Evidence map›Paper›PMID 32605050›Full record

ArticleJournal of clinical medicine2020

Tumor Volume Dynamics as an Early Biomarker for Patient-Specific Evolution of Resistance and Progression in Recurrent High-Grade Glioma.

Daniel J Glazar, G Daniel Grass, John A Arrington, Peter A Forsyth, Natarajan Raghunand, Hsiang-Hsuan Michael Yu, Solmaz Sahebjam, Heiko Enderling

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02313272 (A Phase I Trial of Hypofractionated Stereotactic Irradiation), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 13% 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.

NCT02313272 phase1completednot on this map

A Phase I Trial of Hypofractionated Stereotactic Irradiation (HFSRT) With Pembrolizumab and Bevacizumab in Patients With Recurrent High Grade Gliomas

TypeinterventionalSponsorH. Lee Moffitt Cancer Center and Research InstituteRan2015 to 2021Enrolled32ConditionsMalignant GliomaArmsHypofractionated Stereotactic Irradiation (HFSRT), Pembrolizumab, Bevacizumab
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  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

8 authors at 2 institutions in 1 country.

Daniel J GlazarDepartment of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.ORCID 0000-0003-3031-8629
G Daniel GrassDepartment of Radiation Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
John A ArringtonDepartment of Oncologic Sciences, University of South Florida, Tampa, FL 33612, USA.
Peter A ForsythDepartment of Oncologic Sciences, University of South Florida, Tampa, FL 33612, USA.
Natarajan RaghunandDepartment of Oncologic Sciences, University of South Florida, Tampa, FL 33612, USA.ORCID 0000-0002-8893-7687
Hsiang-Hsuan Michael YuDepartment of Radiation Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.ORCID 0000-0002-0621-9519
Solmaz SahebjamDepartment of Oncologic Sciences, University of South Florida, Tampa, FL 33612, USA.
Heiko EnderlingDepartment of Integrated Mathematical Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.ORCID 0000-0002-9696-6410
University of South Florida · USMoffitt Cancer Center · US

Funding

Developing mathematical model driven optimized recurrent glioblastoma therapiesR21CA263911 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI YU, HSIANG-HSUAN MICHAEL · 2021 to 2022
$420k
American Society of Clinical Oncology Conquer Cancer Foundation Career Development AwardMerck investigator-initiated trial (NCT02313272)NCI NIH HHS R21 CA263911
6 · The paper itself

Abstract

Recurrent high-grade glioma (HGG) remains incurable with inevitable evolution of resistance and high inter-patient heterogeneity in time to progression (TTP). Here, we evaluate if early tumor volume response dynamics can calibrate a mathematical model to predict patient-specific resistance to develop opportunities for treatment adaptation for patients with a high risk of progression. A total of 95 T1-weighted contrast-enhanced (T1post) MRIs from 14 patients treated in a phase I clinical trial with hypo-fractionated stereotactic radiation (HFSRT; 6 Gy × 5) plus pembrolizumab (100 or 200 mg, every 3 weeks) and bevacizumab (10 mg/kg, every 2 weeks; NCT02313272) were delineated to derive longitudinal tumor volumes. We developed, calibrated, and validated a mathematical model that simulates and forecasts tumor volume dynamics with rate of resistance evolution as the single patient-specific parameter. Model prediction performance is evaluated based on how early progression is predicted and the number of false-negative predictions. The model with one patient-specific parameter describing the rate of evolution of resistance to therapy fits untrained data ( R 2 = 0.70 ). In a leave-one-out study, for the nine patients that had T1post tumor volumes ≥1 cm

Indexed as

high-grade gliomamathematical modelpatient-specificresponse prediction

Identifiers

PMID32605050
PMCPMC7409184
OpenAlexW3037264776

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.