Best overall response–associated signature to doxorubicin in soft tissue sarcomas: A transcriptomic analysis from ANNOUNCE Journal Article


Authors: Liu, J.; Moura, D. S.; Jones, R. L.; Aggarwal, A.; Ebert, P. J.; Wagner, A. J.; Wright, J.; Martin-Broto, J.; Tap, W. D.
Article Title: Best overall response–associated signature to doxorubicin in soft tissue sarcomas: A transcriptomic analysis from ANNOUNCE
Abstract: Purpose: 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 (x2 P = 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. © 2024 American Association for Cancer Research.
Keywords: adult; controlled study; treatment outcome; aged; middle aged; gene mutation; major clinical study; overall survival; genetics; doxorubicin; antineoplastic agent; progression free survival; gene expression; gene expression profiling; randomized controlled trial; antineoplastic combined chemotherapy protocols; pathology; tumor marker; monoclonal antibody; sarcoma; antibodies, monoclonal; microarray analysis; soft tissue sarcoma; upregulation; leiomyosarcoma; drug therapy; double blind procedure; transcriptome; disease specific survival; liposarcoma; rna extraction; rna sequence; principal component analysis; estrogen receptor alpha; olaratumab; cancer prognosis; high throughput sequencing; humans; prognosis; human; male; female; article; gene set enrichment analysis; biomarkers, tumor
Journal Title: Clinical Cancer Research
Volume: 30
Issue: 11
ISSN: 1078-0432
Publisher: American Association for Cancer Research  
Date Published: 2024-06-01
Start Page: 2598
End Page: 2608
Language: English
DOI: 10.1158/1078-0432.Ccr-23-3936
PUBMED: 38536068
PROVIDER: scopus
DOI/URL:
Notes: Article -- Source: Scopus
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  1. William Douglas Tap
    372 Tap