Evidence map›Paper›PMID 42609659›Full record

ArticleFrontiers in oncology2026

Cellular variant focal segmental glomerulosclerosis during trastuzumab emtansine treatment in HER2-positive breast cancer: a case report.

Soshi Okada, Sae Aratani, Daisuke Miyamoto, Masujiro Makita, Risa Murasato, Hideko Hoshina, Akio Hirama, Yukako Shintani-Domoto, Tetsuya Kashiwagi, Ryuji Ohashi and 1 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Soshi OkadaDepartment of Endocrinology, Metabolism and Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Sae ArataniDepartment of Endocrinology, Metabolism and Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Daisuke MiyamotoDepartment of Endocrinology, Metabolism and Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Masujiro MakitaDepartment of Breast Surgery and Oncology, Nippon Medical School Musashikosugi Hospital, Kawasaki-shi, Kanagawa, Japan.
Risa MurasatoDepartment of Breast Surgery and Oncology, Nippon Medical School Musashikosugi Hospital, Kawasaki-shi, Kanagawa, Japan.
Hideko HoshinaDepartment of Breast Surgery and Oncology, Nippon Medical School Musashikosugi Hospital, Kawasaki-shi, Kanagawa, Japan.
Akio HiramaDepartment of Endocrinology, Metabolism and Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Yukako Shintani-DomotoDepartment of Diagnostic Pathology, Nippon Medical School, Tokyo, Japan.
Tetsuya KashiwagiDepartment of Endocrinology, Metabolism and Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Ryuji OhashiDepartment of Diagnostic Pathology, Nippon Medical School, Tokyo, Japan.
Masato IwabuDepartment of Endocrinology, Metabolism and Nephrology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Onconephrology is an emerging subspecialty that encompasses comprehensive kidney management in patients with cancer. Trastuzumab emtansine (T-DM1) is an antibody-drug conjugate composed of trastuzumab linked to the microtubule inhibitor. T-DM1 is widely used in the treatment of human epidermal growth factor receptor 2-positive breast cancer, and glomerular disease arising during T-DM1 therapy remains rarely reported. The present report describes the case of a 50-year-old Japanese woman who developed nephrotic-range proteinuria approximately five months after initiating T-DM1 adjuvant therapy. Kidney biopsy confirmed the diagnosis of cellular variant focal segmental glomerulosclerosis. Other secondary causes, including autoimmune disease and infection, were excluded, and the temporal relationship between symptom onset and T-DM1 administration suggested a possible drug-related etiology. Given the absence of alternative treatment regimens for her breast cancer, we decided to continue T-DM1 without immunosuppressive therapy, with careful monitoring of kidney function and proteinuria. The scheduled anticancer treatment course was successfully completed, and proteinuria improved significantly within 7 weeks of treatment completion. This case highlights the importance of recognizing rare glomerular adverse effects of T-DM1 and underscores the need to carefully balance oncological treatment benefits against renal toxicity, emphasizing the value of multidisciplinary collaboration between oncologists and nephrologists.

Indexed as

case reportfocal segmental glomerulosclerosisHER2-positive breast canceronconephrologytrastuzumab emtansine

Identifiers

PMID42609659
PMCPMC13478682

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.