Abstract
BackgroundFor unresectable or metastatic melanoma, first-line ipilimumab has demonstrated long-term survival benefits over a 7-year period. First-line treatment with BRAF inhibitors has demonstrated efficacy in clinical trials with up to 3 years of follow-up. The long-term comparative efficacy and costs of ipilimumab and BRAF inhibitors are unknown.MethodsPatient-level data from 12 clinical studies for ipilimumab were used. Survival data were extracted from included clinical trials for BRAF inhibitors based on a systematic literature review. Different parametric survival models, including exponential, Gompertz, log-normal, and Weibull models, were used to fit reported overall survival (OS) data and to project long-term survival for BRAF inhibitors. Survival benefits were measured in terms of total life-months gained as calculated by the area under the curve of OS Kaplan–Meier curves for the observed ipilimumab data and projected BRAF inhibitor data. Total life-months gained and cumulative costs per life-month gained were compared between ipilimumab and BRAF inhibitors.ResultsThe systematic literature review identified six randomized-controlled trials of BRAF inhibitors for subsequent analyses. With 7-year follow-up, ipilimumab was associated with a total of 28.5 life-months gained. Based on the Weibull model, the extrapolated total life-months gained for BRAF inhibitors were 26.5 months for dabrafenib, 21.3 months for trametinib, 14.3 months for vemurafenib, and 24.6 months for dabrafenib + trametinib. In sensitivity analyses, extrapolated total life-months gained varied across the three other models, ranging from 13.7 to 36.8 months across therapies. Cumulative costs per life-month gained with ipilimumab decreased steadily over time, while the costs remained constant for BRAF inhibitors due to continuous dosing. By year 3, cumulative costs per life-month gained were the lowest with ipilimumab; by year 7, the costs were $4281 for ipilimumab, compared with $8920 for dabrafenib, $10,211 for trametinib, $11,002 for vemurafenib, and $19,132 for the dabrafenib + trametinib combination therapy.ConclusionsIpilimumab was associated with a better long-term cost-per-life month compared to BRAF agents. Long-term extrapolation of survival with BRAF agents was uncertain, and showed no evidence of prolonged survival compared to ipilimumab.Electronic supplementary materialThe online version of this article (doi:10.1186/s40164-016-0039-0) contains supplementary material, which is available to authorized users.
Highlights
For unresectable or metastatic melanoma, first-line ipilimumab has demonstrated long-term survival benefits over a 7-year period
All three agents are approved for use in patients with BRAF V600E or V600K mutations; the combined treatment of dabrafenib + trametinib is associated with significantly better efficacy relative to BRAF monotherapies [12,13,14,15]
Systematic literature review A total of 654 studies were initially identified from database searches and supplemental manual searches of recent American Society of Clinical Oncology (ASCO) and European Society for Medical Oncology (ESMO) conference abstracts (Fig. 1)
Summary
For unresectable or metastatic melanoma, first-line ipilimumab has demonstrated long-term survival benefits over a 7-year period. First-line treatment with BRAF inhibitors has demonstrated efficacy in clinical trials with up to 3 years of follow-up. Ipilimumab, dabrafenib, trametinib, vemurafenib, or dabrafenib + trametinib combination therapy are approved by the US Food and Drug Administration (FDA) as first-line treatments [7]. The targeted therapies dabrafenib, trametinib, and vemurafenib are directed against a specific tumor cell survival pathway, the mitogen activated protein kinase/ extracellular signal-regulated kinase (MEK) pathway [11]. All three agents are approved for use in patients with BRAF V600E or V600K mutations; the combined treatment of dabrafenib + trametinib is associated with significantly better efficacy relative to BRAF monotherapies (e.g., dabrafenib or vemurafenib) [12,13,14,15]
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.