Evidence map›Paper›PMID 25592088›Full record

ReviewClinical therapeutics2015

Exploring the therapeutic rationale for angiogenesis blockade in cervical cancer.

Lauren S Krill, Krishnansu S Tewari

Abstract readReview
In one paragraph

Review in Clinical therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Circular RNAs and Cancers.Advances in experimental medicine and biology · 2025
    Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. The Interaction Between Human Papillomaviruses and the Stromal Microenvironment.Progress in molecular biology and translational science · 2016
    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

2 authors at 1 institution in 1 country.

Lauren S KrillThe Division of Gynecologic Oncology, University of California, Irvine Medical Center, Orange, California.
Krishnansu S TewariThe Division of Gynecologic Oncology, University of California, Irvine Medical Center, Orange, California. Electronic address: ktewari@uci.edu.
University of California, Irvine Medical Center · US

Funding

Novel biologic markers of treatment resistance in locally advanced cervical carciR21CA156032 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI FRUEHAUF, JOHN P, TEWARI, KRISHNANSU SUJATA · 2011 to 2012
$359k
NCI NIH HHS R21 CA156032
6 · The paper itself

Abstract

purposeThis review highlights the molecular and pathologic evidence that cervical cancer is driven by angiogenesis and presents a summary of the recent clinical research in antiangiogenesis therapy for advanced cervical cancer with a focus on the use of bevacizumab.

methodsThe articles chosen for this review reveal the rationale for antiangiogenesis agents in cervical cancer from 3 perspectives: pathologic, molecular, and clinical data.

findingsSeveral translational investigations have revealed that proangiogenic signaling cascades are active in cervical carcinogenesis and can be used to improve patient outcomes in advanced disease. For example, in a recently published study of patients with recurrent and metastatic cervical cancer, bevacizumab was the first targeted agent to improve overall survival in a gynecologic cancer when successfully combined with 2 different chemotherapy regimens. IMPLICATIONS: Because of recent advances in screening, aggressive management of cervical intraepithelial neoplasia, and human papillomavirus vaccination, cervical cancer is preventable and curable with radical surgery plus lymphadenectomy surgery or chemoradiation plus brachytherapy if detected early. Unfortunately, for patients with metastatic or recurrent disease, effective therapeutic options are limited for this aggressive life-threatening condition. However, molecularly targeted agents have provided a critical opportunity to improve patient outcomes beyond optimizing cytotoxic chemotherapy regimens so that they may benefit from other agents or emergent therapies in the future.

Indexed as

Angiogenesis InhibitorsBevacizumabFemaleHumansTreatment OutcomeUterine Cervical NeoplasmsAngiogenesis InhibitorsBevacizumabangiogenesisanti-angiogenesis therapybevacizumabrecurrent cervical cancertherapeutic rationale

Identifiers

PMID25592088
PMCPMC5581982
OpenAlexW2050415197

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.