Background/Aim: The management of elderly patients with advanced non-squamous NSCLC includes several strategies. Patients and Methods: Patients (≥70 years) were randomly assigned to bevacizumab (7.5 mg/kg i.v. on day 1) plus gemcitabine (1,200 mg/m2 i.v. on days 1-8) (arm A) or bevacizumab (7.5 mg/kg i.v.) and cisplatin (60 mg/m2 i.v.) plus gemcitabine (1,000 mg/m2 i.v. on days 1-8) (arm B), to independently evaluate treatments. The primary endpoint was progression-free rate at 6 months; secondary endpoints included progression-free survival (PFS) and safety profiles. Results: At 6 months, 5 (11.6%) patients in arm A and 5 patients (12.5%) in arm B were found to be progression-free. Median PFS was 4.8 months in arm A and 6.5 months in arm B, respectively. Conclusion: In our experience, combination of bevacizumab and chemotherapy had encouraging antitumor efficacy as first-line therapy in elderly patients with non-squamous NSCLC.
De Marinis, F., Bidoli, P., Luciani, A., Amoroso, D., Tonini, G., Bertolini, A., et al. (2017). EAGLES study: First-line bevacizumab in combination with chemotherapy in elderly patients with advanced, metastatic, non-squamous non-small cell lung cancer. ANTICANCER RESEARCH, 37(5), 2457-2464 [10.21873/anticanres.11586].
EAGLES study: First-line bevacizumab in combination with chemotherapy in elderly patients with advanced, metastatic, non-squamous non-small cell lung cancer
Bidoli, P;
2017
Abstract
Background/Aim: The management of elderly patients with advanced non-squamous NSCLC includes several strategies. Patients and Methods: Patients (≥70 years) were randomly assigned to bevacizumab (7.5 mg/kg i.v. on day 1) plus gemcitabine (1,200 mg/m2 i.v. on days 1-8) (arm A) or bevacizumab (7.5 mg/kg i.v.) and cisplatin (60 mg/m2 i.v.) plus gemcitabine (1,000 mg/m2 i.v. on days 1-8) (arm B), to independently evaluate treatments. The primary endpoint was progression-free rate at 6 months; secondary endpoints included progression-free survival (PFS) and safety profiles. Results: At 6 months, 5 (11.6%) patients in arm A and 5 patients (12.5%) in arm B were found to be progression-free. Median PFS was 4.8 months in arm A and 6.5 months in arm B, respectively. Conclusion: In our experience, combination of bevacizumab and chemotherapy had encouraging antitumor efficacy as first-line therapy in elderly patients with non-squamous NSCLC.File | Dimensione | Formato | |
---|---|---|---|
De Marinis F, Bidoli P, Luciani A et al 2017 Anticancer Research.pdf
Solo gestori archivio
Dimensione
300.4 kB
Formato
Adobe PDF
|
300.4 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.