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Best Overall Response-Associated Signature to Doxorubicin in Soft Tissue Sarcomas: A Transcriptomic Analysis from ANNOUNCE.
Liu, Jiangang; Moura, David S; Jones, Robin L; Aggarwal, Amit; Ebert, Philip J; Wagner, Andrew J; Wright, Jennifer; Martin-Broto, Javier; Tap, William D.
Afiliação
  • Liu J; Eli Lilly and Company, Indianapolis, Indiana.
  • Moura DS; Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain.
  • Jones RL; Royal Marsden Hospital and Institute of Cancer Research, London, United Kingdom.
  • Aggarwal A; Eli Lilly and Company, Indianapolis, Indiana.
  • Ebert PJ; Eli Lilly and Company, Indianapolis, Indiana.
  • Wagner AJ; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Wright J; Eli Lilly and Company, Indianapolis, Indiana.
  • Martin-Broto J; Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain.
  • Tap WD; Memorial Sloan Kettering Cancer Center, New York, New York.
Clin Cancer Res ; 30(11): 2598-2608, 2024 Jun 03.
Article em En | MEDLINE | ID: mdl-38536068
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 (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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma / Doxorrubicina / Transcriptoma Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma / Doxorrubicina / Transcriptoma Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article