Evidence map›Paper›PMID 24729732›Full record

ReviewInternational journal of women's health2014

Profile of vintafolide (EC145) and its use in the treatment of platinum-resistant ovarian cancer.

Mathieu Luyckx, Raffaella Votino, Jean-Luc Squifflet, Jean-François Baurain

Open access · goldAbstract readReview
In one paragraph

Review in International journal of women's health, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Delivering living medicines with biomaterials.Nature reviews. Materials · 2025
    Article
  2. Folate Receptor Alpha-A Secret Weapon in Ovarian Cancer Treatment?International journal of molecular sciences · 2024
    Review
  3. Article
  4. Review
  5. Folate Receptor α-TargetedMolecular pharmaceutics · 2019
    Article
  6. Article
  7. Anti-Folate Receptor Alpha-Directed Antibody Therapies Restrict the Growth of Triple-negative Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  8. Article
  9. Article
  10. 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

4 authors at 1 institution in 2 countries.

Mathieu LuyckxGynecology and Andrology Unit, Cliniques Universitaires Saint-Luc, Brussels, Belgium ; Centre du cancer, Gynecologic Oncology Group, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Raffaella VotinoGynecology and Andrology Unit, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Jean-Luc SquiffletGynecology and Andrology Unit, Cliniques Universitaires Saint-Luc, Brussels, Belgium ; Centre du cancer, Gynecologic Oncology Group, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Jean-François BaurainCentre du cancer, Gynecologic Oncology Group, Cliniques Universitaires Saint-Luc, Brussels, Belgium ; Medical Oncology Unit, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Gynecologic Oncology Group · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveOur aim was to review the profile of vintafolide (EC145) and its rationale for use in platinum-resistant ovarian cancer. First we investigated the folate receptors (FRs), folate's pathway into cells, and its expression in normal and cancerous cells, before detailing the mechanism of action of vintafolide, its clinical applications, and the results of different study phases. MATERIALS AND

methodsA literature search was conducted through PubMed/Medline, Google, ClinicalTrials.gov and websites of pharmaceutical companies. Only articles in English were selected. All articles investigating folate receptor expression in ovarian cancer were selected first, than articles reviewing platinum resistance. Papers about vintafolide were collected, while those talking about synthesis and biochemistry concerns were excluded. The different Phase I and II studies were read, and an update on the website of pharmaceuticals companies were added.

resultsFR is a bundle-membrane receptor that is expressed normally in some normal tissues on the apical surface of cells, but highly expressed in ovarian cancer cells (>80%). It collects folate through endocytosis. Chemotherapy does not modify its expression in ovarian cancer cells, and its expression appears to be mostly associated with a poor prognosis and platinum resistance. Vintafolide is a folate-desacetylvinblastine monohydrazide conjugate, allowing a liberation of the drug into the cytoplasm of cancerous cells via the FR-α (FRα) and endocytosis, with high specificity. Phase I studies showed a 2.5 mg bolus dose to be nontoxic, with moderately adverse events. Phase II clinical trials for the first time demonstrated a statistically significant improvement in disease-free survival in patients with platinum-resistant ovarian cancer, and in those with a very poor prognosis who had already received three to four lines of systemic chemotherapy. The greater benefits were observed in patients with highly expressed FRα.

conclusionVintafolide is a promising targeted agent for recurrent platinum-resistant ovarian cancer, first, thanks to its mechanism of action and the characteristics of FRα in ovarian cancer, and, second, because of the favorable results observed in the first clinical trials on platinum-resistant ovarian cancer. Phase III clinical trials are currently ongoing and are expected to confirm these results.

Indexed as

chemotherapyfolate receptorplatinum-resistant ovarian cancer

Identifiers

PMID24729732
PMCPMC3976235
OpenAlexW2045420218

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.