Evidence map›Paper›PMID 23362324›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2013

Efficacy, safety, pharmacokinetics, and biomarkers of cediranib monotherapy in advanced hepatocellular carcinoma: a phase II study.

Andrew X Zhu, Marek Ancukiewicz, Jeffrey G Supko, Dushyant V Sahani, Lawrence S Blaszkowsky, Jeffrey A Meyerhardt, Thomas A Abrams, Nadine Jackson McCleary, Pankaj Bhargava, Alona Muzikansky and 8 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00427973 (A Phase II Study of AZD2171 in Hepatocellular Carcinoma), which is not on this map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
6.2field-weighted citation impact, top 3% 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.

NCT00427973 phase2terminatednot on this map

A Phase II Study of AZD2171 in Hepatocellular Carcinoma

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2009 to 2012Enrolled17ConditionsAdult Primary Hepatocellular Carcinoma, Advanced Adult Primary Liver Cancer, Localized Unresectable Adult Primary Liver Cancer, Recurrent Adult Primary Liver CancerArmscediranib maleate, laboratory biomarker analysis, computed tomography, dynamic contrast-enhanced magnetic resonance imaging, pharmacological study
3 · Its place in the literature

Who cites it

40 citing papers in PubMed, 73 citations in OpenAlex.

  1. Trial
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  3. Role of vascular density and normalization in response to neoadjuvant bevacizumab and chemotherapy in breast cancer patients.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Hepatocellular carcinoma: signaling pathways and therapeutic advances.Signal transduction and targeted therapy · 2025
    Review
  10. Small-molecule-based targeted therapy in liver cancer.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Targeted therapy for hepatocellular carcinoma.Signal transduction and targeted therapy · 2020
    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

18 authors at 3 institutions in 1 country.

Andrew X ZhuMassachusetts General Hospital Cancer Center, Boston, Massachusetts 02114, USA. azhu@partners.org
Marek Ancukiewicz
Jeffrey G Supko
Dushyant V Sahani
Lawrence S Blaszkowsky
Jeffrey A Meyerhardt
Thomas A Abrams
Nadine Jackson McCleary
Pankaj Bhargava
Alona Muzikansky
Susan Sheehan
Eileen Regan
Eamala Vasudev
Michelle Knowles
Charles S Fuchs
David P Ryan
Rakesh K Jain
Dan G Duda
Harvard University · USDana-Farber Cancer Institute · USMassachusetts General Hospital · US

Funding

Vascular Normalization: Rolse of Perivascular CellsP01CA080124 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, RAKESH K. · 2000 to 2016
$35.0M
Probing Tumor Microenvironment Using NanotechnologyR01CA126642 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, RAKESH K. · 2008 to 2012
$8.3M
Role of BMDCs in Solid Tumor Growth and RelapseR01CA115767 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, RAKESH K. · 2006 to 2010
$2.2M
Role of SDF1a pathway in prostate cancer relapse and metastasis post-radiotherapyR01CA159258 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DUDA, DAN GABRIEL · 2011 to 2015
$1.6M
Visualizing Immune Responses in vivo: a systems biology approachR21CA139168 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DUDA, DAN GABRIEL · 2009 to 2010
$412k
NCI NIH HHS P01 CA080124NCI NIH HHS P01-CA80124NCI NIH HHS R01 CA115767NCI NIH HHS R01-CA115767NCI NIH HHS R01 CA126642NCI NIH HHS R01-CA126642NCI NIH HHS R01 CA159258NCI NIH HHS R01-CA159258NCI NIH HHS R21 CA139168NCI NIH HHS R21-CA139168
6 · The paper itself

Abstract

purposeWe conducted a single-arm phase II study of cediranib, a pan-VEGFR tyrosine kinase inhibitor, in patients with advanced hepatocellular carcinoma (HCC). EXPERIMENTAL

designPatients with histologically confirmed measurable advanced HCC and adequate hematologic, hepatic, and renal functions received cediranib 30-mg orally once daily (4 weeks/cycle). The primary endpoint was progression-free survival (PFS) rate at 3 months. Other endpoints included response rates, overall survival (OS), pharmacokinetics (PK), and biomarkers for cediranib.

resultsCediranib treatment resulted in an estimated 3-month PFS rate of 77% (60%, 99%). Median PFS was 5.3 (3.5,9.7) months, stable disease was seen in 5/17 patients (29%), and median OS was 11.7 (7.5-13.6) months. Grade 3 toxicities included hypertension (29%), hyponatremia (29%), and hyperbilirubinemia (18%). Cediranib PK were comparable to those seen in cancer patients with normal hepatic function. Plasma levels of VEGF and PlGF increased and sVEGFR1, sVEGFR2, and Ang-2 decreased after cediranib treatment. PFS was inversely correlated with baseline levels of VEGF, sVEGFR2, and bFGF and with on-treatment levels of bFGF and IGF-1, and directly associated with on-treatment levels of IFN-γ. OS was inversely correlated with baseline levels of sVEGFR1, Ang-2, TNF-α, CAIX, and CD34(+)CD133(+)CD45(dim) circulating progenitor cells and on-treatment levels of sVEGFR2.

conclusionsDespite the limitations of primary endpoint selection, cediranib at 30-mg daily showed a high incidence of toxicity and preliminary evidence of antitumor activity in advanced HCC. Hepatic dysfunction did not seem to affect the steady-state PK of cediranib. Exploratory studies suggested proangiogenic and inflammatory factors as potential biomarkers of anti-VEGF therapy in HCC.

Indexed as

AgedCarcinoma, HepatocellularDisease-Free SurvivalDrug-Related Side Effects and Adverse ReactionsFemaleGene Expression Regulation, NeoplasticHumansIndolesLiver NeoplasmsMaleMiddle AgedNeoplasm ProteinsNeoplasm StagingProtein Kinase InhibitorsQuinazolinesVascular Endothelial Growth Factor Receptor-1cediranibIndolesNeoplasm ProteinsProtein Kinase InhibitorsQuinazolinesVascular Endothelial Growth Factor Receptor-1

Identifiers

PMID23362324
PMCPMC3609423
OpenAlexW2113686775

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Registered trials

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.