Evidence map›Paper›PMID 36338734›Full record

ReviewFrontiers in oncology2022

Circulating tumor DNA - A potential aid in the management of chordomas.

Stephen C Frederico, Corbin Darling, Xiaoran Zhang, Sakibul Huq, Sameer Agnihotri, Paul A Gardner, Carl H Snyderman, Eric W Wang, Georgios A Zenonos

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Ecchordosis Physaliphora: Does It Even Exist?AJNR. American journal of neuroradiology · 2023
    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

9 authors at 2 institutions in 1 country.

Stephen C FredericoSchool of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Corbin DarlingSchool of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
Xiaoran ZhangDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA, United States.
Sakibul HuqDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA, United States.
Sameer AgnihotriDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA, United States.
Paul A GardnerDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA, United States.
Carl H SnydermanDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA, United States.
Eric W WangDepartment of Otolaryngology, University of Pittsburgh, Pittsburgh, PA, United States.
Georgios A ZenonosDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA, United States.
University of Pittsburgh · USNeurological Surgery · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chordomas are a locally invasive, low-grade, CNS malignancy that are primarily found in the skull base, spine, and sacrum. They are thought to be derived from notochordal remnants and remain a significant clinical challenge due to their local invasiveness, resistance to chemoradiation, and difficulty in achieving a complete resection. Adjuvant therapy such as proton beam therapy is critical in preventing recurrence in patients who are at high risk, however this treatment is associated with increased risk of complication. Currently, intraoperative observation and imaging findings are used to determine recurrence and success of gross total resection. These methods can be unreliable due to limited operative view, bony and soft tissue involvement, and complex post-operative changes on MRI. Earlier detection of incomplete resection or recurrence will allow for earlier ability to intervene and potentially improve patient outcomes. Circulating-tumor DNA (ctDNA) is cell-free DNA that is released by tumor cells as they undergo cellular turn-over. Monitoring ctDNA has been shown to be more sensitive at predicting residual tumor than imaging in numerous solid malignancies. Furthermore, ctDNA could be detected earlier in peripheral blood as opposed to imaging changes, allowing for earlier intervention. In this review, we intend to give a brief overview of the current state of molecular diagnosis for skull base chordomas. We will then discuss current advances in the utilization of ctDNA for the management of CNS pathologies such as glioblastoma (GBM) and brain metastases. We will also discuss the role ctDNA has in the management of non-CNS pathologies such as osteosarcoma and Ewing sarcoma (EWS). Finally, we will discuss potential implications of ctDNA monitoring for chordoma management.

Indexed as

chordomaclivusctDNADNAskull basetumor

Identifiers

PMID36338734
PMCPMC9632974
OpenAlexW4306930495

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.