Literature DB >> 33769463

Patterns of Translocation Testing in Patients Enrolling in a Cooperative Group Trial for Newly Diagnosed Metastatic Ewing Sarcoma.

Steven G DuBois1, Mark D Krailo2, Allen Buxton2, Stephen L Lessnick3, Lisa A Teot4, Dinesh Rakheja5, Brian D Crompton1, Katherine A Janeway1, Richard G Gorlick6, Julia Glade-Bender7.   

Abstract

CONTEXT.—: Molecular diagnostics play an increasing role in the diagnosis of Ewing sarcoma. The type of molecular testing used in clinical practice has been poorly described. OBJECTIVE.—: To describe patterns of translocation testing for newly diagnosed Ewing sarcoma. DESIGN.—: Children's Oncology Group (COG) trial AEWS1221 was a phase III randomized trial enrolling patients with newly diagnosed metastatic Ewing sarcoma from 2014 to 2019. Patients were required to have a histologic diagnosis of Ewing sarcoma, but translocation testing was not required. Sites provided types and results of any molecular diagnostics performed. RESULTS.—: Data from 305 enrolled patients were available. The most common type of molecular testing was fluorescence in situ hybridization (FISH) performed on the primary tumor (236 of 305 patients; 77.4%), with positive testing for an EWSR1 or FUS translocation in 211 (89.4%). Reverse transcription-polymerase chain reaction (RT-PCR) on the primary tumor was performed in 61 of 305 patients (20%), with positive results in 48 of 61 patients (78.7%). Next-generation sequencing was reported in 7 patients for the primary tumor and in 3 patients for metastatic sites. For all types of testing on either primary or metastatic tumor, 16 of 305 patients (5.2%) had no reported translocation testing. When evaluating all results from all testing, 44 of 305 patients (14.4%) lacked documentation of an abnormality consistent with a molecular diagnosis of Ewing sarcoma. CONCLUSIONS.—: COG sites enrolling in a Ewing sarcoma trial have high rates of testing by FISH or PCR. A small proportion of patients have no translocation testing on either primary or metastatic sites. Next-generation sequencing techniques are not yet commonly used in this context.

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Year:  2021        PMID: 33769463      PMCID: PMC9048754          DOI: 10.5858/arpa.2020-0671-OA

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.686


  16 in total

1.  The clinical heterogeneity of round cell sarcomas with EWSR1/FUS gene fusions: Impact of gene fusion type on clinical features and outcome.

Authors:  Yusuke Tsuda; Lei Zhang; Paul Meyers; William D Tap; John H Healey; Cristina R Antonescu
Journal:  Genes Chromosomes Cancer       Date:  2020-05-28       Impact factor: 5.006

2.  The use of interval-compressed chemotherapy with the addition of vincristine, irinotecan, and temozolomide for pediatric patients with newly diagnosed desmoplastic small round cell tumor.

Authors:  Kevin X Liu; Natalie B Collins; Katie A Greenzang; Elissa Furutani; Kevin Campbell; Andrew Groves; Elizabeth A Mullen; Suzanne Shusterman; Jennifer Spidle; Karen J Marcus; Brent R Weil; Christopher B Weldon; A Lindsay Frazier; Katherine A Janeway; Allison F O'Neill; Jennifer W Mack; Steven G DuBois; David S Shulman
Journal:  Pediatr Blood Cancer       Date:  2020-07-19       Impact factor: 3.167

Review 3.  Ewing sarcoma.

Authors:  Thomas G P Grünewald; Florencia Cidre-Aranaz; Didier Surdez; Eleni M Tomazou; Enrique de Álava; Heinrich Kovar; Poul H Sorensen; Olivier Delattre; Uta Dirksen
Journal:  Nat Rev Dis Primers       Date:  2018-07-05       Impact factor: 52.329

4.  Novel and established EWSR1 gene fusions and associations identified by next-generation sequencing and fluorescence in-situ hybridization.

Authors:  Melissa Krystel-Whittemore; Martin S Taylor; Miguel Rivera; Jochen K Lennerz; Long P Le; Dora Dias-Santagata; Anthony John Iafrate; Vikram Deshpande; Ivan Chebib; Gunnlaugur Petur Nielsen; Chin-Lee Wu; Valentina Nardi
Journal:  Hum Pathol       Date:  2019-08-17       Impact factor: 3.466

5.  Detailed cytogenetic and array analysis of pediatric primitive sarcomas reveals a recurrent CIC-DUX4 fusion gene event.

Authors:  Maisa Yoshimoto; Cassandra Graham; Susan Chilton-MacNeill; Eric Lee; Mary Shago; Jeremy Squire; Maria Zielenska; Gino R Somers
Journal:  Cancer Genet Cytogenet       Date:  2009-11

6.  Ewing-like sarcomas with BCOR-CCNB3 fusion transcript: a clinical, radiological and pathological retrospective study from the Société Française des Cancers de L'Enfant.

Authors:  Sarah Cohen-Gogo; Cécile Cellier; Jean-Michel Coindre; Véronique Mosseri; Gaëlle Pierron; Cécile Guillemet; Antoine Italiano; Laurence Brugières; Daniel Orbach; Valérie Laurence; Olivier Delattre; Jean Michon
Journal:  Pediatr Blood Cancer       Date:  2014-08-31       Impact factor: 3.167

7.  ChildSeq-RNA: A next-generation sequencing-based diagnostic assay to identify known fusion transcripts in childhood sarcomas.

Authors:  Mohammed A Qadir; Shing H Zhan; Brian Kwok; Jeremy Bruestle; Becky Drees; Oana-Eugenia Popescu; Poul H Sorensen
Journal:  J Mol Diagn       Date:  2014-02-08       Impact factor: 5.568

8.  The spectrum of EWSR1-rearranged neoplasms at a tertiary sarcoma centre; assessing 772 tumour specimens and the value of current ancillary molecular diagnostic modalities.

Authors:  Jonathan Noujaim; Robin L Jones; John Swansbury; David Gonzalez; Charlotte Benson; Ian Judson; Cyril Fisher; Khin Thway
Journal:  Br J Cancer       Date:  2017-01-31       Impact factor: 7.640

9.  A small molecule blocking oncogenic protein EWS-FLI1 interaction with RNA helicase A inhibits growth of Ewing's sarcoma.

Authors:  Hayriye V Erkizan; Yali Kong; Melinda Merchant; Silke Schlottmann; Julie S Barber-Rotenberg; Linshan Yuan; Ogan D Abaan; Tsu-Hang Chou; Sivanesan Dakshanamurthy; Milton L Brown; Aykut Uren; Jeffrey A Toretsky
Journal:  Nat Med       Date:  2009-07-05       Impact factor: 53.440

Review 10.  Breakthrough Technologies Reshape the Ewing Sarcoma Molecular Landscape.

Authors:  Carmen Salguero-Aranda; Ana Teresa Amaral; Joaquín Olmedo-Pelayo; Juan Diaz-Martin; Enrique de Álava
Journal:  Cells       Date:  2020-03-26       Impact factor: 6.600

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  2 in total

1.  Cutaneous Ewing Sarcoma Presenting as a Second Primary Malignancy in a Child.

Authors:  Jessica Daley; Nathan Williams; Claudia M Salgado; Charles Schultz; Julia Meade; John Ozolek; Brock Lindsey; Kelly M Bailey
Journal:  J Pediatr Hematol Oncol       Date:  2022-04-14       Impact factor: 1.170

2.  Rapid and highly sensitive approach for multiplexed somatic fusion detection.

Authors:  Samuel Abbou; Sarah Finstuen-Magro; Brigit McDannell; Michelle Feenstra; Abigail Ward; David S Shulman; Birgit Geoerger; Joadly Duplan; Hannah Comeau; Katherine A Janeway; Kelly Klega; Brian D Crompton
Journal:  Mod Pathol       Date:  2022-03-28       Impact factor: 8.209

  2 in total

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