BACKGROUND: There have been reports suggesting that continuous administration of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) is advantageous for patients in which disease progression was observed after the establishment of clinical benefit from EGFR-TKIs. We retrospectively evaluated the clinical course of patients who received continuous administration of EGFR-TKIs after disease progression was detected solely in bone lesions. PATIENTS AND METHODS: The medical records of patients administered gefitinib or erlotinib between 2002 and 2010 were reviewed. We evaluated the progression-free survival (PFS) and overall survival (OS) in patients who had bone metastases after the establishment of clinical benefit from EGFR-TKI and who received radiation therapy for the bone lesion and continuous treatment with EGFR-TKI. RESULTS: Ten patients were enrolled in this study. The median PFS and OS were 88 days and 330 days, respectively. Furthermore, a longer duration from the start of first EGFR-TKI to detection of bone metastases (p=0.0049) was identified as being significantly associated with a longer PFS. CONCLUSION: Our data suggest that continuous administration of EGFR-TKI is a treatment option for patients with bone metastases who previously benefited from therapy with EGFR-TKI.
BACKGROUND: There have been reports suggesting that continuous administration of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) is advantageous for patients in which disease progression was observed after the establishment of clinical benefit from EGFR-TKIs. We retrospectively evaluated the clinical course of patients who received continuous administration of EGFR-TKIs after disease progression was detected solely in bone lesions. PATIENTS AND METHODS: The medical records of patients administered gefitinib or erlotinib between 2002 and 2010 were reviewed. We evaluated the progression-free survival (PFS) and overall survival (OS) in patients who had bone metastases after the establishment of clinical benefit from EGFR-TKI and who received radiation therapy for the bone lesion and continuous treatment with EGFR-TKI. RESULTS: Ten patients were enrolled in this study. The median PFS and OS were 88 days and 330 days, respectively. Furthermore, a longer duration from the start of first EGFR-TKI to detection of bone metastases (p=0.0049) was identified as being significantly associated with a longer PFS. CONCLUSION: Our data suggest that continuous administration of EGFR-TKI is a treatment option for patients with bone metastases who previously benefited from therapy with EGFR-TKI.
Authors: J B Auliac; C Fournier; C Audigier Valette; M Perol; A Bizieux; F Vinas; C Decroisette Phan van Ho; S Bota Ouchlif; R Corre; G Le Garff; P Fournel; N Baize; R Lamy; A Vergnenegre; D Arpin; B Marin; C Chouaid; R Gervais Journal: Target Oncol Date: 2016-04 Impact factor: 4.493
Authors: D Marquez-Medina; A Chachoua; A Martin-Marco; A M Desai; V Garcia-Reglero; A Salud-Salvia; F Muggia Journal: Clin Transl Oncol Date: 2013-04-20 Impact factor: 3.405
Authors: Olga Y Korolkova; Sarrah E Widatalla; Stephen D Williams; Diva S Whalen; Heather K Beasley; Josiah Ochieng; Thomas Grewal; Amos M Sakwe Journal: Cells Date: 2020-08-07 Impact factor: 6.600