Evidence map›Paper›PMID 42141924›Full record

Trial reportCA: a cancer journal for clinicians

Twenty-year results of the randomized European Organization for Research and Treatment of Cancer trial 22922/10925 evaluating internal mammary chain and medial supraclavicular lymph node irradiation in stage I-III breast cancer.

Orit Kaidar-Person, Caroline G Weltens, Catherine Fortpied, Luc J E E Scheijmans, Carine Y Kirkove, Volker Budach, Karine Peignaux-Casasnovas, Mariacarla Valli, Max Peters, Femke van der Leij and 15 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in CA: a cancer journal for clinicians. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

25 authors.

Orit Kaidar-PersonBreast Radiation Unit, Sheba Medical Center, Ramat Gan, Israel.ORCID https://orcid.org/0000-0003-4023-1869
Caroline G WeltensDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0001-7790-7151
Catherine FortpiedEuropean Organization for Research and Treatment of Cancer, Brussels, Belgium.
Luc J E E ScheijmansDepartment of Radiation Oncology, Institute Verbeeten, Tilburg, Netherlands.ORCID https://orcid.org/0000-0002-6690-6118
Carine Y KirkoveDepartment of Radiation Oncology, University Hospital Saint Luc, Université Catholique de Louvain, Brussels, Belgium.ORCID https://orcid.org/0009-0005-8329-7229
Volker BudachDepartment of Radiation Oncology, Comprehensive Cancer Center, Charite-University Medicine Berlin, Corporate Member of Free University of Berlin and Humboldt University of Berlin, BE, Berlin, Germany.ORCID https://orcid.org/0000-0002-2191-9871
Karine Peignaux-CasasnovasDepartment of Radiation Oncology, Centre Georges François Leclerc, Dijon, France.ORCID https://orcid.org/0000-0002-3718-8524
Mariacarla ValliDepartment of Radiation Oncology, Sant Anna Hospital, Como, Italy.ORCID https://orcid.org/0000-0002-7880-4645
Max PetersDepartment of Radiation Oncology, Radiotherapiegroep, Deventer/Arnhem, Netherlands.ORCID https://orcid.org/0000-0002-7981-5768
Femke van der LeijDepartment of Radiation Oncology, University Medical Centre Utrecht, Utrecht, Netherlands.ORCID https://orcid.org/0009-0009-3914-2958
Sofia RiveraDepartment of Radiation Oncology, Gustave Roussy Cancer Centre, Villejuif, France.
Nicola WeidnerDepartment of Radiation Oncology, University Hospital, Tübingen, Germany.
Desirée H J G van den BongardDepartment of Radiation Oncology, Cancer Center Amsterdam, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, Netherlands.ORCID https://orcid.org/0000-0002-5549-324X
Claudia LinsenmeierDepartment of Radiation Oncology, University Hospital Zürich, University of Zürich, Zürich, Switzerland.
Roxolyana Abdah-BortnyakDepartment of Radiation Oncology, The Joseph Fishman Oncology Center, Rambam Health Care Campus, Haifa, Israel.ORCID https://orcid.org/0009-0006-3471-2809
Shaymaa HosniNottingham University Hospitals National Health Service Trust, Nottingham, UK.
Eveline KoiterDepartment of Radiation Oncology, Medisch Spectrum Twente, Enschede, Netherlands.
Antoine M EngelenDepartment of Radiation Oncology, Institute Verbeeten, Tilburg, Netherlands.
Adinda BatenDepartment of Radiation Oncology, University Hospitals Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0001-7104-7808
Lydia ChampezouEuropean Organization for Research and Treatment of Cancer, Brussels, Belgium.ORCID https://orcid.org/0000-0002-7368-8980
Alain FourquetDepartment of Radiation Oncology, Institut Curie, Paris, France.
Harry G M M BartelinkDepartment of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands.
Henk StruikmansDepartment of Radiation Oncology, Haaglanden Medical Center the Hague, Leidschendam, Netherlands.
Philip M P PoortmansDepartment of Radiation Oncology, Iridium Netwerk, Wilrijk-Antwerp, Belgium.ORCID https://orcid.org/0000-0001-7400-2293
European Organization for Research and Treatment of Cancer Radiation Oncology and Breast Cancer Groups

Funding

EORTC Cancer Research FundKom op tegen KankerKWF Kanker BestrijdingLigue Contre le Cancer
6 · The paper itself

Abstract

European Organization for Research and Treatment of Cancer trial EORTC 22922/10925 evaluated internal mammary and medial supraclavicular (IM-MS) lymph node irradiation (IM-MS-RT) in patients with stage I-III breast cancer. Eligible patients had involved axillary nodes and/or centrally/medially located tumors regardless of nodal involvement. The primary end point was overall survival, secondary end points were disease-free survival, distant metastases-free survival, breast cancer mortality, and any breast recurrence. Between 1996 and 2004, 4004 patients were randomized. The median patient age was 54 years. At a median follow-up of 22.2 years, 1550 (38.7%) patients died, of whom 796 (51.4%) died from breast cancer. At 20 years, the overall survival rate was 61.8% in the control group versus 61.0% in the IM-MS-RT group (hazard ratio [HR], 1.00; p = .967); the disease-free survival rate was 49.0% versus 48.2%, respectively (HR, 0.97; p = .515); and the distant metastases-free survival rate was 59.8% versus 58.9%, respectively (HR, 0.97; p = .578). The breast cancer mortality rate was 22.4% in the control group and 18.6% in the IM-MS-RT group (HR, 0.82; p = .006), whereas the rate of deaths not from breast cancer or from unknown causes was 15.8% versus 20.4%, respectively (HR, 1.26; p = .002). Lung fibrosis, cardiac fibrosis, and cardiac diseases were more frequent after IM-MS-RT versus no IM-MS-RT (6.3% vs. 3.2%, 2.7% vs. 1.7%. and 15.2% vs. 11.7%, respectively); and the rates of severe cardiac and lung morbidities (scores of 3 or 4) were 1.9% versus 1.7% and 0.3% versus 0.0%, respectively. Breast cancer mortality at 20 years was statistically significantly lower after IM-MS-RT, but deaths not from breast cancer increased after 15 years, resulting in no long-term benefit of IM-MS-RT on overall survival. Therefore, the authors strongly call for very long-term follow-up of treatments for prognostically favorable cancers such as breast cancer.

Indexed as

Breast NeoplasmsLymphatic IrradiationLymph NodesAdultAgedDisease-Free SurvivalFemaleFollow-Up StudiesHumansLymphatic MetastasisMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingRadiotherapy, AdjuvantSurvival Ratebreast cancerEuropean Organization for Research and Treatment of Cancer (EORTC)internal mammarylymph nodesradiotherapyrandomized trial

Identifiers

PMID42141924
PMCPMC13179593

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.