Evidence map›Paper›PMID 33107985›Full record

ArticleCancer2021

Activity of sirolimus in patients with progressive epithelioid hemangioendothelioma: A case-series analysis within the Italian Rare Cancer Network.

Silvia Stacchiotti, Noemi Simeone, Salvatore Lo Vullo, Giacomo G Baldi, Antonella Brunello, Bruno Vincenzi, Elena Palassini, GianPaolo Dagrada, Paola Collini, Carlo Morosi and 6 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06408441 (The Observational EURACAN Prospective Clinical Registry Dedicated to Epithelioid Hemangioendothelioma), which is not on this map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.9field-weighted citation impact, top 11% 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.

NCT06408441 recruitingnot on this mapstarted 2023, after this paper: background citation

The Observational EURACAN Prospective Clinical Registry Dedicated to Epithelioid Hemangioendothelioma: the Protocol of an International and Collaborative Effort on an Ultra-rare Entity

Typeobservational_patient_registrySponsorFondazione IRCCS Istituto Nazionale dei Tumori, MilanoRan2023 to 2033Enrolled100ConditionsEpithelioid Hemangioendothelioma, Sarcoma,Soft Tissue
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 48 citations in OpenAlex.

  1. A Single-Arm Phase 2 Trial of Trametinib in Patients with Locally Advanced or Metastatic Epithelioid Hemangioendothelioma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Trial
  2. The TAZ-CAMTA1 Fusion Protein Promotes Tumorigenesis via Connective Tissue Growth Factor and Ras-MAPK Signaling in Epithelioid Hemangioendothelioma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Trial
  3. Review
  4. Article
  5. How I treat soft tissue sarcomas.Future oncology (London, England) · 2026
    Review
  6. Article
  7. Article
  8. Article
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  11. Review
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  14. Review
  15. GDF-15 Predicts Epithelioid Hemangioendothelioma Aggressiveness and Is Downregulated by Sirolimus through ATF4/ATF5 Suppression.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 3 countries.

Silvia StacchiottiDepartment of Medical Oncology, IRCCS Foundation National Cancer Institute, Milan, Italy.ORCID 0000-0002-1742-8666
Noemi SimeoneDepartment of Medical Oncology, IRCCS Foundation National Cancer Institute, Milan, Italy.
Salvatore Lo VulloUnit of Clinical Epidemiology and Trial Organization, IRCCS Foundation National Cancer Institute, Milan, Italy.ORCID 0000-0002-4444-9526
Giacomo G BaldiDepartment of Medical Oncology, Santo Stefano Hospital, Prato, Italy.
Antonella BrunelloDepartment of Oncology, Medical Oncology Unit 1, Veneto Institute of Oncology, IRCCS, Padua, Italy.ORCID 0000-0003-2583-5226
Bruno VincenziDepartment of Medical Oncology, Biomedical Campus, University of Rome, Rome, Italy.
Elena PalassiniDepartment of Medical Oncology, IRCCS Foundation National Cancer Institute, Milan, Italy.
GianPaolo DagradaDepartment of Diagnostic Pathology and Laboratory Medicine, IRCCS Foundation National Cancer Institute, Milan, Italy.
Paola ColliniDepartment of Diagnostic Pathology and Laboratory Medicine, IRCCS Foundation National Cancer Institute, Milan, Italy.
Carlo MorosiDepartment of Radiology, IRCCS Foundation National Cancer Institute, Milan, Italy.
Francesca G GrecoDepartment of Radiology, IRCCS Foundation National Cancer Institute, Milan, Italy.
Marta SbaragliaDepartment of Pathology, University of Padua Foundation, Padua, Italy.
Angelo P Dei TosDepartment of Pathology, University of Padua Foundation, Padua, Italy.
Luigi MarianiUnit of Clinical Epidemiology and Trial Organization, IRCCS Foundation National Cancer Institute, Milan, Italy.
Anna Maria FrezzaDepartment of Medical Oncology, IRCCS Foundation National Cancer Institute, Milan, Italy.ORCID 0000-0003-2335-7224
Paolo G CasaliDepartment of Medical Oncology, IRCCS Foundation National Cancer Institute, Milan, Italy.
National Cancer Institute · UAUniversity of Padua · ITHospital of Prato · ITIstituto Oncologico Veneto · ITUniversità Campus Bio-Medico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe objective of this study was to report on a retrospective series of patients with epithelioid hemangioendothelioma (EHE) who received treatment with sirolimus within the Italian Rare Cancer Network.

methodsFrom January 2005, 38 adult patients with advanced EHE received continuous-dosing sirolimus, 5 mg daily, until they developed either toxicity or disease progression. Disease progression in the 6 months before the start of treatment was required. Each pathologic diagnosis was reviewed. The daily dose of sirolimus was adjusted based on plasma levels. Response was retrospectively assessed by local investigators using Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST). Survival was estimated using the Kaplan-Meier method.

resultsAll 38 patients (WW Domain Containing Transcription Regulator 1 [WWTR1]-positive, n = 37; transcription factor E3 [TFE3]-positive, n = 1) had disease progression before starting sirolimus (at baseline, 13 of 38 patients had the presence of serosal effusions and systemic symptoms). Thirty-seven patients were evaluable for response (there was 1 early interruption). The best RECIST responses were a partial response in 4 patients (10.8%), stable disease in 28 patients (75.7%), and disease progression in 5 patients (13.5%). At a 41.5-month median follow-up (interquartile range [IQR], 23.9-56.8 months), the median PFS was 13 months (95% CI, 3.7 months to not estimated [NE]), and the median OS was 18.8 months (95% CI, 10.6 months to NE). In patients who had serosal effusions at baseline, the median PFS was 4.8 months (IQR, 3.5-11.7 months), and the median OS was 10.6 months (IQR, 5.1-13.0 months), compared with 47.8 months (IQR, 11.4 months to NE) and 47.8 months (IQR, 15.7 months to NE), respectively, in patients without serosal effusions. Overall, sirolimus was fairly well tolerated, with 10 patients reporting irregular menstruation/ovary disfunction.

conclusionsThe current results confirm that sirolimus is active in EHE, leading to prolonged stabilization in most patients who present without serosal effusions. Serosal effusions are confirmed as an unfavorable prognostic sign associated with short survival, and sirolimus displays limited activity in this subgroup.

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsChildDisease ProgressionFemaleHemangioendothelioma, EpithelioidHumansIntracellular Signaling Peptides and ProteinsItalyKaplan-Meier EstimateMaleMiddle AgedPrognosisResponse Evaluation Criteria in Solid TumorsSirolimusIntracellular Signaling Peptides and ProteinsSirolimusTranscriptional Coactivator with PDZ-Binding Motif ProteinsWWTR1 protein, humanchemotherapyepithelioid hemangioendotheliomametastasisprognosissarcomaserosal effusionsirolimus

Identifiers

PMID33107985
OpenAlexW3093617452

What OpenQuestion holds

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Registered trials

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.