[18F]FDG PET/CT in the Evaluation of Melanoma Patients Treated with Immunotherapy

被引:9
作者
Mangas Losada, Maria [1 ]
Romero Robles, Leonardo [1 ]
Mendoza Melero, Alejandro [1 ]
Garcia Megias, Irene [1 ]
Villanueva Torres, Amos [1 ]
Garrastachu Zumaran, Puy [1 ]
Boulvard Chollet, Xavier [1 ]
Lopci, Egesta [2 ]
Ramirez Lasanta, Rafael [1 ]
Delgado Bolton, Roberto C. [1 ]
机构
[1] Univ Hosp San Pedro, Ctr Biomed Res Rioja CIBIR, Dept Diagnost Imaging Radiol & Nucl Med, Logrono 26006, Spain
[2] IRCCS Humanitas Res Hosp, Nucl Med, I-20089 Rozzano, Italy
关键词
FDG PET; CT; immunotherapy; melanoma; response evaluation; adverse events; POSITRON-EMISSION-TOMOGRAPHY; CLINICAL-SIGNIFICANCE; RESPONSE CRITERIA; F-18-FDG PET/CT; GUIDELINES; COLITIS; CANCER;
D O I
10.3390/diagnostics13050978
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Immunotherapy is based on manipulation of the immune system in order to act against tumour cells, with growing evidence especially in melanoma patients. The challenges faced by this new therapeutic tool are (i) finding valid evaluation criteria for response assessment; (ii) knowing and distinguishing between "atypical" response patterns; (iii) using PET biomarkers as predictive and response evaluation parameters and (iv) diagnosis and management of immunorelated adverse effects. This review is focused on melanoma patients analysing (a) the role of [F-18]FDG PET/CT in the mentioned challenges; (b) the evidence of its efficacy. For this purpose, we performed a review of the literature, including original and review articles. In summary, although there are no clearly established or globally accepted criteria, modified response criteria are potentially appropriate for evaluation of immunotherapy benefit. In this context, [F-18]FDG PET/CT biomarkers appear to be promising parameters in prediction and assessment of response to immunotherapy. Moreover, immunorelated adverse effects are recognized as predictors of early response to immunotherapy and may be associated with better prognosis and clinical benefit.
引用
收藏
页数:17
相关论文
共 52 条
[1]   Absolute number of new lesions on 18F-FDG PET/CT is more predictive of clinical response than SUV changes in metastatic melanoma patients receiving ipilimumab [J].
Anwar, Hoda ;
Sachpekidis, Christos ;
Winkler, Julia ;
Kopp-Schneider, Annette ;
Haberkorn, Uwe ;
Hassel, Jessica C. ;
Dimitrakopoulou-Strauss, Antonia .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2018, 45 (03) :376-383
[2]   The value of18F-FDG PET/CT for predicting or monitoring immunotherapy response in patients with metastatic melanoma: a systematic review and meta-analysis [J].
Ayati, Narjess ;
Sadeghi, Ramin ;
Kiamanesh, Zahra ;
Lee, Sze Ting ;
Zakavi, S. Rasoul ;
Scott, Andrew M. .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2021, 48 (02) :428-448
[3]   Patterns of progression in patients treated for immuno-oncology antibodies combination [J].
Bernard-Tessier, Alice ;
Baldini, Capucine ;
Castanon, Eduardo ;
Martin, Patricia ;
Champiat, Stephane ;
Hollebecque, Antoine ;
Postel-Vinay, Sophie ;
Varga, Andreea ;
Bahleda, Rastilav ;
Gazzah, Anas ;
Michot, Jean-Marie ;
Ribrag, Vincent ;
Armand, Jean-Pierre ;
Marabelle, Aurelien ;
Soria, Jean-Charles ;
Massard, Christophe ;
Ammari, Samy .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2021, 70 (01) :221-232
[4]   FDG PET/CT: EANM procedure guidelines for tumour imaging: version 2.0 [J].
Boellaard, Ronald ;
Delgado-Bolton, Roberto ;
Oyen, Wim J. G. ;
Giammarile, Francesco ;
Tatsch, Klaus ;
Eschner, Wolfgang ;
Verzijlbergen, Fred J. ;
Barrington, Sally F. ;
Pike, Lucy C. ;
Weber, Wolfgang A. ;
Stroobants, Sigrid ;
Delbeke, Dominique ;
Donohoe, Kevin J. ;
Holbrook, Scott ;
Graham, Michael M. ;
Testanera, Giorgio ;
Hoekstra, Otto S. ;
Zijlstra, Josee ;
Visser, Eric ;
Hoekstra, Corneline J. ;
Pruim, Jan ;
Willemsen, Antoon ;
Arends, Bertjan ;
Kotzerke, Joerg ;
Bockisch, Andreas ;
Beyer, Thomas ;
Chiti, Arturo ;
Krause, Bernd J. .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2015, 42 (02) :328-354
[5]   Novel patterns of response under immunotherapy [J].
Borcoman, E. ;
Kanjanapan, Y. ;
Champiat, S. ;
Kato, S. ;
Servois, V. ;
Kurzrock, R. ;
Goel, S. ;
Bedard, P. ;
Le Tourneau, C. .
ANNALS OF ONCOLOGY, 2019, 30 (03) :385-396
[6]   Hyperprogressive Disease Is a New Pattern of Progression in Cancer Patients Treated by Anti-PD-1/PD-L1 [J].
Champiat, Stephane ;
Dercle, Laurent ;
Ammari, Samy ;
Massard, Christophe ;
Hollebecque, Antoine ;
Postel-Vinay, Sophie ;
Chaput, Nathalie ;
Eggermont, Alexander ;
Marabelle, Aurelien ;
Soria, Jean-Charles ;
Ferte, Charles .
CLINICAL CANCER RESEARCH, 2017, 23 (08) :1920-1928
[7]   18F-FDG PET/CT features of immune-related adverse events and pitfalls following immunotherapy [J].
Cherk, Martin H. ;
Nadebaum, David P. ;
Barber, Thomas W. ;
Beech, Paul ;
Haydon, Andrew ;
Yap, Kenneth S. .
JOURNAL OF MEDICAL IMAGING AND RADIATION ONCOLOGY, 2022, 66 (04) :483-494
[8]   Prediction of Response to Immune Checkpoint Inhibitor Therapy Using Early-Time-Point 18F-FDG PET/CT Imaging in Patients with Advanced Melanoma [J].
Cho, Steve Y. ;
Lipson, Evan J. ;
Im, Hyung-Jun ;
Rowe, Steven P. ;
Gonzalez, Esther Mena ;
Blackford, Amanda ;
Chirindel, Alin ;
Pardoll, Drew M. ;
Topalian, Suzanne L. ;
Wahl, Richard L. .
JOURNAL OF NUCLEAR MEDICINE, 2017, 58 (09) :1421-1428
[9]   Balancing the good and the bad: controlling immune-related adverse events versus anti-tumor responses in cancer patients treated with immune checkpoint inhibitors [J].
de Britto Evangelista, Guilherme Ferreira ;
Figueiredo, Amanda Braga ;
de Barros E Silva, Milton Jose ;
Gollob, Kenneth J. .
IMMUNOTHERAPY ADVANCES, 2022, 2 (01)
[10]   Therapeutic efficacy of ipilimumab, an anti-CTLA-4 monoclonal antibody, in patients with metastatic melanoma unresponsive to prior systemic treatments: clinical and immunological evidence from three patient cases [J].
Di Giacomo, Anna Maria ;
Danielli, Riccardo ;
Guidoboni, Massimo ;
Calabro, Luana ;
Carlucci, Dora ;
Miracco, Clelia ;
Volterrani, Luca ;
Mazzei, Maria Antonietta ;
Biagioli, Maurizio ;
Altomonte, Maresa ;
Maio, Michele .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2009, 58 (08) :1297-1306