Evidence map›Paper›PMID 26810608›Full record

ArticleBreast cancer research : BCR2016

Lymphocyte depletion and repopulation after chemotherapy for primary breast cancer.

Rashmi Verma, Ruth E Foster, Kieran Horgan, Katherine Mounsey, Helen Nixon, Natuley Smalle, Thomas A Hughes, Clive R D Carter

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 167 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
167citing papers in PubMed, 4 pooled it
5.4field-weighted citation impact, top 3% 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

167 citing papers in PubMed, 4 syntheses or guidelines pooled it, 285 citations in OpenAlex.

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  15. International journal of molecular sciences · 2026
    Article
  16. Overcoming Drug Resistance by Paclitaxel Resistance in Triple-Negative Breast Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  18. Review
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107 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Rashmi VermaSchool of Medicine, University of Leeds, Leeds, UK. docrash12@yahoo.co.uk.
Ruth E FosterDepartment of Transplant Immunology, Leeds Teaching Hospitals NHS Trust, Leeds, UK. ruthfoster5@nhs.net.
Kieran HorganSchool of Medicine, University of Leeds, Leeds, UK. kieran.horgan@nhs.net.
Katherine MounseyDepartment of Transplant Immunology, Leeds Teaching Hospitals NHS Trust, Leeds, UK. katherine.mounsey@nhs.net.
Helen NixonClinical Immunology Laboratories, Leeds Teaching Hospitals NHS Trust, Leeds, UK. helen.nixon5@nhs.net.
Natuley SmalleDepartment of Transplant Immunology, Leeds Teaching Hospitals NHS Trust, Leeds, UK. n.smalle@rbht.nhs.uk.
Thomas A HughesSchool of Medicine, University of Leeds, Leeds, UK. t.hughes@leeds.ac.uk.
Clive R D CarterSchool of Medicine, University of Leeds, Leeds, UK. clivecarter@nhs.net.
Leeds Teaching Hospitals NHS Trust · GBUniversity of Leeds · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApproximately 30 % of breast cancer patients receive chemotherapy, yet little is known about influences of current regimens on circulating lymphocyte levels and phenotypes. Similarly, clinico-pathological factors that modify these influences, and implications for future immune health remain mainly unexplored.

methodsWe used flow-cytometry to assess circulating lymphocyte levels and phenotypes in 88 primary breast cancer patients before chemotherapy and at time-points from 2 weeks to 9 months after chemotherapy completion. We examined circulating titres of antibodies against pneumococcal and tetanus antigens using ELISAs.

resultsLevels of B, T and NK cells were significantly reduced 2 weeks after chemotherapy (p < 0.001). B cells demonstrated particularly dramatic depletion, falling to 5.4 % of pre-chemotherapy levels. Levels of all cells recovered to some extent, although B and CD4(+) T cells remained significantly depleted even 9 months post-chemotherapy (p < 0.001). Phenotypes of repopulating B and CD4(+) T cells were significantly different from, and showed no sign of returning to pre-chemotherapy profiles. Repopulating B cells were highly depleted in memory cells, with proportions of memory cells falling from 38 % to 10 % (p < 0.001). Conversely, repopulating CD4(+) T cells were enriched in memory cells, which increased from 63 % to 75 % (p < 0.001). Differences in chemotherapy regimen and patient smoking were associated with significant differences in depletion extent or repopulation dynamics. Titres of anti-pneumococcal and anti-tetanus antibodies were both significantly reduced post-chemotherapy and did not recover during the study (p < 0.001).

conclusionBreast cancer chemotherapy is associated with long-term changes in immune parameters that should be considered during clinical management.

Indexed as

Lymphocyte DepletionAdultAgedAntibodiesAntigens, CDB-LymphocytesBreast NeoplasmsFemaleFlow CytometryHumansKiller Cells, NaturalLymphocytesMiddle AgedStreptococcus pneumoniaeTetanusT-LymphocytesAntibodiesAntigens, CD

Identifiers

PMID26810608
PMCPMC4727393
OpenAlexW2258061020

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Registered trials

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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.