Evidence map›Paper›PMID 35501755›Full record

Observational studyBMC pulmonary medicine2022

Lymphocyte predominance in blood, pleural fluid, and tumour stroma; a prognostic marker in pleural mesothelioma.

Duneesha De Fonseka, David T Arnold, Anna J Morley, Mary Brett, Nidhi Bhatt, Anthony Edey, Richard Daly, Anna C Bibby, Nick A Maskell

Abstract readObservational Study
In one paragraph

Observational study in BMC pulmonary medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. 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

9 authors.

Duneesha De FonsekaAcademic Respiratory Unit, University of Bristol, Level 2, Learning and Research Building, Southmead Hospital, Bristol, BS10 5NB, UK.
David T ArnoldAcademic Respiratory Unit, University of Bristol, Level 2, Learning and Research Building, Southmead Hospital, Bristol, BS10 5NB, UK. Arnold.dta@gmail.com.
Anna J MorleyAcademic Respiratory Unit, North Bristol NHS Trust, Bristol, UK.
Mary BrettCellular Pathology Department, North Bristol NHS Trust, Bristol, UK.
Nidhi BhattCellular Pathology Department, North Bristol NHS Trust, Bristol, UK.
Anthony EdeyRadiology Department, North Bristol NHS Trust, Bristol, UK.
Richard DalyCellular Pathology Department, North Bristol NHS Trust, Bristol, UK.
Anna C BibbyAcademic Respiratory Unit, University of Bristol, Level 2, Learning and Research Building, Southmead Hospital, Bristol, BS10 5NB, UK.
Nick A MaskellAcademic Respiratory Unit, University of Bristol, Level 2, Learning and Research Building, Southmead Hospital, Bristol, BS10 5NB, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs promising novel treatments develop for malignant pleural mesothelioma (MPM), early prognostication has become increasingly important. Circulating and local inflammatory cells are known to play a significant role in other tumour types. We assessed the proportion of lymphocyte populations within blood, pleural fluid and tumour stroma to prognosticate patients with MPM at diagnosis.

methodsConsecutive patients diagnosed with biopsy-proven MPM were prospectively recruited to an observational cohort study and followed up for a minimum of 7.5 years. Blood and pleural fluid results at presentation were extracted from the medical records. Biopsy specimens were independently reviewed by 2 pathologists who scored the degree of lymphocytic and neutrophilic infiltration.

resultsBaseline results were available for 184 patients. The predominant pleural fluid cell type was calculable for 84 patients and 118 patients had biopsy specimens available for review. A low blood neutrophil/lymphocyte ratio (NLR < 4) inferred a better prognosis with a median survival of 420 days versus 301 days (p < 0.01). Survival was better for patients with a lymphocyte-predominant pleural effusion (430 vs 306 days, p < 0.01). Lymphocyte infiltration of tumour stroma was also associated with improved survival (n = 92, survival 430 days) compared with neutrophilic or acellular samples (n = 26, survival 342 days p < 0.01). In multivariable modelling lymphocyte predominance in blood, pleural fluid and tumour stroma were all associated with a better prognosis.

conclusionsLymphocyte predominance within tumour stroma, pleural fluid or blood infers a better prognosis in patients with MPM.

Indexed as

MesotheliomaMesothelioma, MalignantPleural NeoplasmsHumansLymphocytesPrognosisLymphocytesMesotheliomaNeutrophilsNLRPleural fluid

Identifiers

PMID35501755
PMCPMC9063088

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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.