Efficacy and safety of first-line therapies in EGFR-mutated advanced non-small-cell lung cancer: a network meta-analysis

Author:

Haeussler Katrin1ORCID,Wang Xuan2ORCID,Winfree Katherine B3ORCID,D'yachkova Yulia4ORCID,Traore Sory5ORCID,Puri Tarun6ORCID,Thom Howard7ORCID,Papagiannopoulos Christos2ORCID,Nassim Maria1ORCID,Taipale Kaisa8

Affiliation:

1. ICON plc, Munich, 81829, Germany

2. ICON plc, Stockholm, 111 21, Sweden

3. Eli Lilly & Company, Indianapolis, IN USA

4. Eli Lilly GmbH, Vienna, Austria

5. Eli Lilly & Company, Arlington Square, UK

6. Eli Lilly & Company (India) Pvt Ltd, Gurgaon, India

7. Bristol Medical School Population Health Sciences, University of Bristol, UK

8. Oy Eli Lilly Finland Ab, Helsinki, Finland

Abstract

Aim: To evaluate the comparative efficacy and safety of identified first-line therapies for patients with EGFR mutation-positive ( EGFRm+) advanced non-small-cell lung cancer (NSCLC), with a focus on ramucirumab + erlotinib. Methods: In the absence of head-to-head studies, a Bayesian network meta-analysis was conducted using randomized clinical trial data to evaluate first-line systemic therapies with erlotinib/gefitinib as the reference treatment. Results: For progression-free survival, ramucirumab + erlotinib was comparable to osimertinib and dacomitinib in the primary analysis. Conclusion: The analysis showed ramucirumab + erlotinib efficacy to be comparable to best-in-class treatment options for previously untreated patients with  EGFRm+ advanced NSCLC. Registration information: PROSPERO ID: CRD42020136247

Funder

Eli Lilly & Co., IN, USA

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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