Evidence map›Paper›PMID 40827456›Full record

ArticleCancer medicine2025

Relative Dose Intensity of Trabectedin and Outcome of Advanced L-Sarcomas.

Stephen Poitureau, Marie-Cécile Le Deley, Mehdi Brahmi, Emmanuelle Bompas, Jean-Emmanuel Kurtz, Simon Nannini, Christophe Perrin, Loïc Lebellec, Thomas Ryckewaert, Redha Ould-Ammar and 3 more

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Stephen PoitureauLille University, Medical School, Lille, France.
Marie-Cécile Le DeleyDepartment of Clinical Research and Innovation, Centre Oscar-Lambret, Lille, France.
Mehdi BrahmiDepartment of Medical Oncology, Centre Léon Bérard, University Claude Bernard Lyon I, Lyon, France.
Emmanuelle BompasDepartment of Medical Oncology, Institut de Cancérologie de L'ouest, Nantes, France.ORCID https://orcid.org/0000-0003-4414-7760
Jean-Emmanuel KurtzDepartment of Medical Oncology, Institut de Cancérologie de Strasbourg-Europe, Strasbourg, France.
Simon NanniniDepartment of Medical Oncology, Institut de Cancérologie de Strasbourg-Europe, Strasbourg, France.
Christophe PerrinMedical Oncology Unit, Centre Eugène Marquis, Rennes, France.
Loïc LebellecDepartment of Medical Oncology, Centre Oscar Lambret, Lille, France.
Thomas RyckewaertDepartment of Medical Oncology, Centre Oscar Lambret, Lille, France.
Redha Ould-AmmarDepartment of Clinical Research and Innovation, Centre Oscar Lambret, Lille, France.
Clémence LeguilletteDepartment of Clinical Research and Innovation, Centre Oscar Lambret, Lille, France.
Jean-Yves BlayDepartment of Medical Oncology, Centre Léon Bérard, University Claude Bernard Lyon I, Lyon, France.
Nicolas PenelDepartment of Medical Oncology, Centre Oscar-Lambret, Lille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrabectedin, which is approved for advanced soft tissue sarcoma management, has a complex mechanism of action, but can be classified as an alkylating agent. The need to maintain a high relative dose intensity (RDI) is not clearly established in this clinical setting.

methodsWe conducted a retrospective study in five expert centers to compare the progression-free survival (PFS) and overall survival (OS) of patients with advanced L-Sarcomas (liposarcomas or leiomyosarcoma) according to the RDI calculated over the first three cycles (RDI < 80% and RDI ≥ 80%). Comparisons of patients' characteristics were done using Chi-2, Fisher exact, and Wilcoxon tests. Associations between PFS/OS and RDI were estimated and tested in Cox models.

resultsOut of 332 patients treated with trabectedin between 09/1999 and 12/2021, 244 have received at least 3 cycles before progression. Among these 244 patients, the median RDI during the first 3 cycles was 83% (range, 48%-106%), the mean RDI was 81% (±14%) and 106 patients had RDI < 80%. An RDI < 80% was more frequently observed in patients treated in a center with a high volume of activity (82/169, 49%, vs. 24/75, 32%, p = 0.02), in patients who had previously received pazopanib (12/18, 67%, vs. 94/225, 42%, p = 0.04), and in patients who experienced grade 3 neutropenia during the first cycle (56/77, 73% vs. 35/127, 28%, p < 0.001). PFS did not significantly differ according to RDI (p = 0.08): HR

conclusionThis retrospective study does not support a link between high trabectedin RDI and PFS or OS for advanced L-sarcoma patients.

Indexed as

Antineoplastic Agents, AlkylatingLeiomyosarcomaLiposarcomaTrabectedinAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedProgression-Free SurvivalRetrospective StudiesTreatment OutcomeYoung AdultAntineoplastic Agents, AlkylatingTrabectedindose reductionrelative dose intensitysoft tissue sarcomatoxicitytrabectedin

Identifiers

PMID40827456
PMCPMC12361930

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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.