Evidence map›Paper›PMID 30035251›Full record

ArticleJNCI cancer spectrum2018

Association of Metabolic, Inflammatory, and Tumor Markers With Circulating Tumor Cells in Metastatic Breast Cancer.

Ana Elisa Lohmann, Ryan J O Dowling, Marguerite Ennis, Eitan Amir, Christine Elser, Christine Brezden-Masley, Theodore Vandenberg, Elma Lee, Kamran Fazaee, Vuk Stambolic and 2 more

Open access · goldAbstract read
In one paragraph

Article in JNCI cancer spectrum, 2018. 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
0.7field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Robust anticancer efficacy ofOpen veterinary journal · 2024
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  3. Skeletal muscle omics signatures in cancer cachexia: perspectives and opportunities.Journal of the National Cancer Institute. Monographs · 2023
    Article
  4. Article
  5. Article
  6. Review
  7. 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

12 authors at 6 institutions in 2 countries.

Ana Elisa LohmannLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System.
Ryan J O DowlingUniversity Health Network, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Marguerite EnnisApplied Statistician, Markham, ON, Canada.
Eitan AmirDepartment of Medicine, University of Toronto, Toronto, ON, Canada.
Christine ElserLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System.
Christine Brezden-MasleyDepartment of Medicine, University of Toronto, Toronto, ON, Canada.
Theodore VandenbergLondon Regional Cancer Program, London, ON, Canada.
Elma LeeLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System.
Kamran FazaeeLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System.
Vuk StambolicDepartment of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Pamela J GoodwinLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System.
Martin C ChangLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health System.
Lunenfeld-Tanenbaum Research Institute · CAPrincess Margaret Cancer Centre · CACancer Care Ontario · CAStatistics Canada · CAUniversity Health Network · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCirculating tumor cells (CTCs) are associated with worse prognosis in metastatic breast cancer (BC). We evaluated the association of metabolic, inflammatory, and tumor markers with CTCs in women with metastatic BC before commencing a new systemic therapy.

methodsNinety-six patients with newly diagnosed or progressing metastatic BC without current diabetes or use of anti-inflammatory agents were recruited from four Ontario hospitals. Women provided fasting blood for measurement of metabolic, inflammatory, and tumor markers and CTCs. CTCs were assayed within 72 hours of collection using CellSearch. Other blood was frozen at -80°C, and assays were performed in a single batch. Associations between CTC counts with study factors were evaluated using Spearman correlation, and the chi-square or Fisher exact test. All statistical tests were two-sided and

resultsThe median age was 60.5 years; 90.6% were postmenopausal. The cohort included hormone receptor-positive (87.5%), HER2-positive (15.6%), and triple-negative (10.4%) BCs. Patients were starting firstline (35.5%), second-line (26.0%), or third-or-later-line therapy (38.5%). CTC counts (per 7.5 mL of blood) ranged from 0 to 1238 (median 2); an elevated CTC count, defined as five or more CTCs, was detected in 42 (43.8%) patients. Those with liver metastases (vs not) more frequently had an elevated CTC count (59.0% vs 33.3%,

conclusionsCTC counts were positively associated with tumor and inflammatory markers and inversely associated with some metabolic markers, potentially reflecting tumor burden and cachexia.

Identifiers

PMID30035251
PMCPMC6044231
OpenAlexW2834578332

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.