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A Phase III Randomized Trial of Integrated Genomics and Avatar Models for Personalized Treatment of Pancreatic Cancer: the AVATAR Trial.
Sarno, Francesca; Tenorio, Jair; Perea, Sofia; Medina, Laura; Pazo-Cid, Roberto; Juez, Ignacio; Garcia-Carbonero, Rocio; Feliu, Jaime; Guillen-Ponce, Carmen; Lopez-Casas, Pedro P; Guerra, Carmen; Duran, Yolanda; López-Acosta, Jose Francisco; Alonso, Carolina; Esquivel, Estrella; Dopazo, Ana; Akshinthala, Dipikaa; Muthuswamy, Senthil K; Lapunzina, Pablo; Bockorny, Bruno; Hidalgo, Manuel.
Afiliación
  • Sarno F; Peaches Biotech, Madrid, Madrid, Spain.
  • Tenorio J; Hospital Universitario La Paz, Madrid, Madrid, Spain.
  • Perea S; Freelancer, New York, NY, United States.
  • Medina L; Hospital Universitario Virgen de la Victoria, MALAGA, Spain.
  • Pazo-Cid R; Hospital Universitario Miguel Servet, Zaragoza, Spain.
  • Juez I; Hospital Universitario de Fuenlabrada, Fuenlabrada, Madrid, Spain.
  • Garcia-Carbonero R; Hospital Universitario 12 De Octubre, Madrid, Spain.
  • Feliu J; Hospital Universitario La Paz. CIBERONC. IdiPAZ. Cátedra UAM-AMGEN, Madrid, Spain.
  • Guillen-Ponce C; Hospital Universitario Ramón y Cajal. IRYCIS., Madrid, Madrid, Spain.
  • Lopez-Casas PP; Instituto de Investigacion Sanitaria Hospital 12 de Octubre (imas12), Madrid, Spain.
  • Guerra C; Centro Nacional de Investigaciones Oncológicas, Madrid, Madrid, Spain.
  • Duran Y; Peaches Biotech, Madrid, Madrid, Spain.
  • López-Acosta JF; Hospital Universitario de Fuenlabrada, Spain.
  • Alonso C; Hospital Universitario de Fuenlabrada, Spain.
  • Esquivel E; Unidad de Genómica, Centro Nacional de Investigaciones Cardiovasculares, Madrid, Spain.
  • Dopazo A; CNIC, Madrid, Spain.
  • Akshinthala D; National Institutes of Health, United States.
  • Muthuswamy SK; National Cancer Institute, Bethesda, United States.
  • Lapunzina P; INGEMM-IdiPAZ Institute of Medical and Molecular Genetics, Madrid, Spain.
  • Bockorny B; Beth Israel Deaconess Medical Center, Boston, MA, United States.
  • Hidalgo M; NewYork-Presbyterian Hospital/Weill Cornell Medical Center, New York, United States.
Clin Cancer Res ; 2024 Nov 14.
Article en En | MEDLINE | ID: mdl-39540844
PURPOSE: Pancreatic adenocarcinoma (PDAC) has limited treatment options. We compared the efficacy of comprehensive precision medicine against the conventional treatment in PDAC. METHODS: Phase III trial of advanced PDAC where patients were randomized (1:2) to a conventional treatment treated at physician's discretion (arm A), or to precision medicine (arm B). Subjects randomized to arm B underwent a tumor biopsy for whole exome sequencing (WES) and to generate avatar mouse models and patient derived organoids for phenotypic drug screening, with final treatment recommended by molecular tumor board. The primary objective was median overall survival (OS). RESULTS: 137 patients were enrolled with 125 randomized, 44 to arm A and 81 to Arm B. WES was performed in 80.3% (65/81) patients of arm B, with potentially actionable mutations detected in 21.5% (14/65). Experimental models were generated in 16/81 patients (19.8%). Second-line treatment was administered to 39 patients in the experimental arm, but only 4 (10.2%) received personalized treatment, while 35 could not be receive matched therapy due to rapid clinical deterioration, delays in obtaining study results or absence of actionable targets. Median OS was 8.7 and 8.6 months (p=0.849) and median progression-free survival was 3.8 and 4.3 months (p=0.563) for the conventional and experimental arms, respectively. Notably, the four patients who received personalized treatment had median OS of 19.3 months. CONCLUSIONS: Personalized medicine was challenging to implement in most patients with PDAC, limiting the interpretation of intention to treat analysis. Survival was improved in the subset of patients who did receive matched therapy.

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Clinical_trials Idioma: En Revista: Clin cancer res Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Clinical_trials Idioma: En Revista: Clin cancer res Asunto de la revista: NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: España