Evidence map›Paper›PMID 22047770›Full record

Trial reportGynecologic oncology2012

A phase II study of gemcitabine in combination with tanespimycin in advanced epithelial ovarian and primary peritoneal carcinoma.

Andrea E Wahner Hendrickson, Ann L Oberg, Gretchen Glaser, John K Camoriano, Prema P Peethambaram, Gerardo Colon-Otero, Charles Erlichman, S Percy Ivy, Scott H Kaufmann, Larry M Karnitz and 1 more

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

Trial report in Gynecologic oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
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  13. Interventions for cough in cancer.The Cochrane database of systematic reviews · 2015
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  18. Network analysis identifies an HSP90-central hub susceptible in ovarian cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Article
  19. 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 5 institutions in 1 country.

Andrea E Wahner HendricksonDivision of Medical Oncology, Mayo Clinic, Rochester, MN 55905, USA.
Ann L Oberg
Gretchen Glaser
John K Camoriano
Prema P Peethambaram
Gerardo Colon-Otero
Charles Erlichman
S Percy Ivy
Scott H Kaufmann
Larry M Karnitz
Paul Haluska
Mayo Clinic in Arizona · USMayo Clinic in Florida · USMayo Clinic · USNational Cancer Institute · USWinnMed · US

Funding

Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
Therapeutic targeting of HSP90-dependent singnalingR01CA104378 · NCI · MAYO CLINIC ROCHESTER · PI KARNITZ, LARRY M · 2004 to 2008
$1.4M
NCI NIH HHS K12 CA090628NCI NIH HHS N01 CM062205NCI NIH HHS N01-CM 62205NCI NIH HHS P50 CA136393NCI NIH HHS R01 CA104378
6 · The paper itself

Abstract

objectiveTo evaluate the efficacy and biological effects of the gemcitabine/tanespimycin combination in patients with advanced ovarian and peritoneal cancer. To assess the effect of tanespimycin on tumor cells, levels of the chaperone proteins HSP90 and HSP70 were examined in peripheral blood mononuclear cells (PBMC) and paired tumor biopsy lysates.

methodsTwo-cohort phase II clinical trial. Patients were grouped according to prior gemcitabine therapy. All participants received tanespimycin 154 mg/m(2) on days 1 and 9 of cycle 1 and days 2 and 9 of subsequent cycles. Patients also received gemcitabine 750 mg/m(2) on day 8 of the first treatment cycle and days 1 and 8 of subsequent cycles.

resultsThe tanespimycin/gemcitabine combination induced a partial response in 1 gemcitabine naïve patient and no partial responses in gemcitabine resistant patients. Stable disease was seen in 6 patients (2 gemcitabine naïve and 4 gemcitabine resistant). The most common toxicities were hematologic (anemia and neutropenia) as well as nausea and vomiting. Immunoblotting demonstrated limited upregulation of HSP70 but little or no change in levels of most client proteins in PBMC and paired tumor samples.

conclusionsAlthough well tolerated, the tanespimycin/gemcitabine combination exhibited limited anticancer activity in patients with advanced epithelial ovarian and primary peritoneal carcinoma, perhaps because of failure to significantly downregulate the client proteins at clinically achievable exposures.

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsBenzoquinonesBiomarkers, TumorCarcinoma, Ovarian EpithelialCell Line, TumorCohort StudiesDeoxycytidineFemaleGemcitabineHSP70 Heat-Shock ProteinsHSP90 Heat-Shock ProteinsHumansLactams, MacrocyclicMiddle AgedBenzoquinonesBiomarkers, TumorDeoxycytidineGemcitabineHSP70 Heat-Shock ProteinsHSP90AB1 protein, humanHSP90 Heat-Shock ProteinsLactams, Macrocyclictanespimycin

Identifiers

PMID22047770
PMCPMC3265019
OpenAlexW1998044332

What OpenQuestion holds

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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.