Evidence map›Paper›PMID 28386369›Full record

ArticleAmerican journal of translational research2017

Prognostic role of lymphatic vessel density and lymphovascular invasion in chemotherapy-naive and chemotherapy-treated patients with invasive breast cancer.

Joanna A Niemiec, Agnieszka Adamczyk, Aleksandra Ambicka, Anna Mucha-Małecka, Wojciech M Wysocki, Beata Biesaga, Marek Ziobro, Ida Cedrych, Aleksandra Grela-Wojewoda, Małgorzata Domagała-Haduch and 3 more

Abstract read
In one paragraph

Article in American journal of translational research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. CD45Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2023
    Article
  5. Article
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  7. Review
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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.

Joanna A NiemiecDepartment of Applied Radiobiology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Agnieszka AdamczykDepartment of Applied Radiobiology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Aleksandra AmbickaDepartment of Tumour Pathology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Anna Mucha-MałeckaDepartment of The Oncology Clinic, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Wojciech M WysockiDepartment of Surgical Oncology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Beata BiesagaDepartment of Applied Radiobiology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Marek ZiobroDepartment of Systemic and Generalized Malignancies, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Ida CedrychDepartment of Systemic and Generalized Malignancies, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Aleksandra Grela-WojewodaDepartment of Systemic and Generalized Malignancies, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Małgorzata Domagała-HaduchDepartment of Systemic and Generalized Malignancies, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Joanna WysockaDepartment of Tumour Pathology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Janusz RyśDepartment of Tumour Pathology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.
Beata Sas-KorczyńskaDepartment of The Oncology Clinic, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology Krakow Branch, Krakow, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is assumed that the spread of breast cancer cells via the lymphatic system might be influenced by inflammatory reactions and/or the application of chemotherapy or molecularly targeted therapy. Therefore, we analysed survival according to lymphatic vessel density (LVD), lymphovascular invasion (LVI) (both assessed using podoplanin as immunohistochemical marker of lymphatic endothelium) and well-established clinico-pathological features in a group of 358 patients with invasive ductal breast cancer: 139 chemotherapy-naïve (pT1-2/pN0/M0) and 219 treated with chemotherapy (pT1-4/pN1-3/M0). Univariate analysis revealed that high LVD was related to unfavourable disease-free survival (DFS) in pN0/chemotherapy/trastuzumab-naïve patients (P = 0.028). Conversely, in pN+/chemotherapy-treated individuals high LVD was related to favourable DFS (P = 0.019). LVI was a significant indicator of survival (P = 0.005) only in pN0/chemotherapy/trastuzumab-naïve patients. The following parameters were significant independent adverse prognostic factors for DFS: (i) in pN0/chemotherapy/trastuzumab-naïve patients: high LVD (LVD > 7 vessels/mm

Indexed as

Breast cancerlymphatic vesselspodoplaninprognostic significance

Identifiers

PMID28386369
PMCPMC5376034

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.