Evidence map›Paper›PMID 36503033›Full record

ArticleValue in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research2023

Cost-Effectiveness of Tepotinib Versus Capmatinib for the Treatment of Adult Patients With Metastatic Non-Small Cell Lung Cancer Harboring Mesenchymal-Epithelial Transition Exon 14 Skipping.

Mo Yang, Helene Vioix, Rameet Sachdev, Matthew Stargardter, Jon Tosh, Boris M Pfeiffer, Paul K Paik

Open access · hybridAbstract read
In one paragraph

Article in Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
0.8field-weighted citation impact, top 16% of its field
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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Adagrasib in the treatment of KRASTranslational cancer research · 2025
    Article
  5. Article
  6. Article
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

7 authors at 5 institutions in 3 countries.

Mo YangEMD Serono, Rockland, MA, USA. Electronic address: mo.yang@emdserono.com.
Helene Vioixthe healthcare business of Merck KGaA, Darmstadt, Germany.
Rameet SachdevEvidera, Bethesda, MD, USA.
Matthew StargardterEvidera, Bethesda, MD, USA.
Jon ToshEvidera, London, UK.
Boris M Pfeifferthe healthcare business of Merck KGaA, Darmstadt, Germany.
Paul K PaikMemorial Sloan Kettering Cancer Center, New York City, NY, USA.
Ithaka Harbors · USMerck (Germany) · DEEVRAZ (United Kingdom) · GBMemorial Sloan Kettering Cancer Center · USOno Pharmaceutical (United States) · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

objectivesFrom the US Medicare perspective, this study compared the cost-effectiveness of tepotinib and capmatinib for treating metastatic non-small cell lung cancer with tumors harboring mesenchymal-epithelial transition factor gene exon 14 skipping.

methodsA 3-state partitioned survival model assessed outcomes over a lifetime horizon. Parametric survival analysis of the phase 2 VISION trial informed clinical inputs for tepotinib. Capmatinib inputs were captured using hazard ratios derived from an unanchored matching-adjusted indirect comparison study and published literature. National cost databases, trial data, and literature furnished drug, treatment monitoring, and disease/adverse event management expenditures (2021 US dollars) and utility inputs. Outcomes were discounted at 3% annually.

resultsIn the base case, tepotinib dominated capmatinib in frontline settings (incremental discounted quality-adjusted life-years [QALYs] and costs of 0.2127 and -$47 756, respectively) while realizing an incremental cost-effectiveness ratio of $274 514/QALY in subsequent lines (incremental QALYs and costs of 0.3330 and $91 401, respectively). In a line agnostic context, tepotinib produced an incremental cost-effectiveness ratio of $105 383/QALY (incremental QALYs and costs of 0.2794 and $29 447, respectively). Sensitivity and scenarios analyses for individual lines typically supported the base case, whereas those for the line agnostic setting suggested sensitivity to drug acquisition costs and efficacy inputs.

conclusionsTepotinib could be cost-effective versus capmatinib in frontline and line agnostic contexts, considering the range of willingness-to-pay thresholds recommended by the Institute for Clinical and Economic Review ($100 000-$150 000/QALY). Tepotinib could be cost-effective in subsequent lines at higher willingness-to-pay levels. These results are to be interpreted cautiously, considering uncertainty in key model inputs.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAdultAgedBenzamidesCost-Benefit AnalysisExonsHumansImidazolesMedicarePiperidinesPyridazinesPyrimidinesQuality-Adjusted Life YearsTriazinesUnited StatesBenzamidescapmatinibImidazolesPiperidinesPyridazinesPyrimidinestepotinibTriazinescost-effectivenessmesenchymal–epithelial transition factor gene exon 14 skippingmetastatic non–small cell lung cancertepotinibtyrosine kinase inhibitorsVISION trial

Identifiers

PMID36503033
PMCPMC10424058
OpenAlexW4311087327

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.