Evidence map›Paper›PMID 31285369›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2019

A Phase 0 Trial of Ribociclib in Recurrent Glioblastoma Patients Incorporating a Tumor Pharmacodynamic- and Pharmacokinetic-Guided Expansion Cohort.

An-Chi Tien, Jing Li, Xun Bao, Alanna Derogatis, Seongho Kim, Shwetal Mehta, Nader Sanai

Abstract readClinical Trial
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Guideline
  2. A Phase 0 Trial of Ribociclib in Recurrent Glioblastoma Patients Incorporating a Tumor Pharmacodynamic- and Pharmacokinetic-Guided Expansion Cohort.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
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9 more citing papers are in PubMed but not listed here.

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.

An-Chi TienIvy Brain Tumor Center, Barrow Neurological Institute, Phoenix, Arizona.
Jing LiIvy Brain Tumor Center, Barrow Neurological Institute, Phoenix, Arizona.
Xun BaoKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan.
Alanna DerogatisIvy Brain Tumor Center, Barrow Neurological Institute, Phoenix, Arizona.
Seongho KimKarmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan.
Shwetal MehtaIvy Brain Tumor Center, Barrow Neurological Institute, Phoenix, Arizona.
Nader SanaiIvy Brain Tumor Center, Barrow Neurological Institute, Phoenix, Arizona. Nader.Sanai@barrowbrainandspine.com.
The Barbara Ann Karmanos Cancer Institute · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
UCLA SPORE in Brain CancerP50CA211015 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI David A. Nathanson · 2017 to 2026
$25.2M
NCI NIH HHS P30 CA022453NCI NIH HHS P50 CA211015
6 · The paper itself

Abstract

purposeCDK4/6-dependent cell-cycle regulation is disrupted in most glioblastomas. This study assesses the central nervous system (CNS) pharmacokinetics and tumor pharmacodynamics of ribociclib, a highly selective CDK4/6 inhibitor, in patients with recurrent glioblastoma. PATIENTS AND

methodsPatients with recurrent glioblastoma with intact retinoblastoma protein (RB) expression and

resultsTwelve patients were enrolled. The mean unbound ribociclib concentrations in CSF, nonenhancing, and enhancing tumor regions were 0.374 μmol/L, 0.560, and 2.152 μmol/kg, respectively, which were more than 5-fold the

conclusionsRibociclib exhibited good CNS penetration, and target modulation was indicated by inhibition of RB phosphorylation and tumor proliferation. Ribociclib monotherapy showed limited clinical efficacy in patients with recurrent glioblastoma. Combination therapy with CDK4/6 and PI3K/mTOR inhibitors may be explored for treating recurrent glioblastoma.

Indexed as

AdultAgedAged, 80 and overAminopyridinesBiomarkers, TumorBrain NeoplasmsCell ProliferationCohort StudiesFemaleGlioblastomaHumansMaleMiddle AgedNeoplasm Recurrence, LocalPhosphorylationProgression-Free SurvivalAminopyridinesBiomarkers, TumorProtein Kinase InhibitorsPurinesRB1 protein, humanRetinoblastoma Binding ProteinsribociclibUbiquitin-Protein Ligases

Identifiers

PMID31285369
PMCPMC6863147
OpenAlexW2961134062

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.