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Advanced non‑squamous NSCLC with no actionable oncogenic driver in Spain: a cross‑sectional descriptive analysis of data from the Thoracic Tumor Registry

    1. [1] Complejo Hospitalario Universitario Insular - Materno Infantil de Canarias

      Complejo Hospitalario Universitario Insular - Materno Infantil de Canarias

      Gran Canaria, España

    2. [2] Hospital Universitario de Valladolid

      Hospital Universitario de Valladolid

      Valladolid, España

    3. [3] Hospital General Universitario de Elche

      Hospital General Universitario de Elche

      Elche, España

    4. [4] Hospital General Universitario de Alicante

      Hospital General Universitario de Alicante

      Alicante, España

    5. [5] Hospital Regional Universitario de Málaga

      Hospital Regional Universitario de Málaga

      Málaga, España

    6. [6] Hospital General Universitario de Valencia

      Hospital General Universitario de Valencia

      Valencia, España

    7. [7] Hospital Universitario de Salamanca

      Hospital Universitario de Salamanca

      Salamanca, España

    8. [8] Hospital Universitario de Jaén

      Hospital Universitario de Jaén

      Jaén, España

    9. [9] Complexo Hospitalario Universitario da Coruña

      Complexo Hospitalario Universitario da Coruña

      A Coruña, España

    10. [10] Hospital Universitario Virgen del Rocío

      Hospital Universitario Virgen del Rocío

      Sevilla, España

    11. [11] Hospital Clínico San Carlos de Madrid

      Hospital Clínico San Carlos de Madrid

      Madrid, España

    12. [12] Hospital de Fuenlabrada

      Hospital de Fuenlabrada

      Fuenlabrada, España

    13. [13] Complexo Hospitalario Universitario de Vigo

      Complexo Hospitalario Universitario de Vigo

      Vigo, España

    14. [14] Institut Català D’oncologia Badalona- Hospital Germans Trias I Pujol, B-Argo Group, Badalona, Spain
    15. [15] Hospital Universitario Puerta de Hierro-Majadahonda, Madrid, Spain
    16. [16] Hospital Universitari I Politècnic La Fe, Valencia, Spain
    17. [17] OSI Bilbao Basurto, Bilbao, Spain
    18. [18] Josep Trueta and Precision Oncology Group (OncoGIR-Pro), Institut d’Investigacions Biomèdiques de Girona (IDIBGI), Catalan Institute of Oncology, Hospital Universitari Dr, Girona, Spain
    19. [19] Hospital Universitario, Nuestra Señora De La Candelaria, Santa Cruz de Tenerife, Spain
    20. [20] Hospital Provincial de Castellón, Castellón, Spain
  • Localización: Clinical & translational oncology, ISSN 1699-048X, Vol. 26, Nº. 12, 2024, págs. 3218-3225
  • Idioma: inglés
  • Texto completo no disponible (Saber más ...)
  • Resumen
    • Background Non-small cell lung cancer (NSCLC) accounts for the vast majority of all diagnosed lung cancers. According to their histology, most NSCLCs are considered non-squamous cell carcinoma (NSCC), and up to 85% of the latter may lack either one of the two main actionable oncogenic drivers (i.e., EGFR mutations and ALK rearrangements).

      Objective Our analysis aimed to describe the clinical and epidemiological characteristics of Spanish patients sufering from NSCC with no actionable oncogenic driver in daily clinical practice. Design A retrospective, cross-sectional, descriptive analysis.

      Methods We analyzed the records of all Spanish patients with advanced NSCC diagnosed between January 2011 and January 2020 and included in the Spanish Thoracic Tumor Registry database. We evaluated the presence of metastasis and molecular profling at the time of diagnosis and treatments received. We also assessed overall survival (OS) and progression-free survival (PFS) according to frst-line treatment.

      Results One thousand seven hundred ninety-seven Spanish patients with NSCC were included. They were mainly men (73.2%), smokers (current [44.4%] and former [44.4%]) and presented adenocarcinoma histology (97.6%). Most patients had at least one comorbidity (80.4%) and one metastatic site (96.8%), and a non-negligible number of those tested were PD-L1 positive (35.2%). Notably, the presence of liver metastasis indicated a shorter median OS and PFS than metastasis in other locations (p<0.001). Chemotherapy was more often prescribed than immunotherapy as frst-, second-, and third-line treatment in that period. In frst-line, the OS rates were similar in patients receiving either regimen, but PFS rates signifcantly better in patients treated with immunotherapy (p=0.026). Also, a high number of patients did not reach second- and thirdline treatment, suggesting the failure of current early diagnostic measures and therapies.

      Conclusions This analysis of the most lethal tumor in Spain could highlight the strengths and the weaknesses of its clinical management and set the ground for further advances and research.


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