Evidence map›Paper›PMID 19399750›Full record

ArticleHead & neck2009

Sequence dependence of cell growth inhibition by EGFR-tyrosine kinase inhibitor ZD1839, docetaxel, and cisplatin in head and neck cancer.

Carmen M Klass, Mi Sun Choe, Selwyn J Hurwitz, Mourad Tighiouart, Xin Zhang, Zhuo Georgia Chen, Dong M Shin

Open access · greenAbstract read
In one paragraph

Article in Head & neck, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. EGFR inhibitor enhances cisplatin sensitivity of human glioma cells.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2011
    Article
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 3 institutions in 1 country.

Carmen M KlassDepartment of Hematology and Medical Oncology, Winship Cancer Institute, Atlanta, Georgia 30322, USA.
Mi Sun Choe
Selwyn J Hurwitz
Mourad Tighiouart
Xin Zhang
Zhuo Georgia Chen
Dong M Shin
Piedmont Cancer Institute · USEmory University · USWinship Cancer Institute

Funding

TARGETING DEATH RECEPTOR-MEDIATED APOPTOSIS FOR HEAD AND NECK CANCERP50CA128613 · NCI · EMORY UNIVERSITY · PI SHIN, DONG M · 2007 to 2011
$12.0M
Chemoprevention of the Head and Neck Cancer with ZD1839*U01CA101244 · NCI · EMORY UNIVERSITY · PI SHIN, DONG M · 2004 to 2008
$3.1M
Second Primary Tumor Prevention w/EGFR TKIs & COX-2 inhibitors in H & N CancerR01CA112643 · NCI · EMORY UNIVERSITY · PI SHIN, DONG M · 2006 to 2011
$1.6M
NCI NIH HHS P50 CA128613NCI NIH HHS R01 CA112643NCI NIH HHS U01 CA101244PHS HHS U01 101244
6 · The paper itself

Abstract

backgroundThis study was to explore whether the efficacy of the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor ZD1839 (Z, Iressa, gefitinib) plus chemotherapeutic agents docetaxel (D) and cisplatin (P) may benefit from sequencing of the combination.

methodsThree head and neck cancer cell lines were used to study the effect of various combinations of and relative sequencing of D, P, and Z in cell growth inhibition. A population pharmacokinetic stimulation study was conducted on Z in silico and used together with the growth inhibition data to derive principles for future in vivo use of this drug combination.

resultsThe inhibitory effects of Z on combinations of D and P were sequence dependent. Treatment simultaneously with DPZ or with DP followed by Z (DP-->Z) showed synergistic effects in all 3 cell lines. However, sequencing with Z followed by DP (Z-->DP), gave an antagonistic effect, suggesting that D and P should be administered when the effect of Z is low. The induction of apoptosis was also sequence dependent. The in silico pharmacokinetic study suggested the feasibility of deriving a 5-day-on/2-day-off regimen for Z, in which D and P administration commences when levels of Z are low, allowing levels of Z to accumulate sufficiently during the remainder of the cycle.

conclusionThese data suggests that it is feasible to design clinical trials with these settings to maximize the efficacy of this combined drug regimen.

Indexed as

Annexin A5Antineoplastic AgentsApoptosisCell CycleCell Line, TumorCisplatinDocetaxelDose-Response Relationship, DrugEnzyme InhibitorsErbB ReceptorsGefitinibHumansPhosphorylationProtein Kinase InhibitorsQuinazolinesSignal TransductionAnnexin A5Antineoplastic AgentsCisplatinDocetaxelEnzyme InhibitorsErbB ReceptorsGefitinibProtein Kinase InhibitorsQuinazolinesTaxoids

Identifiers

PMID19399750
PMCPMC3600558
OpenAlexW2165375378

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.