Evidence map›Paper›PMID 38993253›Full record

ArticleWorld journal of oncology2024

Risk Stratification Tools to Aid Decisions on Adjuvant Chemotherapy Usage in Resected Soft Tissue Sarcomas: A Ten-Year Review of an Irish Sarcoma Center Experience.

Catherine S Weadick, Caitriona Goggin, Rachel J Keogh, Jake F Murphy, Linda Feeley, Michael W Bennett, Seamus O'Reilly, H Paul Redmond, Jason Kelly, Deirdre O'Mahony and 3 more

Abstract read
In one paragraph

Article in World journal of oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Catherine S WeadickDepartment of Medical Oncology, Cork University Hospital, Wilton, Cork, Ireland.
Caitriona GogginDepartment of Medical Oncology, Cork University Hospital, Wilton, Cork, Ireland.
Rachel J KeoghDepartment of Medical Oncology, Cork University Hospital, Wilton, Cork, Ireland.
Jake F MurphyDepartment of Radiation Oncology, Cork University Hospital, Wilton, Cork, Ireland.
Linda FeeleyDepartment of Histopathology, Cork University Hospital, Wilton, Cork, Ireland.
Michael W BennettDepartment of Histopathology, Cork University Hospital, Wilton, Cork, Ireland.
Seamus O'ReillyDepartment of Medical Oncology, Cork University Hospital, Wilton, Cork, Ireland.
H Paul RedmondDepartment of Surgery, Cork University Hospital, Wilton, Cork, Ireland.
Jason KellyDepartment of Surgery, Cork University Hospital, Wilton, Cork, Ireland.
Deirdre O'MahonyDepartment of Medical Oncology, Cork University Hospital, Wilton, Cork, Ireland.
Sinead NoonanDepartment of Medical Oncology, Cork University Hospital, Wilton, Cork, Ireland.
A James P CloverDepartment of Plastic Surgery, Cork University Hospital, Wilton, Cork, Ireland.
Richard M BamburyDepartment of Medical Oncology, Cork University Hospital, Wilton, Cork, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Soft tissue sarcoma (STS) is comprised of approximately 80 subtypes, with an incidence of 4 - 5 per 100,000 annually in Europe. The National Comprehensive Cancer Network (NCCN) guidelines recommend consideration of neoadjuvant/adjuvant chemotherapy in tumors at high risk of recurrence based on the American Joint Committee on Cancer (AJCC) staging. Alternatively, the Sarculator is a risk prediction tool that has identified a threshold of risk, above which chemotherapy may provide an overall survival (OS) benefit. Using this nomogram, patients with a 10-year predicted OS < 60% are classified as high risk and should be considered for chemotherapy. The aim of this study was to assess the prognostic accuracy of these two risk prediction methods in an Irish population. Methods: All newly diagnosed patients with resected STS discussed in the STS tumor board in Cork University Hospital between January 2012 and December 2021 were identified. Clinicopathological data were collected. Risk assessment using AJCC and Sarculator nomogram was performed on all patients with an extremity/trunk sarcoma. The OS was calculated including Kaplan-Meier method for time to event analysis. Results: In total, 200 STS patients were reviewed, of whom 134 had truncal or extremity tumors. Sarculator score was calculated for 60 of these (well differentiated liposarcomas, desmoid tumors and dermatofibrosarcoma protuberans were excluded). Using the Sarculator nomogram to calculate 10-year predicted OS, 19 patients were categorized as high risk and 41 were categorized as low risk. Using AJCC staging, 25 patients were categorized as high risk and 35 as low risk. The 5-year OS rate in the Sarculator high-risk group was 60.2%, compared with 87.1% in the low-risk group (P = 0.009). The 5-year OS rate in the AJCC high-risk group was 67.6%, compared with 86.3% in the low-risk group (P = 0.083). Conclusions: Our cohort is representative of the broad histological subtypes expected. In our population, Sarculator score results correlate with international outcomes and higher scores were associated with increased mortality. The Sarculator was more predictive of clinical outcome than AJCC staging, and its use would lower the proportion of patients being considered for adjuvant chemotherapy thereby sparing toxicity, which is important in the setting of uncertain clinical benefit.

Indexed as

Adjuvant chemotherapyNeoadjuvant chemotherapySarculatorSoft tissue sarcoma

Identifiers

PMID38993253
PMCPMC11236376

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.