Evidence map›Paper›PMID 21154746›Full record

Trial reportInternational journal of cancer2011

Phase II study of sunitinib malate, a multitargeted tyrosine kinase inhibitor in patients with relapsed or refractory soft tissue sarcomas. Focus on three prevalent histologies: leiomyosarcoma, liposarcoma and malignant fibrous histiocytoma.

S Tariq Mahmood, Samuel Agresta, Carlos E Vigil, Xiuhua Zhao, Gang Han, Gina D'Amato, Ciara E Calitri, Michelle Dean, Christopher Garrett, Michael J Schell and 2 more

Open access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in International journal of cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 3% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 citations in OpenAlex.

  1. Pooled it
  2. A phase II study of tivozanib in patients with metastatic and nonresectable soft-tissue sarcomas.Annals of oncology : official journal of the European Society for Medical Oncology · 2017
    Trial
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  6. Review
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  14. Regorafenib for the Treatment of Sarcoma.Current treatment options in oncology · 2022
    Review
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  20. Article

8 more citing papers are in PubMed but not listed here.

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

12 authors at 2 institutions in 1 country.

S Tariq MahmoodSarcoma Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Samuel Agresta
Carlos E Vigil
Xiuhua Zhao
Gang Han
Gina D'Amato
Ciara E Calitri
Michelle Dean
Christopher Garrett
Michael J Schell
Scott Antonia
Alberto Chiappori
Moffitt Cancer Center · USIn-Q-Tel · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI John L. Cleveland · 1998 to 2026
$93.5M
Development of Immunotherapeutic Strategies in the Treatment of Lung CancerK24CA128953 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI ANTONIA, SCOTT J. · 2008 to 2012
$946k
NCI NIH HHS K24 CA128953NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

Soft tissue sarcomas (STS) represent a diverse group of histologic subtypes with targetable molecular alterations, often treated as a single disease. Sunitinib malate is a multitargeted receptor tyrosine kinase inhibitor active in other solid tumors carrying similar alterations (i.e., imatinib mesylate-refractory gastrointestinal stromal tumors). This single-institution phase II study investigated the safety and efficacy of sunitinib malate in three common STS subtypes. Patients with documented unresectable or metastatic STS (liposarcoma, leiomyosarcoma and malignant fibrous histiocytoma [MFH]), measurable disease, and 3 or less prior lines of therapy were eligible. Treatment consisted of sunitinib malate, 50 mg daily, for 4 weeks every 6 weeks. Forty-eight patients were enrolled, and 35% were heavily pretreated (≥ 2 prior lines of chemotherapy). The safety profile resembled previously known sunitinib malate toxicities. Median progression-free and overall survivals for liposarcoma, leiomyosarcoma, and MFH were 3.9 and 18.6, 4.2 and 10.1 and 2.5 and 13.6 months, respectively. The 3-month progression-free rates in the untreated and pretreated (chemotherapy) patients with liposarcoma, leiomyosarcoma and MFH were 75% and 69.2%, 60%, and 62.5% and 25% and 44.4%, respectively. With the caveats that a minority of patients with potentially indolent or low-grade disease could have been included and the small numbers, a 3-month progression-free rate of >40% suggests activity for sunitinib malate at least in liposarcomas and leiomyosarcomas. Thus, we believe that further investigation in these susceptible STS subtypes is warranted.

Indexed as

Disease-Free SurvivalDrug Administration ScheduleDrug Resistance, NeoplasmFemaleHistiocytoma, Malignant FibrousHumansIndolesLeiomyosarcomaLiposarcomaMaleNeoplasm MetastasisProtein Kinase InhibitorsPyrrolesRecurrenceRetreatmentSarcomaIndolesProtein Kinase InhibitorsPyrrolesSunitinib

Identifiers

PMID21154746
PMCPMC3776586
OpenAlexW1971610159

What OpenQuestion holds

Textmetadata
LicenceTDM
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.