042), consistent with increased clonal homogeneity. The increase in mutation CCF was significant in CS-converted (P = 0.04) but not in IS-converted (P = 0.48) metastases. Clonal remodelling was highest in metastases from hormone receptor-positive and human epidermal growth factor 2 (HER2)-positive tumours (P = 0.006). Mutations in BC metastases showed significantly higher estimated CCF than primary tumours. CCF changes were more prominent in metastases with CS conversion. Our findings suggest that changes in BC subtypes are linked to clonal remodelling during BC evolution.

Sections du résumé

BACKGROUND
Changes in the clinical subtype (CS) and intrinsic subtype (IS) between breast cancer (BC) metastases and corresponding primary tumours have been reported. However, their relationship with tumour genomic changes remains poorly characterised. Here, we analysed the association between genomic remodelling and subtype conversion in paired primary and metastatic BC samples.
METHODS
A total of 57 paired primary and metastatic tumours from GEICAM/2009-03 (ConvertHER, NCT01377363) study participants with centrally assessed CS (n = 57) and IS (n = 46) were analysed. Targeted capture and next-generation sequencing of 202 genes on formalin-fixed paraffin-embedded samples was performed. The cancer cell fraction (CCF) of mutations in primary and metastatic pairs was estimated as a surrogate of tumour clonal architecture. Changes in mutation CCF between matched primary and metastatic tumours were analysed in the presence or absence of subtype conversion.
FINDINGS
CS conversion occurred in 24.6% and IS conversion occurred in 36.9% of metastases. Primary tumours and metastases had a median of 11 (range, 3-29) and 9 (range, 1-38) mutations, respectively (P = 0.05). Overall, mutations in metastases showed a higher estimated CCF than in primary tumours (median CCF, 0.51 and 0.47, respectively; P = 0.042), consistent with increased clonal homogeneity. The increase in mutation CCF was significant in CS-converted (P = 0.04) but not in IS-converted (P = 0.48) metastases. Clonal remodelling was highest in metastases from hormone receptor-positive and human epidermal growth factor 2 (HER2)-positive tumours (P = 0.006).
CONCLUSIONS
Mutations in BC metastases showed significantly higher estimated CCF than primary tumours. CCF changes were more prominent in metastases with CS conversion. Our findings suggest that changes in BC subtypes are linked to clonal remodelling during BC evolution.

Identifiants

pubmed: 31491604
pii: S0959-8049(19)30403-4
doi: 10.1016/j.ejca.2019.07.003
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

54-64

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Ana Lluch (A)

Hospital Clínico Universitario de Valencia, Valencia, Spain; GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Centro de Investigación Biomédica en Red de Oncología, CIBERONC-ISCIII, Spain; Universidad de Valencia, Valencia, Spain; Instituto de Investigación Sanitaria INCLIVA, Valencia, Spain.

Ana M González-Angulo (AM)

MD Anderson Cancer Center, Houston, TX 77030, USA.

David Casadevall (D)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Centro de Investigación Biomédica en Red de Oncología, CIBERONC-ISCIII, Spain; IMIM Hospital del Mar Medical Research Institute; Barcelona, Spain; Medical Oncology Department Hospital del Mar, Barcelona, Barcelona, Spain.

Agda K Eterovic (AK)

MD Anderson Cancer Center, Houston, TX 77030, USA.

Eduardo Martínez de Dueñas (E)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Hospital Provincial de Castellón, Castellón, Spain.

Xiaofeng Zheng (X)

MD Anderson Cancer Center, Houston, TX 77030, USA.

Ángel Guerrero-Zotano (Á)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Instituto Valenciano de Oncología, Valencia, Spain.

Shuying Liu (S)

MD Anderson Cancer Center, Houston, TX 77030, USA.

Ramón Pérez (R)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Hospital Universitario Quirón de Madrid, Madrid, Spain.

Ken Chen (K)

MD Anderson Cancer Center, Houston, TX 77030, USA.

Jose Ignacio Chacón (JI)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Hospital Virgen de la Salud, Toledo, Spain.

Gordon B Mills (GB)

MD Anderson Cancer Center, Houston, TX 77030, USA; Department of Systems Biology and Institute of Personalized Cancer Therapy, The University of Texas, USA.

Silvia Antolín (S)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Complejo Hospitalario Universitario A Coruña, A Coruña, Spain.

Isabel Blancas (I)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Hospital Clínico San Cecilio, Granada, Spain.

Paula López-Serra (P)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain.

Eva Carrasco (E)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain.

Rosalía Caballero (R)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain.

Aleix Prat (A)

Medical Oncology Department, Hospital Clínic of Barcelona, Barcelona, Spain.

Federico Rojo (F)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Centro de Investigación Biomédica en Red de Oncología, CIBERONC-ISCIII, Spain; Fundación Jiménez Díaz, Madrid, Spain.

Abel Gonzalez-Perez (A)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Institut de Recerca Biomedica Barcelona, Spain. Electronic address: abel.gonzalez@irbbarcelona.org.

Funda Meric-Bernstam (F)

MD Anderson Cancer Center, Houston, TX 77030, USA. Electronic address: fmeric@mdanderson.org.

Joan Albanell (J)

GEICAM (Grupo GEICAM de Investigación en Cáncer de Mama), Madrid, Spain; Centro de Investigación Biomédica en Red de Oncología, CIBERONC-ISCIII, Spain; IMIM Hospital del Mar Medical Research Institute; Barcelona, Spain; Medical Oncology Department Hospital del Mar, Barcelona, Barcelona, Spain; Universitat Pompeu Fabra, Barcelona, Spain. Electronic address: 96087@parcdesalutmar.cat.

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