Evidence map›Paper›PMID 38978352›Full record

Trial reportMolecular oncology2025

Circulating tumor cells in metastatic breast cancer patients treated with immune checkpoint inhibitors - a biomarker analysis of the ALICE and ICON trials.

Nikolai Kragøe Andresen, Andreas Hagen Røssevold, Elin Borgen, Cecilie Bendigtsen Schirmer, Bjørnar Gilje, Øystein Garred, Jon Lømo, Marius Stensland, Oddmund Nordgård, Ragnhild Sørum Falk and 4 more

Abstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Molecular oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Do Metastatic Cells Arise from PD-L1International journal of molecular sciences · 2026
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  5. Article
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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

14 authors.

Nikolai Kragøe AndresenDepartment of Clinical Cancer Research, Oslo University Hospital, Norway.ORCID https://orcid.org/0000-0001-9386-1368
Andreas Hagen RøssevoldDepartment of Clinical Cancer Research, Oslo University Hospital, Norway.
Elin BorgenDepartment of Pathology, Oslo University Hospital, Norway.
Cecilie Bendigtsen SchirmerDepartment of Pathology, Oslo University Hospital, Norway.
Bjørnar GiljeDepartment of Hematology and Oncology, Stavanger University Hospital, Norway.
Øystein GarredDepartment of Pathology, Oslo University Hospital, Norway.
Jon LømoDepartment of Pathology, Oslo University Hospital, Norway.
Marius StenslandDepartment of Hematology and Oncology, Stavanger University Hospital, Norway.
Oddmund NordgårdDepartment of Hematology and Oncology, Stavanger University Hospital, Norway.ORCID https://orcid.org/0000-0002-5847-6752
Ragnhild Sørum FalkOslo Centre for Biostatistics and Epidemiology, Oslo University Hospital, Norway.
Randi R MathiesenDepartment of Oncology, Oslo University Hospital, Norway.
Hege G RussnesInstitute of Clinical Medicine, University of Oslo, Norway.
Jon Amund KyteDepartment of Clinical Cancer Research, Oslo University Hospital, Norway.ORCID https://orcid.org/0000-0002-2854-3694
Bjørn NaumeInstitute of Clinical Medicine, University of Oslo, Norway.ORCID https://orcid.org/0000-0002-6811-9476

Funding

Bristol Myers SquibbCancer-ID Consortium 115749Helse Sør-Øst RHF 2017100Helse Sør-Øst RHF 2018090Kreftforeningen 182632RocheWellcome Trust 214972
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) have been introduced in breast cancer (BC) treatment and better biomarkers are needed to predict benefit. Circulating tumor cells (CTCs) are prognostic in BC, but knowledge is limited on CTCs in the context of ICI therapy. In this study, serial sampling of CTCs (CellSearch system) was evaluated in 82 patients with metastatic BC enrolled in two randomized trials investigating ICI plus chemotherapy. Programmed death-ligand 1 (PD-L1) expression on CTCs was also measured. Patients with ≥ 2 CTCs per 7.5 mL at baseline had gene expression profiles in tumor suggestive of increased T-cell activity, including increased tumor inflammation signature (TIS) in both triple-negative (P = 0.010) and hormone receptor-positive (P = 0.024) disease. Patients with luminal A BC had higher CTC levels. The association between CTC status and outcome was most apparent 4 weeks into therapy. PD-L1 expression in CTCs was observed in 6/17 CTC-positive patients and was associated with inferior survival. In conclusion, our study indicates that CTC numbers may inform on tumor immune composition, as well as prognosis. These findings suggest a potential of using CTCs as an accessible biomarker source in BC patients treated with immunotherapy.

Indexed as

Biomarkers, TumorBreast NeoplasmsImmune Checkpoint InhibitorsNeoplastic Cells, CirculatingAdultAgedB7-H1 AntigenFemaleHumansMiddle AgedNeoplasm MetastasisB7-H1 AntigenBiomarkers, TumorCD274 protein, humanImmune Checkpoint Inhibitorsbreast cancercirculating tumor cellsimmune checkpoint inhibitorsliquid biopsy

Identifiers

PMID38978352
PMCPMC12234385

What OpenQuestion holds

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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.