The Nanocind Signature Is an Independent Prognosticator of Recurrence and Death in Uterine Leiomyosarcomas.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
15 02 2020
Historique:
received: 03 09 2019
revised: 18 10 2019
accepted: 26 11 2019
pubmed: 5 12 2019
medline: 18 11 2020
entrez: 5 12 2019
Statut: ppublish

Résumé

Uterine leiomyosarcoma, which accounts for 7% of all soft-tissue sarcomas and 1%-3% of all uterine malignancies, is an aggressive tumor responsible for a significant proportion of uterine cancer-related deaths. While Federation Internationale des Gynaecologistes et Obstetristes (FIGO) stage is the most important prognostic factor, metastatic and relapse rates at stage I exceed 50% so it is currently impossible to predict the clinical outcome of stage I leiomyosarcomas. In 2010, our team published a transcriptomic signature composed of 67 genes related to chromosome biogenesis, mitosis control, and chromosome segregation. It has demonstrated its prognostic value in many cancer types and was recently successfully applied to formalin-fixed, paraffin-embedded sarcomas by NanoCind on NanoString technology, making another step forward toward its use in routine practice. Sixty uterine leiomyosarcomas at any stage, including 40 localized in the uterus (stage I), were analyzed with the NanoCind (CINSARC with NanoString) signature. Its prognostic value was evaluated for overall survival and relapse-free survival and compared in multivariate analysis with other prognostic markers like FIGO staging and genomic index. The NanoCind signature was able to split the heterogeneous group of uterine leiomyosarcomas of any stage including stage I into two distinct groups with different relapse-free survival and overall survival. These results were validated on an independent cohort of uterine leiomyosarcomas in The Cancer Genome Atlas consortium. The NanoCind signature is a powerful prognosticator that outperforms FIGO staging and the genomic index. The CINSARC signature is platform independent and "ready to use" and should now be used for randomization in future therapeutic trials.

Identifiants

pubmed: 31796515
pii: 1078-0432.CCR-19-2891
doi: 10.1158/1078-0432.CCR-19-2891
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

855-861

Informations de copyright

©2019 American Association for Cancer Research.

Auteurs

Sabrina Croce (S)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France. s.croce@bordeaux.unicancer.fr.
INSERM U1218, Bordeaux, France.

Tom Lesluyes (T)

University of Bordeaux, Bordeaux, France.
Oncosarc, INSERM UMR1037, Cancer Research Center of Toulouse, Toulouse, France.
Department of Pathology, Institut Claudius Regaud, IUCT-Oncopole, Toulouse France.

Carine Valle (C)

Plateau Génomique et Transcriptomique, INSERM U1037, Cancer Research Center of Toulouse, Toulouse, France.

Loubna M'Hamdi (L)

Department of Pathology, Institut Claudius Regaud, IUCT-Oncopole, Toulouse France.

Noémie Thébault (N)

Oncosarc, INSERM UMR1037, Cancer Research Center of Toulouse, Toulouse, France.

Gaëlle Pérot (G)

Oncosarc, INSERM UMR1037, Cancer Research Center of Toulouse, Toulouse, France.
Department of Pathology, Institut Claudius Regaud, IUCT-Oncopole, Toulouse France.

Eberhard Stoeckle (E)

Department of Surgery, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.

Jean-Christophe Noël (JC)

Department of Pathology, Clinic of Gynecopathology and Senology, Erasme University Hospital, Brussels, Belgium.

Quitterie Fontanges (Q)

Department of Pathology, Clinic of Gynecopathology and Senology, Erasme University Hospital, Brussels, Belgium.

Mojgan Devouassoux-Shisheboran (M)

Department of Pathology, CHU Lyon Sud, Pierrebenite, France.

Denis Querleu (D)

Department of Surgery, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.

Frédéric Guyon (F)

Department of Surgery, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.

Anne Floquet (A)

Department of Oncology, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.

Camille Chakiba (C)

Department of Oncology, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.

Laetitia Mayeur (L)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.

Flora Rebier (F)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.

Gaëtan Marie MacGrogan (GM)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.

Isabelle Soubeyran (I)

Department of Biopathology, Institut Bergonié, Comprehensive Cancer Center, Bordeaux, France.
INSERM U1218, Bordeaux, France.

Sophie Le Guellec (S)

Oncosarc, INSERM UMR1037, Cancer Research Center of Toulouse, Toulouse, France.
Department of Pathology, Institut Claudius Regaud, IUCT-Oncopole, Toulouse France.

Frédéric Chibon (F)

Oncosarc, INSERM UMR1037, Cancer Research Center of Toulouse, Toulouse, France.
Department of Pathology, Institut Claudius Regaud, IUCT-Oncopole, Toulouse France.

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