Evidence map›Paper›PMID 42840281›Full record

ArticleiScience2026

Lymphocyte-to-monocyte ratio predicts survival in localized osteosarcoma in Vietnamese patients.

Tran Thi Thu Hien, Dat Nguyen Quoc, Tran Duc Thanh, Tran Tuyet Thanh Hai, Nguyen Tran Quang Sang, Tran Trung Dung, Xuan-Hung Nguyen, Son Hai Vu

Abstract read
In one paragraph

Article in iScience, 2026. 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

8 authors.

Tran Thi Thu HienCollege of Health Sciences, VinUniversity, Hanoi, Vietnam.
Dat Nguyen QuocInstitute of Biomedical Data and Science Research (BIODAS), Hanoi, Vietnam.
Tran Duc ThanhSarcoma Center, Vinmec Healthcare System, Hanoi, Vietnam.
Tran Tuyet Thanh HaiSarcoma Center, Vinmec Healthcare System, Hanoi, Vietnam.
Nguyen Tran Quang SangSarcoma Center, Vinmec Healthcare System, Hanoi, Vietnam.
Tran Trung DungSarcoma Center, Vinmec Healthcare System, Hanoi, Vietnam.
Xuan-Hung NguyenCenter for Regenerative Medicine and Cell Therapy, Vinmec Healthcare System, Hanoi, Vietnam.
Son Hai VuVinmec-VinUni Institute of Immunology, College of Health Sciences, VinUniversity, Hanoi, Vietnam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory markers such as the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR), alongside hemoglobin (Hgb) levels, have been proposed as prognostic tools in osteosarcoma, though their reliability remains unclear. We retrospectively evaluated the prognostic significance of these pre-operative markers in a cohort of 100 Vietnamese patients with stage IB-IIB osteosarcoma, specifically focusing on the post-neoadjuvant, pre-operative window, a clinically critical yet underexplored time frame. In the primary dichotomized multivariable analysis, LMR emerged as an independent predictor of poor overall survival, whereas PLR showed only univariable associations, and NLR and Hgb were not statistically significant. While LMR demonstrated robust prognostic value for overall survival, it failed to predict disease progression within 24 months. To address cutpoint bias, sensitivity analyses modeling these markers as continuous variables combined with internal bootstrap validation (1000 resamples) confirmed parameter stability only for LMR, but not PLR and NLR. Reflecting these continuous trends, the final multivariable model achieved an apparent C-index of 0.729, which adjusted to an optimism-corrected C-index of 0.628. External literature-derived median cutoffs did not show significant associations when applied to this post-neoadjuvant cohort, highlighting key population- and timing-specific limitations. Although these peripheral blood markers demonstrate prognostic potential, our findings remain exploratory, and validation in independent multi-center cohorts with longitudinal prospective evaluation is required before their clinical utility can be established.

Indexed as

inflammatory markersLMRosteosarcomaprognosis

Identifiers

PMID42840281
PMCPMC13638794

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.