Evidence map›Paper›PMID 17383529›Full record

ArticleSurgery2007

Use of an oncolytic virus secreting GM-CSF as combined oncolytic and immunotherapy for treatment of colorectal and hepatic adenocarcinomas.

Sandeep Malhotra, Teresa Kim, Jonathan Zager, Joseph Bennett, Michael Ebright, Michael D'Angelica, Yuman Fong

Open access · greenAbstract read
In one paragraph

Article in Surgery, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Review
  3. Molecular Circuits of Immune Sensing and Response to Oncolytic Virotherapy.International journal of molecular sciences · 2024
    Review
  4. Review
  5. Construction and application of adenoviral vectors.Molecular therapy. Nucleic acids · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Strategies to sensitize cancer cells to immunotherapy.Human vaccines & immunotherapeutics · 2021
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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 1 institution in 1 country.

Sandeep MalhotraDepartment of Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Teresa Kim
Jonathan Zager
Joseph Bennett
Michael Ebright
Michael D'Angelica
Yuman Fong
Memorial Sloan Kettering Cancer Center · US

Funding

Liver Regeneration in Man--Effects or Adjuvant TherapyR01CA075416 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI FONG, YUMAN · 1997 to 2005
$1.5M
CLINICAL AND BIOLOGICAL BASIS OF 18F-FDG PET IN CANCERR01CA080982 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI FONG, YUMAN · 1999 to 2001
$843k
ACCELERATION OF TUMOR GROWTH BY LIVER RESECTIONR01CA072632 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI FONG, YUMAN · 1997 to 1999
–
NCI NIH HHS R01 CA072632NCI NIH HHS R01 CA075416
6 · The paper itself

Abstract

backgroundOncolytic cancer therapy using herpes simplex viruses (HSV) that have direct tumoricidal effects and cancer immunotherapy using the cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF) have each been effective in preclinical testing. NV1034 is a multimutated oncolytic HSV carrying the gene for murine GM-CSF that attempts to combine these 2 anticancer strategies. The purpose of this study was to compare NV1034 to NV1023, the parent HSV mutants lacking GM-CSF, to determine if such combined oncolytic and immunotherapy using a single vector has advantages over oncolytic therapy alone.

methodsExpression GM-CSF in vitro did not alter the infectivity, cytotoxicity, or replication of NV1034 compared to the noncytokine-secreting control. Tumors infected with NV1034 produced GM-CSF in picogram quantities. In vivo efficacy of the viruses against murine colorectal carcinoma CT26 and murine hepatoma Hepa l-6 was then tested in subcutaneous tumors in syngeneic Balb/c and C57 L/J mice, respectively. In these immune-competent models, NV1034 and NV1023 each demonstrated potent antitumor activity.

resultsTreatment with NV1034 had significantly better antitumor effect compared to treatment with NV1023. Furthermore, there was no difference in the antitumor efficacy of these viruses in mice depleted of CD4+ and CD8+ T lymphocytes.

conclusionsViral vectors combining oncolytic and immunotherapy are promising agents in treatment of colorectal carcinoma and hepatoma.

Indexed as

Oncolytic VirotherapyAdenocarcinomaAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorColorectal NeoplasmsGranulocyte-Macrophage Colony-Stimulating FactorImmunotherapyLiver NeoplasmsLymphocyte DepletionMiceMice, Inbred BALB CNeoplasms, ExperimentalSecondary PreventionSimplexvirusGranulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID17383529
PMCPMC2559995
OpenAlexW2062490338

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.