Evidence map›Paper›PMID 27494111›Full record

ArticlePloS one2016

Prognostic Impact of Time to Ipsilateral Breast Tumor Recurrence after Breast Conserving Surgery.

Marie Gosset, Anne-Sophie Hamy, Peter Mallon, Myriam Delomenie, Delphine Mouttet, Jean-Yves Pierga, Marick Lae, Alain Fourquet, Roman Rouzier, Fabien Reyal and 1 more

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Occult breast cancer in an older woman: A case report.Experimental and therapeutic medicine · 2025
    Article
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  7. Is invasion a necessary step for metastases in breast cancer?Breast cancer research and treatment · 2018
    Review
  8. 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

11 authors.

Marie GossetDepartment of Surgery, Institut Curie, 75005, Paris, France.
Anne-Sophie HamyDepartment of Surgery, Institut Curie, 75005, Paris, France.
Peter MallonBreast Unit, Belfast City Hospital, Lisburn Road, Belfast, BT9 7AB, Northern Ireland.
Myriam DelomenieDepartment of Surgery, Institut Curie, 75005, Paris, France.
Delphine MouttetDepartment of Surgery, Institut Curie, 75005, Paris, France.
Jean-Yves PiergaDepartment of Medical Oncology, 75005, Institut Curie, Paris, France.
Marick LaeDepartment of Tumor Biology, Institut Curie, 75005, Paris, France.
Alain FourquetDepartment of Radiotherapy, Institut Curie, 75005, Paris, France.
Roman RouzierDepartment of Surgery, Institut Curie, 75005, Paris, France.
Fabien ReyalDepartment of Surgery, Institut Curie, 75005, Paris, France.
Jean-Guillaume FeronDepartment of Surgery, Institut Curie, 75005, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe poor prognosis of patients who experience ipsilateral breast tumor recurrence (IBTR) after breast conserving surgery (BCS) is established. A short time between primary cancer and IBTR is a prognostic factor but no clinically relevant threshold was determined. Classification of IBTR may help tailor treatment strategies. PURPOSE: We determined a specific time frame, which differentiates IBTR into early and late recurrence, and identified prognostic factors for patients with IBTR at time of the recurrence.

methodsWe analyzed 2209 patients with IBTR after BCS. We applied the optimal cut-points method for survival data to determine the cut-off times to IBTR. A subgroup analysis was performed by hormone receptor (HR) status. Survival analyses were performed using a Cox proportional hazard model to determine clinical features associated with distant-disease-free survival (DDFS) after IBTR. We therefor built decision trees.

resultsOn the 828 metastatic events observed, the majority occurred within the first 3 months after IBTR: 157 in the HR positive group, 98 in the HR negative group. We found different prognostic times to IBTR: 49 months in the HR positive group, 33 in the HR negative group. After multivariate analysis, time to IBTR was the first discriminant prognostic factor in both groups (HR 0.65 CI95% [0.54-0.79] and 0.42 [0.30-0.57] respectively). The other following variables were significantly correlated with the DDFS: the initial number of positive lymph nodes for both groups, the initial tumor size and grade for HR positive tumors.

conclusionA short interval time to IBTR is the strongest factor of poor prognosis and reflects occult distant disease. It would appear that prognosis after IBTR depends more on clinical and histological parameters than on surgical treatment. A prospective trial in a low-risk group of patients to validate the safety of salvage BCS instead of mastectomy in IBTR is needed.

Indexed as

Neoplasm Recurrence, LocalAdultAgedAntineoplastic AgentsBreast NeoplasmsDisease-Free SurvivalFemaleHumansKaplan-Meier EstimateLymphatic MetastasisMastectomyMiddle AgedNeoplasm GradingPrognosisProportional Hazards ModelsReceptors, EstrogenAntineoplastic AgentsReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID27494111
PMCPMC4975471

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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.