RET Fusion Testing in Patients With NSCLC: The RETING Study

dc.contributor.authorConde, Esther
dc.contributor.authorHernández, Susana
dc.contributor.authorRodríguez Carrillo, Jose Luis
dc.contributor.authorMartínez, Rebeca
dc.contributor.authorAlonso, Marta
dc.contributor.authorCurto, Daniel
dc.contributor.authorJiménez, Beatriz
dc.contributor.authorCaminoa, Alejandra
dc.contributor.authorBenito, Amparo
dc.contributor.authorGarrido, Pilar
dc.contributor.authorClave, Sergi
dc.contributor.authorArriola, Edurne
dc.contributor.authorEsteban Rodríguez, Isabel
dc.contributor.authorCastro, Javier de
dc.contributor.authorSansano, Irene
dc.contributor.authorFelip, Enriqueta
dc.contributor.authorRojo, Federico
dc.contributor.authorDómine, Manuel
dc.contributor.authorAbdulkader, Ihab
dc.contributor.authorGarcía González, Jorge
dc.contributor.authorTeixidó, Cristina
dc.contributor.authorReguart, Noemí
dc.contributor.authorCompañ, Desamparados
dc.contributor.authorInsa, Amelia
dc.contributor.authorMancheño, Nuria
dc.contributor.authorPalanca, Sarai
dc.contributor.authorJuan Vidal, Oscar
dc.contributor.authorBaixeras, Nuria
dc.contributor.authorNadal, Ernest
dc.contributor.authorCebollero, Maria
dc.contributor.authorCalles Blanco, Antonio
dc.contributor.authorMartín, Paloma
dc.contributor.authorSalas, Clara
dc.contributor.authorProvencio, Mariano
dc.contributor.authorAranda, Ignacio
dc.contributor.authorMassuti, Bartomeu
dc.contributor.authorLópez Vilaro, Laura
dc.contributor.authorMajem, Margarita
dc.contributor.authorPaz-Ares, Luis
dc.contributor.authorLópez Rios, Fernando
dc.date.accessioned2024-07-02T15:07:28Z
dc.date.available2024-07-02T15:07:28Z
dc.date.issued2024-04-01
dc.date.updated2024-06-20T15:01:11Z
dc.description.abstractIntroduction: RET inhibitors with impressive overall response rates are now available for patients with NSCLC, yet the identi fication of RET fusions remains a dif ficult challenge. Most guidelines encourage the upfront use of next -generation sequencing (NGS), or alternatively, fluorescence in situ hybridization (FISH) or reverse transcriptase-polymerase chain reaction (RT-PCR) when NGS is not possible or available. Taken together, the suboptimal performance of single-analyte assays to detect RET fusions, although consistent with the notion of encouraging universal NGS, is currently widening some of the clinical practice gaps in the implementation of predictive biomarkers in patients with advanced NSCLC. Methods: This situation prompted us to evaluate several RET assays in a large multicenter cohort of RET fusion -positive NSCLC (n 1 / 4 38) to obtain real -world data. In addition to RNA -based NGS (the criterion standard method), all positive specimens underwent break -apart RET FISH with two different assays and were also tested by an RT-PCR assay. Results: The most common RET partners were KIF5B (78.9%), followed by CCDC6 (15.8%). The two RET NGSpositive but FISH -negative samples contained a KIF5B(15)RET(12) fusion. The three RET fusions not identi fied with RT-PCR were AKAP13(35)-RET(12) , KIF5B(24)-RET(9) and KIF5B(24)-RET(11) . All three false -negative RT-PCR cases were FISH -positive, exhibited a typical break -apart pattern, and contained a very high number of positive tumor cells with both FISH assays. Signet ring cells, psammoma bodies, and pleomorphic features were frequently observed (in 34.2%, 39.5%, and 39.5% of tumors, respectively). Conclusions: In-depth knowledge of the advantages and disadvantages of the different RET testing methodologies could help clinical and molecular tumor boards implement and maintain sensible algorithms for the rapid and effective detection of RET fusions in patients with NSCLC. The likelihood of RET false -negative results with both FISH and RT-PCR reinforces the need for upfront NGS in patients with NSCLC. (c) 2024 The Authors. Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
dc.format.extent13 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn1556-1380
dc.identifier.pmid38525319
dc.identifier.urihttps://hdl.handle.net/2445/214201
dc.language.isoeng
dc.publisherElsevier BV
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1016/j.jtocrr.2024.100653
dc.relation.ispartofJTO Clinical and Research Reports, 2024, vol. 5, num. 4
dc.relation.urihttps://doi.org/10.1016/j.jtocrr.2024.100653
dc.rightscc by (c) Conde, Esther et al, 2024
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationCàncer de pulmó
dc.subject.classificationCreatina quinasa
dc.subject.otherLung cancer
dc.subject.otherCreatine kinase
dc.titleRET Fusion Testing in Patients With NSCLC: The RETING Study
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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