Healthy tissue metabolism assessed by [18F]FDG PET/CT as a marker of prognosis and adverse events in advanced Hodgkin lymphoma patients

被引:0
作者
Malaih, Afnan A. [1 ,2 ,3 ]
Kirkwood, Amy A. [4 ]
Johnson, Peter [5 ]
Radhakrishnan, Vivek [6 ]
Fischer, Barbara M. [1 ,2 ,7 ]
Barrington, Sally F. [1 ,2 ]
机构
[1] Kings Coll London, London, England
[2] Kings Coll London, Guys & St ThomasPET Ctr, Sch Biomed Engn & Imaging Sci, Kings Hlth Partners, London, England
[3] King Abdulaziz Univ, Fac Appl Med Sci, Radiol Sci, Jeddah, Saudi Arabia
[4] UCL, UCL Canc Inst, Canc Res UK & UCL Canc Trials Ctr, London, England
[5] Univ Southampton, Canc Res UK Ctr, Southampton, England
[6] Univ Hosp Southampton, Canc Care Grp, Southampton, England
[7] Univ Copenhagen, Dept Clin Physiol & Nucl Med, Rigshosp, Copenhagen, Denmark
关键词
CELL LUNG-CANCER; MARROW F-18-FDG UPTAKE; BONE-MARROW; TUMOR VOLUME; EARLY RESPONSE; BLOOD-POOL; FDG UPTAKE; LIVER; CHEMOTHERAPY; REPEATABILITY;
D O I
10.1038/s41598-024-63349-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The aim of the study was to assess healthy tissue metabolism (HTM) using 2-deoxy-2-[F-18]fluoro-D-glucose ([F-18]FDG) positron emission tomography/computed tomography (PET/CT) during chemotherapy in Hodgkin lymphoma (HL) and the association of HTM with baseline metabolic tumour volume (MTV), haematological parameters, adverse events (AEs), early response and progression-free survival (PFS). We retrospectively identified 200 patients with advanced HL from the RATHL trial with [F-18]FDG-PET/CT before (PET0) and following 2 cycles of chemotherapy (PET2). [F-18]FDG-uptake was measured in bone marrow (BM), spleen, liver and mediastinal blood pool (MBP). Deauville score (DS) 1-3 was used to classify responders and DS 4-5, non-responders. [F-18]FDG-uptake decreased significantly in BM and spleen and increased in liver and MBP at PET2 (all p < 0.0001), but was not associated with MTV. Higher BM uptake at PET0 was associated with lower baseline haemoglobin and higher absolute neutrophil counts, platelets, and white blood cells. High BM, spleen, and liver uptake at PET0 was associated with neutropenia after cycles 1-2. BM uptake at PET0 was associated with treatment failure at PET2 and non-responders with higher BM uptake at PET2 had significantly inferior PFS (p = 0.023; hazard ratio = 2.31). Based on these results, we concluded that the change in HTM during chemotherapy was most likely a direct impact of chemotherapy rather than a change in MTV. BM uptake has prognostic value in HL.
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页数:9
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