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Record W4410709097 · doi:10.1016/j.eclinm.2025.103261

Modelling the potential financial impacts of expanding access to immune checkpoint inhibitors as monotherapy for treating advanced non-small cell lung cancer

2025· article· en· W4410709097 on OpenAlexfundaboutno aff
Kiu Tay-Teo, Dario Trapani, Manju Sengar, Zeba Aziz, Filip Meheus, André Ilbawi, Elisabeth G.E. de Vries, Lorenzo Moja

Bibliographic record

VenueEClinicalMedicine · 2025
Typearticle
Languageen
FieldEconomics, Econometrics and Finance
TopicEconomic and Financial Impacts of Cancer
Canadian institutionsnot available
FundersEuropean Society for Medical OncologyIrish AidEuropean CommissionGovernment of CanadaMinistère de l'Europe et des Affaires ÉtrangèresWorld Health Organization
KeywordsMedicineLung cancerOncologyIntensive care medicineInternal medicine

Abstract

fetched live from OpenAlex

Background: Access to immune checkpoint inhibitors remains limited due to cost-effectiveness and affordability concerns. This study evaluates the financial impacts of expanding global access to PD1/PD-L1 inhibitors as first-line monotherapy for patients aged 40-74 years with advanced unresectable non-small cell lung cancer (NSCLC), with wildtype EGFR and ≥50% of tumour cells with PD-L1 expression. Methods: The potential usage and associated costs were assessed from 2024 to 2040 through repeated cross-sectional assessments. The base case assumed treatment rates in countries with access to PD1/PD-L1 inhibitors in 2023, while expanded-access scenarios projected coverage increases to 30% in low-income, 50% in lower-middle-income, 80% in upper-middle-income (UMICs), and 95% in high-income countries over 10 years. Findings: The model estimated that 200,000-250,000 individuals are treatment-eligible, with only about one-fifth receiving PD1/PD-L1 inhibitors in the base case. Expanding access would increase global treatment coverage to 75% by 2040, particularly in middle-income countries. The largest increases would be in UMICs (+100,700) and the Western Pacific region (+82,400). At an estimated per-patient lifetime cost of US$37,600-US$75,100, total costs could reach US$14,087 million with fixed dosing, or US$9080 million with weight-based dosing. PD-L1 testing costs would add <1% to the total. Interpretation: Expanding access to PD1/PD-L1 inhibitors for advanced NSCLC over 10 years demands significant funding, making equitable access in lower-income countries doubtful without a significant price reduction. Policymakers should negotiate lower prices to ensure cost-effectiveness and affordability, improve spending efficiency by optimised dosing and treatment duration, and enhance health system capacity, including ensuring appropriate use and introducing biosimilars. Funding: This publication was made available as open access through WHO funding provided by two projects: the Universal Health Coverage Partnership (Award 74812, the European Union, the Grand Duchy of Luxembourg, Irish Aid, the Government of Japan, the French Ministry for Europe and Foreign Affairs, the United Kingdom's Foreign, Commonwealth & Development Office, the Government of Belgium, the Government of Canada, and the Government of Germany) and the Increasing Global Equitable Access to Health Products & Health Technologies project (Award 72913, the Government of Belgium).

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Simulation or modeling · Consensus signal: Simulation or modeling
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.143
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.030
GPT teacher head0.330
Teacher spread0.300 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designSimulation or modeling
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations11
Published2025
Admission routes2
Has abstractyes

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