Cost-effectiveness and budget impact of venetoclax in combination with rituximab in relapsed/refractory chronic lymphocytic leukemia in Switzerland

被引:15
作者
Barbier, Michaela [1 ]
Durno, Nicholas [2 ]
Bennison, Craig [2 ]
Ortli, Mathias [3 ]
Knapp, Christian [3 ]
Schwenkglenks, Matthias [1 ]
机构
[1] Univ Basel, Inst Pharmaceut Med ECPM, Klingelbergstr 61, CH-4056 Basel, Switzerland
[2] OPEN Hlth, Oxford, England
[3] AbbVie AG, Alte Steinhauserstr 14, CH-6330 Cham, Switzerland
关键词
Rituximab; Venetoclax; Chronic lymphocytic leukemia; Cost-effectiveness; Partitioned survival model; EVPI; IBRUTINIB; CLL;
D O I
10.1007/s10198-021-01398-7
中图分类号
F [经济];
学科分类号
02 ;
摘要
Introduction Venetoclax in combination with rituximab (VEN + R) demonstrated prolonged overall survival (OS) and progression-free survival (PFS) for patients with relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) in comparison to standard chemoimmunotherapy [bendamustine + rituximab (BR)]. We conducted a cost-effectiveness and budget impact analysis comparing VEN + R versus six comparators from the Swiss healthcare payer perspective. Methods A three-state partitioned survival model, developed in accordance with NICE and ISPOR decision modelling guidelines, was adapted to Switzerland. Model inputs were informed by the MURANO trial (survival data, patient characteristics), publicly available Swiss sources (drug prices, inpatient and outpatient costs), Swiss National Institute of Cancer Epidemiology and Registration data (incidence and prevalence values), and Swiss medical expert feedback. We used published (dis-)utility values and adverse event probabilities. Results Over a lifetime, VEN + R resulted in an expected gain of 2.60 quality-adjusted life years (QALYs) per patient and incremental costs of Swiss Francs (CHF) 147,851 compared to BR, leading to an incremental cost-effectiveness ratio of CHF 56,881/QALY gained. Other treatment strategies (for example ibrutinib versus VEN + R) resulted in higher costs and lower QALYs. Results were not different for subgroups of patients with/without deletion of chromosome 17p/tumour protein 53 mutation. In scenario analysis, changes in post-progression treatment costs demonstrated a high impact on results. We estimated an expected value of perfect information of CHF 3,318/patient. A moderate VEN + R uptake was estimated to save CHF 12.3 million during 5 years. Conclusions Using a threshold of CHF 100,000 per QALY, VEN + R was projected to be cost-effective vs BR.
引用
收藏
页码:837 / 846
页数:10
相关论文
共 37 条
[1]  
[Anonymous], 2013, Guide to the Methods of Technology Appraisal
[2]   Fludarabine, cyclophosphamide, and rituximab chemoimmunotherapy is highly effective treatment for relapsed patients with CLL [J].
Badoux, Xavier C. ;
Keating, Michael J. ;
Wang, Xuemei ;
O'Brien, Susan M. ;
Ferrajoli, Alessandra ;
Faderl, Stefan ;
Burger, Jan ;
Koller, Charles ;
Lerner, Susan ;
Kantarjian, Hagop ;
Wierda, William G. .
BLOOD, 2011, 117 (11) :3016-3024
[3]   A cost-effectiveness analysis of pembrolizumab with or without chemotherapy for the treatment of patients with metastatic, non-squamous non-small cell lung cancer and high PD-L1 expression in Switzerland [J].
Barbier, Michaela Carla ;
Pardo, Esther ;
Panje, Cedric Michael ;
Gautschi, Oliver ;
Lupatsch, Judith Eva .
EUROPEAN JOURNAL OF HEALTH ECONOMICS, 2021, 22 (05) :669-677
[4]  
Blutspende SRK Zurich, BLUTSP ZUR PREISL VE
[5]   Ibrutinib versus Ofatumumab in Previously Treated Chronic Lymphoid Leukemia [J].
Byrd, J. C. ;
Brown, J. R. ;
O'Brien, S. ;
Barrientos, J. C. ;
Kay, N. E. ;
Reddy, N. M. ;
Coutre, S. ;
Tam, C. S. ;
Mulligan, S. P. ;
Jaeger, U. ;
Devereux, S. ;
Barr, P. M. ;
Furman, R. R. ;
Kipps, T. J. ;
Cymbalista, F. ;
Pocock, C. ;
Thornton, P. ;
Caligaris-Cappio, F. ;
Robak, T. ;
Delgado, J. ;
Schuster, S. J. ;
Montillo, M. ;
Schuh, A. ;
de Vos, S. ;
Gill, D. ;
Bloor, A. ;
Dearden, C. ;
Moreno, C. ;
Jones, J. J. ;
Chu, A. D. ;
Fardis, M. ;
McGreivy, J. ;
Clow, F. ;
James, D. F. ;
Hillmen, P. .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (03) :213-223
[6]   Long-term efficacy and safety with ibrutinib (ibr) in previously treated chronic lymphocytic leukemia (CLL): Up to four years follow-up of the RESONATE study. [J].
Byrd, John C. ;
Hillmen, Peter ;
O'Brien, Susan Mary ;
Barrientos, Jacqueline Claudia ;
Reddy, Nishitha M. ;
Coutre, Steven ;
Tam, Constantine S. ;
Mulligan, Stephen P. ;
Jager, Ulrich ;
Barr, Paul M. ;
Furman, Richard R. ;
Kipps, Thomas J. ;
Thornton, Patrick ;
Pagel, John M. ;
Burger, Jan Andreas ;
Jones, Jeffrey Alan ;
Dai, Sandra ;
Vezan, Remus N. ;
James, Danelle Frances ;
Brown, Jennifer R. .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
[7]   Ibrutinib combined with bendamustine and rituximab compared with placebo, bendamustine, and rituximab for previously treated chronic lymphocytic leukaemia or small lymphocytic lymphoma (HELIOS): a randomised, double-blind, phase 3 study [J].
Chanan-Khan, Asher ;
Cramer, Paula ;
Demirkan, Fatih ;
Fraser, Graeme ;
Silva, Rodrigo Santucci ;
Grosicki, Sebastian ;
Pristupa, Aleksander ;
Janssens, Ann ;
Mayer, Jiri ;
Bartlett, Nancy L. ;
Dilhuydy, Marie-Sarah ;
Pylypenko, Halyna ;
Loscertales, Javier ;
Avigdor, Abraham ;
Rule, Simon ;
Villa, Diego ;
Samoilova, Olga ;
Panagiotidis, Panagiots ;
Goy, Andre ;
Mato, Anthony ;
Pavlovsky, Miguel A. ;
Karlsson, Claes ;
Mahler, Michelle ;
Salman, Mariya ;
Sun, Steven ;
Phelps, Charles ;
Balasubramanian, Sriram ;
Howes, Angela ;
Hallek, Michael ;
Assouline, S. ;
Bence-Bruckler, I. ;
Buckstein, R. ;
Fraser, G. ;
Larratt, L. ;
Minuk, L. ;
Villa, D. ;
Angevine, A. ;
Bartlett, N. ;
Bixby, D. ;
Caimi, P. ;
Chanan-Khan, A. ;
Craig, M. ;
Forero-Torres, A. ;
Ganguly, S. ;
Goy, A. ;
Heffner, L. ;
Hermann, R. ;
Lansigan, F. ;
Leis, J. ;
Letzer, J. .
LANCET ONCOLOGY, 2016, 17 (02) :200-211
[8]  
ClinicalTrials.gov, PHAS 2 OP LAB STUD E
[9]  
Durno N, INT WORKSH CLL 2019
[10]   Chronic lymohocytic leukaemia: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Eichhorst, B. ;
Robak, T. ;
Montserrat, E. ;
Ghia, P. ;
Niemann, C. U. ;
Kater, A. P. ;
Gregor, M. ;
Cymbalista, F. ;
Buske, C. ;
Hillmen, P. ;
Hallek, M. ;
Mey, U. .
ANNALS OF ONCOLOGY, 2021, 32 (01) :23-33