HER2 Immunohistochemistry in Invasive Micropapillary Breast Carcinoma: Complete Assessment of an Incomplete Pattern.


Journal

Archives of pathology & laboratory medicine
ISSN: 1543-2165
Titre abrégé: Arch Pathol Lab Med
Pays: United States
ID NLM: 7607091

Informations de publication

Date de publication:
01 08 2021
Historique:
accepted: 17 09 2020
pubmed: 20 11 2020
medline: 14 9 2021
entrez: 19 11 2020
Statut: ppublish

Résumé

Invasive micropapillary carcinoma (IMPC) is a rare variant of breast carcinoma, composed of avascular morula-like tumor clusters surrounded by stromal spaces, which can affect the HER2 immunohistochemical (IHC) staining pattern. The 2013 American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) HER2 testing guideline suggests moderate to intense but incomplete (basolateral) staining be considered equivocal. To perform a detailed assessment of HER2 IHC staining patterns in IMPC. Hematoxylin-eosin and HER2 IHC slides were retrospectively reviewed to assess the morphology and HER2 IHC characteristics of IMPC. The 2018 ASCO/CAP guideline was applied. The cohort consisted of 187 IMPCs from 181 patients with median age of 58 years. Homogeneous (≥90%) micropapillary component was found in 40% (75 of 187) of cases. Receptor profile was as follows: 75% (140 of 187) ER+ HER2-, 19% (37 of 187) ER+ HER2+, 4% (7 of 187) ER- HER2+, and 2% (3 of 187) ER- HER2-. Of 26 cases with HER2 IHC 3+, 65% (17 of 26) showed a basolateral staining pattern with strong intensity. HER2 fluorescence in situ hybridization (FISH) showed amplification in 26% (17 of 66) of HER2 IHC equivocal cases: 76% (13 of 17) showed basolateral staining pattern and 24% (4 of 17) complete staining, with weak to moderate (2), moderate (14), or moderate to strong (1) intensity. The most frequent staining pattern was basolateral, seen in 49% of cases, including 65% HER2 IHC positive and 76% HER2 IHC equivocal/FISH amplified. If a basolateral pattern and weak to moderate staining is observed in IMPC, alternative testing should be performed to confirm the HER2 status.

Identifiants

pubmed: 33212478
pii: 448207
doi: 10.5858/arpa.2020-0288-OA
pmc: PMC9382909
mid: NIHMS1828214
doi:

Substances chimiques

Biomarkers, Tumor 0
Receptors, Estrogen 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

979-987

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Déclaration de conflit d'intérêts

The authors have no relevant financial interest in the products or companies described in this article.

Références

Am J Clin Pathol. 2004 Jun;121(6):857-66
pubmed: 15198358
Br J Cancer. 2014 Jul 29;111(3):619-22
pubmed: 24921921
Mod Pathol. 2009 Mar;22(3):403-9
pubmed: 19060846
Arch Pathol Lab Med. 2005 Oct;129(10):1277-82
pubmed: 16196516
Breast. 2010 Jun;19(3):231-7
pubmed: 20304650
Jpn J Clin Oncol. 2010 Aug;40(8):781-7
pubmed: 20444748
J Pathol. 2009 Jul;218(3):301-15
pubmed: 19479727
Appl Immunohistochem Mol Morphol. 2016 Mar;24(3):151-8
pubmed: 26200840
Arch Pathol Lab Med. 2015 Aug;139(8):970-1
pubmed: 25884371
J Cancer. 2019 Nov 1;10(27):6801-6812
pubmed: 31839814
Mod Pathol. 1993 Nov;6(6):660-2
pubmed: 8302807
Pathol Int. 2004 Feb;54(2):90-6
pubmed: 14720138
Arch Pathol Lab Med. 2007;131(1):18-43
pubmed: 19548375
J Clin Oncol. 2017 Feb;35(4):446-464
pubmed: 28129524
Histopathology. 2008 Jun;52(7):797-805
pubmed: 18422971
Histopathology. 2013 Aug;63(2):217-24
pubmed: 23763700
J Pathol. 2008 Aug;215(4):398-410
pubmed: 18484683
Arch Pathol Lab Med. 2018 Nov;142(11):1364-1382
pubmed: 29846104
Breast Cancer Res Treat. 2015 Jun;151(2):443-51
pubmed: 25953688
Breast J. 2019 Nov;25(6):1171-1176
pubmed: 31321854
Arch Pathol Lab Med. 2014 Feb;138(2):241-56
pubmed: 24099077
Mod Pathol. 2020 Jul;33(7):1275-1286
pubmed: 31974492
Mod Pathol. 2018 Apr;31(4):685
pubmed: 29666481
Zhonghua Bing Li Xue Za Zhi. 2015 Jan;44(1):48-52
pubmed: 25765031
BMC Cancer. 2017 Dec 11;17(1):839
pubmed: 29228910
Histopathology. 2004 Apr;44(4):332-8
pubmed: 15049898
Mod Pathol. 2017 Nov;30(11):1561-1566
pubmed: 28752841
Mod Pathol. 2018 Apr;31(4):686
pubmed: 29666479
Cancer Med. 2017 Dec;6(12):2775-2786
pubmed: 29072365
Pathol Res Pract. 2000;196(1):35-9
pubmed: 10674270
BMC Res Notes. 2018 Jul 31;11(1):531
pubmed: 30064485
Oncotarget. 2017 Jun 27;8(26):42455-42465
pubmed: 28418916
Breast Cancer. 2004;11(3):301-6
pubmed: 15550850

Auteurs

Marjorie Perron (M)

From the Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

Hannah Y Wen (HY)

From the Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

Matthew G Hanna (MG)

From the Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

Edi Brogi (E)

From the Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

Dara S Ross (DS)

From the Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.

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Classifications MeSH