Evidence map›Paper›PMID 41468687›Full record

ArticleESMO open2026

A multiomic framework for predicting laryngo-esophageal dysfunction following induction chemotherapy in hypopharyngeal-laryngeal carcinoma.

D Mattavelli, M Compagnoni, S Calza, M Ravanelli, M Plana, G Wichmann, A Paderno, Y Zhan, D Smussi, P Rondi and 15 more

Abstract readMulticenter Study
In one paragraph

Article in ESMO open, 2026. 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

25 authors.

D MattavelliUnit of Otorhinolaryngology-Head and Neck Surgery, ASST Spedali Civili di Brescia, Brescia, Italy; Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy.
M CompagnoniDepartment of Experimental Oncology, IEO, European Institute of Oncology, IRCCS, Milan, Italy.
S CalzaUnit of Biostatistics and Bioinformatics, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
M RavanelliDepartment of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy; Unit of Radiology, ASST Spedali Civili di Brescia, Brescia, Italy.
M PlanaMedical Oncology Department, Institut Català d'Oncologia (ICO-Hospitalet), IDIBELL, Hospitalet de Llobregat, Barcelona, Spain.
G WichmannClinic of Otolaryngology, Head and Neck Surgery, Department of Head Medicine and Oral Health, University Hospital Leipzig, Leipzig, Germany.
A PadernoDepartment of Biomedical Sciences, Humanitas University, Milan, Italy; Otorhinolaryngology Head & Neck Surgery Unit, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Y ZhanDepartment of Experimental Oncology, IEO, European Institute of Oncology, IRCCS, Milan, Italy.
D SmussiDepartment of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy; Unit of Medical Oncology, ASST Spedali Civili di Brescia, Brescia, Italy.
P RondiDepartment of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy; Unit of Radiology, ASST Spedali Civili di Brescia, Brescia, Italy.
A PinacoliUnit of Otorhinolaryngology-Head and Neck Surgery, ASST Spedali Civili di Brescia, Brescia, Italy; Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy.
A MeddaDepartment of Experimental Oncology, IEO, European Institute of Oncology, IRCCS, Milan, Italy.
L LoriniMedical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Milan, Italy.
K KhelikCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway.
E HovigCentre for Bioinformatics, Department of Informatics, University of Oslo, Oslo, Norway; Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
F A MaffiniDepartment of Surgical Pathology, IEO, European Institute of Oncology, IRCCS, Milan, Italy.
M KalogeriniAthens Technology Center S.A., Athens, Greece.
A AlbertiUnit of Medical Oncology, ASST Spedali Civili di Brescia, Brescia, Italy.
D FarinaDepartment of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy; Unit of Radiology, ASST Spedali Civili di Brescia, Brescia, Italy.
A DietzClinic of Otolaryngology, Head and Neck Surgery, Department of Head Medicine and Oral Health, University Hospital Leipzig, Leipzig, Germany.
R MesiaInstitut Català d'Oncologia (ICO-Badalona), B-ARGO Group, Care Program, IGTP, Barcelona, Spain.
C PiazzaUnit of Otorhinolaryngology-Head and Neck Surgery, ASST Spedali Civili di Brescia, Brescia, Italy; Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, Brescia, Italy.
S ChioccaDepartment of Experimental Oncology, IEO, European Institute of Oncology, IRCCS, Milan, Italy.
P BossiDepartment of Biomedical Sciences, Humanitas University, Milan, Italy; Medical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Milan, Italy. Electronic address: paolo.bossi@hunimed.eu.
PRESERVE Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPre-treatment predictors of laryngeal preservation (LP) and survival in advanced laryngeal-hypopharyngeal squamous-cell carcinoma (LHSCC) represent an unmet clinical need. MATERIALS AND

methodsA multicentric, international, retrospective series of LHSCC patients undergoing induction chemotherapy (IC) within an LP protocol was analyzed. The primary objective was to develop a predictive model by exploiting multiomics data (clinical, genomics, radiomics). Endpoints were laryngo-esophageal dysfunction (LED), response to IC, overall survival (OS), and progression-free survival (PFS). Patients were divided into three groups: group A (no LED); group B (responders to IC with LED); group C (non-responders to IC with LED). Several algorithms (support vector machine, random forest, C5.0, k-nearest neighbors, XGBoost, and naive Bayes) were run and compared in terms of multiclass area under the curve (AUC) score and classification error.

resultsOne hundred and ninety-one LHSCC patients were included (median age 60 years, 72% laryngeal, 80% T1-T3, and 58% N+). Responders to IC were 85%, while 66% suffered from LED. The 5-year PFS and OS were 58.4% and 64.7%, respectively. When comparing the three predictive models (clinical, clinical + genomics, clinical + radiomics), the addition of genomics provided the highest AUC. Then, we selected a 64-gene signature and 6 clinical variables (comorbidities, primary site, smoking, T category, N category, performance status) to build up the PRESERVE model. It showed a classification error of 28.9% and an AUC of 87.4%. Risks of major misclassification were low (group A to C, 1.13%; group C to A, 7.38%). Decision analysis confirmed the efficiency of the model.

conclusionsThe PRESERVE model proved to be efficient and accurate in predicting LED and response to IC in LHSCC. External validation is needed before clinical application.

Indexed as

Hypopharyngeal NeoplasmsInduction ChemotherapyLaryngeal NeoplasmsLarynxSquamous Cell Carcinoma of Head and NeckAgedEsophagusFemaleHumansMaleMiddle AgedRetrospective Studieslaryngeal cancerlaryngo-esophageal dysfunctionorgan preservation protocolspredictionpredictive modelsquamous-cell carcinoma

Identifiers

PMID41468687
PMCPMC12804047

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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.