Evidence map›Paper›PMID 42371064›Full record

ArticleEuropean journal of clinical pharmacology2026

Comparing National Health Technology Assessment approaches and the new European Joint Clinical Assessment framework: The case of onco-hematological medicines.

Benedetta Starinieri, Eleonora Allocati, Chiara Gerardi, Roberta Joppi, Rita Banzi

Abstract readComparative Study
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In one paragraph

Article in European journal of clinical pharmacology, 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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0citing papers in PubMed
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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

5 authors.

Benedetta StarinieriLaboratory for Health Regulatory Policies, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Via Mario Negri, 2, Milano, 20156, Milan, Italy. benedetta.starinieri@marionegri.it.ORCID http://orcid.org/0009-0006-4872-1685
Eleonora AllocatiLaboratory for Health Regulatory Policies, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Via Mario Negri, 2, Milano, 20156, Milan, Italy.ORCID http://orcid.org/0000-0002-6917-1495
Chiara GerardiLaboratory for Health Regulatory Policies, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Via Mario Negri, 2, Milano, 20156, Milan, Italy.ORCID http://orcid.org/0000-0002-2459-4769
Roberta JoppiPharmaceutical Department, Central Hospital of Bolzano, Azienda Sanitaria dell'Alto Adige, Via Lorenz Böhler 5, Bolzano, Italy.ORCID http://orcid.org/0000-0002-9085-3626
Rita BanziLaboratory for Health Regulatory Policies, Istituto di Ricerche Farmacologiche "Mario Negri" IRCCS, Via Mario Negri, 2, Milano, 20156, Milan, Italy.ORCID http://orcid.org/0000-0002-2211-3300

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo analyze national-level evaluations conducted by selected Health Technology Assessment (HTA) bodies and compare them with the methodological framework outlined in the European HTA Regulation for Joint Clinical Assessment (JCA), in order to assess whether JCA would improve alignment among national practices.

methodsWe used onco-hematological medicines as a case model. From the European Medicine Agency (EMA) website, we identified onco-hematological medicines licensed from January 2023 to April 2025 and the pivotal trials supporting their marketing authorization (MA). We retrieved the reports of seven national HTA agencies and examined the rationale and evidence underlying the agencies' evaluation and their final recommendations. To estimate how the JCA opinion would have changed compared to those taken by the national HTA authorities, we developed a set of possible Population, Intervention, Comparators, and Outcomes (PICOs) and applied JCA criteria to selected medicines.

resultsWe assessed ten trials supporting the MA of eight medicines. All except momelotinib were approved based on one single pivotal trial. Six were single-arm studies. By June 2025, 22 national HTA reports were available for six medicines, incorporating pivotal trial data and indirect treatment comparisons for five medicines. Overall, recommendations from HTA agencies varied. The PICO scoping process generated at least four PICOs per medicine, reflecting high heterogeneity across countries. The limited evidence at the time of MA was insufficient to address all the PICOs.

conclusionAlthough JCA strengthens procedural harmonization, the current HTA fragmentation may persist due to the proliferation of PICOs and divergent interpretations of evidence.

Indexed as

Antineoplastic AgentsTechnology Assessment, BiomedicalDrug ApprovalEuropeHumansAntineoplastic AgentsEuropean HTA RegulationHealth technology assessmentIndirect comparisonsJoint Clinical AssessmentOnco-hematology

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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.