Evidence map›Paper›PMID 23891158›Full record

Trial reportClinical genitourinary cancer2013

A phase II safety and efficacy study of the vascular endothelial growth factor receptor tyrosine kinase inhibitor pazopanib in patients with metastatic urothelial cancer.

Roberto Pili, Rui Qin, P J Flynn, Joel Picus, Michael Millward, Wing Ming Ho, Henry Pitot, Winston Tan, Kiersten M Miles, Charles Erlichman and 1 more

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Clinical genitourinary cancer, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
7.6field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 60 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Review
  8. Article
  9. Landscape of targeted therapies for advanced urothelial carcinoma.Exploration of targeted anti-tumor therapy · 2024
    Review
  10. Article
  11. Article
  12. Review
  13. Novel Tyrosine Kinase Targets in Urothelial Carcinoma.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Incorporating VEGF-targeted therapy in advanced urothelial cancer.Therapeutic advances in medical oncology · 2017
    Review
  17. Article
  18. Article
  19. Review
  20. Review
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

11 authors at 8 institutions in 3 countries.

Roberto PiliRoswell Park Cancer Institute, Buffalo, NY. Electronic address: Roberto.Pili@RoswellPark.org.
Rui Qin
P J Flynn
Joel Picus
Michael Millward
Wing Ming Ho
Henry Pitot
Winston Tan
Kiersten M Miles
Charles Erlichman
Ulka Vaishampayan
Mayo Clinic · USRoswell Park Comprehensive Cancer Center · USChinese University of Hong Kong · CNMayo Clinic in Florida · USMinnesota Oncology · USSir Charles Gairdner Hospital · AUThe Barbara Ann Karmanos Cancer Institute · USWashington University in St. Louis · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Keith L. Knutson · 1985 to 2026
$151.3M
Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Jennifer L Beebe-Dimmer · 1985 to 2026
$68.4M
NCI NIH HHS N01 CM062205NCI NIH HHS N01-CM62205NCI NIH HHS P30 CA015083NCI NIH HHS P30 CA022453
6 · The paper itself

Abstract

backgroundVascular endothelial growth factor (VEGF) is produced by bladder cancer cell lines in vitro and expressed in human bladder tumor tissues. Pazopanib is a vascular endothelial receptor tyrosine kinase inhibitor with anti-angiogenesis and anti-tumor activity in several preclinical models. A 2-stage phase II study was conducted to assess the activity and toxicity profile of pazopanib in patients with metastatic, urothelial carcinoma.

methodsPatients with one prior systemic therapy for metastatic urothelial carcinoma were eligible. Patients received pazopanib at a dose of 800 mg orally for a 4-week cycle.

resultsNineteen patients were enrolled. No grade 4 or 5 events were experienced. Nine patients experienced 11 grade 3 adverse events. Most common toxicities were anemia, thrombocytopenia, leucopenia, and fatigue. For stage I, none of the first 16 evaluable patients were deemed a success (complete response or partial response) by the Response Evaluation Criteria In Solid Tumors criteria during the first four 4-week cycles of treatment. Median progression-free survival was 1.9 months. This met the futility stopping rule of interim analysis, and therefore the trial was recommended to be permanently closed.

conclusionsPazopanib did not show significant activity in patients with urothelial carcinoma. The role of anti-VEGF therapies in urothelial carcinoma may need further evaluation in rational combination strategies.

Indexed as

AdultAgedAged, 80 and overAngiogenesis InhibitorsCarcinoma, Transitional CellDisease-Free SurvivalFemaleHumansIndazolesMaleMiddle AgedNeovascularization, PathologicPyrimidinesReceptors, Vascular Endothelial Growth FactorSulfonamidesTreatment FailureAngiogenesis InhibitorsIndazolespazopanibPyrimidinesReceptors, Vascular Endothelial Growth FactorSulfonamidesPazopanibUrothelial cancerVEGF tyrosine kinase inhibitors

Identifiers

PMID23891158
PMCPMC4102930
OpenAlexW2145526926

What OpenQuestion holds

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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.