Evidence map›Paper›PMID 17237909›Full record

Trial reportInvestigational new drugs2007

A phase II and pharmacological study of the matrix metalloproteinase inhibitor (MMPI) COL-3 in patients with advanced soft tissue sarcomas.

Quincy S C Chu, Bahram Forouzesh, Samira Syed, Monica Mita, Garry Schwartz, Joshua Cooper, Joshua Copper, Janet Curtright, Eric K Rowinsky

Erratum issuedAbstract readClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Investigational new drugs, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 60 citations in OpenAlex.

  1. Matrix Metalloproteinase Inhibition in Melanoma.Experimental dermatology · 2026
    Review
  2. Review
  3. Article
  4. Computational drug discovery for castration-resistant prostate cancers through in vitro drug response modeling.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Targeting Tumor Microenvironment for Cancer Therapy.International journal of molecular sciences · 2019
    Review
  12. Article
  13. Tetracycline repurposing in neurodegeneration: focus on Parkinson's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2018
    Review
  14. Matrix metalloproteinases in the brain and blood-brain barrier: Versatile breakers and makers.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2016
    Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Matrix metalloproteinase inhibitor COL-3 prevents the development of paclitaxel-induced hyperalgesia in mice.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2013
    Article
  20. Targeting angiogenesis for treatment of human cancer.Indian journal of pharmaceutical sciences · 2013
    Article
4 · The record

Corrections and comments

  • Erratum issued
    Copper, Joshua [corrected to Cooper, Joshua]
5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Quincy S C ChuCross Cancer Institute, 11560 University Avenue, Edmonton, AB T6G 1Z2, Canada. quincchu@cancerboard.ab.ca
Bahram Forouzesh
Samira Syed
Monica Mita
Garry Schwartz
Joshua Cooper
Joshua Copper
Janet Curtright
Eric K Rowinsky
The University of Texas Health Science Center at San Antonio · USCollege of the Holy Cross · USSan Antonio Military Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This phase II study evaluated the antitumor activity of the tetracycline analog COL-3, a potent inhibitor of metalloproteinases (MMPs), particularly MMP-2 and MMP-9, on a continuous oral schedule at a dose of 50 mg/m2 daily in patients with advanced and/or metastatic soft tissue sarcoma (STS). The principal endpoints were the rate of objective tumor regression and the proportion of patients who did not experience disease progression during the first 8 weeks of treatment. Other study objectives included an assessment of pharmacology of COL-3, time to progression (TTP), and overall survival. A Simon two-stage design with multinomial stopping rule was employed, with 15 patients enrolled during the first stage of the study. Although COL-3 was generally well-tolerated, there were no objective responses and 5(33%) patients experienced disease progression during the first 8 weeks of treatment, which exceeded the criteria established a priori with regard to pursuing further evaluations of COL-3 in STS. The median values for TTP and survival were 109 and 279 days, respectively. Based on these results, further studies of COL-3 on this administration schedule in patients with STS are not warranted.

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsDisease ProgressionEndpoint DeterminationFemaleGastrointestinal Stromal TumorsHumansMaleMatrix Metalloproteinase InhibitorsMiddle AgedNeoplasm Recurrence, LocalSarcomaTetracyclinesTreatment OutcomeAntineoplastic AgentsMatrix Metalloproteinase Inhibitorstetracycline CMT-3Tetracyclines

Identifiers

PMID17237909
OpenAlexW2095397887

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.