Evidence map›Paper›PMID 30810980›Full record

Trial reportAnnals of nuclear medicine2019

The use of 3'-deoxy-3'-

Benjamin E Ueberroth, Jawana M Lawhorn-Crews, Lance K Heilbrun, Daryn W Smith, Janice Akoury, Rouba Ali-Fehmi, Nicole T Eiseler, Anthony F Shields

Abstract readClinical Trial
In one paragraph

Trial report in Annals of nuclear medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Observational
  2. Review
  3. Article
  4. Article
  5. STING-driven interferon signaling triggers metabolic alterations in pancreas cancer cells visualized by [Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  6. Breast cancer research : BCR · 2021
    Article
  7. Interest and Limits of [Frontiers in oncology · 2021
    Review
  8. 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.

Benjamin E UeberrothWayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA. fx4638@wayne.edu.ORCID http://orcid.org/0000-0001-8882-2348
Jawana M Lawhorn-CrewsWayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA.
Lance K HeilbrunWayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA.
Daryn W SmithKarmanos Cancer Institute, 4100 John R St, Detroit, MI, 48201, USA.
Janice AkouryWayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA.
Rouba Ali-FehmiWayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA.
Nicole T EiselerWayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA.
Anthony F ShieldsWayne State University School of Medicine, 540 E Canfield St, Detroit, MI, 48201, USA.

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
NCI NIH HHS P30 CA022453
6 · The paper itself

Abstract

objectiveTo assess the role of serial FLT-PET scans during early neoadjuvant treatment as a prognostic marker of response to treatment and survival.

methodsThis study is a prospective cohort study which draws from a larger original study which examined the utility of FLT-PET imaging across multiple cancers. Our cohort consisted of patients who had biopsy-confirmed breast cancer amenable to surgical resection. These patients underwent serial FLT-PET scans: the first scan prior to starting neoadjuvant chemotherapy (NAC), and a second scan shortly after starting NAC. SUV

results16 patients (n = 16) met criteria for inclusion and successfully underwent FLT-PET scans in the prescribed sequence of events. Seven of these patients had a decrease of 20% or larger between the two serial PET scans, making them "responders". The remaining nine patients were "non-responders" to NAC based on PET imaging. Between responders and non-responders, there was no significant difference in median PFS (7.9 years versus 3.7 years; p = 0.425) and median OS (7.5 years versus 5.0 years; p = 0.944). In the 14 patients who underwent surgical resection (n = 14), there was no significant difference in the rate of achieving pCR (33% vs. 14%; p = 0.5846) between responders and non-responders.

conclusionFurther study of a larger sample size is needed to examine the potential role for FLT-PET in predicting response to neoadjuvant treatment, particularly in correlating with long-term overall and progression-free survival. Our study is limited by small sample size, but does suggest that FLT-PET has a role in the long-term prognosis of breast cancer treated with NAC and surgical resection which is worthy of further study.

Indexed as

DideoxynucleosidesNeoadjuvant TherapyPositron-Emission TomographyAdultBreast NeoplasmsDisease-Free SurvivalFemaleHumansMiddle AgedProspective StudiesSurvival AnalysisalovudineDideoxynucleosidesBreast cancerFLT-PETNeoadjuvantSurvival

Identifiers

PMID30810980
PMCPMC6859000

What OpenQuestion holds

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Registered trials

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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.