Evidence map›Paper›PMID 31780778›Full record

ArticleBritish journal of cancer2020

Integration of Ki-67 index into AJCC 2018 staging provides additional prognostic information in breast tumours candidate for genomic profiling.

Elena Vissio, Jasna Metovic, Simona Osella-Abate, Luca Bertero, Giuseppe Migliaretti, Fulvio Borella, Chiara Benedetto, Anna Sapino, Paola Cassoni, Isabella Castellano

Abstract read
In one paragraph

Article in British journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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  9. Concomitant use ofGland surgery · 2021
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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

10 authors.

Elena VissioDepartment of Medical Sciences, University of Turin, Via Santena 7, 10126, Turin, Italy.
Jasna MetovicDepartment of Oncology, Pathology Unit, University of Turin, Via Santena 7, 10126, Turin, Italy.
Simona Osella-AbateDepartment of Medical Sciences, University of Turin, Via Santena 7, 10126, Turin, Italy.
Luca BerteroDepartment of Medical Sciences, University of Turin, Via Santena 7, 10126, Turin, Italy.
Giuseppe MigliarettiDepartment of Public Health and Pediatric Sciences, School of Medicine, University of Turin, 10126, Turin, Italy.
Fulvio BorellaDepartment of Surgical Sciences, Gynecology and Obstetrics 1, AOU Città della Salute, 10126, Turin, Italy.
Chiara BenedettoDepartment of Surgical Sciences, Gynecology and Obstetrics 1, AOU Città della Salute, 10126, Turin, Italy.
Anna SapinoDepartment of Medical Sciences, University of Turin, Via Santena 7, 10126, Turin, Italy.
Paola CassoniDepartment of Medical Sciences, University of Turin, Via Santena 7, 10126, Turin, Italy.
Isabella CastellanoDepartment of Medical Sciences, University of Turin, Via Santena 7, 10126, Turin, Italy. isabella.castellano@unito.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Eighth edition of the American Joint Committee on Cancer (AJCC) staging system (2018) for breast cancer (BC) introduced the prognostic stage. Moreover, multigene assessment has been indicated to tailor staging in T1/T2/N0, ER-positive/HER2-negative BC. However, many National Health Systems do not provide reimbursement for routine testing. The aim of this study was to assess whether Ki67 proliferation index is prognostically relevant for patients' candidacy for molecular testing.

methodsA retrospective series of 686 ER+/HER2- BC were reclassified using AJCC 2018, and in the group of 521 patients for which AJCC 2018 recommends molecular evaluation, we assessed the prognostic efficacy of a prognostic stage enriched by Ki67 (Ki67-PS), considering Ki67 <20% an alternative to recurrence score <11 provided by Oncotype DX.

resultsWe found that a group of BCs (35.6%, 58/163) assigned to IB stage by prognostic score were down classified to IA with Ki67-PS. The outcome of these 58 cases overlapped with that of lesions classified as stage IA using prognostic stage, showing a significantly better prognosis compared to IB tumours (HR = 2.79, p = 0.003).

conclusionsThese data suggest that Ki67 may be a reliable marker to enrich the 2018 AJCC prognostic score in BC patients' candidacy for genomic profiling.

Indexed as

Breast NeoplasmsCell ProliferationErb-b2 Receptor Tyrosine KinasesFemaleGenomicsHumansImmunohistochemistryKi-67 AntigenMolecular Diagnostic TechniquesNeoplasm StagingPrognosisProportional Hazards ModelsReceptors, EstrogenReceptors, ProgesteroneRetrospective StudiesErb-b2 Receptor Tyrosine KinasesKi-67 AntigenMKI67 protein, humanReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID31780778
PMCPMC7000715

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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.