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Transcriptomic definition of molecular subgroups of small round cell sarcomas

Journal of pathology and bacteriology, 2018-05, Vol.245 (1), p.29-40

2018

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Grading of soft tissue sarcomas: review and update

Archives of pathology & laboratory medicine (1976), 2006-10, Vol.130 (10), p.1448-1453

Coindre, Jean-Michel

2006

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Tazemetostat, an EZH2 inhibitor, in relapsed or refractory B-cell non-Hodgkin lymphoma and advanced solid tumours: a first-in-human, open-label, phase 1 study

The lancet oncology, 2018-05, Vol.19 (5), p.649-659

2018

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The value of research collaborations and consortia in rare cancers

The lancet oncology, 2016-02, Vol.17 (2), p.e62-e69

2016

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High prevalence of CIC fusion with double-homeobox (DUX4) transcription factors in EWSR1-negative undifferentiated small blue round cell sarcomas

Genes chromosomes & cancer, 2012-03, Vol.51 (3), p.207-218

2012

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The 2015 World Health Organization Classification of Tumors of the Thymus: Continuity and Changes

Journal of thoracic oncology, 2015-10, Vol.10 (10), p.1383-1395

2015

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Well-differentiated and dedifferentiated liposarcomas

American journal of human genetics, 2010-02, Vol.456 (2), p.167-179

2010

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A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion

Nature genetics, 2012-04, Vol.44 (4), p.461-466

2012

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ETV4 is a useful marker for the diagnosis of CIC-rearranged undifferentiated round-cell sarcomas: a study of 127 cases including mimicking lesions

Modern pathology, 2016-12, Vol.29 (12), p.1523-1531

2016

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Incidence of Soft Tissue Sarcoma and Beyond: A Population-Based Prospective Study in 3 European Regions

Cancer, 2012-11, Vol.118 (21), p.5339-5348

2012

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Overall and net survival of patients with sarcoma between 2005 and 2010: Results from the French Network of Cancer Registries (FRANCIM)

Cancer, 2022-07, Vol.128 (13), p.2483-2492

2022

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Prognostic Factors Influencing Progression-Free Survival Determined From a Series of Sporadic Desmoid Tumors: A Wait-and-See Policy According to Tumor Presentation

Journal of clinical oncology, 2011-09, Vol.29 (26), p.3553-3558

2011

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Recurrent MALAT1-GLI1 oncogenic fusion and GLI1 up-regulation define a subset of plexiform fibromyxoma

The Journal of pathology, 2016-07, Vol.239 (3), p.335-343

2016

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Trends in survival for patients with metastatic soft‐tissue sarcoma

Cancer, 2011-03, Vol.117 (5), p.1049-1054

2011

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Grading of soft tissue sarcomas: from histological to molecular assessment

Pathology, 2014-02, Vol.46 (2), p.113-120

2014

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A subset of so‐called dermal non‐neural granular cell tumours are underlined by ALK fusions, further supporting the idea that they represent a variant of epithelioid fibrous histiocytoma

Histopathology, 2018-09, Vol.73 (3), p.532-534

2018

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Tumor genotype is an independent prognostic factor in primary gastrointestinal stromal tumors of gastric origin: a european multicenter analysis based on ConticaGIST

Clinical cancer research, 2014-12, Vol.20 (23), p.6105-6116

2014

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Incidence of soft tissue sarcoma and beyond

Cancer, 2012-11, Vol.118 (21), p.5339-5348

2012

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Evaluation of eight melanocytic and neural crest‐associated markers in a well‐characterised series of 124 malignant peripheral nerve sheath tumours (MPNST): useful to distinguish MPNST from melanoma?

Histopathology, 2018-12, Vol.73 (6), p.969-982

2018

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Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material

Genes chromosomes & cancer, 2014-06, Vol.53 (6), p.475-486

2014

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Transcriptomic definition of molecular subgroups of small round cell sarcomas

Grading of soft tissue sarcomas: review and update

Tazemetostat, an EZH2 inhibitor, in relapsed or refractory B-cell non-Hodgkin lymphoma and advanced solid tumours: a first-in-human, open-label, phase 1 study

The value of research collaborations and consortia in rare cancers

High prevalence of CIC fusion with double-homeobox (DUX4) transcription factors in EWSR1-negative undifferentiated small blue round cell sarcomas

The 2015 World Health Organization Classification of Tumors of the Thymus: Continuity and Changes

Well-differentiated and dedifferentiated liposarcomas

A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion

Clinical effect of molecular methods in sarcoma diagnosis (GENSARC): a prospective, multicentre, observational study

ETV4 is a useful marker for the diagnosis of CIC-rearranged undifferentiated round-cell sarcomas: a study of 127 cases including mimicking lesions

Superficial CD34‐positive fibroblastic tumor and PRDM10‐rearranged soft tissue tumor are overlapping entities: a comprehensive study of 20 cases

Incidence of Soft Tissue Sarcoma and Beyond: A Population-Based Prospective Study in 3 European Regions

Presentation and outcome of frequent and rare sarcoma histologic subtypes: A study of 10,262 patients with localized visceral/soft tissue sarcoma managed in reference centers

Overall and net survival of patients with sarcoma between 2005 and 2010: Results from the French Network of Cancer Registries (FRANCIM)

Prognostic Factors Influencing Progression-Free Survival Determined From a Series of Sporadic Desmoid Tumors: A Wait-and-See Policy According to Tumor Presentation

Recurrent MALAT1-GLI1 oncogenic fusion and GLI1 up-regulation define a subset of plexiform fibromyxoma

Trends in survival for patients with metastatic soft‐tissue sarcoma

Watch and Wait Approach for Re-excision After Unplanned Yet Macroscopically Complete Excision of Extremity and Superficial Truncal Soft Tissue Sarcoma is Safe and Does Not Affect Metastatic Risk or Amputation Rate

Grading of soft tissue sarcomas: from histological to molecular assessment

A subset of so‐called dermal non‐neural granular cell tumours are underlined by ALK fusions, further supporting the idea that they represent a variant of epithelioid fibrous histiocytoma

Tumor genotype is an independent prognostic factor in primary gastrointestinal stromal tumors of gastric origin: a european multicenter analysis based on ConticaGIST

Incidence of soft tissue sarcoma and beyond

Validated prediction of clinical outcome in sarcomas and multiple types of cancer on the basis of a gene expression signature related to genome complexity

Evaluation of eight melanocytic and neural crest‐associated markers in a well‐characterised series of 124 malignant peripheral nerve sheath tumours (MPNST): useful to distinguish MPNST from melanoma?

Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material

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