Evidence map›Paper›PMID 25605928›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2015

Improved tumor vascularization after anti-VEGF therapy with carboplatin and nab-paclitaxel associates with survival in lung cancer.

Rebecca S Heist, Dan G Duda, Dushyant V Sahani, Marek Ancukiewicz, Panos Fidias, Lecia V Sequist, Jennifer S Temel, Alice T Shaw, Nathan A Pennell, Joel W Neal and 4 more

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

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
10.9field-weighted citation impact, top 1% 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

71 citing papers in PubMed, 123 citations in OpenAlex.

  1. Trial
  2. A Phase II and Biomarker Study of Sorafenib Combined with Modified FOLFOX in Patients with Advanced Hepatocellular Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Trial
  3. Trial
  4. 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
  5. Review
  6. Detecting vascular normalization in epithelial ovarian cancer.Medical oncology (Northwood, London, England) · 2025
    Review
  7. Review
  8. Article
  9. Current trends in the characterization and monitoring of vascular response to cancer therapy.Cancer imaging : the official publication of the International Cancer Imaging Society · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Molecular Mechanisms and Future Implications of VEGF/VEGFR in Cancer Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Review
  14. Article
  15. Multiphoton Phosphorescence Quenching Microscopy Reveals Kinetics of Tumor Oxygenation during Antiangiogenesis and Angiotensin Signaling Inhibition.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  16. Towards Immunotherapy-Induced Normalization of the Tumor Microenvironment.Frontiers in cell and developmental biology · 2022
    Review
  17. Article
  18. Review
  19. Review
  20. Review

11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 1 country.

Rebecca S HeistDepartments of Medicine, rheist@partners.org jain@steele.mgh.harvard.edu.
Dan G DudaRadiation Oncology, and.
Dushyant V SahaniRadiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114;
Marek AncukiewiczRadiation Oncology, and.
Panos FidiasDepartment of Medical Oncology, University of Arizona Cancer Center at Dignity, Phoenix, AZ 85013;
Lecia V SequistDepartments of Medicine.
Jennifer S TemelDepartments of Medicine.
Alice T ShawDepartments of Medicine.
Nathan A PennellDepartment of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH 44195;
Joel W NealDepartment of Medicine, Division of Oncology, Stanford University/Stanford Cancer Institute, Palo Alto, CA 94305;
Leena GandhiDepartment of Adult Oncology, Dana-Farber Cancer Institute, Boston, MA 02115; and.
Thomas J LynchDepartment of Medical Oncology, Yale Cancer Center, New Haven, CT 06520.
Jeffrey A EngelmanDepartments of Medicine.
Rakesh K JainRadiation Oncology, and rheist@partners.org jain@steele.mgh.harvard.edu.
Radiation Oncology Associates · USCleveland Clinic · USDana-Farber Cancer Institute · USMassachusetts General Hospital · USStanford Cancer InstituteUniversity of Arizona · USYale Cancer Center · US

Funding

Vascular Normalization: Rolse of Perivascular CellsP01CA080124 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, RAKESH K. · 2000 to 2016
$35.0M
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
NCI NIH HHS P01 CA080124NCI NIH HHS P01CA080124NCI NIH HHS R01 CA159258NCI NIH HHS R01CA159258
6 · The paper itself

Abstract

Addition of anti-VEGF antibody therapy to standard chemotherapies has improved survival and is an accepted standard of care for advanced non-small cell lung cancer (NSCLC). However, the mechanisms by which anti-VEGF therapy increases survival remain unclear. We evaluated dynamic CT-based vascular parameters and plasma cytokines after bevacizumab alone and after bevacizumab plus chemotherapy with carboplatin and nab-paclitaxel in advanced NSCLC patients to explore potential biomarkers of treatment response and resistance to this regimen. Thirty-six patients were enrolled in this study. The primary end point was 6-mo progression-free survival rate, which was 74% (95% CI: 57, 97). This regimen has a promising overall response rate of 36% and median time to progression of 8.5 (6.0, 38.7) mo and overall survival of 12.2 (9.6, 44.1) mo. We found that anti-VEGF therapy led to a sustained increase in plasma PlGF, a potential pharmacodynamic marker. We also found that higher levels of soluble VEGFR1 measured before starting bevacizumab with chemotherapy were associated with worse survival, supporting its potential role as biomarker of treatment resistance. Our imaging biomarker studies indicate that bevacizumab-based treatment-while reducing blood flow, volume, and permeability in the overall population-may be associated with improved survival in patients with improved tumor vasculature and blood perfusion after treatment. This hypothesis-generating study supports the notion that excessively decreasing vascular permeability and pruning/rarefaction after bevacizumab therapy may negatively impact the outcome of combination therapy in NSCLC patients. This hypothesis warrants further dose-titration studies of bevacizumab to examine the dose effect on tumor vasculature and treatment efficacy.

Indexed as

AlbuminsAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBevacizumabBiomarkers, TumorCarboplatinCarcinoma, Non-Small-Cell LungFemaleHumansLung NeoplasmsMaleMiddle AgedNeovascularization, PathologicPaclitaxelVascular Endothelial Growth Factor A130-nm albumin-bound paclitaxelAlbuminsAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedBevacizumabBiomarkers, TumorCarboplatinPaclitaxelVascular Endothelial Growth Factor Aantiangiogenesisbioimaginglung cancer

Identifiers

PMID25605928
PMCPMC4321320
OpenAlexW1981486151

What OpenQuestion holds

Textmetadata
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.