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Noninvasive Assessment of Acute Graft-Versus-Host Disease of the Gastrointestinal Tract After Allogeneic Hemopoietic Stem Cell Transplantation Using 18F-FDG PET.
Cherk, Martin H; Khor, Robert; Barber, Thomas W; Yap, Kenneth S K; Patil, Sushrut; Walker, Patricia; Avery, Sharon; Roberts, Stuart; Kemp, William; Pham, Alan; Bailey, Michael; Kalff, Victor.
Afiliação
  • Cherk MH; Department of Nuclear Medicine & PET, Alfred Hospital, Melbourne Australia; m.cherk@alfred.org.au.
  • Khor R; Monash University, Melbourne, Australia.
  • Barber TW; Department of Nuclear Medicine & PET, Alfred Hospital, Melbourne Australia.
  • Yap KSK; Department of Nuclear Medicine & PET, Alfred Hospital, Melbourne Australia.
  • Patil S; Monash University, Melbourne, Australia.
  • Walker P; Department of Nuclear Medicine & PET, Alfred Hospital, Melbourne Australia.
  • Avery S; Monash University, Melbourne, Australia.
  • Roberts S; Monash University, Melbourne, Australia.
  • Kemp W; Department of Haematology, Alfred Hospital, Melbourne, Australia.
  • Pham A; Department of Haematology, Alfred Hospital, Melbourne, Australia.
  • Bailey M; Monash University, Melbourne, Australia.
  • Kalff V; Department of Haematology, Alfred Hospital, Melbourne, Australia.
J Nucl Med ; 63(12): 1899-1905, 2022 12.
Article em En | MEDLINE | ID: mdl-35450959
ABSTRACT
Acute graft-versus-host disease of the gastrointestinal tract (acute GIT-GVHD) often complicates allogeneic hemopoietic stem cell transplantation (AHSCT). 18F-FDG PET/CT is known to detect active inflammation and may be a useful noninvasive test for acute GIT-GVHD. The objective of this study was to evaluate the diagnostic utility of 18F-FDG PET/CT to noninvasively assess patients with clinically suspected acute GIT-GVHD. Fifty-one AHSCT patients with clinically suspected acute GIT-GVHD prospectively underwent 18F-FDG PET/CT scanning followed by upper and lower GIT endoscopy within 7 d. Endoscopic biopsies of 4 upper GIT and 4 colonic segments were obtained for histology to compare with corresponding quantitative segmental 18F-FDG PET/CT SUVmax Receiver-operating-characteristic curve (ROC) analysis was performed to determine predictive capacity of 18F-FDG PET/CT SUVmax for acute GIT-GVHD. A separate qualitative visual 18F-FDG PET/CT analysis was also performed for comparison.

Results:

Twenty-three of 51 (45.1%) patients had biopsy-confirmed acute GIT-GVHD, with 19 of 23 (82.6%) having upper GIT and 22 of 22 (100%) colonic involvement. One of 23 patients did not undergo a colonoscopy. GVHD involved the entire colon contiguously in 21 of 22 patients. For quantitative analysis, histology from 4 upper GIT and 4 colonic segments were compared with 18F-FDG PET/CT SUVmax Colonic segments positive for GVHD had a higher SUVmax (4.1 [95% CI, 3.6-4.5]) than did normal colonic segments (2.3 [1.9-2.7], P = 0.006). No difference was demonstrated in upper GIT segments. Quantitative 18F-FDG PET/CT yielded a 69% sensitivity, 57% specificity, 73% negative predictive value, and 59% positive predictive value for the detection of GVHD compared with 70%, 76%, 76%, and 68%, respectively, for qualitative analysis.

Conclusion:

18F-FDG PET is a useful noninvasive diagnostic test for acute GIT-GVHD, which when present always involves the colon and usually in its entirety, suggesting colonic biopsy obtained by sigmoidoscopy is adequate for histologic confirmation when acute GIT-GVHD is suspected. Of note, 18F-FDG PET cannot distinguish acute GIT-GVHD from non-GVHD inflammatory changes in the colon.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article