Evidence map›Paper›PMID 41968610›Full record

Observational studyCancer medicine2026

Endocrinologist-Led Management of Endocrine Immune-Related Adverse Events: Real-World Evidence Supporting the Japan Endocrine Society Guidelines.

Kota Nishihama, Hajime Fujimoto, Kanako Saito, Chisa Inoue, Yuko Okano, Atsuro Takeshita, Mei Uemura, Corina N D'Alessandro-Gabazza, Esteban C Gabazza, Yutaka Yano and 1 more

Abstract readObservational Study
In one paragraph

Observational study in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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.

Kota NishihamaDepartment of Diabetes, Metabolism and Endocrinology, Mie University Graduate School of Medicine, Tsu, Japan.ORCID https://orcid.org/0000-0002-0471-5164
Hajime FujimotoDepartment of Pulmonary and Critical Care Medicine, Mie University Graduate School of Medicine, Tsu, Japan.
Kanako SaitoDepartment of Medical Oncology, Mie University Hospital, Tsu, Japan.ORCID https://orcid.org/0000-0001-7420-563X
Chisa InoueDepartment of Diabetes, Metabolism and Endocrinology, Mie University Graduate School of Medicine, Tsu, Japan.
Yuko OkanoDepartment of Diabetes, Metabolism and Endocrinology, Mie University Graduate School of Medicine, Tsu, Japan.
Atsuro TakeshitaDepartment of Diabetes, Metabolism and Endocrinology, Mie University Graduate School of Medicine, Tsu, Japan.
Mei UemuraDepartment of Diabetes, Metabolism and Endocrinology, Mie University Graduate School of Medicine, Tsu, Japan.
Corina N D'Alessandro-GabazzaDepartment of Immunology, Mie University Graduate School of Medicine, Tsu, Japan.
Esteban C GabazzaDepartment of Immunology, Mie University Graduate School of Medicine, Tsu, Japan.
Yutaka YanoDepartment of Diabetes, Metabolism and Endocrinology, Mie University Graduate School of Medicine, Tsu, Japan.
Taro YasumaDepartment of Diabetes, Metabolism and Endocrinology, Mie University Graduate School of Medicine, Tsu, Japan.

Funding

Public Interest Incorporated Foundation Mie Health Care Business Service Center
6 · The paper itself

Abstract

This retrospective observational study assessed the real-world management of endocrine immune-related adverse events (irAEs) in 84 patients treated with immune checkpoint inhibitors (ICIs) at a single center in Japan. Care was provided by endocrinologists and evaluated for consistency with the Japan Endocrine Society (JES) guidelines. Thyroid dysfunction (64.3%) and adrenal insufficiency (42.9%) were the most frequent irAEs, followed by hypophysitis and insulin-dependent diabetes mellitus (each 8.3%). Management generally conformed to JES recommendations, including levothyroxine and hydrocortisone replacement at guideline-recommended doses. More than 80% of patients received maintenance therapy as recommended in the JES guidelines. In some cases, higher hydrocortisone doses were administered based on clinical judgment, particularly in patients with malignancy-related poor general condition. No hospitalizations occurred for thyroid dysfunction, whereas four patients were admitted for adrenal insufficiency-related sick day management. For the treatment of hypophysitis, continuous hydrocortisone replacement therapy was commonly administered. All cases of ICI-induced diabetes presented with severe hyperglycemia, highlighting the importance of early recognition. Survival analysis indicated a trend toward improved prognosis in patients with renal cell carcinoma who developed endocrine irAEs. Notably, the occurrence of endocrine irAE did not directly necessitate switching or discontinuation of ICI therapy. Although limited by its single-center design and the possibility of underreporting, this study provides valuable clinical insights into endocrine irAE management and supports the feasibility of JES guidelines. These findings underscore the importance of specialized endocrine care and guideline-based management in optimizing safety and long-term outcomes in ICI-treated cancer patients, particularly in settings with limited endocrinology resources.

Indexed as

Endocrine System DiseasesEndocrinologistsImmune Checkpoint InhibitorsNeoplasmsAdrenal InsufficiencyAgedAged, 80 and overFemaleHumansHydrocortisoneHypophysitisJapanMaleMiddle AgedPractice Guidelines as TopicRetrospective StudiesHydrocortisoneImmune Checkpoint Inhibitorsadrenal insufficiencyhypophysitishypothyroidismimmune checkpoint inhibitorsimmune‐related adverse events

Identifiers

PMID41968610
PMCPMC13071169

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.