Cost Effectiveness of Dabrafenib as a First-Line Treatment in Patients with BRAF V600 Mutation-Positive Unresectable or Metastatic Melanoma in Canada

被引:19
作者
Delea, Thomas E. [1 ]
Amdahl, Jordan [1 ]
Wang, Alice [1 ]
Amonkar, Mayur M. [2 ]
Thabane, Marroon [3 ]
机构
[1] PAI, Brookline, MA 02445 USA
[2] GlaxoSmithKline, Collegeville, PA 19426 USA
[3] GlaxoSmithKline, Mississauga, ON L5N 6L4, Canada
关键词
Overall Survival; Ipilimumab; Dacarbazine; Vemurafenib; Probabilistic Sensitivity Analysis;
D O I
10.1007/s40273-014-0241-z
中图分类号
F [经济];
学科分类号
02 ;
摘要
To evaluate the cost effectiveness of dabrafenib versus dacarbazine and vemurafenib as first-line treatments in patients with BRAF V600 mutation-positive unresectable or metastatic melanoma from a Canadian healthcare system perspective. A partitioned-survival analysis model with three mutually exclusive health states (pre-progression, post-progression, and dead) was used. The proportion of patients in each state was calculated using survival distributions for progression-free and overall survival derived from pivotal trials of dabrafenib and vemurafenib. For each treatment, expected progression-free, post-progression, overall, and quality-adjusted life-years (QALYs), and costs were calculated. Costs were based on list prices, a clinician survey, and published sources. A 5-year time horizon was used in the base case. Costs (in 2012 Canadian dollars [CA$]) and QALYs were discounted at 5 % annually. Deterministic and probabilistic sensitivity analyses were conducted. Dabrafenib was estimated to yield 0.2055 more QALYs at higher cost than dacarbazine. The incremental cost-effectiveness ratio was CA$363,136/QALY. In probabilistic sensitivity analyses, at a threshold of CA$200,000/QALY, there was an 8.2 % probability that dabrafenib is cost effective versus dacarbazine. In deterministic sensitivity analyses, cost effectiveness was sensitive to survival distributions, utilities, and time horizon, with the hazard ratio for overall survival for dabrafenib versus dacarbazine being the most sensitive parameter. Assuming a class effect for efficacy of BRAF inhibitors, dabrafenib was dominant versus vemurafenib (less costly, equally effective), reflecting its assumed lower daily cost. Assuming no class effect, dabrafenib yielded 0.0486 more QALYs than vemurafenib. At a threshold of CA$200,000/QALY, dabrafenib is unlikely to be cost effective compared with dacarbazine. It is not possible to make reliable conclusions regarding the relative cost effectiveness of dabrafenib versus vemurafenib based on available information.
引用
收藏
页码:367 / 380
页数:14
相关论文
共 50 条
[21]   Cost-Effectiveness of Pembrolizumab Versus Carboplatin and Paclitaxel in Patients With Unresectable or Metastatic Melanoma After First-Line Treatment in China [J].
Tang, Wen-Xi ;
Shao, Rong-Jie ;
Wang, Jingshu ;
Scherrer, Emilie ;
Ma, Ai-Xia ;
Aguiar-Ibanez, Raquel .
VALUE IN HEALTH REGIONAL ISSUES, 2022, 27 :99-107
[22]   Cobimetinib Plus Vemurafenib: A Review in BRAFV600 Mutation-Positive Unresectable or Metastatic Melanoma [J].
Gillian M. Keating .
Drugs, 2016, 76 :605-615
[23]   Cobimetinib Plus Vemurafenib: A Review in BRAFV600 Mutation-Positive Unresectable or Metastatic Melanoma [J].
Keating, Gillian M. .
DRUGS, 2016, 76 (05) :605-615
[24]   Safety of vemurafenib in patients with BRAF V600 mutated metastatic melanoma: the Spanish experience [J].
Arance, A. M. ;
Berrocal, A. ;
Lopez-Martin, J. A. ;
de la Cruz-Merino, L. ;
Soriano, V. ;
Martin Algarra, S. ;
Alonso, L. ;
Cerezuela, P. ;
La Orden, B. ;
Espinosa, E. .
CLINICAL & TRANSLATIONAL ONCOLOGY, 2016, 18 (11) :1147-1157
[25]   The European Medicines Agency review of vemurafenib (Zelboraf®) for the treatment of adult patients with BRAF 600 mutation-positive unresectable or metastatic melanoma: Summary of the scientific assessment of the Committee for Medicinal Products for Human Use [J].
Dias, Silvy da Rocha ;
Salmonson, Tomas ;
van Zwieten-Boot, Barbara ;
Jonsson, Bertil ;
Marchetti, Serena ;
Schellens, Jan H. M. ;
Giuliani, Rosa ;
Pignatti, Francesco .
EUROPEAN JOURNAL OF CANCER, 2013, 49 (07) :1654-1661
[26]   Safety and efficacy of vemurafenib in BRAF V600E mutation-positive metastatic melanomas [J].
Andrea P Sponghini ;
David Rondonotti ;
Marco Giavarra ;
Roberto Giorgione ;
Francesca Platini .
Journal of Translational Medicine, 13 (Suppl 1)
[27]   Budget Impact of Dabrafenib and Trametinib in Combination as Adjuvant Treatment of BRAF V600E/K Mutation-Positive Melanoma from a US Commercial Payer Perspective [J].
Stellato, Daniel ;
Gerbasi, Margaret E. ;
Ndife, Briana ;
Ghate, Sameer R. ;
Moynahan, Aaron ;
Mishra, Dinesh ;
Gunda, Praveen ;
Koruth, Roy ;
Delea, Thomas E. .
JOURNAL OF MANAGED CARE & SPECIALTY PHARMACY, 2019, 25 (11) :1227-+
[28]   Skin toxicity in BRAF(V600) mutated metastatic cutaneous melanoma patients treated with vemurafenib [J].
Nowara, Elzbieta ;
Huszno, Joanna ;
Slomian, Grzegorz ;
Nieckula, Jaroslaw .
POSTEPY DERMATOLOGII I ALERGOLOGII, 2016, 33 (01) :52-56
[29]   Efficacy and safety of dabrafenib-trametinib in the treatment of unresectable advanced/metastatic melanoma with BRAF-V600 mutation: A systematic review and network meta-analysis [J].
Garzon-Orjuela, Nathaly ;
Prieto-Pinto, Laura ;
Lasalvia, Pieralessandro ;
Herrera, Daniel ;
Castrillon, Johanna ;
Gonzalez-Bravo, Diana ;
Castaneda-Cardona, Camilo ;
Rosselli, Diego .
DERMATOLOGIC THERAPY, 2020, 33 (02)
[30]   A population-based study of the treatment effect of first-line ipilimumab for metastatic or unresectable melanoma [J].
Drysdale, Erik ;
Peng, Yingwei ;
Nguyen, Paul ;
Baetz, Tara ;
Hanna, Timothy P. .
MELANOMA RESEARCH, 2019, 29 (06) :635-642