作者
Jordi Remón,Benjamin Lacas,Roy S. Herbst,Martin Reck,Edward B. Garon,Giorgio V. Scagliotti,Rodryg Ramlau,Nasser H. Hanna,Johan Vansteenkiste,Kiyotaka Yoh,Harry J.M. Groen,John V. Heymach,Sumithra J. Mandrekar,Isamu Okamoto,Joel W. Neal,Rebecca S. Heist,David Planchard,Jean‐Pierre Pignon,Benjamin Besse,Benjamin Besse,Benjamin Lacas,Jean‐Pierre Pignon,Jordi Remón,T. Berghmans,Suzanne E. Dahlberg,Enriqueta Felip,Thierry Berghmans,Benjamin Besse,Suzanne E. Dahlberg,Enriqueta Felip,Edward B. Garon,Harry J.M. Groen,Nasser H. Hanna,Rebecca S. Heist,Roy S. Herbst,John V. Heymach,Benjamin Lacas,Alex A. Adjei,Rebecca S. Heist,Sumithra J. Mandrekar,Joel W. Neal,Isamu Okamoto,Jean‐Pierre Pignon,Rodryg Ramlau,Jordi Remón,Martin Reck,Giorgio V. Scagliotti,Johan Vansteenkiste,Kiyotaka Yoh
摘要
Background: Now that immunotherapy plus chemotherapy (CT) is one standard option in first-line treatment of advanced non-small cell lung cancer (NSCLC), there exists a medical need to assess the efficacy of second-line treatments (2LT) with antiangiogenics (AA).We performed an individual patient data meta-analysis to validate the efficacy of these combinations as 2LT.Methods: Randomised trials of AA plus standard 2LT compared to 2LT alone that ended accrual before 2015 were eligible.Fixed-effect models were used to compute pooled hazard ratios (HRs) for overall survival (OS, main end-point), progression-free survival (PFS) and subgroup analyses.Results: Sixteen trials were available (8,629 patients, 64% adenocarcinoma).AA significantly prolonged OS (HR Z 0.93 [95% confidence interval {CI}: 0.89; 0.98], p Z 0.005) and PFS (0.80 [0.77; 0.84], p < 0.0001) compared with 2LT alone.Absolute 1-year OS and PFS benefit for AA were þ1.8% [À0.4; þ4.0] and þ3.5% [þ1.9; þ5.1], respectively.The OS benefit of AA was higher in younger patients (HR Z 0.87 [95% CI: 0.76; 1.00], 0.89 [0.81; 0.97], 0.94 [0.87; 1.02] and 1,04 [0.93; 1.17] for patients <50, 50e59, 60e69 and !70 years old, respectively; trend test: p Z 0.02) and in patients who started AA within 9 months after starting the first-line therapy (0.88 [0.82; 0.99]) than in patients who started AA later (0.99 [0.91; 1.08]) (interaction: p Z 0.03).Results were similar for PFS.AA increased the risk of hypertension (p < 0.0001), but not the risk of pulmonary thromboembolic events (p Z 0.21).Conclusions: In the 2LT of advanced NSCLC, adding AA significantly prolongs OS and PFS, but the benefit is clinically limited, mainly observed in younger patients and after shorter time since the start of first-line therapy.