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Long-term survival in advanced non-squamous NSCLC patients treated with first-line bevacizumab-based therapy

  • J. De Castro [1] ; J. L. González-Larriba [2] ; S. Vázquez [3] ; B. Massutí [4] ; J. M. Sanchez-Torres [24] ; M. Dómine [5] ; P. Garrido [6] ; A. Calles [25] ; A. Artal [7] ; R. Collado [8] ; R. García [9] ; M. Sereno [10] ; M. Majem [11] ; J. A. Macías [12] ; O. Juan [26] ; J. Gómez-Codina [27] ; B. Hernández [13] ; M. Lázaro [14] ; A. L. Ortega [28] ; M. Cobo [15] ; J. M. Trigo [16] ; E. Carcereny [17] ; C. Rolfo [29] ; S. Macia [18] ; J. Muñoz [19] ; P. Diz [30] ; M. Méndez [20] ; F. Rosillo [21] ; L. Paz-Ares [22] ; J. V. Cardona [31] ; D. Isla [23]
    1. [1] Hospital Universitario La Paz

      Hospital Universitario La Paz

      Madrid, España

    2. [2] Hospital Clínico San Carlos de Madrid

      Hospital Clínico San Carlos de Madrid

      Madrid, España

    3. [3] Hospital Universitario Lucus Augusti

      Hospital Universitario Lucus Augusti

      Lugo, España

    4. [4] Hospital General Universitario de Alicante

      Hospital General Universitario de Alicante

      Alicante, España

    5. [5] Fundación Jiménez Díaz

      Fundación Jiménez Díaz

      Madrid, España

    6. [6] Hospital Ramón y Cajal

      Hospital Ramón y Cajal

      Madrid, España

    7. [7] Hospital Miguel Servet

      Hospital Miguel Servet

      Zaragoza, España

    8. [8] Hospital San Pedro de Alcántara

      Hospital San Pedro de Alcántara

      Cáceres, España

    9. [9] Hospital General Universitario Gregorio Marañón

      Hospital General Universitario Gregorio Marañón

      Madrid, España

    10. [10] Hospital Infanta Sofia

      Hospital Infanta Sofia

      Madrid, España

    11. [11] Hospital de la Santa Creu i Sant Pau

      Hospital de la Santa Creu i Sant Pau

      Barcelona, España

    12. [12] Hospital Morales Meseguer

      Hospital Morales Meseguer

      Murcia, España

    13. [13] Gobierno de Navarra

      Gobierno de Navarra

      Pamplona, España

    14. [14] Complexo Hospitalario Universitario de Vigo

      Complexo Hospitalario Universitario de Vigo

      Vigo, España

    15. [15] Hospital Regional Universitario de Málaga

      Hospital Regional Universitario de Málaga

      Málaga, España

    16. [16] Hospital Universitario Virgen de la Victoria

      Hospital Universitario Virgen de la Victoria

      Málaga, España

    17. [17] Institute Catalá Oncología

      Institute Catalá Oncología

      Barcelona, España

    18. [18] Hospital General de Elda

      Hospital General de Elda

      Elda, España

    19. [19] Hospital Universitario Doctor Peset

      Hospital Universitario Doctor Peset

      Valencia, España

    20. [20] Hospital de Móstoles

      Hospital de Móstoles

      Móstoles, España

    21. [21] Complejo Hospitalario Torrecárdenas de Almería

      Complejo Hospitalario Torrecárdenas de Almería

      Almería, España

    22. [22] Hospital Universitario Virgen del Rocío

      Hospital Universitario Virgen del Rocío

      Sevilla, España

    23. [23] Hospital Clínico Universitario Lozano Blesa

      Hospital Clínico Universitario Lozano Blesa

      Zaragoza, España

    24. [24] MD Anderson Cancer Center Madrid, España
    25. [25] Centro Integral Oncológico Clara Campal, España
    26. [26] Hospital Arnau Vilanova, España
    27. [27] Hospital La Fe, España
    28. [28] Complejo Hospitalario de Jaén, España
    29. [29] University Hospital of Antwerp, Bélgica
    30. [30] Complejo Asistencial Universitario de León, España
    31. [31] Roche Farma, España
  • Localización: Clinical & translational oncology, ISSN 1699-048X, Vol. 19, Nº. 2 (February 2017), 2017, págs. 219-226
  • Idioma: inglés
  • Texto completo no disponible (Saber más ...)
  • Resumen
    • Background/Aim First-line bevacizumab-based therapies have been shown to improve clinical outcomes in patients with non-squamous non-small-cell lung cancer (NSCLC). We aimed to descriptively analyse patients with non-squamous NSCLC who received a long-term period of maintenance bevacizumab.

      Patients and methods This retrospective study included 104 patients who had already reached a progression-free survival (PFS) of at least 9 months.

      Results Median overall survival and PFS were 30.7 and 15.1 months, respectively. The overall response rate was 83 %. Weight loss ≤5 %, ECOG PS = 0, or low number of metastatic sites seem to be predictive factors of good evolution. The incidence of bevacizumab-related adverse events appeared to be similar as the previous studies.

      Conclusion Our findings show that there is a long-term survivor group whom the administration of bevacizumab resulted in a relevant prolongation of response without new safety signals. Due to the population heterogeneity, it was not possible to identify the standardised predictive factors.


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