Clinical-grade autonomous cytopathology through whole-slide edge tomography

N Nao Nitta Y Yuko Sugiyama T Takeaki Sugimura T Takahiko Ito K Koichi Ikebata H Hitoshi Abe S Shuhei Ishii H Hiroyuki Kanao N Nagisa Hosoya R Raihan Ull Islam A Aditya Jain M Meisam Hasani J Joseph Zonghi P Peter Koh Y Yukihito Mase M Miki Kanematsu N Noureldin M. Z. Ali Y Yoshihiko Murata A Ayumi Shikama Y Yusuke Kobayashi D Daisuke Matsubara Y Yukari Himeji H Hiroshi Nakamura A Akane Hashizume M Miyaka Umemori H Hiroyuki Ohsaki Y Yingdong Luo T Tianben Ding F Fernando C. Schmitt R Robert Y. Osamura T Tomohiro Chiba K Keisuke Goda

Abstract

Abstract Cytopathology, often abbreviated as cytology, has a central role in the early detection of cancer, such as cervical, lung and bladder cancers, owing to its speed, simplicity and minimally invasive nature 1–9 . However, its effectiveness is limited by variability in diagnostic accuracy stemming from subjective visual interpretation 10–21 . Although many artificial intelligence (AI)-powered systems have been proposed to improve consistency 22–26 , none have achieved fully autonomous, clinical-grade performance. Existing approaches serve as assistive tools and still rely on human oversight for interpretation and decision-making 22–26 . Here we present a clinical-grade autonomous cytopathology pipeline that combines high-resolution, real-time optical whole-slide tomography with edge computing to deliver end-to-end automation. The system achieves practical performance in imaging speed, quality and data volume, with localized data compression enabling streamlined storage and accelerated AI-driven analysis. In addition to supporting cell-level classification, the platform enables flow cytometry-like, population-wide morphological profiling for comprehensive interpretation of cellular distributions and patterns. A vision transformer achieved area under the receiver operating characteristic (ROC) curve (AUC) values exceeding 0.99 at the single-cell level for detecting low-grade squamous intraepithelial lesions (LSILs), high-grade squamous intraepithelial lesions (HSILs) and adenocarcinoma. In a multicentre evaluation of 1,124 cervical liquid-based cytology samples across four centres, the AI model achieved slide-level AUC values of 0.86–0.91 for LSIL + and 0.89–0.97 for HSIL + , with LSIL counts correlating strongly with human papillomavirus positivity and HSIL counts scaling with diagnostic severity. The system enables autonomous triage cytology, offering a foundation for routine, scalable and objective diagnostics.

Article Details

Journal Nature
Volume / Issue Vol. 651, Issue 8105
Published March 12, 2026
Pages 472-481
ISSN 0028-0836
Publisher Nature Portfolio

Journal Info

Nature

Nature Portfolio

ISSN: 0028-0836 Health Sciences

Authors (32)

N

Nao Nitta

Y

Yuko Sugiyama

T

Takeaki Sugimura

T

Takahiko Ito

K

Koichi Ikebata

H

Hitoshi Abe

S

Shuhei Ishii

H

Hiroyuki Kanao

N

Nagisa Hosoya

R

Raihan Ull Islam

A

Aditya Jain

M

Meisam Hasani

J

Joseph Zonghi

P

Peter Koh

Y

Yukihito Mase

M

Miki Kanematsu

N

Noureldin M. Z. Ali

Y

Yoshihiko Murata

A

Ayumi Shikama

Y

Yusuke Kobayashi

D

Daisuke Matsubara

Y

Yukari Himeji

H

Hiroshi Nakamura

A

Akane Hashizume

M

Miyaka Umemori

H

Hiroyuki Ohsaki

Y

Yingdong Luo

T

Tianben Ding

F

Fernando C. Schmitt

R

Robert Y. Osamura

T

Tomohiro Chiba

K

Keisuke Goda