Evidence map›Paper›PMID 33289298›Full record

ArticleThe oncologist2021

Evaluating the Soft Tissue Sarcoma Paradigm for the Local Management of Extraskeletal Ewing Sarcoma.

David Boyce-Fappiano, B Ashleigh Guadagnolo, Ravin Ratan, Wei-Lien Wang, Michael J Wagner, Shreyaskumar Patel, John A Livingston, Patrick P Lin, Kevin Diao, Devarati Mitra and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The oncologist, 2021. 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
1.1field-weighted citation impact, top 18% 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, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. A case report of retroperitoneal Ewing sarcoma requiring adrenalectomy.International journal of surgery case reports · 2022
    Article
  4. Article
  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

14 authors at 2 institutions in 1 country.

David Boyce-FappianoDepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-6044-758X
B Ashleigh GuadagnoloDepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Ravin RatanDepartments of Sarcoma Medical Oncology, , The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Wei-Lien WangDepartments of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Michael J WagnerDivision of Medical Oncology, University of Washington, Seattle, Washington, USA.
Shreyaskumar PatelDepartments of Sarcoma Medical Oncology, , The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
John A LivingstonDepartments of Sarcoma Medical Oncology, , The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Patrick P LinDepartments of Orthopedic Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Kevin DiaoDepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Devarati MitraDepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Ahsan FarooqiDepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Alexander J LazarDepartments of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Christina L RolandDepartments of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Andrew J BishopDepartments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
The University of Texas MD Anderson Cancer Center · USUniversity of Washington Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe reviewed our experience treating patients with localized extraskeletal Ewing sarcoma (EES) to determine optimal local management strategies for this rare disease.

methodsSixty patients with localized EES treated at our institution between 1994 and 2018 were reviewed. The Kaplan-Meier method was used to estimates disease outcomes.

resultsThe median follow-up time was 74 months (interquartile range [IQR], 17-121). Half the patients (n = 30) received combined-modality local therapy (CMT) with both surgery and radiation therapy (RT), whereas the other half received single-modality local therapy (SMT) with either surgery or RT. All patients received chemotherapy. The 5-year overall survival was 76%. Twenty-two patients (37%) developed recurrence at a median time of 15 months (IQR, 5-56 months) resulting in 3-year progression-free survival (PFS) of 65%. On univariate analysis, the use of both neoadjuvant and adjuvant chemotherapy was associated with improved 5-year PFS (71% vs. 50%, p = .04) compared with those who received one or the other. Furthermore, 11 patients (18%) developed local recurrences at a median time of 14 months (IQR, 2-19 months), resulting in a 5-year local control (LC) rate of 77%. Use of CMT was not associated with improved LC (83% vs. 72% SMT, p = .41). Also, use of CMT was the only factor associated with poorer disease-specific survival (vs. SMT; hazard ratio, 3.4; p = .047; 95% confidence interval, 1.01-11.4).

conclusionFor patients with EES, CMT was not associated with a decreased rate of local relapse. These data suggest that SMT alone may be sufficient for LC in select patients. A multi-institutional collaborative effort should be considered to validate these findings. IMPLICATIONS FOR PRACTICE: Extraskeletal Ewing sarcoma is a rare chemosensitive sarcoma whose clinical course more closely follows Ewing sarcoma of bone rather than that of other soft tissue sarcomas. Based on this study, combined-modality local therapy did not confer a local control advantage compared with single-modality local therapy. Therefore, single-modality local therapy is likely adequate in select patients with favorable disease features, which has the advantage of ensuring prompt administration of systemic therapy. A multi-institutional collaborative effort is warranted to determine which patients may benefit from de-escalated local therapy.

Indexed as

Bone NeoplasmsSarcomaSarcoma, EwingSoft Tissue NeoplasmsCombined Modality TherapyHumansNeoplasm Recurrence, LocalRetrospective StudiesTreatment OutcomeExtraskeletal Ewing sarcomaLocal therapyRadiation therapySarcoma

Identifiers

PMID33289298
PMCPMC7930399
OpenAlexW3108474212

What OpenQuestion holds

Textmetadata
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.