Fully Automated Artificial Intelligence Solution for Human Epidermal Growth Factor Receptor 2 Immunohistochemistry Scoring in Breast Cancer: A Multireader Study
The proven efficacy of human epidermal growth factor receptor 2 (HER2) antibody-drug conjugate therapy for treating HER2-low breast cancers necessitates more accurate and reproducible HER2 immunohistochemistry (IHC) scoring. We aimed to validate performance and utility of a fully automated artificia...
Saved in:
Published in: | JCO precision oncology Vol. 8; p. e2400353 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
01-10-2024
|
Subjects: | |
Online Access: | Get more information |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | The proven efficacy of human epidermal growth factor receptor 2 (HER2) antibody-drug conjugate therapy for treating HER2-low breast cancers necessitates more accurate and reproducible HER2 immunohistochemistry (IHC) scoring. We aimed to validate performance and utility of a fully automated artificial intelligence (AI) solution for interpreting HER2 IHC in breast carcinoma.
A two-arm multireader study of 120 HER2 IHC whole-slide images from four sites assessed HER2 scoring by four surgical pathologists without and with the aid of an AI HER2 solution. Both arms were compared with high-confidence ground truth (GT) established by agreement of at least four of five breast pathology subspecialists according to ASCO/College of American Pathologists (CAP) 2018/2023 guidelines.
The mean interobserver agreement among GT pathologists across all HER2 scores was 72.4% (N = 120). The AI solution demonstrated high accuracy for HER2 scoring, with 92.1% agreement on slides with high confidence GT (n = 92). The use of the AI tool led to improved performance by readers, interobserver agreement increased from 75.0% for digital manual read to 83.7% for AI-assisted review, and scoring accuracy improved from 85.3% to 88.0%. For the distinction of HER2 0 from 1+ cases (n = 58), pathologists supported by AI showed significantly higher interobserver agreement (69.8% without AI
87.4% with AI) and accuracy (81.9% without AI
88.8% with AI).
This study demonstrated utility of a fully automated AI solution to aid in scoring HER2 IHC accurately according to ASCO/CAP 2018/2023 guidelines. Pathologists supported by AI showed improvements in HER2 IHC scoring consistency and accuracy, especially for distinguishing HER2 0 from 1+ cases. This AI solution could be used by pathologists as a decision support tool for enhancing reproducibility and consistency of HER2 scoring and particularly for identifying HER2-low breast cancers. |
---|---|
AbstractList | The proven efficacy of human epidermal growth factor receptor 2 (HER2) antibody-drug conjugate therapy for treating HER2-low breast cancers necessitates more accurate and reproducible HER2 immunohistochemistry (IHC) scoring. We aimed to validate performance and utility of a fully automated artificial intelligence (AI) solution for interpreting HER2 IHC in breast carcinoma.
A two-arm multireader study of 120 HER2 IHC whole-slide images from four sites assessed HER2 scoring by four surgical pathologists without and with the aid of an AI HER2 solution. Both arms were compared with high-confidence ground truth (GT) established by agreement of at least four of five breast pathology subspecialists according to ASCO/College of American Pathologists (CAP) 2018/2023 guidelines.
The mean interobserver agreement among GT pathologists across all HER2 scores was 72.4% (N = 120). The AI solution demonstrated high accuracy for HER2 scoring, with 92.1% agreement on slides with high confidence GT (n = 92). The use of the AI tool led to improved performance by readers, interobserver agreement increased from 75.0% for digital manual read to 83.7% for AI-assisted review, and scoring accuracy improved from 85.3% to 88.0%. For the distinction of HER2 0 from 1+ cases (n = 58), pathologists supported by AI showed significantly higher interobserver agreement (69.8% without AI
87.4% with AI) and accuracy (81.9% without AI
88.8% with AI).
This study demonstrated utility of a fully automated AI solution to aid in scoring HER2 IHC accurately according to ASCO/CAP 2018/2023 guidelines. Pathologists supported by AI showed improvements in HER2 IHC scoring consistency and accuracy, especially for distinguishing HER2 0 from 1+ cases. This AI solution could be used by pathologists as a decision support tool for enhancing reproducibility and consistency of HER2 scoring and particularly for identifying HER2-low breast cancers. |
Author | Thomassin, Jeanne Sandbank, Judith Kantekure, Kanchan Mallel, Giuseppe Finck, Wilfrid Vincent-Salomon, Anne Canas-Marques, Rita Krishnamurthy, Savitri Linhart, Chaim Vecsler, Manuela Maklakovski, Marina Colon, Eugenia Bien, Lilach Grinwald, Maya Schnitt, Stuart J Globerson, Yuval |
Author_xml | – sequence: 1 givenname: Savitri orcidid: 0000-0001-9030-4136 surname: Krishnamurthy fullname: Krishnamurthy, Savitri organization: Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX – sequence: 2 givenname: Stuart J surname: Schnitt fullname: Schnitt, Stuart J organization: Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA – sequence: 3 givenname: Anne orcidid: 0000-0001-5754-5771 surname: Vincent-Salomon fullname: Vincent-Salomon, Anne organization: Department of Pathology, Institut Curie, PSL University, Paris, France – sequence: 4 givenname: Rita surname: Canas-Marques fullname: Canas-Marques, Rita organization: Department of Pathology, Champalimaud Foundation, Lisbon, Portugal – sequence: 5 givenname: Eugenia surname: Colon fullname: Colon, Eugenia organization: Department of Pathology, Unilabs, St Görans Hospital, Stockholm, Sweden – sequence: 6 givenname: Kanchan surname: Kantekure fullname: Kantekure, Kanchan organization: Beth Israel Deaconess, Harvard Medical School, Boston, MA – sequence: 7 givenname: Marina surname: Maklakovski fullname: Maklakovski, Marina organization: Department of Pathology, Assuta Ashdod Medical Center, Ashdod, Israel – sequence: 8 givenname: Wilfrid surname: Finck fullname: Finck, Wilfrid organization: MediPath, Frejus, France – sequence: 9 givenname: Jeanne surname: Thomassin fullname: Thomassin, Jeanne organization: MediPath, Frejus, France – sequence: 10 givenname: Yuval surname: Globerson fullname: Globerson, Yuval organization: Ibex Medical Analytics, Tel Aviv, Israel – sequence: 11 givenname: Lilach surname: Bien fullname: Bien, Lilach organization: Ibex Medical Analytics, Tel Aviv, Israel – sequence: 12 givenname: Giuseppe orcidid: 0000-0002-8673-7526 surname: Mallel fullname: Mallel, Giuseppe organization: Ibex Medical Analytics, Tel Aviv, Israel – sequence: 13 givenname: Maya surname: Grinwald fullname: Grinwald, Maya organization: Ibex Medical Analytics, Tel Aviv, Israel – sequence: 14 givenname: Chaim surname: Linhart fullname: Linhart, Chaim organization: Ibex Medical Analytics, Tel Aviv, Israel – sequence: 15 givenname: Judith surname: Sandbank fullname: Sandbank, Judith organization: Institute of Pathology, Maccabi Healthcare Services, Rehovot, Israel – sequence: 16 givenname: Manuela orcidid: 0000-0002-7951-4885 surname: Vecsler fullname: Vecsler, Manuela organization: Ibex Medical Analytics, Tel Aviv, Israel |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39393036$$D View this record in MEDLINE/PubMed |
BookMark | eNo1kF9LwzAUxYMobs49-S75Ap35t6b1rY79g8nE6fNIk3SLNElJU6Tfxo9qReU8_C7nXs6FcwMunXcagDuMZpgg9PCynxE2Q4jO6QUYE8ZpwkjGRmDath8IIUIxwTy9BiOaD0I0HYOvVVfXPSy66K2IWsEiRFMZaUQNty7qujYn7aSGB1930XgHKx_gprPCwWVjlA52uFwH_xnPcCVkHLavWurmZyBwa23n_Nm00cuztgNDDw_SB-NO0Dj4FLRoI1yI4UV4hAV87upoBnMIhofYqf4WXFWibvX0jxPwvlq-LTbJbr_eLopdIjHLaEIyklaY8XQuFEEak1wiJSkjPOVM6AqVPNdclDjNclEqNucUl1zTvFIp4yQnE3D_m9t0pdXq2ARjReiP_1WRbzFEbTs |
ContentType | Journal Article |
DBID | CGR CUY CVF ECM EIF NPM |
DOI | 10.1200/PO.24.00353 |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) |
DatabaseTitleList | MEDLINE |
Database_xml | – sequence: 1 dbid: ECM name: MEDLINE url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live sourceTypes: Index Database |
DeliveryMethod | no_fulltext_linktorsrc |
EISSN | 2473-4284 |
ExternalDocumentID | 39393036 |
Genre | Journal Article |
GroupedDBID | 0R~ 53G ABDBF ALMA_UNASSIGNED_HOLDINGS C45 CGR CUY CVF EBS ECM EIF FBNNL H13 NPM O9- OVD RLZ RUC TEORI |
ID | FETCH-LOGICAL-c1483-2826f14765ad20e129c0dc3427674aef0b79e7ab1689abd45731b7e39fd647292 |
IngestDate | Sat Nov 02 11:58:18 EDT 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c1483-2826f14765ad20e129c0dc3427674aef0b79e7ab1689abd45731b7e39fd647292 |
ORCID | 0000-0002-7951-4885 0000-0001-5754-5771 0000-0002-8673-7526 0000-0001-9030-4136 |
OpenAccessLink | https://pubmed.ncbi.nlm.nih.gov/PMC11485213 |
PMID | 39393036 |
ParticipantIDs | pubmed_primary_39393036 |
PublicationCentury | 2000 |
PublicationDate | 2024-Oct |
PublicationDateYYYYMMDD | 2024-10-01 |
PublicationDate_xml | – month: 10 year: 2024 text: 2024-Oct |
PublicationDecade | 2020 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | JCO precision oncology |
PublicationTitleAlternate | JCO Precis Oncol |
PublicationYear | 2024 |
SSID | ssj0002312176 |
Score | 2.3207097 |
Snippet | The proven efficacy of human epidermal growth factor receptor 2 (HER2) antibody-drug conjugate therapy for treating HER2-low breast cancers necessitates more... |
SourceID | pubmed |
SourceType | Index Database |
StartPage | e2400353 |
SubjectTerms | Artificial Intelligence Breast Neoplasms - pathology Female Humans Immunohistochemistry - methods Observer Variation Receptor, ErbB-2 - analysis |
Title | Fully Automated Artificial Intelligence Solution for Human Epidermal Growth Factor Receptor 2 Immunohistochemistry Scoring in Breast Cancer: A Multireader Study |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39393036 |
Volume | 8 |
hasFullText | |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3di9NAEF9aBbkXUfw6T2UefAvRZpMmjW-l9jiF84Se4tux2d3QwHVTcqly_41_qjO7-br6gT5IIYTdNCw7PyYzszO_YexloCgAlk79SMbKj1Kh_TSXuR-EGs3_MEu5pHrnk1Xy4cvs7TJajkYtD3E_9l8ljWMoa6qc_Qdpdy_FAbxHmeMVpY7Xv5I7-ZTX3nxXl2iLojU5r2w2kOPUGNJvNquweYYulL-kbrGoqC8pIvWtXnvHthkPmZZ6Szfce0flJKUlKZZtqzjUDy6LrzAIFeoF5C0IS5WrerclvpXNmLZZizfOkd8vzoimwPX58Uojb0T5SQOtjdjsqtqBYSW-FnVV9KdHa9OcbuGbcTP6Q67PhaG8U38lLstN0zfb9CkERMpw5Z-Kij6LjmCgFsMICI-6XDr8gFlNyaMk9NGPioZqfTZQy5oyZUPHSvzTN4Pbdtgfz15xIlLfewp3aruxUAlT_E0cW8ufZ_cIvNupMRujOUYW--K0CwOieY1OYdxUjuJSXg8WcsDutH_e83qs9XN-j91t3BaYO7zdZyNtHrDvFmvQYQ16rMEQa9BiDRBrYLEGHdbAYQ0c1qDFGnD4FdagwRoUBhzWwGHtDcxhgDSwSHvIPh0vzxcnftPxw5foloc--v9xHkRJPBWoQzTaonKiZBhxopwSOp9kSaoTkQXxLBWZiqZJGGSJDtNcURuElD9it0xp9BMGWqmEC64Un2pinRQyk-i6ZEpO0lkQykP22G3oxdbRuly0W_30tzNH7KDH3zN2O0edoZ-z8ZXavbBi_QFUN5QW |
link.rule.ids | 782 |
linkProvider | EBSCOhost |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Fully+Automated+Artificial+Intelligence+Solution+for+Human+Epidermal+Growth+Factor+Receptor+2+Immunohistochemistry+Scoring+in+Breast+Cancer%3A+A+Multireader+Study&rft.jtitle=JCO+precision+oncology&rft.au=Krishnamurthy%2C+Savitri&rft.au=Schnitt%2C+Stuart+J&rft.au=Vincent-Salomon%2C+Anne&rft.au=Canas-Marques%2C+Rita&rft.date=2024-10-01&rft.eissn=2473-4284&rft.volume=8&rft.spage=e2400353&rft_id=info:doi/10.1200%2FPO.24.00353&rft_id=info%3Apmid%2F39393036&rft_id=info%3Apmid%2F39393036&rft.externalDocID=39393036 |