Evidence map›Paper›PMID 42435159›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Expert opinion document on the management of desmoid tumours in adult patients in Spain.

Rosa María Álvarez Álvarez, Javier Zenón Martín Broto, Javier Martínez Trufero, Ana Sebio García, Claudia María Valverde Morales, Jorge García López, Celia Martín Machín, Alicia Gil

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Rosa María Álvarez ÁlvarezMedical Oncology Service, Instituto de Investigación Sanitaria Gregorio Marañón, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Javier Zenón Martín BrotoMedical Oncology Service. Hospital General de Villalba, Madrid, Spain.
Javier Martínez TruferoMedical Oncology Service. Hospital, Universitario Miguel Servet, Zaragoza, Spain.
Ana Sebio GarcíaMedical Oncology Service, Hospital de La Santa Creu I Sant Pau, Barcelona, Spain.
Claudia María Valverde MoralesMedical Oncology Service. Hospital, Universitari Vall d'Hebron, Barcelona, Spain.
Jorge García LópezOmakase Consulting S.L., Barcelona and Madrid, Spain.
Celia Martín MachínOmakase Consulting S.L., Barcelona and Madrid, Spain.
Alicia GilOmakase Consulting S.L., Barcelona and Madrid, Spain. agil@omakaseconsulting.com.ORCID http://orcid.org/0000-0003-3006-7858

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDesmoid tumours (DT), or aggressive fibromatosis are rare, nonmetastatic soft tissue neoplasms characterized by monoclonal fibroblast proliferation and infiltrative local behaviour that can affect organs and adjacent structures, resulting in sustained clinical burden and impacting patient's quality of life. PURPOSE: The aim of this work is to determine the current management of DT in Spain, including unmet needs and to propose the positioning of nirogacestat in the current treatment algorithm. METHODOLOGY: A literature review was conducted in June 2025 to identify published evidence on the epidemiology, diagnosis, management and unmet needs of DT in Spain. An expert panel of five Spanish oncologists specialized in sarcomas was convened. Each expert completed a questionnaire relating to research topics. Responses were consolidated and analysed, with a consensus threshold set at 80%. Findings were discussed and consensus reached at two virtual meetings.

resultsThe therapeutic approach to DT is currently based on an individualized strategy according to symptoms and tumour's biological behaviour. In asymptomatic patients, active surveillance represents the first recommended strategy, given the potential for spontaneous tumour stabilization or regression. Symptomatic, functionally limiting, or documented progression cases require active treatment. The current unmet needs include lack of systemic treatments with approved indication and favourable safety profile. Nirogacestat, the first treatment authorised for patients with progressing DT who require systemic therapy, should be positioned as standard of care in the treatment algorithm.

conclusionsThis first Spanish expert opinion document on DT management addresses evidence gaps and proposes a treatment algorithm to harmonise clinical practice.

Indexed as

Aggressive fibromatosisDesmoid tumoursExpert opinionNirogacestatSystemic treatment

Identifiers

PMID42435159

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.