Evidence map›Paper›PMID 37781501›Full record

ArticleTherapeutic advances in medical oncology2023

Clinico-demographic characteristics and outcomes of radiation-induced sarcomas (RIS): a CanSaRCC study.

Mauricio Fernando Ribeiro, Hagit Peretz Soroka, Zainab Bhura, Ian Hirsch, Jay Wunder, Peter Ferguson, Kim Tsoi, Savtaj Brar, Rebecca Gladdy, Carol Swallow and 7 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  3. Review
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  5. 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

17 authors at 2 institutions in 1 country.

Mauricio Fernando RibeiroDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.ORCID https://orcid.org/0000-0002-5602-164X
Hagit Peretz SorokaDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.
Zainab BhuraDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.
Ian HirschDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.
Jay WunderDepartment of Surgery, Mount Sinai Hospital, Sinai Health, Toronto, ON, Canada.
Peter FergusonDepartment of Surgery, Mount Sinai Hospital, Sinai Health, Toronto, ON, Canada.
Kim TsoiDepartment of Surgery, Mount Sinai Hospital, Sinai Health, Toronto, ON, Canada.
Savtaj BrarDepartment of Surgery, Mount Sinai Hospital, Sinai Health, Toronto, ON, Canada.
Rebecca GladdyDepartment of Surgery, Mount Sinai Hospital, Sinai Health, Toronto, ON, Canada.
Carol SwallowDepartment of Surgery, Mount Sinai Hospital, Sinai Health, Toronto, ON, Canada.
Peter ChungDepartment of Radiation Oncology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.
Charles CattonDepartment of Radiation Oncology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.
Philip WongDepartment of Radiation Oncology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.ORCID https://orcid.org/0000-0002-7761-0283
Geoffrey WatsonDivision of Medical Oncology, Mount Sinai Hospital, Sinai Health, Toronto, ON, Canada.
Albiruni Ryan Abdul RazakDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.
Abha A GuptaDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, ON, Canada.
David ShultzDepartment of Radiation Oncology, Princess Margaret Cancer Centre - University of Toronto, 610 University Avenue, Toronto, ON M5G 2M9, Canada.
University of Toronto · CAMount Sinai Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Radiation-induced sarcomas (RIS) tend to have aggressive behaviour and because of their rarity, the most appropriate management for these malignancies is uncertain. Objectives: Using the Canadian Sarcoma Research and Clinical Collaboration (CanSaRCC) database, a national sarcoma registry, we aimed to investigate prognostic factors and outcomes for RIS. Design: Retrospective study of RIS patients treated from 1996 to 2021 at three Canadian centres. Methods: RIS was defined as a sarcoma arising in a previously irradiated field following a 3+ year latency period, whose histology was distinct from the initially irradiated tumour. Clinicopathologic and treatment-related information was extracted from the CanSaRCC database. Overall survival (OS) was defined as the time from RIS diagnosis to death from any cause. Response rate (RR) to neoadjuvant chemotherapy (NACT) was based on physician assessment. Time-to-event analyses were estimated using the Kaplan-Meier method, with Cox regression for multivariate analysis. We considered a two-tailed Results: One hundred seven tumours met the criteria for RIS and were divided into three subgroups: breast angiosarcoma (BAS, Conclusion: Surgery is standard, and NACT might be useful to downsize large lesions, especially in BAS patients. Raising RIS awareness is fundamental to promoting appropriate management and fostering research through multi-institutional collaborations.

Indexed as

angiosarcomabreast sarcomaradiation-induced cancersradiation-induced sarcomaradiotherapysoft-tissue sarcoma

Identifiers

PMID37781501
PMCPMC10540571
OpenAlexW4387133870

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.