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dc.contributor.authorLiu, J
dc.contributor.authorMoura, DS
dc.contributor.authorJones, RL
dc.contributor.authorAggarwal, A
dc.contributor.authorEbert, PJ
dc.contributor.authorWagner, AJ
dc.contributor.authorWright, J
dc.contributor.authorMartin-Broto, J
dc.contributor.authorTap, WD
dc.coverage.spatialUnited States
dc.date.accessioned2024-06-25T11:20:42Z
dc.date.available2024-06-25T11:20:42Z
dc.date.issued2024-06-03
dc.identifier742031
dc.identifier.citationClinical Cancer Research, 2024, 30 (11), pp. 2598 - 2608
dc.identifier.issn1078-0432
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6268
dc.identifier.eissn1557-3265
dc.identifier.eissn1557-3265
dc.identifier.doi10.1158/1078-0432.CCR-23-3936
dc.identifier.doi10.1158/1078-0432.CCR-23-3936
dc.description.abstractPURPOSE: This exploratory analysis evaluated the tumor samples of the patients treated with doxorubicin (with or without olaratumab) in a negative phase III ANNOUNCE trial to better understand the complexity of advanced soft tissue sarcomas (STS) and to potentially identify its predictive markers. EXPERIMENTAL DESIGN: RNA sequencing was performed on pretreatment tumor samples (n = 273) from the ANNOUNCE trial to evaluate response patterns and identify potential predictive treatment markers for doxorubicin. A BOR-associated signature to doxorubicin (REDSARC) was created by evaluating tumors with radiographic response versus progression. An external cohort of doxorubicin-treated patients from the Spanish Group for Research on Sarcomas (GEIS) was used for refinement and validation. RESULTS: A total of 259 samples from the trial were considered for analysis. Comparative analyses by the treatment arm did not explain the negative trial. However, there was an association between the BOR signature and histologic subtype (χ2P = 2.0e-7) and grade (P = 0.002). There were no associations between the BOR signature and gender, age, ethnicity, or stage. Applied to survival outcomes, REDSARC was also predictive for progression-free survival (PFS) and overall survival (OS). Using the GEIS cohort, a refined 25-gene signature was identified and applied to the ANNOUNCE cohort, where it was predictive of PFS and OS in leiomyosarcoma, liposarcoma, and other sarcoma subtypes, but not in undifferentiated pleomorphic sarcoma. CONCLUSIONS: The refined REDSARC signature provides a potential tool to direct the application of doxorubicin in sarcomas and other malignancies. Validation and further refinement of the signature in other potentially subtype specific prospective cohorts is recommended.
dc.formatPrint
dc.format.extent2598 - 2608
dc.languageeng
dc.language.isoeng
dc.publisherAMER ASSOC CANCER RESEARCH
dc.relation.ispartofClinical Cancer Research
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectHumans
dc.subjectDoxorubicin
dc.subjectSarcoma
dc.subjectFemale
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectTranscriptome
dc.subjectGene Expression Profiling
dc.subjectAdult
dc.subjectAged
dc.subjectBiomarkers, Tumor
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectPrognosis
dc.subjectAntibodies, Monoclonal
dc.subjectTreatment Outcome
dc.titleBest Overall Response-Associated Signature to Doxorubicin in Soft Tissue Sarcomas: A Transcriptomic Analysis from ANNOUNCE.
dc.typeJournal Article
dcterms.dateAccepted2024-03-22
dc.date.updated2024-06-25T11:18:36Z
rioxxterms.versionAM
rioxxterms.versionofrecord10.1158/1078-0432.CCR-23-3936
rioxxterms.licenseref.startdate2024-06-03
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38536068
pubs.issue11
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials (R Jones)
pubs.organisational-groupICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials (R Jones)/Sarcoma Clinical Trials (R Jones) (hon.)
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1158/1078-0432.ccr-23-3936
pubs.volume30
dc.contributor.icrauthorJones, Robin
icr.provenanceDeposited by Mr Arek Surman on 2024-06-25. Deposit type is initial. No. of files: 1. Files: ccr-23-3936.pdf


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