Evidence map›Paper›PMID 37025260›Full record

ArticleTherapeutic advances in medical oncology2023

A transcriptomics approach to expand therapeutic options and optimize clinical trials in oncology.

Vladimir Lazar, Baolin Zhang, Shai Magidi, Christophe Le Tourneau, Eric Raymond, Michel Ducreux, Catherine Bresson, Jacques Raynaud, Fanny Wunder, Amir Onn and 6 more

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

16 authors.

Vladimir LazarWorldwide Innovative Network (WIN) Association-WIN Consortium, 24 rue Albert Thuret, Villejuif 94550, France.
Baolin ZhangOffice of Biotechnology Products (OBP), Center for Drug Evaluation and Research (CDER), Food and Drug Administration (FDA), Silver Spring, MA, USA.
Shai MagidiWorldwide Innovative Network (WIN) Association-WIN Consortium, Villejuif, France.
Christophe Le TourneauDepartment of Drug Development and Innovation (D3i), INSERM U900 Research Unit, Paris-Saclay University, Institut Curie, Paris, France.
Eric RaymondOncology Department, Groupe Hospitalier Paris Saint Joseph, Paris, France.
Michel DucreuxDepartment of Medical Oncology, Gustave Roussy, Université Paris-Saclay, Inserm U1279, Villejuif, France.
Catherine BressonWorldwide Innovative Network (WIN) Association-WIN Consortium, Villejuif, France.
Jacques RaynaudWorldwide Innovative Network (WIN) Association-WIN Consortium, Villejuif, France.
Fanny WunderWorldwide Innovative Network (WIN) Association-WIN Consortium, Villejuif, France.
Amir OnnInstitute of Pulmonology, Sheba Medical Center, Tel-Hashomer, Israel.
Enriqueta FelipOncology Department, Vall d'Hebron Hospital Campus and Institute of Oncology (VHIO), UVic-UCC, Barcelona, Spain.
Josep TaberneroOncology Department, Vall d'Hebron Hospital Campus and Institute of Oncology (VHIO), UVic-UCC, Barcelona, Spain.
Gerald BatistDepartment of Oncology, Segal Cancer Centre, Jewish General Hospital, McGill University, Montréal, Canada.
Razelle KurzrockWorldwide Innovative Network (WIN) Association-WIN Consortium, Villejuif, France.
Eitan RubinShraga Segal Department of Microbiology and Immunology, Faculty of Health Sciences Ben-Gurion University of the Negev, Beer-Sheeva, Israel.
Richard L SchilskyWorldwide Innovative Network (WIN) Association-WIN Consortium, Villejuif, France.

Funding

VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jesse Nodora · 1985 to 2026
$124.9M
NCI NIH HHS P30 CA023100
6 · The paper itself

Abstract

Background: The current model of clinical drug development in oncology displays major limitations due to a high attrition rate in patient enrollment in early phase trials and a high failure rate of drugs in phase III studies. Objective: Integrating transcriptomics for selection of patients has the potential to achieve enhanced speed and efficacy of precision oncology trials for any targeted therapies or immunotherapies. Methods: Relative gene expression level in the metastasis and normal organ-matched tissues from the WINTHER database was used to estimate Results: As example, high mRNA expression in tumor tissue compared to analogous normal tissue of Conclusion: This

Indexed as

analogous normal tissue biopsiesclinical trialsoncologytranscriptomicstumor biopsies

Identifiers

PMID37025260
PMCPMC10071163

What OpenQuestion holds

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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.