Adrenal disease

Prognostic impact of anatomic site in pheochromocytomas and paragangliomas: a population-based cohort study

Eur J EndocrinolPublished Retrospective cohort study

Main finding · Survival by anatomic siteResult — go to the resultHR, event not stated (higher = poorer prognosis) 2.26 95% CI 1.14–4.48

Authors' conclusion

The prognostic effect of anatomic site in PPGLs is stage-dependent. While location does not influence outcomes in localized disease, it becomes clinically meaningful with progression-favoring head and neck tumors and disadvantaging adrenal primaries in advanced stages. Incorporating site into stage-aware risk stratification and tailoring multimodal care for high-risk thoraco-abdominal/adrenal disease are warranted. Prospective, genotype-annotated registries should validate and refine these findings.

Study context

Population
Patients with histologically confirmed pheochromocytomas and paragangliomas (PPGLs), SEER 17 (2000–2022)
Participants
1,468 patients
Exposure
Anatomic site of PPGL: adrenal vs head and neck vs thorax vs abdomen
Outcome
Overall and cancer-specific survival
Methodological detailspopulation-based, SEER 17 (2000-2022), propensity score matching, stage-stratified analyses
  • Population-based
  • SEER 17 (2000-2022)
  • Propensity score matching
  • Stage-stratified analyses

Main finding

Survival by anatomic site

HR, event not stated (higher = poorer prognosis)

2.26

95% CI 1.14–4.48

Adrenal
HR, event not stated (higher = poorer prognosis) 2.26 (95% CI 1.14–4.48)

As reported in the abstract

Survival outcomes varied by site; head and neck PGLs had the most favorable prognosis
P = 0.004

Observational data: associations, not effects.

Further findings

Distribution of primary site

Original publication

Prognostic impact of anatomic site in pheochromocytomas and paragangliomas: a population-based cohort study. Eur J Endocrinol. Published 18 May 2026. doi:10.1093/ejendo/lvag084

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