Spotlight on Ki67 as a prognostic marker in early breast cancer: all that glitters may not be gold.


Journal

Diagnostic pathology
ISSN: 1746-1596
Titre abrégé: Diagn Pathol
Pays: England
ID NLM: 101251558

Informations de publication

Date de publication:
11 09 2020
Historique:
received: 23 07 2020
accepted: 03 09 2020
entrez: 12 9 2020
pubmed: 13 9 2020
medline: 13 7 2021
Statut: epublish

Résumé

Kang and colleagues evaluated on a case series of 1848 breast cancer (BC) patients operated for a first primary ER positive HER2 negative BC if Ki67 expression is a significant prognostic factor only when PgR expression is low. The authors concluded that Ki67 with 10% cut off value is a prognostic factor only under low PgR expression level in early BC. We would like to underline, that as already stated in our previous papers, we believe that proliferation is important to define the decision-making of adjuvant therapies in early BC. The issue on Ki67 detection is the poor reproducibility due to different antibody clones, platforms and scoring methods. Not less important is that different Ki67 cut off values have been used by San Gallen guidelines and changed overtime. Then, despite the interesting results, we believe it would be better to use Ki67 biomarker in according to the standard Ki67 cut off according to San Gallen guidelines. Nowadays, standardization and optimization of Ki67 is still an urgent need.

Identifiants

pubmed: 32917222
doi: 10.1186/s13000-020-01024-9
pii: 10.1186/s13000-020-01024-9
pmc: PMC7488398
doi:

Substances chimiques

Ki-67 Antigen 0
Receptors, Estrogen 0
Gold 7440-57-5
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Letter Comment

Langues

eng

Sous-ensembles de citation

IM

Pagination

109

Commentaires et corrections

Type : CommentOn

Références

J Oncol. 2019 Dec 28;2019:7386734
pubmed: 31975992
Mod Pathol. 2015 Jun;28(6):778-86
pubmed: 25698062
Breast Cancer Res Treat. 2014 May;145(1):177-83
pubmed: 24658893
Breast Cancer Res Treat. 2008 Mar;108(2):259-64
pubmed: 17530429
Ther Adv Med Oncol. 2020 Feb 27;12:1758835919888999
pubmed: 32158505

Auteurs

Roberta Maltoni (R)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Via P. Maroncelli 40, 47014, Meldola (FC), Italy.

Michela Palleschi (M)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Via P. Maroncelli 40, 47014, Meldola (FC), Italy.

Sara Ravaioli (S)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Via P. Maroncelli 40, 47014, Meldola (FC), Italy. sara.ravaioli@irst.emr.it.

Maria Maddalena Tumedei (MM)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Via P. Maroncelli 40, 47014, Meldola (FC), Italy.

Mattia Altini (M)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Via P. Maroncelli 40, 47014, Meldola (FC), Italy.

Sara Bravaccini (S)

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Via P. Maroncelli 40, 47014, Meldola (FC), Italy.

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Classifications MeSH