Evidence map›Paper›PMID 38335904›Full record

ArticleESMO open2024

Clinical benefit of anti-PD-(L)1 immunotherapies in advanced cancer in France: a population-based estimate from 2014 to 2021.

V Grumberg, F-E Cotté, E Giroux-Leprieur, A-F Gaudin, C Lebbé, I Borget

Open access · goldAbstract read
In one paragraph

Article in ESMO open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Advances in lymphatic metastasis of non-small cell lung cancer.Cell communication and signaling : CCS · 2024
    Review
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

6 authors at 3 institutions in 2 countries.

V GrumbergBristol Myers Squibb France, Rueil-Malmaison; Oncostat, U1018, CESP, Inserm, Paris-Saclay University, 'Ligue Contre le Cancer' Team, Villejuif. Electronic address: Valentine.grumberg@bms.com.
F-E CottéBristol Myers Squibb France, Rueil-Malmaison.
E Giroux-LeprieurDepartment of Respiratory Diseases and Thoracic Oncology, Paris-Saclay University, UVSQ, EA4340, APHP-Hôpital Ambroise Paré, Boulogne Billancourt.
A-F GaudinBristol Myers Squibb France, Rueil-Malmaison.
C LebbéUniversité Paris Cite, APHP Dermato-oncology, Cancer Institute APHP Nord Paris Cité, INSERM U976, Saint Louis Hospital, Paris.
I BorgetOncostat, U1018, CESP, Inserm, Paris-Saclay University, 'Ligue Contre le Cancer' Team, Villejuif; Biostatistics and Epidemiology Office, Gustave Roussy, Paris-Saclay University, Villejuif, France.
Inserm · FRBristol-Myers Squibb (France) · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn France, the potential benefit of new treatments is initially evaluated by the Haute Autorité de Santé to determine reimbursement and pricing, but rarely afterwards. Although immunotherapies (ITs) have considerably improved the survival of patients, few data are available on their long-term benefit at a population-treated level. The present retrospective study aimed to assess the clinical benefit of ITs compared to the previous standards of care (SoCs) in France from 2014 to 2021. MATERIALS AND

methodsTo do this, we analyzed all ITs from the anti-programmed cell death protein 1/programmed death-ligand 1 [anti-PD-(L)1] class used in monotherapy or in association with another treatment available in early access or reimbursed in France between 2014 and 2021, regardless of indication. The number of patients initiating an IT was retrieved by year, drug and indication. Using extrapolated Kaplan-Meier curves, utility scores and the population treated, the clinical benefit was expressed as the number of deaths prevented (DP), life-years (LYs) and quality-adjusted life years (QALYs) gained compared to previous SoC.

resultsAcross the period, five ITs were marketed in 21 indications related to eight primary tumor sites. Between 2014 and 2021, 132 924 patients initiated an IT. By December 2021, 16 173 (13 804-17 141) deaths were delayed compared to previous SoC, mainly in lung cancer. Compared to their SoC, ITs provided a gain of 37 316 (33 581-41 048) additional LYs and 27 709 (23 784-30 450) additional QALYs. Lung cancer was the driver indication with 70.6% of LYs and 68.4% of QALYs gained followed by melanoma with 18.7% and 20.4% of the gain, respectively.

conclusionsSignificant gains in DP, LYs and QALYs have been observed in France following the introduction of ITs.

Indexed as

Lung NeoplasmsCost-Benefit AnalysisFranceHumansImmunotherapyRetrospective Studiesclinical benefitimmunotherapieslife-yearsoncology

Identifiers

PMID38335904
PMCPMC10937192
OpenAlexW4391689850

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.