Cost-effectiveness of FOLFIRI plus cetuximab vs FOLFIRI plus bevacizumab in the first-line treatment of RAS wild-type metastatic colorectal cancer in Germany: data from the FIRE-3 (AIO KRK-0306) study

被引:12
作者
Stintzing, Sebastian [1 ]
van Oostrum, Ilse [2 ]
Pescott, Chris P. [3 ]
Ronga, Philippe [3 ]
Heeg, Bart [2 ]
Heinemann, Volker [4 ]
机构
[1] Charite, Med Dept, Div Hematol Oncol & Tumor Immunol CCM, Berlin, Germany
[2] Ingress Hlth, Rotterdam, Netherlands
[3] Merck KGaA, Darmstadt, Germany
[4] Ludwig Maximilians Univ Munchen, Dept Med 3, Univ Hosp, Munich, Germany
关键词
FIRE-3; cetuximab; metastatic colorectal cancer; FOLFIRI; cost-effectiveness; PHASE-III TRIAL; PRIMARY TUMOR; PANITUMUMAB PLUS; OPEN-LABEL; CHEMOTHERAPY; FLUOROURACIL; LEUCOVORIN; IRINOTECAN; ANTIBODIES; SITE;
D O I
10.1080/13696998.2019.1709848
中图分类号
F [经济];
学科分类号
02 ;
摘要
Aims: This analysis evaluates the cost-effectiveness of first-line treatment with FOLFIRI + cetuximab vs FOLFIRI + bevacizumab for patients with RAS wild-type (wt) metastatic colorectal cancer (mCRC) in Germany based on the randomized phase 3 FIRE-3 trial. For patients with RAS wt mCRC, FOLFIRI + cetuximab yielded statistically significant median overall survival gains over FOLFIRI + bevacizumab. Materials and methods: A standard 3-state partitioned survival cost-utility model was developed to compare the health benefits and costs of treatment from a German social health insurance perspective using individual patient-level trial data. Health outcomes were reported in life-years (LYs) and quality-adjusted life-years (QALYs) gained. Survival was estimated based on Kaplan-Meier (KM) curves supplemented with best-fitting parametric survival model extrapolations. Subgroup analyses of patients with a left-sided primary tumor location or patients with metastases confined to the liver were performed. Results: In the modified intention-to-treat analysis, FOLFIRI + cetuximab, providing 0.68 additional LYs (0.53 QALYs), yielded incremental cost-effectiveness ratios (ICERs) of euro36,360/LY and euro47,250/QALY. In subgroup analyses, patients experienced improved survival gains without a corresponding increase in costs, resulting in lower ICERs. Our model was most sensitive to changes in treatment duration across all lines of therapy, utility of progressive disease, as well as patients' weight and body surface area. Limitations: This cost-effectiveness analysis was based on patient-level data from the FIRE-3 trial. Trial outcomes may not adequately reflect those in the real-world setting. Additionally, resource use and costs were obtained from tariff lists, which do not account for differences in treatment practice. These considerations limit generalizability of outcomes to other countries, or within the German healthcare setting. Conclusions: Based on our analyses, FOLFIRI + cetuximab is cost-effective compared with FOLFIRI + bevacizumab in patients with RAS wt mCRC, with ICERs well below willingness-to-pay thresholds for diseases with a high burden.
引用
收藏
页码:448 / 455
页数:8
相关论文
共 35 条
[1]  
Adam R, 2004, ANN SURG, V240, P644, DOI 10.1097/01.sla.0000141198.92114.16
[2]  
[Anonymous], 2012, Globocan 2012: Estimated cancer incidence, mortality and prevalence worldwide in 2012
[3]   Prognostic and predictive value of primary tumour side in patients with RAS wild-type metastatic colorectal cancer treated with chemotherapy and EGFR directed antibodies in six randomized trials [J].
Arnold, D. ;
Lueza, B. ;
Douillard, J. -Y. ;
Peeters, M. ;
Lenz, H. -J. ;
Venook, A. ;
Heinemann, V. ;
Van Cutsem, E. ;
Pignon, J. -P. ;
Tabernero, J. ;
Cervantes, A. ;
Ciardiello, F. .
ANNALS OF ONCOLOGY, 2017, 28 (08) :1713-1729
[4]   Comparison of Site of Death, Health Care Utilization, and Hospital Expenditures for Patients Dying With Cancer in 7 Developed Countries [J].
Bekelman, Justin E. ;
Halpern, Scott D. ;
Blankart, Carl Rudolf ;
Bynum, Julie P. ;
Cohen, Joachim ;
Fowler, Robert ;
Kaasa, Stein ;
Kwietniewski, Lukas ;
Melberg, Hans Olav ;
Onwuteaka-Philipsen, Bregje ;
Oosterveld-Vlug, Mariska ;
Pring, Andrew ;
Schreyoegg, Jonas ;
Ulrich, Connie M. ;
Verne, Julia ;
Wunsch, Hannah ;
Emanuel, Ezekiel J. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 315 (03) :272-283
[5]   Comparison of 17,641 Patients With Right- and Left-Sided Colon Cancer: Differences in Epidemiology, Perioperative Course, Histology, and Survival [J].
Benedix, Frank ;
Kube, Rainer ;
Meyer, Frank ;
Schmidt, Uwe ;
Gastinger, Ingo ;
Lippert, Hans .
DISEASES OF THE COLON & RECTUM, 2010, 53 (01) :57-64
[6]   Global estimates of cancer prevalence for 27 sites in the adult population in 2008 [J].
Bray, Freddie ;
Ren, Jian-Song ;
Masuyer, Eric ;
Ferlay, Jacques .
INTERNATIONAL JOURNAL OF CANCER, 2013, 132 (05) :1133-1145
[7]   Primary tumor site is a useful predictor of cetuximab efficacy in the third-line or salvage treatment of KRAS wild-type (exon 2 non-mutant) metastatic colorectal cancer: a nationwide cohort study [J].
Chen, Kuo-Hsing ;
Shao, Yu-Yun ;
Chen, Ho-Min ;
Lin, Yu-Lin ;
Lin, Zhong-Zhe ;
Lai, Mei-Shu ;
Cheng, Ann-Lii ;
Yeh, Kun-Huei .
BMC CANCER, 2016, 16
[8]   Randomized, Phase III Trial of Panitumumab With Infusional Fluorouracil, Leucovorin, and Oxaliplatin (FOLFOX4) Versus FOLFOX4 Alone As First-Line Treatment in Patients With Previously Untreated Metastatic Colorectal Cancer: The PRIME Study [J].
Douillard, Jean-Yves ;
Siena, Salvatore ;
Cassidy, James ;
Tabernero, Josep ;
Burkes, Ronald ;
Barugel, Mario ;
Humblet, Yves ;
Bodoky, Gyoergy ;
Cunningham, David ;
Jassem, Jacek ;
Rivera, Fernando ;
Kocakova, Ilona ;
Ruff, Paul ;
Blasinska-Morawiec, Maria ;
Smakal, Martin ;
Canon, Jean-Luc ;
Rother, Mark ;
Oliner, Kelly S. ;
Wolf, Michael ;
Gansert, Jennifer .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (31) :4697-4705
[9]  
*GGPO, 2019, GERMAN GUIDELINE PRO
[10]   Economic Analysis of Panitumumab Compared With Cetuximab in Patients With Wild-type KRAS Metastatic Colorectal Cancer That Progressed After Standard Chemotherapy [J].
Graham, Christopher N. ;
Maglinte, Gregory A. ;
Schwartzberg, Lee S. ;
Price, Timothy J. ;
Knox, Hediyyih N. ;
Hechmati, Guy ;
Hjelmgren, Jonas ;
Barber, Beth ;
Fakih, Marwan G. .
CLINICAL THERAPEUTICS, 2016, 38 (06) :1376-1391