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Erschienen in: PharmacoEconomics 9/2016

01.09.2016 | Systematic Review

Use of Intermediate Endpoints in the Economic Evaluation of New Treatments for Advanced Cancer and Methods Adopted When Suitable Overall Survival Data are Not Available

verfasst von: Catherine Beauchemin, Marie-Ève Lapierre, Nathalie Letarte, Louise Yelle, Jean Lachaine

Erschienen in: PharmacoEconomics | Ausgabe 9/2016

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Abstract

Objectives

This study assessed the use of intermediate endpoints in the economic evaluation of new treatments for advanced cancer and the methodological approaches adopted when overall survival (OS) data are unavailable or of limited use.

Methods

A systematic literature review was conducted to identify economic evaluations of treatments for advanced cancer published between 2003 and 2013. Cost-effectiveness and cost-utility analyses expressed in cost per life-year gained and cost per quality-adjusted life-year using an intermediate endpoint as an outcome measure were eligible. Characteristics of selected studies were extracted and comprised population, treatment of interest, comparator, line of treatment, study perspective, and time horizon. Use of intermediate endpoints and methods adopted when OS data were lacking were analyzed.

Results

In total, 7219 studies were identified and 100 fulfilled the eligibility criteria. Intermediate endpoints mostly used were progression-free survival and time to progression, accounting for 92 % of included studies. OS data were unavailable for analysis in nearly 25 % of economic evaluations. In the absence of OS data, studies most commonly assumed an equal risk of death for all treatment groups. Other methods included use of indirect comparison based on numerous assumptions, use of a proxy for OS, consultation with clinical experts, and use of published external information from different treatment settings.

Conclusion

Intermediate endpoints are widely used in the economic evaluation of new treatments for advanced cancer in order to estimate OS. Currently, different methods are used in the absence of suitable OS data and the choice of an appropriate method depends on many factors including the data availability.
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Literatur
1.
Zurück zum Zitat Lebwohl D, et al. Progression-free survival: gaining on overall survival as a gold standard and accelerating drug development. Cancer J. 2009;15(5):386–94.CrossRefPubMed Lebwohl D, et al. Progression-free survival: gaining on overall survival as a gold standard and accelerating drug development. Cancer J. 2009;15(5):386–94.CrossRefPubMed
2.
Zurück zum Zitat Saad ED, Buyse M. Overall survival: patient outcome, therapeutic objective, clinical trial end point, or public health measure? J Clin Oncol. 2012;30(15):1750–4.CrossRefPubMed Saad ED, Buyse M. Overall survival: patient outcome, therapeutic objective, clinical trial end point, or public health measure? J Clin Oncol. 2012;30(15):1750–4.CrossRefPubMed
3.
Zurück zum Zitat Zhuang SH, Xiu L, Elsayed YA. Overall survival: a gold standard in search of a surrogate: the value of progression-free survival and time to progression as end points of drug efficacy. Cancer J. 2009;15(5):395–400.CrossRefPubMed Zhuang SH, Xiu L, Elsayed YA. Overall survival: a gold standard in search of a surrogate: the value of progression-free survival and time to progression as end points of drug efficacy. Cancer J. 2009;15(5):395–400.CrossRefPubMed
4.
Zurück zum Zitat Pazdur R. Endpoints for assessing drug activity in clinical trials. Oncologist. 2008;13(Suppl 2):19–21.CrossRefPubMed Pazdur R. Endpoints for assessing drug activity in clinical trials. Oncologist. 2008;13(Suppl 2):19–21.CrossRefPubMed
5.
Zurück zum Zitat US Department of Health and Human Services: Food and Drug Administration: Center for Drug Evaluation and Research (CDER): Center for Biologics Evaluation and Research (CBER), Guidance for Industry. Clinical Trial Endpoints for the Approval of Cancer Drugs and Biologics. Rockville: Food and Drug Administration (FDA); 2007. Available from: http://www.fda.gov/downloads/Drugs/Guidances/ucm071590.pdf. Accessed Dec 2015. US Department of Health and Human Services: Food and Drug Administration: Center for Drug Evaluation and Research (CDER): Center for Biologics Evaluation and Research (CBER), Guidance for Industry. Clinical Trial Endpoints for the Approval of Cancer Drugs and Biologics. Rockville: Food and Drug Administration (FDA); 2007. Available from: http://​www.​fda.​gov/​downloads/​Drugs/​Guidances/​ucm071590.​pdf. Accessed Dec 2015.
7.
Zurück zum Zitat Booth CM, Eisenhauer EA. Progression-free survival: meaningful or simply measurable? J Clin Oncol. 2012;30(10):1030–3.CrossRefPubMed Booth CM, Eisenhauer EA. Progression-free survival: meaningful or simply measurable? J Clin Oncol. 2012;30(10):1030–3.CrossRefPubMed
8.
Zurück zum Zitat Kay A, et al. Randomized controlled trials in the era of molecular oncology: methodology, biomarkers, and end points. Ann Oncol. 2012;23(6):1646–51.CrossRefPubMed Kay A, et al. Randomized controlled trials in the era of molecular oncology: methodology, biomarkers, and end points. Ann Oncol. 2012;23(6):1646–51.CrossRefPubMed
9.
Zurück zum Zitat Saad ED, Katz A. Progression-free survival and time to progression as primary end points in advanced breast cancer: often used, sometimes loosely defined. Ann Oncol. 2009;20(3):460–4.CrossRefPubMed Saad ED, Katz A. Progression-free survival and time to progression as primary end points in advanced breast cancer: often used, sometimes loosely defined. Ann Oncol. 2009;20(3):460–4.CrossRefPubMed
10.
Zurück zum Zitat Davis S, Tappenden P, Cantrell A, A review of studies examining the relationship between progression-free survival and overall survival in advanced or metastatic cancer—a report by the Decision Support Unit. School of Health and Related Research, University of Sheffield; 2012. Davis S, Tappenden P, Cantrell A, A review of studies examining the relationship between progression-free survival and overall survival in advanced or metastatic cancer—a report by the Decision Support Unit. School of Health and Related Research, University of Sheffield; 2012.
11.
Zurück zum Zitat Sridhara R, et al. Review of oncology and hematology drug product approvals at the US Food and Drug Administration between July 2005 and December 2007. J Natl Cancer Inst. 2010;102(4):230–43.CrossRefPubMed Sridhara R, et al. Review of oncology and hematology drug product approvals at the US Food and Drug Administration between July 2005 and December 2007. J Natl Cancer Inst. 2010;102(4):230–43.CrossRefPubMed
12.
Zurück zum Zitat Conde-Estevez D, et al. An overview of randomized clinical trials in metastatic breast cancer: variables affecting regulatory drug approval. Anticancer Drugs. 2014;25(9):992–7.CrossRefPubMed Conde-Estevez D, et al. An overview of randomized clinical trials in metastatic breast cancer: variables affecting regulatory drug approval. Anticancer Drugs. 2014;25(9):992–7.CrossRefPubMed
13.
Zurück zum Zitat Chabot I, Rocchi A. Oncology drug health technology assessment recommendations: Canadian versus UK experiences. Clinicoecon Outcomes Res. 2014;6:357–67.CrossRefPubMedPubMedCentral Chabot I, Rocchi A. Oncology drug health technology assessment recommendations: Canadian versus UK experiences. Clinicoecon Outcomes Res. 2014;6:357–67.CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Center for Reviews and Dissemination. Systematic reviews: CRD’s guidance for undertaking reviews in health care. University of York; 2008. Center for Reviews and Dissemination. Systematic reviews: CRD’s guidance for undertaking reviews in health care. University of York; 2008.
15.
16.
Zurück zum Zitat Lewis G, et al. Cost-effectiveness of erlotinib versus docetaxel for second-line treatment of advanced non-small-cell lung cancer in the United Kingdom. J Int Med Res. 2010;38(1):9–21.CrossRefPubMed Lewis G, et al. Cost-effectiveness of erlotinib versus docetaxel for second-line treatment of advanced non-small-cell lung cancer in the United Kingdom. J Int Med Res. 2010;38(1):9–21.CrossRefPubMed
17.
Zurück zum Zitat Carlson JJ, et al. The potential clinical and economic outcomes of pharmacogenomic approaches to EGFR-tyrosine kinase inhibitor therapy in non-small-cell lung cancer. Value Health. 2009;12(1):20–7.CrossRefPubMed Carlson JJ, et al. The potential clinical and economic outcomes of pharmacogenomic approaches to EGFR-tyrosine kinase inhibitor therapy in non-small-cell lung cancer. Value Health. 2009;12(1):20–7.CrossRefPubMed
18.
Zurück zum Zitat Carlson JJ, et al. Comparative clinical and economic outcomes of treatments for refractory non-small cell lung cancer (NSCLC). Lung Cancer. 2008;61(3):405–15.CrossRefPubMed Carlson JJ, et al. Comparative clinical and economic outcomes of treatments for refractory non-small cell lung cancer (NSCLC). Lung Cancer. 2008;61(3):405–15.CrossRefPubMed
19.
Zurück zum Zitat Lesnock JL, et al. Consolidation paclitaxel is more cost-effective than bevacizumab following upfront treatment of advanced epithelial ovarian cancer. Gynecol Oncol. 2011;122(3):473–8.CrossRefPubMedPubMedCentral Lesnock JL, et al. Consolidation paclitaxel is more cost-effective than bevacizumab following upfront treatment of advanced epithelial ovarian cancer. Gynecol Oncol. 2011;122(3):473–8.CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Le QA, Hay JW. Cost-effectiveness analysis of lapatinib in HER-2-positive advanced breast cancer. Cancer. 2009;115(3):489–98.CrossRefPubMed Le QA, Hay JW. Cost-effectiveness analysis of lapatinib in HER-2-positive advanced breast cancer. Cancer. 2009;115(3):489–98.CrossRefPubMed
21.
Zurück zum Zitat Giuliani G, et al. Cost-effectiveness analysis of bevacizumab versus pemetrexed for advanced non-squamous NSCLC in Italy. Lung Cancer. 2010;69(SUPPL. 1):S11–7.CrossRefPubMed Giuliani G, et al. Cost-effectiveness analysis of bevacizumab versus pemetrexed for advanced non-squamous NSCLC in Italy. Lung Cancer. 2010;69(SUPPL. 1):S11–7.CrossRefPubMed
22.
Zurück zum Zitat Zeng X, et al. Cost-effectiveness of continuation maintenance pemetrexed after cisplatin and pemetrexed chemotherapy for advanced nonsquamous non-small-cell lung cancer: estimates from the perspective of the chinese health care system. Clin Ther. 2013;35(1):54–65.CrossRefPubMed Zeng X, et al. Cost-effectiveness of continuation maintenance pemetrexed after cisplatin and pemetrexed chemotherapy for advanced nonsquamous non-small-cell lung cancer: estimates from the perspective of the chinese health care system. Clin Ther. 2013;35(1):54–65.CrossRefPubMed
24.
Zurück zum Zitat Rocconi RP, et al. Role of chemotherapy for patients with recurrent platinum-resistant advanced epithelial ovarian cancer: a cost-effectiveness analysis. Cancer. 2006;107(3):536–43.CrossRefPubMed Rocconi RP, et al. Role of chemotherapy for patients with recurrent platinum-resistant advanced epithelial ovarian cancer: a cost-effectiveness analysis. Cancer. 2006;107(3):536–43.CrossRefPubMed
25.
Zurück zum Zitat Spackman E, et al. Trastuzumab for the treatment of HER2-positive metastatic gastric cancer: a NICE single technology appraisal. Pharmacoeconomics. 2013;31(3):185–94.CrossRefPubMed Spackman E, et al. Trastuzumab for the treatment of HER2-positive metastatic gastric cancer: a NICE single technology appraisal. Pharmacoeconomics. 2013;31(3):185–94.CrossRefPubMed
26.
Zurück zum Zitat Hoyle M, et al. Cost-effectiveness of cetuximab, cetuximab plus irinotecan, and panitumumab for third and further lines of treatment for KRAS wild-type patients with metastatic colorectal cancer. Value Health. 2013;16(2):288–96.CrossRefPubMed Hoyle M, et al. Cost-effectiveness of cetuximab, cetuximab plus irinotecan, and panitumumab for third and further lines of treatment for KRAS wild-type patients with metastatic colorectal cancer. Value Health. 2013;16(2):288–96.CrossRefPubMed
27.
Zurück zum Zitat Asseburg C, et al. Cost-effectiveness of targeted therapy with cetuximab in patients with K-ras wild-type colorectal cancer presenting with initially unresectable metastases limited to the liver in a German setting. Clin Ther. 2011;33(4):482–97.CrossRefPubMed Asseburg C, et al. Cost-effectiveness of targeted therapy with cetuximab in patients with K-ras wild-type colorectal cancer presenting with initially unresectable metastases limited to the liver in a German setting. Clin Ther. 2011;33(4):482–97.CrossRefPubMed
28.
Zurück zum Zitat Benedict A, et al. An economic evaluation of docetaxel and paclitaxel regimens in metastatic breast cancer in the UK. PharmacoEconomics. 2009;27(10):847–59.CrossRefPubMed Benedict A, et al. An economic evaluation of docetaxel and paclitaxel regimens in metastatic breast cancer in the UK. PharmacoEconomics. 2009;27(10):847–59.CrossRefPubMed
29.
Zurück zum Zitat Benedict A, et al. Economic evaluation of new targeted therapies for the first-line treatment of patients with metastatic renal cell carcinoma. BJU Int. 2011;108(5):665–72.PubMed Benedict A, et al. Economic evaluation of new targeted therapies for the first-line treatment of patients with metastatic renal cell carcinoma. BJU Int. 2011;108(5):665–72.PubMed
30.
Zurück zum Zitat Calvo Aller E, et al. Cost-effectiveness evaluation of sunitinib as first-line targeted therapy for metastatic renal cell carcinoma in Spain. Clin Transl Oncol. 2011;13(12):869–77.CrossRefPubMed Calvo Aller E, et al. Cost-effectiveness evaluation of sunitinib as first-line targeted therapy for metastatic renal cell carcinoma in Spain. Clin Transl Oncol. 2011;13(12):869–77.CrossRefPubMed
31.
Zurück zum Zitat Karnon J, et al. A trial-based cost-effectiveness analysis of letrozole followed by tamoxifen versus tamoxifen followed by letrozole for postmenopausal advanced breast cancer. Ann Oncol. 2003;14(11):1629–33.CrossRefPubMed Karnon J, et al. A trial-based cost-effectiveness analysis of letrozole followed by tamoxifen versus tamoxifen followed by letrozole for postmenopausal advanced breast cancer. Ann Oncol. 2003;14(11):1629–33.CrossRefPubMed
32.
Zurück zum Zitat Shiroiwa T, Fukuda T, Tsutani K. Cost-effectiveness analysis of XELOX for metastatic colorectal cancer based on the NO16966 and NO16967 trials. Br J Cancer. 2009;101(1):12–8.CrossRefPubMedPubMedCentral Shiroiwa T, Fukuda T, Tsutani K. Cost-effectiveness analysis of XELOX for metastatic colorectal cancer based on the NO16966 and NO16967 trials. Br J Cancer. 2009;101(1):12–8.CrossRefPubMedPubMedCentral
33.
Zurück zum Zitat Reed SD, et al. Cost effectiveness of ixabepilone plus capecitabine for metastatic breast cancer progressing after anthracycline and taxane treatment. J Clin Oncol. 2009;27(13):2185–91.CrossRefPubMed Reed SD, et al. Cost effectiveness of ixabepilone plus capecitabine for metastatic breast cancer progressing after anthracycline and taxane treatment. J Clin Oncol. 2009;27(13):2185–91.CrossRefPubMed
34.
Zurück zum Zitat Cameron DA, et al. Economic evaluation of fulvestrant as an extra step in the treatment sequence for ER-positive advanced breast cancer. Br J Cancer. 2008;99(12):1984–90.CrossRefPubMedPubMedCentral Cameron DA, et al. Economic evaluation of fulvestrant as an extra step in the treatment sequence for ER-positive advanced breast cancer. Br J Cancer. 2008;99(12):1984–90.CrossRefPubMedPubMedCentral
35.
Zurück zum Zitat Lux MP, et al. Cost-utility analysis for advanced breast cancer therapy in Germany: results of the fulvestrant sequencing model. Breast Cancer Res Treat. 2009;117(2):305–17.CrossRefPubMed Lux MP, et al. Cost-utility analysis for advanced breast cancer therapy in Germany: results of the fulvestrant sequencing model. Breast Cancer Res Treat. 2009;117(2):305–17.CrossRefPubMed
36.
Zurück zum Zitat Remak E, et al. Economic evaluation of sunitinib malate for the first-line treatment of metastatic renal cell carcinoma. J Clin Oncol. 2008;26(24):3995–4000.CrossRefPubMed Remak E, et al. Economic evaluation of sunitinib malate for the first-line treatment of metastatic renal cell carcinoma. J Clin Oncol. 2008;26(24):3995–4000.CrossRefPubMed
37.
Zurück zum Zitat Greenhalgh J, et al. Rituximab for the first-line maintenance treatment of follicular non-Hodgkin’s lymphoma: a NICE single technology appraisal. PharmacoEconomics. 2013;31(5):403–13.CrossRefPubMedPubMedCentral Greenhalgh J, et al. Rituximab for the first-line maintenance treatment of follicular non-Hodgkin’s lymphoma: a NICE single technology appraisal. PharmacoEconomics. 2013;31(5):403–13.CrossRefPubMedPubMedCentral
38.
Zurück zum Zitat Chabot I, Rocchi A. How do cost-effectiveness analyses inform reimbursement decisions for oncology medicines in Canada? The example of Sunitinib for first-line treatment of metastatic renal cell carcinoma. Value Health. 2010;13(6):837–45.CrossRefPubMed Chabot I, Rocchi A. How do cost-effectiveness analyses inform reimbursement decisions for oncology medicines in Canada? The example of Sunitinib for first-line treatment of metastatic renal cell carcinoma. Value Health. 2010;13(6):837–45.CrossRefPubMed
39.
Zurück zum Zitat Zhu J, et al. Gene-guided Gefitinib switch maintenance therapy for patients with advanced EGFR mutation-positive Non-small cell lung cancer: an economic analysis. BMC Cancer. 2013;13(39):1–11. Zhu J, et al. Gene-guided Gefitinib switch maintenance therapy for patients with advanced EGFR mutation-positive Non-small cell lung cancer: an economic analysis. BMC Cancer. 2013;13(39):1–11.
40.
Zurück zum Zitat Bowater RJ, Bridge LJ, Lilford RJ. The relationship between progression-free and post-progression survival in treating four types of metastatic cancer. Cancer Lett. 2008;262(1):48–53.CrossRefPubMed Bowater RJ, Bridge LJ, Lilford RJ. The relationship between progression-free and post-progression survival in treating four types of metastatic cancer. Cancer Lett. 2008;262(1):48–53.CrossRefPubMed
41.
Zurück zum Zitat Jansen JP, et al. Interpreting indirect treatment comparisons and network meta-analysis for health-care decision making: report of the ISPOR Task Force on Indirect Treatment Comparisons Good Research Practices: part 1. Value Health. 2011;14(4):417–28.CrossRefPubMed Jansen JP, et al. Interpreting indirect treatment comparisons and network meta-analysis for health-care decision making: report of the ISPOR Task Force on Indirect Treatment Comparisons Good Research Practices: part 1. Value Health. 2011;14(4):417–28.CrossRefPubMed
42.
Zurück zum Zitat Hoaglin DC, et al. Conducting indirect-treatment-comparison and network-meta-analysis studies: report of the ISPOR Task Force on Indirect Treatment Comparisons Good Research Practices: part 2. Value Health. 2011;14(4):429–37.CrossRefPubMed Hoaglin DC, et al. Conducting indirect-treatment-comparison and network-meta-analysis studies: report of the ISPOR Task Force on Indirect Treatment Comparisons Good Research Practices: part 2. Value Health. 2011;14(4):429–37.CrossRefPubMed
43.
Zurück zum Zitat Delea TE, et al. Cost-effectiveness of lapatinib plus capecitabine in women with HER2+ metastatic breast cancer who have received prior therapy with trastuzumab. Eur J Health Econ. 2012;13(5):589–603.CrossRefPubMed Delea TE, et al. Cost-effectiveness of lapatinib plus capecitabine in women with HER2+ metastatic breast cancer who have received prior therapy with trastuzumab. Eur J Health Econ. 2012;13(5):589–603.CrossRefPubMed
44.
Zurück zum Zitat Kilonzo M, et al. Pazopanib for the first-line treatment of patients with advanced and/or metastatic renal cell carcinoma: a NICE single technology appraisal. PharmacoEconomics. 2013;31(1):15–24.CrossRefPubMed Kilonzo M, et al. Pazopanib for the first-line treatment of patients with advanced and/or metastatic renal cell carcinoma: a NICE single technology appraisal. PharmacoEconomics. 2013;31(1):15–24.CrossRefPubMed
45.
Zurück zum Zitat Lidgren M, et al. Cost-effectiveness of HER2 testing and trastuzumab therapy for metastatic breast cancer. Acta Oncol. 2008;47(6):1018–28.CrossRefPubMed Lidgren M, et al. Cost-effectiveness of HER2 testing and trastuzumab therapy for metastatic breast cancer. Acta Oncol. 2008;47(6):1018–28.CrossRefPubMed
46.
Zurück zum Zitat Machado M, Einarson TR. Lapatinib in patients with metastatic breast cancer following initial treatment with trastuzumab: an economic analysis from the Brazilian public health care perspective. Breast Cancer Targets Therapy. 2012;4:173–82. Machado M, Einarson TR. Lapatinib in patients with metastatic breast cancer following initial treatment with trastuzumab: an economic analysis from the Brazilian public health care perspective. Breast Cancer Targets Therapy. 2012;4:173–82.
47.
Zurück zum Zitat Ishak KJ, et al. Methods for adjusting for bias due to crossover in oncology trials. Pharmacoeconomics. 2014;32(6):533–46.CrossRefPubMed Ishak KJ, et al. Methods for adjusting for bias due to crossover in oncology trials. Pharmacoeconomics. 2014;32(6):533–46.CrossRefPubMed
48.
Zurück zum Zitat Jonsson L, et al. Analyzing overall survival in randomized controlled trials with crossover and implications for economic evaluation. Value Health. 2014;17(6):707–13.CrossRefPubMed Jonsson L, et al. Analyzing overall survival in randomized controlled trials with crossover and implications for economic evaluation. Value Health. 2014;17(6):707–13.CrossRefPubMed
49.
Zurück zum Zitat Davies A, et al. The ends justify the means: outcome measures for estimating the value of new cancer therapies. Health Outcomes Res Med. 2012;3(1):e25–36.CrossRef Davies A, et al. The ends justify the means: outcome measures for estimating the value of new cancer therapies. Health Outcomes Res Med. 2012;3(1):e25–36.CrossRef
50.
Zurück zum Zitat Wu B, et al. Cost-effectiveness of adding Rh-endostatin to first-line chemotherapy in patients with advanced non-small-cell lung cancer in China. Clin Ther. 2011;33(10):1446–55.CrossRefPubMed Wu B, et al. Cost-effectiveness of adding Rh-endostatin to first-line chemotherapy in patients with advanced non-small-cell lung cancer in China. Clin Ther. 2011;33(10):1446–55.CrossRefPubMed
51.
Zurück zum Zitat Lazzaro C, et al. An Italian cost-effectiveness analysis of paclitaxel albumin (nab-paclitaxel) versus conventional paclitaxel for metastatic breast cancer patients: the COSTANza study. ClinicoEcon Outcomes Res. 2013;5(1):125–35.CrossRefPubMedPubMedCentral Lazzaro C, et al. An Italian cost-effectiveness analysis of paclitaxel albumin (nab-paclitaxel) versus conventional paclitaxel for metastatic breast cancer patients: the COSTANza study. ClinicoEcon Outcomes Res. 2013;5(1):125–35.CrossRefPubMedPubMedCentral
52.
Zurück zum Zitat Spolverato G, et al. Hepatic resection for disappearing liver metastasis: a cost-utility analysis. J Gastrointest Surg. 2015;19(9):1668–75.CrossRefPubMed Spolverato G, et al. Hepatic resection for disappearing liver metastasis: a cost-utility analysis. J Gastrointest Surg. 2015;19(9):1668–75.CrossRefPubMed
53.
Zurück zum Zitat Delea TE, et al. Cost effectiveness of dabrafenib as a first-line treatment in patients with BRAF V600 mutation-positive unresectable or metastatic melanoma in Canada. Pharmacoeconomics. 2015;33(4):367–80.CrossRefPubMed Delea TE, et al. Cost effectiveness of dabrafenib as a first-line treatment in patients with BRAF V600 mutation-positive unresectable or metastatic melanoma in Canada. Pharmacoeconomics. 2015;33(4):367–80.CrossRefPubMed
Metadaten
Titel
Use of Intermediate Endpoints in the Economic Evaluation of New Treatments for Advanced Cancer and Methods Adopted When Suitable Overall Survival Data are Not Available
verfasst von
Catherine Beauchemin
Marie-Ève Lapierre
Nathalie Letarte
Louise Yelle
Jean Lachaine
Publikationsdatum
01.09.2016
Verlag
Springer International Publishing
Erschienen in
PharmacoEconomics / Ausgabe 9/2016
Print ISSN: 1170-7690
Elektronische ISSN: 1179-2027
DOI
https://doi.org/10.1007/s40273-016-0401-4

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