Evidence map›Paper›PMID 39284953›Full record

Trial reportNature medicine2024

Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple-negative breast cancer: a phase 2 adaptive trial.

Iris Nederlof, Olga I Isaeva, Manon de Graaf, Robbert C A M Gielen, Noor A M Bakker, Adrianne L Rolfes, Hannah Garner, Bram Boeckx, Joleen J H Traets, Ingrid A M Mandjes and 28 more

Registry-linked trialAbstract readClinical Trial, Phase IIAdaptive Clinical Trial
In one paragraph

Trial report in Nature medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07055399 (Neoadjuvant Therapy of Iparomlimab and Tuvonralimab Combined With Chemotherapy-eclipse for Locally Advanced Cervical Cancer:A Single-arm, Open-label, Phase II Trial), which is not on this map. Cited by 48 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 2 pooled it
–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.

NCT07055399 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

Neoadjuvant Therapy of Iparomlimab and Tuvonralimab Combined With Chemotherapy-eclipse for Locally Advanced Cervical Cancer:A Single-arm, Open-label, Phase II Trial

TypeinterventionalSponsorFujian Cancer HospitalRan2025 to 2029Enrolled43ConditionsLocally Advanced Cervical CancerArmsneoadjuvant chemo-immunotherapy: Iparomlimab and tuvonralimab plus cisplatin,nab-paclitaxel for 1 cycle and Iparomlimab and tuvonralimab for 2 cycles
3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Cancer-related fatigue during treatment with neoadjuvant and/or adjuvant immune checkpoint inhibitors: a systematic review and meta-analysis.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Pooled it
  2. Pooled it
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  5. The immunology of human breast cancer.Nature reviews. Immunology · 2026
    Review
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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

38 authors.

Iris Nederlof *Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0001-7608-6515
Olga I Isaeva *Division of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0001-7377-0944
Manon de GraafDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Robbert C A M GielenDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Noor A M BakkerDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Adrianne L RolfesDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Hannah GarnerDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-6804-5040
Bram BoeckxLaboratory for Translational Genetics, Department of Human Genetics, KU Leuven, Leuven, Belgium.
Joleen J H TraetsDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Ingrid A M MandjesBiometrics Department, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Michiel de MaakerCore Facility Molecular Pathology & Biobanking, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Thomas van BrusselLaboratory for Translational Genetics, Department of Human Genetics, KU Leuven, Leuven, Belgium.
Maksim ChelushkinDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-4284-9294
Elisa ChampanhetDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Marta Lopez-YurdaBiometrics Department, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0003-3678-3222
Koen van de VijverDepartment of Pathology, UZ Gent - Universitair Ziekenhuis Gent, Gent, Belgium.ORCID http://orcid.org/0000-0002-2026-9790
José G van den BergDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Ingrid HoflandCore Facility Molecular Pathology & Biobanking, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Natasja KliouevaDepartment of Pathology, OLVG Hospital, Amsterdam, the Netherlands.
Ritse M MannDepartment of Radiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Claudette E LooDepartment of Radiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Frederieke H van DuijnhovenDepartment of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Victoria SkinnerDepartment of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Sylvia LuykxMedical Oncology Department, Tergooi Hospital - locatie Hilversum, Hilversum, the Netherlands.
Emile KerverDepartment of Oncology, OLVG Hospital, Amsterdam, the Netherlands.
Ekaterina KalashnikovaNatera, San Carlos, CA, USA.
Marloes G J van DongenDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Gabe S SonkeDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0001-8088-9628
Sabine C LinnDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0001-5541-0347
Christian U BlankDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-7945-5846
Karin E de VisserDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-0293-868X
Roberto SalgadoDepartment of Pathology, ZAS hospitals, Antwerp, Belgium.ORCID http://orcid.org/0000-0002-1110-3801
Lodewyk F A WesselsOncode Institute, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-1656-6995
Caroline A DrukkerDepartment of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Ton N SchumacherOncode Institute, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0003-0517-8804
Hugo M HorlingsDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0003-4782-8828
Diether LambrechtsLaboratory for Translational Genetics, Department of Human Genetics, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-3429-302X
Marleen KokDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands. m.kok@nki.nl.ORCID http://orcid.org/0000-0001-9043-9815

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek (Netherlands Organisation for Scientific Research) 09150172010043
6 · The paper itself

Abstract

Immune checkpoint inhibition (ICI) with chemotherapy is now the standard of care for stage II-III triple-negative breast cancer; however, it is largely unknown for which patients ICI without chemotherapy could be an option and what the benefit of combination ICI could be. The adaptive BELLINI trial explored whether short combination ICI induces immune activation (primary end point, twofold increase in CD8

Indexed as

CD8-Positive T-LymphocytesIpilimumabLymphocytes, Tumor-InfiltratingNeoadjuvant TherapyNivolumabTriple Negative Breast NeoplasmsAdultAgedAntineoplastic Combined Chemotherapy ProtocolsCTLA-4 AntigenFemaleHumansImmune Checkpoint InhibitorsMiddle AgedNeoplasm StagingProgrammed Cell Death 1 ReceptorCTLA-4 AntigenImmune Checkpoint InhibitorsIpilimumabNivolumabProgrammed Cell Death 1 Receptor

Identifiers

PMID39284953
PMCPMC11564107

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.