Evidence map›Paper›PMID 26043723›Full record

ArticleOncology2015

Outcomes of Systemic Therapy for Patients with Metastatic Angiosarcoma.

Sandra P D'Angelo, Rodrigo R Munhoz, Deborah Kuk, Johnathan Landa, Eliza W Hartley, Michael Bonafede, Mark A Dickson, Mrinal Gounder, Mary L Keohan, Aimee M Crago and 2 more

Open access · greenAbstract read
In one paragraph

Article in Oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 14% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Phase II study of MLN8237 (Alisertib) in advanced/metastatic sarcoma.Annals of oncology : official journal of the European Society for Medical Oncology · 2016
    Trial
  5. Article
  6. Review
  7. Article
  8. Article
  9. miR-497 Target Gene Regulatory Network in Angiosarcoma.Molecular cancer research : MCR · 2024
    Article
  10. Review
  11. Article
  12. Target gene regulatory network of miR-497 in angiosarcoma.bioRxiv : the preprint server for biology · 2023
    Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

12 authors at 5 institutions in 2 countries.

Sandra P D'AngeloDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, N.Y., USA.
Rodrigo R Munhoz
Deborah Kuk
Johnathan Landa
Eliza W Hartley
Michael Bonafede
Mark A Dickson
Mrinal Gounder
Mary L Keohan
Aimee M Crago
Cristina R Antonescu
William D Tap
Cornell University · USMemorial Sloan Kettering Cancer Center · USCancer Research And Biostatistics · USHospital Sírio-Libanês · BRUniversity Radiology · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundAngiosarcomas (AS) are rare tumors of vascular origin with a variable behavior and overall poor prognosis. We sought to assess the outcomes of patients treated for metastatic disease.

methodsWe performed a retrospective analysis of 119 patients treated for metastatic AS. Outcomes and efficacy measurements of the first and subsequent lines of treatment were analyzed.

resultsMedian age was 61 years, and the most frequent primary sites were chest wall/breast (31%), viscera (22%) and head/neck (20%). Seventy-three (61%) and 46 (39%) patients received ≥ 2 and ≥ 3 lines of therapy, respectively. The most commonly used agents included taxanes and anthracyclines. Median overall survival was 12.1 months. Median times to tumor progression were 3.5 months for first line, 3.7 months for second line and 2.7 months for third line. Among 48 patients evaluable per RECIST, the overall response rate to first line was 30% and <10% in subsequent lines. Doxorubicin, liposomal doxorubicin and taxanes resulted in similar response rates and survival, and there was no apparent benefit for combination chemotherapy.

conclusionDespite reasonable response rates in the first-line setting, benefit from systemic therapy is short-lived in metastatic AS, and outcomes are poor. Doxorubicin, liposomal doxorubicin and taxanes are reasonable and appropriate choices for monotherapy.

Indexed as

AdultAgedAged, 80 and overAnthracyclinesAntineoplastic AgentsDisease ProgressionDoxorubicinFemaleHemangiosarcomaHumansMaleMiddle AgedPolyethylene GlycolsRetrospective StudiesTaxoidsTreatment OutcomeAnthracyclinesAntineoplastic AgentsDoxorubicinliposomal doxorubicinPolyethylene GlycolsTaxoids

Identifiers

PMID26043723
PMCPMC5587158
OpenAlexW1536751072

What OpenQuestion holds

Textmetadata
LicenceTDM
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.