Evidence map›Paper›PMID 36979853›Full record

ReviewBiomedicines2023

Shifting from a Biological-Agnostic Approach to a Molecular-Driven Strategy in Rare Cancers: Ewing Sarcoma Archetype.

Aldo Caltavituro, Roberto Buonaiuto, Erica Pietroluongo, Rocco Morra, Fabio Salomone, Pietro De Placido, Martina Pagliuca, Angelo Vaia, Margaret Ottaviano, Marianna Tortora and 3 more

Open access · goldFull text readReview
In one paragraph

Review in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 31% of its field
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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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 at 4 institutions in 2 countries.

Aldo CaltavituroDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.
Roberto BuonaiutoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.ORCID 0000-0002-5495-3224
Erica PietroluongoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.
Rocco MorraDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.ORCID 0000-0002-2516-076X
Fabio SalomoneDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.
Pietro De PlacidoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.
Martina PagliucaScuola Superiore Meridionale (SSM), Clinical and Translational Oncology, 80138 Naples, Italy.ORCID 0000-0001-8114-2577
Angelo VaiaMedical Oncology Unit, "San Carlo" Hospital, 85100 Napoli, Italy.
Margaret OttavianoUnit of Melanoma, Cancer Immunotherapy and Development Therapeutics, Istituto Nazionale Tumori IRCCS Fondazione Pascale, Campania, 80131 Napoli, Italy.ORCID 0000-0001-9589-0808
Marianna TortoraCRCTR Coordinating Rare Tumors Reference Center of Campania Region, 80131 Naples, Italy.ORCID 0000-0002-9853-9594
Sabino De PlacidoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.
Giovannella PalmieriCRCTR Coordinating Rare Tumors Reference Center of Campania Region, 80131 Naples, Italy.
Mario GiulianoDepartment of Clinical Medicine and Surgery, University of Naples Federico II, 80131 Naples, Italy.
University of Naples Federico II · ITRegione Campania · ITInstitut Gustave Roussy · FROspedale San Carlo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcomas of the thoracic cavity are rare entities that predominantly affect children and young adults. They can be very heterogeneous encompassing several different histological entities. Ewing Sarcoma (ES) can potentially arise from every bone, soft tissue, or visceral site in the body. However, it represents an extremely rare finding when it affects the thoracic cavity. It represents the second most frequent type of thoracic sarcoma, after chondrosarcoma. ES arises more frequently in sites that differ from the thoracic cavity, but it displays the same biological features and behavior of extra-thoracic ones. Current management of ES often requires a multidisciplinary treatment approach including surgery, radiotherapy, and systemic therapy, as it can guarantee local and distant disease control, at least transiently, although the long-term outcome remains poor. Unfortunately, due to the paucity of clinical trials purposely designed for this rare malignancy, there are no optimal strategies that can be used for disease recurrence. As a result of its complex biological features, ES might be suitable for emerging biology-based therapeutic strategies. However, a deeper understanding of the molecular mechanisms driving tumor growth and treatment resistance, including those related to oncogenic pathways, epigenetic landscape, and immune microenvironment, is necessary in order to develop new valid therapeutic opportunities. Here, we provide an overview of the most recent therapeutic advances for ES in both the preclinical and clinical settings. We performed a review of the current available literature and of the ongoing clinical trials focusing on new treatment strategies, after failure of conventional multimodal treatments.

Indexed as

biologyepigeneticsewing sarcomaimmunotherapyrare thoracic tumors

Identifiers

PMID36979853
PMCPMC10045500
OpenAlexW4324054304

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read17
identifiers read4
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 Socratic graph.