Evidence map›Paper›PMID 39087065›Full record

ArticleJournal of radiosurgery and SBRT2024

Impact of

Jim X Leng, Chang Su, David J Carpenter, Warren Floyd, Eugene Vaios, Rachel Shenker, Peter G Hendrickson, Will Giles, Trey Mullikin, Scott R Floyd and 3 more

Abstract read
In one paragraph

Article in Journal of radiosurgery and SBRT, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Jim X LengDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Chang SuDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
David J CarpenterDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Warren FloydDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Eugene VaiosDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Rachel ShenkerDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Peter G HendricksonDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Will GilesDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Trey MullikinDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Scott R FloydDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
John P KirkpatrickDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.
Michelle GreenDepartment of Pathology, Duke University Medical Center, Durham, NC, 27710, USA.
Zachary J ReitmanDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27710, USA.

Funding

Duke Radiation Oncology and Radiology Stimulating Access to Research in ResidencyR38CA245204 · NCI · DUKE UNIVERSITY · PI FLOYD, SCOTT R · 2020 to 2023
$1.4M
Enhancing the efficacy of Radiation Therapy for brainstem glioma by targeting ATMK08CA256045 · NCI · DUKE UNIVERSITY · PI Zachary Reitman · 2022 to 2026
$1.1M
NCI NIH HHS K08 CA256045NCI NIH HHS R38 CA245204
6 · The paper itself

Abstract

Purpose: To investigate whether TP53 variants may be correlated with overall survival and local control following stereotactic radiosurgery (SRS) for brain metastases (BMs) from non-small cell lung cancer (NSCLC). Methods: Patients undergoing an initial course of SRS for NSCLC brain metastases between 1/2015 and 12/2020 were retrospectively identified. Overall survival and freedom from local intracranial progression (FFLIP) were estimated via Kaplan-Meier method. Cox models assessed TP53 variant status (pathogenic variant, PV; variant not detected, ND). Results: 255 patients underwent molecular profiling for TP53, among whom 144 (56%) had a TP53 PV. Median follow-up was 11.6 months. OS was not significantly different across TP53 status. A trend toward superior FFLIP was observed for PV (95% CI 62.9 months-NR) versus ND patients (95% CI 29.4 months-NR; p=0.06). Superior FFLIP was observed for patients with one TP53 variant versus those with TP53 ND. Conclusion: Among NSCLC patients with BMs, the potential association between TP53 status and post-SRS FFLIP warrants further investigation in a larger prospective cohort.

Indexed as

brain metastasesNSCLCSRSTP53

Identifiers

PMID39087065
PMCPMC11288656

What OpenQuestion holds

Textmetadata
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.