Evidence map›Paper›PMID 38858721›Full record

ArticleBreast cancer research : BCR2024

Pre-treatment peripheral blood immunophenotyping and response to neoadjuvant chemotherapy in operable breast cancer.

Roberto A Leon-Ferre, Kaitlyn R Whitaker, Vera J Suman, Tanya Hoskin, Karthik V Giridhar, Raymond M Moore, Ahmad Al-Jarrad, Sarah A McLaughlin, Donald W Northfelt, Katie N Hunt and 12 more

Registry-linked trialAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02022202 (Breast Cancer Genome Guided Therapy Study), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

NCT02022202 completednot on this map

Breast Cancer Genome Guided Therapy Study (BEAUTY)

TypeobservationalSponsorMayo ClinicRan2012 to 2020Enrolled140ConditionsInvasive Breast Cancer
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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

22 authors.

Roberto A Leon-FerreDepartment of Oncology, Mayo Clinic, Rochester, MN, USA. leonferre.roberto@mayo.edu.
Kaitlyn R WhitakerDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Vera J SumanDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Tanya HoskinDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Karthik V GiridharDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Raymond M MooreDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Ahmad Al-JarradDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Sarah A McLaughlinDepartment of Surgery, Mayo Clinic, Jacksonville, FL, USA.
Donald W NorthfeltDivision of Hematology and Oncology, Mayo Clinic, Scottsdale, AZ, USA.
Katie N HuntDepartment of Radiology, Mayo Clinic, Rochester, MN, USA.
Amy Lynn ConnersDepartment of Radiology, Mayo Clinic, Rochester, MN, USA.
Ann MoyerDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Jodi M CarterDepartment of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
Krishna KalariDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
Richard WeinshilboumSchulze Center for Novel Therapeutics, Mayo Clinic, Rochester, MN, USA.
Liewei WangDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA.
James N IngleDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Keith L KnutsonDepartment of Immunology, Mayo Clinic, Jacksonville, FL, USA.
Stephen M AnsellDivision of Hematology, Mayo Clinic, Rochester, MN, USA.
Judy C BougheyDepartment of Surgery, Mayo Clinic, Rochester, MN, USA.
Matthew P Goetz *Department of Oncology, Mayo Clinic, Rochester, MN, USA.
Jose C Villasboas *Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
Pharmacogenetics of Phase II Drug Metabolizing EnzymesU19GM061388 · NIGMS · MAYO CLINIC ROCHESTER · PI WEINSHILBOUM, RICHARD M. · 2010 to 2014
$15.8M
Institutional Career Development CoreKL2TR002379 · NCATS · MAYO CLINIC ROCHESTER · PI NILUFER ERTEKIN-TANER · 2017 to 2026
$14.9M
Investigate the role of TPD52-AMPK pathway in tumorigenesis and cancer therapyR01CA196648 · NCI · MAYO CLINIC ROCHESTER · PI WANG, LIEWEI · 2016 to 2020
$1.7M
Mayo Clinic Breast Cancer Specialized Program of Research Excellence Grant P50CA 116201Mayo Clinic Cancer Center Support Grant P30 CA15083-40A2NCATS NIH HHS CTSA Grant Number KL2 TR002379NCATS NIH HHS KL2 TR002379NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA116201NCI NIH HHS R01 CA196648NIGMS NIH HHS U19 GM061388Pharmacogenomics Research Network U19 GM61388
6 · The paper itself

Abstract

backgroundTumor immune infiltration and peripheral blood immune signatures have prognostic and predictive value in breast cancer. Whether distinct peripheral blood immune phenotypes are associated with response to neoadjuvant chemotherapy (NAC) remains understudied.

methodsPeripheral blood mononuclear cells from 126 breast cancer patients enrolled in a prospective clinical trial (NCT02022202) were analyzed using Cytometry by time-of-flight with a panel of 29 immune cell surface protein markers. Kruskal-Wallis tests or Wilcoxon rank-sum tests were used to evaluate differences in immune cell subpopulations according to breast cancer subtype and response to NAC.

resultsThere were 122 evaluable samples: 47 (38.5%) from patients with hormone receptor-positive, 39 (32%) triple-negative (TNBC), and 36 (29.5%) HER2-positive breast cancer. The relative abundances of pre-treatment peripheral blood T, B, myeloid, NK, and unclassified cells did not differ according to breast cancer subtype. In TNBC, higher pre-treatment myeloid cells were associated with lower pathologic complete response (pCR) rates. In hormone receptor-positive breast cancer, lower pre-treatment CD8 + naïve and CD4 + effector memory cells re-expressing CD45RA (T

conclusionsPre-treatment peripheral blood immune cell populations (myeloid in TNBC; CD8 + naïve T cells and CD4 + T

trial registrationNCT02022202 . Registered 20 December 2013.

Indexed as

Breast NeoplasmsImmunophenotypingNeoadjuvant TherapyAdultAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorChemotherapy, AdjuvantErb-b2 Receptor Tyrosine KinasesFemaleHumansLeukocytes, MononuclearLymphocytes, Tumor-InfiltratingMiddle AgedPrognosisProspective StudiesBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesBiomarkersBreast cancerChemotherapyImmunologySingle cell technologiesTranslational research

Identifiers

PMID38858721
PMCPMC11165781

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Registered trials

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.