Journal Article DZNE-2026-01141

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Baseline body composition and early PRRT outcome in GEP-NETs: an exploratory analysis.

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2026
Springer-Verl. Heidelberg [u.a.]

European journal of nuclear medicine and molecular imaging 53(13), 8621 - 8629 () [10.1007/s00259-026-08182-w]

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Abstract: Early progression after PRRT occurs in a subset of patients with somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (GEP-NETs). Associations between body composition and early PET-based progression after PRRT were assessed.In this retrospective analysis, 321 patients undergoing PRRT were screened. Body composition parameters were assessed on the CT component at the L3/L4 level. Myosteatosis was defined using BMI-adjusted psoas muscle attenuation cut-offs. The primary endpoint was early SSTR-targeted PET-based progression after up to four consecutive PRRT cycles, dichotomized as progressive disease versus disease control, which was available in 301 patients.Early PET-based progression occurred in 24/301 patients (8.0%). Traditional quantity-based body composition parameters were not associated with early progression. Baseline myosteatosis was present in only 8/301 patients (2.7%) and showed a nominal association with early progression in univariable analysis (OR 7.8, 95% CI 1.74-34.78; p = 0.0073), but this association did not remain significant after Benjamini-Hochberg correction for multiple testing (FDR-adjusted p = 0.1073). In a separately specified baseline-adjusted model, myosteatosis remained nominally associated with early progression (OR 8.1, 95% CI 1.69-38.75; p = 0.0090). In an exploratory model additionally including the number of completed PRRT cycles as a post-baseline treatment-exposure variable, the association was attenuated and narrowly missed conventional statistical significance (OR 5.7, 95% CI 0.97-32.86; p = 0.0538).Traditional quantity-based body composition parameters were not associated with early PET-based progression after PRRT. Although baseline myosteatosis showed a nominal association with early progression, this finding was based on only eight patients and did not remain significant after correction for multiple testing. The results should therefore be regarded as exploratory and hypothesis-generating and do not establish clinical utility of myosteatosis for individual risk stratification.

Keyword(s): Humans (MeSH) ; Body Composition (MeSH) ; Neuroendocrine Tumors: diagnostic imaging (MeSH) ; Neuroendocrine Tumors: metabolism (MeSH) ; Neuroendocrine Tumors: drug therapy (MeSH) ; Female (MeSH) ; Pancreatic Neoplasms: diagnostic imaging (MeSH) ; Pancreatic Neoplasms: metabolism (MeSH) ; Retrospective Studies (MeSH) ; Male (MeSH) ; Stomach Neoplasms: diagnostic imaging (MeSH) ; Stomach Neoplasms: metabolism (MeSH) ; Stomach Neoplasms: drug therapy (MeSH) ; Disease Progression (MeSH) ; Middle Aged (MeSH) ; Treatment Outcome (MeSH) ; Aged (MeSH) ; Receptors, Somatostatin: metabolism (MeSH) ; Positron-Emission Tomography (MeSH) ; Intestinal Neoplasms (MeSH) ; Body composition ; Early progression ; Myosteatosis ; NET ; PRRT ; Receptors, Somatostatin

Classification:

Contributing Institute(s):
  1. Molecular Neurodegeneration (AG Haass)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)

Database coverage:
Medline ; Clarivate Analytics Master Journal List ; Current Contents - Clinical Medicine ; Current Contents - Life Sciences ; DEAL Springer ; DEAL Springer ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2026-11-04, last modified 2026-11-04


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