Evidence map›Paper›PMID 39404995›Full record

ArticleBioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy2024

Advanced Therapy Medicinal Products: Availability, Access and Expenditure in Italy.

Pia Rivetti di Val Cervo, Eva Alessi, Marilena Lastella, Antonio La Greca, Francesco Trotta

Abstract read
In one paragraph

Article in BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
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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.

Pia Rivetti di Val CervoHTA and Pharmaceutical Economics Department, Italian Medicines Agency, Via del Tritone 181, 00187, Rome, Italy. p.rivettidivalcervo@aifa.gov.it.ORCID http://orcid.org/0000-0001-5999-1230
Eva AlessiHTA and Pharmaceutical Economics Department, Italian Medicines Agency, Via del Tritone 181, 00187, Rome, Italy.
Marilena LastellaHTA and Pharmaceutical Economics Department, Italian Medicines Agency, Via del Tritone 181, 00187, Rome, Italy.
Antonio La GrecaHTA and Pharmaceutical Economics Department, Italian Medicines Agency, Via del Tritone 181, 00187, Rome, Italy.
Francesco TrottaHTA and Pharmaceutical Economics Department, Italian Medicines Agency, Via del Tritone 181, 00187, Rome, Italy.ORCID http://orcid.org/0000-0001-6889-8484

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdvanced therapy medicinal products (ATMPs) are an innovative output of biomedical research, characterized by a high level of uncertainty on long-term efficacy and safety, elevated price tags and often complex administration. All these elements compounded make their European authorization, national price negotiation for reimbursement and subsequent dispensation and administration to the patient less straightforward and often less successful than for less innovative drugs. To assess if these hurdles have affected patient access and how are ATMPs used in Italy, we have analysed availability, access and expenditure of ATMPs in the period spanning from 2016 to 2023.

methodsWe have analysed real world data on the duration of ATMP regulatory evaluations for authorisation and reimbursement, time to first patient access and expenditure for ATMPs through the Italian National Health System (INHS) expenditure data flow, as well as information on patient mobility and availability of health facilities specialized in administering ATMPs.

findingsOf the 18 ATMPs currently authorized in Europe, 9 are reimbursed by the INHS, but only 6 were actually used, generating a cumulative expenditure of roughly 300 Mln€ from 2016 to 2023, largely owing to CAR-T therapies. Time to patient access reaches an average of 340.6 days from the day publication in the official Gazette of the reimbursement decision to first patient treatment in one of the 107 health facilities authorized for ATMP administration, after an even longer evaluation time by regulatory agencies.

conclusionSince the first reimbursement decision for an ATMP in Italy, back in 2016, these innovative drugs became progressively more and more available, both in terms of numbers and in terms of coverage across the country. Almost all Italian regions have at least one centre for ATMP administration and has performed a treatment in 2023. Notwithstanding their high per-treatment prices, ATMPs currently have a rather contained expenditure, however it is bound to keep growing in the next few years.

Indexed as

Health ExpendituresHealth Services AccessibilityHumansItaly

Identifiers

PMID39404995
PMCPMC11530470

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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.