Clinical management and outcome of patients with advanced NSCLC carrying EGFR mutations in Spain


Por: Arriola E, Garcia Gomez R, Diz P, Majem M, Martinez Aguillo M, Valdivia J, Paredes A, Sanchez-Torres JM, Peralta Muñoz S, Barneto I, Gutierrez V, Andrade Santiago JM, Aparisi F, Isla D, Ponce S, Vicente Baz D, Artal A, Amador M and Provencio M

Publicada: 30 ene 2018 Ahead of Print: 30 ene 2018
Resumen:
Background: Although the benefit of first-line epidermal growth factor receptor (EGFR) tyrosine-kinase inhibitors (TKIs) over chemotherapy has been demonstrated in several clinical trials, data from clinical practice is lacking and the optimal EGFR TKI to be used remains unclear. This study aims to assess the real-life diagnostic and clinical management and outcome of patients with advanced non-small-cell lung cancer (NSCLC) carrying EGFR mutations in Spain. Methods: All consecutive patients recently diagnosed with advanced or metastatic NSCLC from April 2010 to December 2011 in 18 Spanish hospitals and carrying EGFR mutations were retrospectively evaluated. Results: Between March and November 2013, a total of 187 patients were enrolled (98.3% Caucasian, 61.9% female, 54.9% never-smokers, 89.0% adenocarcinoma). Mutation testing was mainly performed on biopsy tumour tissue specimens (69.0%) using a qPCR-based test (90%) (47.0% Therascreen EGFR PCR Kit). Common sensitising mutations were detected in 79.8% of patients: 57.1% had exon 19 deletions and 22.6% exon 21 L858R point mutations. The vast majority of patients received first-line therapy (n = 168; 92.8%). EGFR TKIs were the most commonly used first-line treatment (81.5%), while chemotherapy was more frequently administered as a second-and third-line option (51.9% and 56.0%, respectively). Of 141 patients who experienced disease progression, 79 (56.0%) received second-line treatment. After disease progression on first-line TKIs (n = 112), 33.9% received chemotherapy, 8.9% chemotherapy and a TKI, and 9.8% continued TKI therapy. Most patients received first-line gefitinib (83.0%), while erlotinib was more frequently used in the second-line setting (83.0%). Progression-free survival (PFS) and overall survival (OS) in patients harbouring common mutations were 11.1 months and 20.1 months respectively (exon 19 deletions: 12.4 and 21.4 months; L858R: 8.3 and 14.5 months), and 3.9 months and 11.1 months respectively for those with rare mutations. Conclusion: EGFR TKIs (gefitinib and erlotinib) are used as the preferred first-line treatment while chemotherapy is more frequently administered as a second-and third-line option in routine clinical practice in Spain. In addition, efficacy data obtained in the real-life setting seem to concur with data from EGFR TKI phase III pivotal studies in NSCLC.

Filiaciones:
Arriola E:
 Medical Oncology Department, Hospital del Mar, Passeig Marítim, 25-29, 08018, Barcelona, Spain.

Garcia Gomez R:
 Hospital General Universitario Gregorio Marañón, Madrid, Spain

 Hospital General Universitario Gregorio Maranon, Madrid, Spain

Diz P:
 Hospital Universitario de León, León, Spain

Majem M:
 Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

Martinez Aguillo M:
 Complejo Hospitalario de Navarra, Pamplona, Spain

Valdivia J:
 Hospital Universitario Virgen de las Nieves, Granada, Spain

Paredes A:
 Hospital Universitario Donostia, San Sebastián, Spain

Sanchez-Torres JM:
 Hospital Universitario de La Princesa, Madrid, Spain

Peralta Muñoz S:
 Hospital Universitari Sant Joan de Reus, Reus, Tarragona, Spain

Barneto I:
 Hospital Universitario Reina Sofía, Córdoba, Spain

Gutierrez V:
 Hospital Regional Universitario Carlos Haya, Málaga, Spain

Andrade Santiago JM:
 Hospital Virgen de la Salud, Toledo, Spain

:
 Hospital Virgen de los Lirios, Alcoy, Alicante, Spain

Isla D:
 Hospital Clinico Universitario Lozano Blesa, Zaragoza, Spain

Ponce S:
 Hospital Universitario 12 de Octubre, Madrid, Spain

Vicente Baz D:
 Hospital Universitario Virgen Macarena, Sevilla, Spain

Artal A:
 Hospital Universitario Miguel Servet, Zaragoza, Spain

Amador M:
 AstraZeneca, Madrid, Spain

Provencio M:
 Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain
ISSN: 14712407





BMC Cancer
Editorial
BIOMED CENTRAL LTD, 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 18 Número:
Páginas: 106-106
WOS Id: 000423880600001
ID de PubMed: 29382302
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