Evidence map›Paper›PMID 26466893›Full record

ArticleBMC cancer2015

Immunohistochemical subtypes predict the clinical outcome in high-risk node-negative breast cancer patients treated with adjuvant FEC regimen: results of a single-center retrospective study.

S Rahal, J M Boher, J M Extra, C Tarpin, E Charafe-Jauffret, E Lambaudie, R Sabatier, J Thomassin-Piana, A Tallet, M Resbeut and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. 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
0.2field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  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

15 authors at 2 institutions in 1 country.

S RahalDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Bd. Sainte-Marguerite, 13009, Marseille, France. rahalsoraya@hotmail.com.
J M BoherDepartment of Biostatistics, Institut Paoli-Calmettes, Marseille, France. boherjm@ipc.unicancer.fr.
J M ExtraDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Bd. Sainte-Marguerite, 13009, Marseille, France. extrajm@ipc.unicancer.fr.
C TarpinDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Bd. Sainte-Marguerite, 13009, Marseille, France. tarpinc@ipc.unicancer.fr.
E Charafe-JauffretDepartment of Biopathology, Institut Paoli-Calmettes, Marseille, France. jauffrete@ipc.unicancer.fr.
E LambaudieDepartment of Surgical Oncology, Institut Paoli-Calmettes, Marseille, France. lambaudiee@ipc.unicancer.fr.
R SabatierDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Bd. Sainte-Marguerite, 13009, Marseille, France. sabatierr@ipc.unicancer.fr.
J Thomassin-PianaDepartment of Biopathology, Institut Paoli-Calmettes, Marseille, France. THOMASSINJ@ipc.unicancer.fr.
A TalletDepartment of Radiation Oncology, Institut Paoli-Calmettes, Marseille, France. TALLETA@ipc.unicancer.fr.
M ResbeutDepartment of Radiation Oncology, Institut Paoli-Calmettes, Marseille, France. resbeutm@ipc.unicancer.fr.
G HouvenaeghelDepartment of Surgical Oncology, Institut Paoli-Calmettes, Marseille, France. HOUVENAEGHELG@ipc.unicancer.fr.
L LabordeData Management and Analysis Center, Institut Paoli-Calmettes, Marseille, France. labordel@ipc.unicancer.fr.
F BertucciDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Bd. Sainte-Marguerite, 13009, Marseille, France. bertuccif@ipc.unicancer.fr.
P ViensDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Bd. Sainte-Marguerite, 13009, Marseille, France. viensp@ipc.unicancer.fr.
A GonçalvesDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Bd. Sainte-Marguerite, 13009, Marseille, France. goncalvesa@ipc.unicancer.fr.
Institut Paoli-Calmettes · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnthracycline-based adjuvant chemotherapy improves survival in patients with high-risk node-negative breast cancer (BC). In this setting, prognostic factors predicting for treatment failure might help selecting among the different available cytotoxic combinations.

methodsBetween 1998 and 2008, 757 consecutive patients with node-negative BC treated in our institution with adjuvant FEC (5FU, epirubicin, cyclophosphamide) chemotherapy were identified. Data collection included demographic, clinico-pathological characteristics and treatment information. Molecular subtypes were derived from estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) status and Scarff-Bloom-Richardson (SBR) grade. Disease-free survival (DFS), distant disease-free survival (DDFS) and overall survival (OS) were estimated using the Kaplan-Meier Method, and prognostic factors were examined by multivariate Cox analysis.

resultsAfter a median follow-up of 70 months, the 5-year DFS, DDFS and OS were 90.6 % (95 % confidence interval (CI): 88.2-93.1), 92.8 % (95 % CI: 90.7-95) and 95.1 % (95 % CI, 93.3-96.9), respectively. In the multivariate analysis including classical clinico-pathological parameters, only grade 3 maintained a significant and independent adverse prognostic impact. In an alternative multivariate model where ER, PR and grade were replaced by molecular subtypes, only luminal B/HER2-negative and triple-negative subtypes were associated with reduced DFS and DDFS.

conclusionsNode-negative BC patients receiving adjuvant FEC regimen have a favorable outcome. Luminal B/HER2-negative and triple-negative subtypes identify patients with a higher risk of treatment failure, which might warrant more aggressive systemic treatment.

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorBreast NeoplasmsChemotherapy, AdjuvantCombined Modality TherapyCyclophosphamideEpirubicinFemaleFluorouracilFollow-Up StudiesHumansImmunohistochemistryMiddle AgedNeoplasm GradingBiomarkers, TumorCyclophosphamideEpirubicinFluorouracil

Identifiers

PMID26466893
PMCPMC4607139
OpenAlexW1942534287

What OpenQuestion holds

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LicenceCC BY
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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.