Metabolic patterns on [18F]FDG PET/CT in patients with unresectable stage III NSCLC undergoing chemoradiotherapy ± durvalumab maintenance treatment

被引:8
作者
Holzgreve, Adrien [1 ]
Taugner, Julian [2 ]
Kaesmann, Lukas [2 ,3 ,4 ]
Mueller, Philipp [5 ]
Tufman, Amanda [3 ,6 ]
Reinmuth, Niels [7 ]
Li, Minglun [2 ]
Winkelmann, Michael [5 ]
Unterrainer, Lena M. [1 ]
Nieto, Alexander E. [2 ]
Bartenstein, Peter [1 ,4 ]
Kunz, Wolfgang G. [5 ]
Ricke, Jens [5 ]
Belka, Claus [2 ,3 ,4 ]
Eze, Chukwuka [2 ]
Unterrainer, Marcus [1 ,4 ,5 ]
Manapov, Farkhad [2 ,3 ,4 ]
机构
[1] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Nucl Med, Marchioninistr 15, D-81377 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Radiat Oncol, Munich, Germany
[3] Comprehens Pneumol Ctr Munich CPC M, German Ctr Lung Res DZL, Munich, Germany
[4] German Canc Consortium DKTK, Partner Site Munich, Munich, Germany
[5] Univ Hosp, LMU Munich, Dept Radiol, Munich, Germany
[6] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Internal Medicine5, Munich, Germany
[7] Asklepios Lung Clin, Gauting, Germany
关键词
Non-small-cell lung cancer (NSCLC); F-18]FDG PET; CT; Durvalumab immune checkpoint inhibitor consolidation; Durvalumab maintenance treatment; Immunotherapy-related adverse events (irAE); CELL LUNG-CANCER; PREDICTION; SURVIVAL;
D O I
10.1007/s00259-023-06192-6
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
PurposeIn patients with unresectable stage III non-small-cell lung cancer (NSCLC), durvalumab maintenance treatment after chemoradiotherapy (CRT) significantly improves survival. So far, however, metabolic changes of tumoral lesions and secondary lymphoid organs under durvalumab are unknown. Hence, we assessed changes on [F-18]FDG PET/CT in comparison to patients undergoing CRT alone.MethodsForty-three patients with [F-18]FDG PET/CT both before and after standard CRT for unresectable stage III NSCLC were included, in 16/43 patients durvalumab maintenance treatment was initiated (CRT-IO) prior to the second PET/CT. Uptake of tumor sites and secondary lymphoid organs was compared between CRT and CRT-IO. Also, readers were blinded for durvalumab administration and reviewed scans for findings suspicious for immunotherapy-related adverse events (irAE).ResultsInitial uptake characteristics were comparable. However, under durvalumab, diverging metabolic patterns were noted: There was a significantly higher reduction of tumoral uptake intensity in CRT-IO compared to CRT, e.g. median decrease of SUVmax -70.0% vs. -24.8%, p = 0.009. In contrast, the spleen uptake increased in CRT-IO while it dropped in CRT (median + 12.5% vs. -4.4%, p = 0.029). Overall survival was significantly longer in CRT-IO compared to CRT with few events (progression/death) noted in CRT-IO. Findings suggestive of irAE were present on PET/CT more often in CRT-IO (12/16) compared to CRT (8/27 patients), p = 0.005.ConclusionDurvalumab maintenance treatment after CRT leads to diverging tumoral metabolic changes, but also increases splenic metabolism and leads to a higher proportion of findings suggestive of irAE compared to patients without durvalumab. Due to significantly prolonged survival with durvalumab, survival analysis will be substantiated in correlation to metabolic changes as soon as more clinical events are present.
引用
收藏
页码:2466 / 2476
页数:11
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