Evidence map›Paper›PMID 39335124›Full record

ReviewCancers2024

Therapeutic Opportunities for Biomarkers in Metastatic Spine Tumors.

Christian Schroeder, Beatrice Campilan, Owen P Leary, Jonathan Arditi, Madison J Michles, Rafael De La Garza Ramos, Oluwaseun O Akinduro, Ziya L Gokaslan, Margot Martinez Moreno, Patricia L Zadnik Sullivan

Abstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Christian SchroederDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
Beatrice CampilanDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.ORCID 0000-0003-1687-3474
Owen P LearyDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
Jonathan ArditiDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
Madison J MichlesDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
Rafael De La Garza RamosDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.ORCID 0000-0002-5536-2514
Oluwaseun O AkinduroDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
Ziya L GokaslanDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
Margot Martinez MorenoDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.ORCID 0000-0003-1137-1651
Patricia L Zadnik SullivanDepartment of Neurosurgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For many spine surgeons, patients with metastatic cancer are often present in an emergent situation with rapidly progressive neurological dysfunction. Since the Patchell trial, scoring systems such as NOMS and SINS have emerged to guide the extent of surgical excision and fusion in the context of chemotherapy and radiation therapy. Yet, while multidisciplinary decision-making is the gold standard of cancer care, in the middle of the night, when a patient needs spinal surgery, the wealth of chemotherapy data, clinical trials, and other medical advances can feel overwhelming. The goal of this review is to provide an overview of the relevant molecular biomarkers and therapies driving patient survival in lung, breast, prostate, and renal cell cancer. We highlight the molecular differences between primary tumors (i.e., the patient's original lung cancer) and the subsequent spinal metastasis. This distinction is crucial, as there are limited data investigating how metastases respond to their primary tumor's targeted molecular therapies. Integrating information from primary and metastatic markers allows for a more comprehensive and personalized approach to cancer treatment.

Indexed as

molecular markersmolecular therapyprimary tumorspinal metastasestargeted therapy

Identifiers

PMID39335124
PMCPMC11430692

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.