Evidence map›Paper›PMID 39995768›Full record

ArticleLung Cancer (Auckland, N.Z.)2025

Genomic Profiling of Extensive Stage Small-Cell Lung Cancer Patients Identifies Molecular Factors Associated with Survival.

Matteo Canale, Milena Urbini, Elisabetta Petracci, Davide Angeli, Gianluca Tedaldi, Ilaria Priano, Paola Cravero, Michele Flospergher, Kalliopi Andrikou, Chiara Bennati and 9 more

Abstract read
In one paragraph

Article in Lung Cancer (Auckland, N.Z.), 2025. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

19 authors.

Matteo CanaleBiosciences Laboratory, IRCCS Istituto Romagnolo per Lo Studio Dei Tumori (IRST) "dino Amadori", Meldola, Italy.ORCID 0000-0002-9768-7149
Milena UrbiniBiosciences Laboratory, IRCCS Istituto Romagnolo per Lo Studio Dei Tumori (IRST) "dino Amadori", Meldola, Italy.
Elisabetta PetracciUnit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Davide AngeliUnit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Gianluca TedaldiBiosciences Laboratory, IRCCS Istituto Romagnolo per Lo Studio Dei Tumori (IRST) "dino Amadori", Meldola, Italy.ORCID 0000-0003-0540-6694
Ilaria PrianoDepartment of Medical Oncology, Vall d´Hebron Institute of Oncology (VHIO), Vall d'Hebron Hospital Universitari, Barcelona, Spain.
Paola CraveroDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, 47014, Italy.
Michele FlospergherDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, 47014, Italy.
Kalliopi AndrikouDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, 47014, Italy.
Chiara BennatiDepartment of Onco-Hematology, Santa Maria Delle Croci Hospital, Ravenna, Italy.
Davide TassinariDepartment of Medical Oncology, Infermi Hospital, Rimini, Italy.
Alessandra DubiniDepartment of Pathology, Morgagni-Pierantoni Hospital, Forlì, Italy.
Giulio RossiFondazione Poliambulanza, Brescia, Italy.
Riccardo PanzacchiDepartment of Pathology, Ospedale S. Maria Della Scaletta, Imola, Italy.
Mirca ValliDepartment of Pathology, Infermi Hospital, Rimini, Italy.
Giuseppe BronteDepartment of Medicina Traslazionale E per la Romagna, University of Ferrara, Ferrara, Italy.
Lucio CrinòDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, 47014, Italy.ORCID 0000-0001-5745-6429
Angelo DelmonteDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, 47014, Italy.
Paola UliviBiosciences Laboratory, IRCCS Istituto Romagnolo per Lo Studio Dei Tumori (IRST) "dino Amadori", Meldola, Italy.ORCID 0000-0002-4334-9662

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Extensive stage Small-Cell Lung Cancer (ES-SCLC) is the most lethal lung cancer, and the addition of immunotherapy conferred a slight survival benefit for patients. Extensive molecular profiling of patients treated with chemotherapy (CT) or chemotherapy plus immunotherapy (CT+IO) would be able to identify molecular factors associated with patients' survival. Material and Methods: In this retrospective study, 99 ES-SCLC patients were considered. Of the 79 includible patients, 42 received CT (median age 71 y/o, I-IIIQ: 65-76), and 37 received CT+IO (median age 71 y/o, I-IIIQ 66-75). The FoundationOne CDx assay was performed on patients' tumor tissues. Results: The most mutated genes were Conclusion: In ES-SCLC, TMB is associated with worse survival in patients treated with CT alone, and with better survival in patients treated with CT+IO, whether considered as a continuous or a dichotomized variable, at different cut-offs. Alterations in epigenetic factors are also associated to better patient prognosis.

Indexed as

immunotherapypatients prognosispredictive biomarkerssmall-cell lung cancertumor mutation burden

Identifiers

PMID39995768
PMCPMC11849429

What OpenQuestion holds

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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.