Evidence map›Paper›PMID 35403159›Full record

ArticleCancer diagnosis & prognosis

The Systemic Immune Markers at Diagnosis Can Predict the Survival Benefit in Advanced Breast Cancer.

Shogo Nakamoto, Masahiko Ikeda, Shinichiro Kubo, Mari Yamamoto, Tetsumasa Yamashita, Chihiro Kuwahara

Open access · greenAbstract read
In one paragraph

Article in Cancer diagnosis & prognosis. 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
0.1field-weighted citation impact, top 51% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

6 authors at 1 institution in 1 country.

Shogo NakamotoDivision of Breast and Thyroid Gland Surgery, Fukuyama City Hospital, Hiroshima, Japan.
Masahiko IkedaDivision of Breast and Thyroid Gland Surgery, Fukuyama City Hospital, Hiroshima, Japan.
Shinichiro KuboDivision of Breast and Thyroid Gland Surgery, Fukuyama City Hospital, Hiroshima, Japan.
Mari YamamotoDivision of Breast and Thyroid Gland Surgery, Fukuyama City Hospital, Hiroshima, Japan.
Tetsumasa YamashitaDivision of Breast and Thyroid Gland Surgery, Fukuyama City Hospital, Hiroshima, Japan.
Chihiro KuwaharaDivision of Breast and Thyroid Gland Surgery, Fukuyama City Hospital, Hiroshima, Japan.
Fukuyama City Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aim: It has been difficult to establish prognostic markers for overall survival (OS) in patients with advanced breast cancer (ABC). Although systemic immune markers were reported as prognostic markers in several cancers, their utility in ABC remains unclear. Patients and Methods: We retrospectively analyzed 331 ABC patients, who received treatment at Fukuyama City Hospital between April 2009 and December 2020. Results: Patients with high absolute lymphocyte count (ALC), low neutrophil-to-lymphocyte ratio (NLR), and high lymphocyte-to-monocyte ratio (LMR) had significantly longer OS (p=0.025, p=0.010, and p<0.001, respectively). High ALC and high LMR were independently associated with longer OS (p=0.020 and p=0.015, respectively). High ALC was also independently associated with longer time to treatment failure (p=0.014). Conclusion: These systemic immune markers at diagnosis can predict not only a better OS but also a better TTF after first-line treatment.

Indexed as

absolute lymphocyte countAdvanced breast cancerlymphocyte-to-monocyte rationeutrophil-to-lymphocyte ratioprognostic marker

Identifiers

PMID35403159
PMCPMC8962865
OpenAlexW3211800475

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.