Evidence map›Paper›PMID 36724001›Full record

Trial reportThe oncologist2023

Outcome of Patients With Malignant Peripheral Nerve Sheath Tumors Enrolled on Sarcoma Alliance for Research Through Collaboration (SARC) Phase II Trials.

Srivandana Akshintala, Nicole C Mallory, Yao Lu, Karla V Ballman, Scott M Schuetze, Rashmi Chugh, Robert G Maki, Denise K Reinke, Brigitte C Widemann, AeRang Kim

Registry-linked trialAbstract readClinical Trial, Phase II
In one paragraph

Trial report in The oncologist, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00304083 (Phase II Trial of Chemotherapy in Sporadic and Neurofibromatosis Type 1 Associated High Grade Malignant Peripheral Nerve Sheath Tumors), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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.

NCT00304083 phase2completednot on this map

Phase II Trial of Chemotherapy in Sporadic and Neurofibromatosis Type 1 Associated High Grade Malignant Peripheral Nerve Sheath Tumors

TypeinterventionalSponsorSarcoma Alliance for Research through CollaborationRan2005 to 2014Enrolled48ConditionsNeurofibromatosis Type 1, SarcomaArmsfilgrastim, doxorubicin hydrochloride, etoposide, ifosfamide, conventional surgery
3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. SARC031: A Phase II Trial of Selumetinib and Sirolimus for Patients with Unresectable or Metastatic Malignant Peripheral Nerve Sheath Tumors (MPNST).Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
  2. Article
  3. Review
  4. Review
  5. MTA-Cooperative PRMT5 Inhibitors Are Efficacious in MTAP-Deleted Malignant Peripheral Nerve Sheath Tumor Models.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  6. Review
  7. Article
  8. Histology-Specific Clinical Trial of Lenvatinib and Pembrolizumab in Patients with Sarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Contemporary Approach to Neurofibromatosis Type 1-Associated Malignant Peripheral Nerve Sheath Tumors.American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

10 authors.

Srivandana AkshintalaDivision of Pediatric Hematology-Oncology, New York University Langone Health, New York, NY, USA.ORCID 0000-0002-3478-9893
Nicole C MalloryDivision of Pediatric Hematology-Oncology, New York University Langone Health, New York, NY, USA.
Yao LuDivision of Biostatistics, Weill Cornell Medicine, New York, NY, USA.
Karla V BallmanDivision of Biostatistics, Weill Cornell Medicine, New York, NY, USA.
Scott M SchuetzeDivision of Hematology/Oncology, University of Michigan, Ann Arbor, MI, USA.
Rashmi ChughDivision of Hematology/Oncology, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-4633-6971
Robert G MakiDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Denise K ReinkeDivision of Hematology/Oncology, University of Michigan, Ann Arbor, MI, USA.
Brigitte C WidemannPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
AeRang KimCenter for Cancer and Blood Disorders, Children's National Medical Center, Washington, DC, USA.ORCID 0000-0002-7813-5568

Funding

Therapies for patients with rare tumors and genetic tumor predispositionZIASC010354 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WIDEMANN, BRIGITTE · 2009 to 2025
$19.2M
6 · The paper itself

Abstract

backgroundEvaluation of prior phase II trials for malignant peripheral nerve sheath tumors (MPNST) may help develop more suitable trial endpoints in future studies.

methodsWe analyzed outcomes of patients with recurrent or unresectable/metastatic MPNST enrolled on prior Sarcoma Alliance for Research through Collaboration (SARC) phase II trials and estimated the progression-free survival (PFS). PFS from SARC006 (NCT00304083), the phase II trial of upfront chemotherapy in chemotherapy naïve patients, was analyzed separately. Impact of baseline enrollment characteristics on PFS was evaluated.

resultsSixty-four patients (29 male, 35 female, median age 39 years (range 15-81)) with MPNST were enrolled on 1 of 5 trials of single agent or combination therapy that were determined to be inactive. Patients had received a median of 1 (range 0-5) prior systemic therapy, and most had undergone prior surgery (77%) and radiation (61%). Seventy-three percent had metastatic disease at enrollment. Median PFS was 1.77 months (95% CI, 1.61-3.45), and the PFS rate at 4 months was 15%. Greater number of prior systemic therapies and worse performance status were associated with inferior PFS. There was no significant difference in PFS based on age at enrollment, treatment trial, response criteria, presence of metastatic disease, disease site at enrollment, and prior surgery or radiation. In comparison, on the SARC006 trial the PFS rate at 4 months was 94% in 40 patients.

conclusionThese data provide a historical baseline PFS that may be used as a comparator in future clinical trials for patients with MPNST.

Indexed as

NeurofibrosarcomaSarcomaSoft Tissue NeoplasmsAdolescentAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyFemaleHumansMaleMiddle AgedProgression-Free SurvivalYoung Adultmalignant peripheral nerve sheath tumorsoutcomesphase II trialsprogression-free survival

Identifiers

PMID36724001
PMCPMC10166173

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.