Evidence map›Paper›PMID 41781348›Full record

ArticleJournal of internal medicine2026

Who can safely discontinue lifelong follow-up among patients with sporadic pheochromocytoma and paraganglioma?

Min Jeong Park, Seung Shin Park, Won Woong Kim, Su-Jin Kim, Yu-Mi Lee, Kyu Eun Lee, Tae-Yon Sung, Jae-Kyung Won, Dong Eun Song, Jung-Min Koh and 6 more

Abstract read
In one paragraph

Article in Journal of internal medicine, 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
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1 · What the graph read from it

What it found

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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

16 authors.

Min Jeong ParkDepartment of Internal Medicine, Korea University Medical Center Guro Hospital, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-2204-2901
Seung Shin ParkDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-5719-1539
Won Woong KimDepartment of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Su-Jin KimDepartment of Surgery, Seoul National University College of Medicine, Seoul, Republic of Korea.
Yu-Mi LeeDepartment of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Kyu Eun LeeDepartment of Surgery, Seoul National University College of Medicine, Seoul, Republic of Korea.
Tae-Yon SungDepartment of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Jae-Kyung WonDepartment of Pathology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Dong Eun SongDepartment of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Jung-Min KohDivision of Endocrinology and Metabolism, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Sara TalvacchioAKESO Center for Adrenal Endocrine Tumors, Prague, Czech Republic.
Tamara ProdanovAKESO Center for Adrenal Endocrine Tumors, Prague, Czech Republic.ORCID https://orcid.org/0009-0007-3887-5303
Hussam AlkaissiNational Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland, USA.
Karel PacakAKESO Center for Adrenal Endocrine Tumors, Prague, Czech Republic.
Seung Hun LeeDivision of Endocrinology and Metabolism, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-0496-247X
Jung Hee KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-1932-0234

Funding

Korea Health Industry Development InstituteMinistry of Health and Welfare of the Republic of Korea RS-2024-00397426Ministry of Health and Welfare of the Republic of Korea RS-2024-00406806Ministry of Health and Welfare of the Republic of Korea RS-2025-02233101
6 · The paper itself

Abstract

backgroundCurrent guidelines recommend at least 10 years of follow-up for all pheochromocytoma and paraganglioma (PPGL) patients and lifelong monitoring for high-risk individuals. Nonetheless, data identifying patients who may not require routine lifelong follow-up are scarce.

methodsAmong 999 patients with PPGL, 703 who were non-metastatic, non-hereditary, and had undergone complete resection were included. Variables that significantly differed between the recurrence (n = 50) and non-recurrence groups over 10 years (n = 83) were identified, and cutoff values were determined using receiver-operating characteristic curve analysis. These very low-risk criteria were validated in an internal cohort and an external dataset from the National Institutes of Health.

resultsThe non-recurrence group was older and had smaller pheochromocytomas (PCCs) than the recurrence group, with cutoffs of 37 years and 5.7 cm, respectively. The non-recurrence group had a higher percentage of patients with pheochromocytoma of the adrenal gland scaled score (PASS) <4 or grading system for adrenal pheochromocytoma and paraganglioma (GAPP) score <3 (p = 0.027). Age >40 years (hazard ratio [HR] [95% confidence intervals] of 0.36 [0.17-0.76]), PCC size <6 cm (HR = 0.43 [0.19-0.98]), and PASS <4 or GAPP score <3 (HR = 0.37 [0.16-0.89]) were associated with lower recurrence risk. None of the patients meeting all these criteria in the internal (n = 114) and external (n = 13) validation sets experienced recurrence.

conclusionThis study suggests that routine lifelong follow-up may be unnecessary for patients with sporadic PCC aged >40 years, size <6 cm, and PASS <4 or GAPP score <3.

Indexed as

Adrenal Gland NeoplasmsNeoplasm Recurrence, LocalParagangliomaPheochromocytomaAdultAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedYoung Adultcriteriafollow‐upmetastasisparagangliomapheochromocytomarecurrence

Identifiers

PMID41781348
PMCPMC13061095

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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.