Frontiers in Oncology (Nov 2021)

First Nationwide Molecular Screening Program in Spain for Patients With Advanced Breast Cancer: Results From the AGATA SOLTI-1301 Study

  • Sonia Pernas,
  • Sonia Pernas,
  • Patricia Villagrasa,
  • Ana Vivancos,
  • Maurizio Scaltriti,
  • Jordi Rodón,
  • Jordi Rodón,
  • Octavio Burgués,
  • Paolo Nuciforo,
  • Jordi Canes,
  • Laia Paré,
  • Marta Dueñas,
  • Marta Dueñas,
  • Maria Vidal,
  • Maria Vidal,
  • Maria Vidal,
  • Juan Miguel Cejalvo,
  • Juan Miguel Cejalvo,
  • Juan Miguel Cejalvo,
  • Antonia Perelló,
  • Antonio Llommbard-Cussac,
  • Joan Dorca,
  • Alvaro Montaño,
  • Tomás Pascual,
  • Mafalda Oliveira,
  • Mafalda Oliveira,
  • Gloria Ribas,
  • Gloria Ribas,
  • Inmaculada Rapado,
  • Aleix Prat,
  • Aleix Prat,
  • Aleix Prat,
  • Aleix Prat,
  • Eva Ciruelos,
  • Eva Ciruelos

DOI
https://doi.org/10.3389/fonc.2021.744112
Journal volume & issue
Vol. 11

Abstract

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BackgroundThe SOLTI-1301 AGATA study aimed to assess the feasibility of a multi-institutional molecular screening program to better characterize the genomic landscape of advanced breast cancer (ABC) and to facilitate patient access to matched-targeted therapies in Spain.MethodsDNA sequencing of 74 cancer-related genes was performed using FFPE tumor samples in three different laboratories with three different gene panels. A multidisciplinary advisory board prospectively recommended potential targeted treatments. The primary objective was to determine the success of matching somatic DNA alteration to an experimental drug/drug class.ResultsBetween September 2014 and July 2017, 305 patients with ABC from 10 institutions were enrolled. Tumor sequencing was successful in 260 (85.3%) patients. Median age was 54 (29-80); most tumors were hormone receptor-positive/HER2-negative (74%), followed by triple-negative (14.5%) and HER2-positive (11.5%). Ninety-seven (37%) tumor samples analyzed proceeded from metastatic sites. Somatic mutations were identified in 163 (62.7%) patients, mostly in PIK3CA (34%), TP53 (22%), AKT1 (5%), ESR1 (3%), and ERBB2 (3%) genes. Significant enrichment of AKT1 mutation was observed in metastatic versus primary samples (9% vs. 2%; p=0.01). Genome-driven cancer therapy was recommended in 45% (n=116) of successfully screened patients, 11% (n=13) of whom finally received it. Among these patients, 46.2% had a PFS of ≥6 months on matched therapy.ConclusionsAGATA is the first nationwide molecular screening program carried out in Spain and we proved that implementing molecular data in the management of ABC is feasible. Although these results are promising, only 11% of the patients with genome-driven cancer therapy received it.

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