Evidence map›Paper›PMID 22083229›Full record

Trial reportBreast cancer research and treatment2012

A phase II study of 17-allylamino-17-demethoxygeldanamycin in metastatic or locally advanced, unresectable breast cancer.

Elaina M Gartner, Paula Silverman, Michael Simon, Lawrence Flaherty, Judith Abrams, Percy Ivy, Patricia M Lorusso

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Breast cancer research and treatment, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Combination of Anti-Cancer Drugs with Molecular Chaperone Inhibitors.International journal of molecular sciences · 2019
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. The HSP90 inhibitor 17-AAG exhibits potent antitumor activity for pheochromocytoma in a xenograft model.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    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

7 authors at 4 institutions in 1 country.

Elaina M GartnerKarmanos Cancer Institute, Wayne State University, 4100 John R, 4HWCRC, Detroit, MI 48201, USA. gartnere@karmanos.org
Paula Silverman
Michael Simon
Lawrence Flaherty
Judith Abrams
Percy Ivy
Patricia M Lorusso
Wayne State University · USCase Western Reserve University · USNational Institutes of Health · USThe Barbara Ann Karmanos Cancer Institute · US

Funding

PHASE I TRIALS OF NEW ANTICANCER AGENTSU01CA062487 · NCI · WAYNE STATE UNIVERSITY · PI LORUSSO, PATRICIA M. · 1994 to 2013
$8.4M
NCI National Clinical Trials Network-Network Lead Academic Participating SiteU10CA180835 · NCI · WAYNE STATE UNIVERSITY · PI FLAHERTY, LAWRENCE E · 2014 to 2018
$3.1M
NCI NIH HHS U01 CA062487NCI NIH HHS U10 CA180835
6 · The paper itself

Abstract

Heat shock protein 90 (Hsp90) is an attractive target for breast cancer treatment, as it is required for the proper folding and stabilization of several proteins known to be involved in breast cancer growth and development. These proteins include the epidermal growth factor receptor, human epidermal growth factor receptor 2 (HER2), estrogen receptor (ER), progesterone receptor (PR), and src. 17-Allylamino-17-demethoxygeldanamycin (17-AAG) is an intravenous Hsp90 inhibitor in development for breast cancer treatment. We conducted a phase II study of 17-AAG 220 mg/m(2) on days 1, 4, 8, and 11 every 21 days in patients with metastatic and locally advanced breast cancer. Since we expected the molecular effects of Hsp90 inhibition to extend beyond just ER, PR, and HER2 down regulation and to impact a variety of other cellular proteins, patients were not selected based on ER, PR, or HER2 status. Eleven patients, including 6 patients with triple negative breast cancer, were enrolled and treated. There were no responses and 3 patients had stable disease as their best response. Five patients developed grade 3/4 toxicities, which were primarily hepatic and pulmonary. Based on these results, we do not recommend further study of 17-AAG at this dosing schedule or in unselected breast cancer patients.

Indexed as

AdultAgedAntineoplastic AgentsBenzoquinonesBreast NeoplasmsFemaleHSP90 Heat-Shock ProteinsHumansLactams, MacrocyclicMiddle AgedNeoplasm MetastasisNeoplasm StagingTreatment OutcomeAntineoplastic AgentsBenzoquinonesHSP90 Heat-Shock ProteinsLactams, Macrocyclictanespimycin

Identifiers

PMID22083229
PMCPMC3839045
OpenAlexW2014220379

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.