Evidence map›Paper›PMID 40940991›Full record

ArticleCancers2025

ESFT13: A Phase II Study Evaluating the Addition of Window and Maintenance Therapy to a Standard Chemotherapy Backbone for the Treatment of High-Risk Ewing Sarcoma.

Jessica Gartrell, Fariba Navid, Xiaomeng Yuan, Kirsten K Ness, Mikhail Dubrovin, Fang Wang, Haitao Pan, Mary Beth McCarville, Barry L Shulkin, Sara Helmig and 9 more

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Jessica GartrellDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-1722-2924
Fariba NavidCancer and Blood Disease Institute, Children's Hospital Los Angeles, Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, CA 90027, USA.ORCID 0000-0002-7916-6382
Xiaomeng YuanDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-6435-8525
Kirsten K NessDepartment of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Mikhail DubrovinDepartment of Radiology, Columbia University, New York, NY 10032, USA.
Fang WangDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0001-8764-9387
Haitao PanDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0003-4457-7349
Mary Beth McCarvilleDepartment of Radiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Barry L ShulkinDepartment of Radiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Sara HelmigDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Matthew J KrasinDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0001-5421-765X
Michael D NeelDepartment of Surgery, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Andrew M DavidoffDepartment of Surgery, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Belinda N MandrellDepartment of Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-6041-7559
Deena R LevineDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-3206-5648
Zhongheng CaiDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-0000-3389
Michael W BishopDepartment of Pediatric Hematology-Oncology, Arkansas Children's Hospital, Little Rock, AR 72202, USA.
Alberto S PappoDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-5338-3979
Sara M FedericoDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.ORCID 0000-0002-5807-4876

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Shondra Michelle Miller · 1985 to 2026
$166.9M
American Lebanese Syrian Associated Charities xxx-xxxNCI NIH HHS P30 CA021765St. Jude Children's Research Hospital xxx-xxx
6 · The paper itself

Abstract

STUDY

aimPatients with high-risk Ewing sarcoma (ES) have dismal outcomes despite aggressive multimodal therapy. This phase II, single-institution study evaluated the response rate to two up-front cycles of irinotecan, temozolomide, and temsirolimus (ITT) and assessed the tolerability of maintenance therapy following standard treatment in high-risk ES.

methodsEligible patients had newly diagnosed high-risk ES (age ≥14 years old, metastatic disease, or primary pelvic tumor). The therapy included two cycles of window therapy (ITT) followed by interval-compressed chemotherapy (vincristine, doxorubicin, and cyclophosphamide alternating with ifosfamide and etoposide) and maintenance therapy (cyclophosphamide, sorafenib, and bevacizumab). A two-stage sequential design was employed to assess a >50% WHO response (CR or PR) with 80% power. Patients who required emergent radiation were excluded from receiving window therapy.

resultsSixteen patients (median age 12.2 years; range 4.8-23.6 years) were enrolled (12 evaluable for overall response, 10 for primary tumor response). Only three achieved a PR to window therapy, leading to study closure. All evaluable patients demonstrated a decline in their primary tumor volume (mean decline: 32.5%, standard deviation: 17.6%,

conclusionsITT did not achieve the prespecified response rate of 50%, according to WHO criteria; however, all patients exhibited decreased volume and metabolic activity, highlighting the limitations of conventional response assessments. Maintenance therapy was feasible and well tolerated. Although limited by small sample size, heterogeneous disease presentations, and the absence of a control arm, this study supports further evaluation of ITT and a maintenance approach in larger, randomized trials for high-risk ES.

Indexed as

Ewing sarcomairinotecanmaintenance chemotherapypediatricstemozolomidetemsirolimus

Identifiers

PMID40940991
PMCPMC12428418

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Registered trials

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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.