Evidence map›Paper›PMID 33468209›Full record

ArticleBreast cancer research : BCR2021

Characteristics and outcome of breast cancer-related microangiopathic haemolytic anaemia: a multicentre study.

Marion Alhenc-Gelas, Luc Cabel, Frederique Berger, Suzette Delaloge, Jean-Sebastien Frenel, Christelle Levy, Nelly Firmin, Sylvain Ladoire, Isabelle Desmoulins, Pierre-Etienne Heudel and 13 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Breast cancer research : BCR, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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

23 authors at 11 institutions in 1 country.

Marion Alhenc-GelasDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.
Luc CabelDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.
Frederique BergerInstitut Curie, Biometry Unit, Paris and Saint-Cloud, France.
Suzette DelalogeDepartment of Cancer Medicine, Institut Gustave Roussy, Villejuif, France.
Jean-Sebastien FrenelDepartment of Medical Oncology, Institut de Cancérologie de l'Ouest, Saint-Herblain, France.
Christelle LevyDepartment of Medical Oncology, Centre François Baclesse, Caen, France.
Nelly FirminDepartment of Medical Oncology, Institut du Cancer de Montpellier, Institut de cancérologie de Montpellier INSERM U1194, Montpellier, France.
Sylvain LadoireDepartment of Medical Oncology, Centre Georges-François Leclerc, Dijon, France.
Isabelle DesmoulinsDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France.
Pierre-Etienne HeudelDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France.
Florence DalencDepartment of Medical Oncology, Institut Claudius Regaud, Institut Universitaire du Cancer de Toulouse-Oncopole (IUCT-Oncopole), Toulouse, France.
Delphine LoiratDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.
Coraline DubotDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.
Perrine VuagnatDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.
Elise DelucheDepartment of Cancer Medicine, Institut Gustave Roussy, Villejuif, France.
Meriem Mokdad-AdiDepartment of Cancer Medicine, Institut Gustave Roussy, Villejuif, France.
Anne PatsourisDepartment of Medical Oncology, Institut de Cancérologie de l'Ouest, Saint-Herblain, France.
Josselin AnnicDepartment of Medical Oncology, Institut de Cancérologie de l'Ouest, Saint-Herblain, France.
Lounes DjerroudiDepartment of Pathology, Institut Curie, Paris, France.
Marion LavigneDepartment of Pathology, Institut Curie, Paris, France.
Jean-Yves PiergaDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France.
Paul CoppoReference Center for Thrombotic Microangiopathies (CNR-MAT), AP-HP.SU, INSERM UMRS, 1138, Paris, France.
Francois-Clement BidardDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, France. fcbidard@curie.fr.ORCID 0000-0001-5932-8949
Institut Curie · FRInstitut de Cancérologie de l'Ouest · FRInstitut Gustave Roussy · FRCentre Léon Bérard · FRInserm · FRUniversité de Versailles Saint-Quentin-en-Yvelines · FRCentre François Baclesse · FRCentre Georges François Leclerc · FRInstitut Claudius Regaud · FRUniversité Paris Cité · FRZimmer Biomet (France) · FR

Funding

Institut Curie Siric 2 INCa-DGOS-4654Novartis N/A
6 · The paper itself

Abstract

backgroundCancer-related microangiopathic haemolytic anaemia (MAHA) is a rare but life-threatening paraneoplastic syndrome. Only single cases or small series have been reported to date. We set up a retrospective multicentre study focusing on breast cancer-related MAHA.

methodsMain inclusion criteria were known diagnosis of breast cancer, presence of schistocytes and either low haptoglobin or cytopenia and absence of any causes of MAHA other than breast cancer, including gemcitabine- or bevacizumab-based treatment. Patient characteristics, treatments and outcome were retrieved from digital medical records.

resultsIndividual data from 54 patients with breast cancer-related MAHA were obtained from 7 centres. Twenty-three (44%) patients had a breast tumour with lobular features, and most primary tumours were low grade (grade I/II, N = 39, 75%). ER+/HER2-, HER2+ and triple-negative phenotypes accounted for N = 33 (69%), N = 7 (15%) and N = 8 (17%) cases, respectively. All patients had stage IV cancer at the time of MAHA diagnosis. Median overall survival (OS) was 28 days (range 0-1035; Q1:10, Q3:186). Independent prognostic factors for early death (≤ 28 days) were PS > 2 (OR = 7.0 [1.6; 31.8]), elevated bilirubin (OR = 6.9 [1.1; 42.6]), haemoglobin < 8.0 g/dL (OR = 3.7 [0.9; 16.7]) and prothrombin time < 50% (OR = 9.1 [1.2; 50.0]). A score to predict early death displayed a sensitivity of 86% (95% CI [0.67; 0.96]), a specificity of 73% (95% CI [0.52; 0.88]) and an area under the curve of 0.90 (95% CI [0.83; 0.97]).

conclusionsBreast cancer-related MAHA appears to be a new feature of invasive lobular breast carcinoma. Prognostic factors and scores may guide clinical decision-making in this serious but not always fatal condition.

Indexed as

Anemia, HemolyticArea Under CurveBiomarkers, TumorBreast NeoplasmsDisease ManagementDisease SusceptibilityFemaleFranceHumansNeoplasm GradingNeoplasm StagingPhenotypePrognosisSeverity of Illness IndexSurvival AnalysisBiomarkers, TumorBreast cancerMicroangiopathic haemolytic anaemiaPrognostic factorsSurvival

Identifiers

PMID33468209
PMCPMC7814553
OpenAlexW3122891089

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