Evidence map›Paper›PMID 41636995›Full record

ArticlePharmacoEconomics2026

Bevacizumab for Metastatic Colorectal Cancer with Chromosomal Instability: Cost-Effectiveness Analysis for a Novel Precision Treatment Approach in Germany, Ireland and Spain.

Jonathan Briody, Ian S Miller, James F O'Mahony, Lesley Tilson, Alice C O'Farrell, Qiushi Chen, Verena Murphy, Orla Casey, Nadine Schulte, Matthias P Ebert and 6 more

Abstract read
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In one paragraph

Article in PharmacoEconomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Jonathan BriodyData Science Centre, School of Population Health, RCSI University of Medicine and Health Sciences, Beaux Lane House, Lower Mercer St, Dublin 2, Ireland. jonathanbriody@rcsi.ie.ORCID http://orcid.org/0000-0002-0641-1551
Ian S MillerDepartment of Physiology and Medical Physics, RCSI University of Medicine and Health Sciences, Dublin, Ireland.ORCID http://orcid.org/0000-0002-2673-9618
James F O'MahonySchool of Economics, University College Dublin, Dublin, Ireland.ORCID http://orcid.org/0000-0003-3414-7388
Lesley TilsonSt James Hospital, National Centre for Pharmacoeconomics, Dublin, Ireland.
Alice C O'FarrellDepartment of Physiology and Medical Physics, RCSI University of Medicine and Health Sciences, Dublin, Ireland.ORCID http://orcid.org/0000-0002-6732-2966
Qiushi ChenThe Pennsylvania State University Libraries, Penn State Abington, Abington, PA, USA.ORCID http://orcid.org/0000-0003-4031-2669
Verena MurphyCancer Trials Ireland, Dublin, Ireland.ORCID http://orcid.org/0000-0003-3113-7854
Orla CaseyCancer Trials Ireland, Dublin, Ireland.ORCID http://orcid.org/0000-0003-0097-1248
Nadine SchulteDepartment of Medicine II, Medical Faculty Mannheim, University Medical Center Mannheim, Heidelberg University, Mannheim, Germany.ORCID http://orcid.org/0009-0002-4729-458X
Matthias P EbertDepartment of Medicine II, Medical Faculty Mannheim, University Medical Center Mannheim, Heidelberg University, Mannheim, Germany.ORCID http://orcid.org/0000-0003-3228-5138
Jochen H M PrehnDepartment of Physiology and Medical Physics, RCSI University of Medicine and Health Sciences, Dublin, Ireland.ORCID http://orcid.org/0000-0003-3479-7794
Diether LambrechtsDepartment of Human Genetics, Laboratory for Translational Genetics, VIB Center for Cancer Biology, Katholieke Universiteit Leuven, 3000, Leuven, Belgium.ORCID http://orcid.org/0000-0002-3429-302X
Bauke YlstraDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9479-3010
Rodrigo DienstmannOncology Data Science (ODysSey) Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.ORCID http://orcid.org/0000-0001-5997-318X
Annette T ByrneDepartment of Physiology and Medical Physics, RCSI University of Medicine and Health Sciences, Dublin, Ireland.ORCID http://orcid.org/0000-0003-0287-8899
Kathleen BennettData Science Centre, School of Population Health, RCSI University of Medicine and Health Sciences, Beaux Lane House, Lower Mercer St, Dublin 2, Ireland.ORCID http://orcid.org/0000-0002-2861-7665

Funding

Horizon 2020 754923
6 · The paper itself

Abstract

objectivesBevacizumab was approved for first-line treatment of metastatic colorectal cancer (mCRC) in 2004. However, adding bevacizumab to treatment consistently fails to be cost-effective owing to modest response rates. Recently, the European Commission (EC) funded ANGIOPREDICT consortium ( www.angiopredict.com ) identified a link between bevacizumab treatment response and intermediate-to-high chromosomal instability (CIN) in mCRC. Thus, the objective of the current study was to compare the cost-effectiveness of adding bevacizumab with first-line chemotherapy in the bevacizumab responsive CIN subtype across three European countries (Germany, Ireland and Spain) with varying costs of care and reimbursement policies.

methodsWe developed an open-source health economic model to estimate cost-effectiveness. The ANGIOPREDICT cohort informed progression risks and cause-specific mortality. Health utilities and adverse events probabilities were obtained from the literature. Costs were derived from surveys of collaborating consortium hospitals in Germany, Ireland, and Spain that participated in the recently completed EC funded COLOSSUS translational study (ANGIOPREDICT successor initiative) and the literature. Sensitivity analyses included individual and simultaneous variation of input parameters from a priori defined distributions.

resultsBevacizumab was not cost effective even at willingness-to-pay (WTP) thresholds that are appreciably higher than those considered realistic. The highest incremental cost-effectiveness ratio (ICER) was in Germany at €241,188 per quality-adjusted life year (QALY), while the lowest was in Ireland at €180,477 per QALY. All deterministic and probabilistic sensitivity analyses demonstrated that these results were robust.

conclusionsEven for patients with mCRC manifesting improved outcomes, adding bevacizumab to first-line chemotherapy is invariably not cost-effective in any of the countries examined. Variability in pricing, healthcare costs and WTP thresholds across countries did not commute this result.

Indexed as

Antineoplastic Agents, ImmunologicalBevacizumabChromosomal InstabilityColorectal NeoplasmsModels, EconomicAntineoplastic Combined Chemotherapy ProtocolsCost-Benefit AnalysisCost-Effectiveness AnalysisGermanyHumansIrelandNeoplasm MetastasisPrecision MedicineQuality-Adjusted Life YearsSpainAntineoplastic Agents, ImmunologicalBevacizumab

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.