[Pseudoprogression after start of immunotherapy].
1/5 보강
[CLINICAL/METHODICAL ISSUE] Distinguishing pseudoprogression from true progression represents a considerable challenge in both clinical practice and radiological imaging.
APA
Winkelmann M, Kassube M, et al. (2026). [Pseudoprogression after start of immunotherapy].. Radiologie (Heidelberg, Germany), 66(1), 24-32. https://doi.org/10.1007/s00117-025-01544-9
MLA
Winkelmann M, et al.. "[Pseudoprogression after start of immunotherapy].." Radiologie (Heidelberg, Germany), vol. 66, no. 1, 2026, pp. 24-32.
PMID
41364195 ↗
Abstract 한글 요약
[CLINICAL/METHODICAL ISSUE] Distinguishing pseudoprogression from true progression represents a considerable challenge in both clinical practice and radiological imaging.
[STANDARD RADIOLOGICAL METHODS] Established radiological methods include computed tomography (CT) and magnetic resonance imaging (MRI), complemented by fluorodeoxyglucose-positron emission tomography (FDG-PET)/CT from nuclear medicine.
[METHODICAL INNOVATIONS] Novel PET/CT tracers, liquid biopsies, and radiomics are considered innovative approaches that may facilitate the detection of pseudoprogression but still need clinical validation.
[PERFORMANCE] CT, MRI, and PET/CT can provide valuable clues for distinguishing pseudoprogression from true progression, but are often inconclusive. Novel imaging approaches are currently under investigation in clinical studies.
[ACHIEVEMENTS] The use of laboratory markers and radiomics has shown promising improvements in several studies, but has not yet been adopted into clinical routine.
[PRACTICAL RECOMMENDATIONS] In clinically stable patients, suspected pseudoprogression early after start of immunotherapy justifies continuation of therapy with close imaging follow-up (early follow-up after 4-8 weeks).
[STANDARD RADIOLOGICAL METHODS] Established radiological methods include computed tomography (CT) and magnetic resonance imaging (MRI), complemented by fluorodeoxyglucose-positron emission tomography (FDG-PET)/CT from nuclear medicine.
[METHODICAL INNOVATIONS] Novel PET/CT tracers, liquid biopsies, and radiomics are considered innovative approaches that may facilitate the detection of pseudoprogression but still need clinical validation.
[PERFORMANCE] CT, MRI, and PET/CT can provide valuable clues for distinguishing pseudoprogression from true progression, but are often inconclusive. Novel imaging approaches are currently under investigation in clinical studies.
[ACHIEVEMENTS] The use of laboratory markers and radiomics has shown promising improvements in several studies, but has not yet been adopted into clinical routine.
[PRACTICAL RECOMMENDATIONS] In clinically stable patients, suspected pseudoprogression early after start of immunotherapy justifies continuation of therapy with close imaging follow-up (early follow-up after 4-8 weeks).
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