Evidence map›Paper›PMID 29218795›Full record

ArticleCPT: pharmacometrics & systems pharmacology2018

Revisiting Bevacizumab + Cytotoxics Scheduling Using Mathematical Modeling: Proof of Concept Study in Experimental Non-Small Cell Lung Carcinoma.

Diane-Charlotte Imbs, Raouf El Cheikh, Arnaud Boyer, Joseph Ciccolini, Céline Mascaux, Bruno Lacarelle, Fabrice Barlesi, Dominique Barbolosi, Sébastien Benzekry

Abstract read
In one paragraph

Article in CPT: pharmacometrics & systems pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Efficient simulation of clinical target response surfaces.CPT: pharmacometrics & systems pharmacology · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Pharmacodynamic Drug-Drug Interactions.Clinical pharmacology and therapeutics · 2019
    Review
  13. 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

9 authors.

Diane-Charlotte ImbsSMARTc Unit, Inserm S_911 CRO2, Aix-Marseille University, Marseille, France.
Raouf El CheikhSMARTc Unit, Inserm S_911 CRO2, Aix-Marseille University, Marseille, France.
Arnaud BoyerSMARTc Unit, Inserm S_911 CRO2, Aix-Marseille University, Marseille, France.
Joseph CiccoliniSMARTc Unit, Inserm S_911 CRO2, Aix-Marseille University, Marseille, France.
Céline MascauxSMARTc Unit, Inserm S_911 CRO2, Aix-Marseille University, Marseille, France.
Bruno LacarelleSMARTc Unit, Inserm S_911 CRO2, Aix-Marseille University, Marseille, France.
Fabrice BarlesiSMARTc Unit, Inserm S_911 CRO2, Aix-Marseille University, Marseille, France.
Dominique BarbolosiSMARTc Unit, Inserm S_911 CRO2, Aix-Marseille University, Marseille, France.
Sébastien BenzekryMONC Team, Inria Bordeaux Sud-Ouest, Talence, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Concomitant administration of bevacizumab and pemetrexed-cisplatin is a common treatment for advanced nonsquamous non-small cell lung cancer (NSCLC). Vascular normalization following bevacizumab administration may transiently enhance drug delivery, suggesting improved efficacy with sequential administration. To investigate optimal scheduling, we conducted a study in NSCLC-bearing mice. First, experiments demonstrated improved efficacy when using sequential vs. concomitant scheduling of bevacizumab and chemotherapy. Combining this data with a mathematical model of tumor growth under therapy accounting for the normalization effect, we predicted an optimal delay of 2.8 days between bevacizumab and chemotherapy. This prediction was confirmed experimentally, with reduced tumor growth of 38% as compared to concomitant scheduling, and prolonged survival (74 vs. 70 days). Alternate sequencing of 8 days failed in achieving a similar increase in efficacy, thus emphasizing the utility of modeling support to identify optimal scheduling. The model could also be a useful tool in the clinic to personally tailor regimen sequences.

Indexed as

Models, TheoreticalAnimalsAntineoplastic Combined Chemotherapy ProtocolsBevacizumabCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationDrug Administration ScheduleHumansLung NeoplasmsMiceProof of Concept StudyXenograft Model Antitumor AssaysBevacizumab

Identifiers

PMID29218795
PMCPMC5784740

What OpenQuestion holds

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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.