Evidence map›Paper›PMID 42250196›Full record

ArticleClinical drug investigation2026

Assessing the Impact on Health and Productivity Outcomes of Anti-PD-(L)1 Agents to Treat Early-Stage Cancers in Italy.

Andrea Marcellusi, Fabio Calabrò, Anna Maria Di Giacomo, Fabio Puglisi, Alessio Cortellini, Isobel Thornton, Yan Zhi Tan, Alessandro Catanzaro, Catarina Neves, Fabrizio Ascone and 4 more

Abstract read
In one paragraph

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

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Andrea MarcellusiDepartment of Pharmaceutical Sciences-DISFARM, University of Milan, Milan, Italy.
Fabio CalabròDepartment of Medical Oncology 1, National Cancer Institute Regina Elena, IRCCS, Rome, Italy.
Anna Maria Di GiacomoCenter for Immuno-Oncology, University Hospital of Siena, University of Siena, Siena, Italy.
Fabio PuglisiDepartment of Medical Oncology, National Cancer Institute, Centro di Riferimento Oncologico RCCS, Aviano, Italy.
Alessio CortelliniDepartment of Medicine and Surgery, Università Campus Bio-Medico di Roma, Rome, Italy.
Isobel ThorntonLumanity, London, UK.
Yan Zhi TanLumanity, Utrecht, The Netherlands.
Alessandro CatanzaroLumanity, Utrecht, The Netherlands.
Catarina NevesLumanity, Utrecht, The Netherlands.
Fabrizio AsconeMSD Ltd, Rome, Italy.
Matilde FranceschiniMSD Ltd, Rome, Italy.
Mario CalandrielloMSD Ltd, Rome, Italy.
Raquel Aguiar-IbáñezMerck Canada Inc., Kirkland, QC, Canada.
Yizhen LaiMerck & Co., Inc., Rahway, NJ, USA. joyce.lai2@merck.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnti-programmed cell death-(ligand) 1 (anti-PD-[L]1) agents are approved for advanced and early-stage cancers. While they may offer clinical and economic benefits in the neoadjuvant and/or adjuvant setting, their population-level impact in Italy has not been thoroughly evaluated.

objectiveThis study aims to estimate health and productivity outcomes of introducing anti‑PD‑(L)1 agents for neoadjuvant and/or adjuvant therapy in early‑stage cancers in Italy (melanoma Stage IIB/C, melanoma Stage III, renal cell carcinoma, triple‑negative breast cancer and resectable non‑small‑cell lung cancer) over a 10-year horizon.

methodsWe developed a model synthesising outputs from five indication-specific Markov models comparing two worlds: one without anti-PD-(L)1 agents use in the neoadjuvant and/or adjuvant settings versus one with their use. Italian-specific population and incidence inputs were used, with clinical and quality-of-life data from individual trials, from a societal perspective with 3% annual discount. Outcomes included total life years (LYs), recurrence- free (RF)/event-free (EF)/disease-free (DF) LYs, quality-adjusted LYs (QALYs), number of recurrences/events, metastatic treatments, total deaths and deaths after first event/recurrence. Productivity gains were estimated using a human capital approach.

resultsBetween 2025 and 2034, 118,329 patients with early-stage cancer were estimated to be eligible for anti-PD-(L)1 agents in Italy. Compared with no early-stage use, neoadjuvant/adjuvant use was associated with increased total LYs (+ 20,458, + 5%), RF/EF/DF LYs (+ 60,631, + 19%), QALYs (+ 21,093, + 6%) and fewer recurrences/events (- 20,209, - 33%), metastatic treatments (- 25,220, - 38%), total deaths (- 7137, - 24%) and deaths after first event/recurrence (- 8021, - 32%). Productive years gained were 35,897 (+ 30%).

conclusionsOur study suggests that the use of anti-PD-(L)1 agents in early-stage cancers is associated with substantial health and societal gains in Italy. Expanding their use across approved indications translates trial benefits into fewer recurrences, deaths and productivity losses, informing national planning and access decision.

Indexed as

Immune Checkpoint InhibitorsNeoplasmsCost-Benefit AnalysisFemaleHumansItalyMarkov ChainsNeoadjuvant TherapyNeoplasm StagingQuality-Adjusted Life YearsQuality of LifeImmune Checkpoint Inhibitors

Identifiers

PMID42250196
PMCPMC13356081

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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.