Abstract:Peripheral T-cell lymphoma (PTCL) is a heterogeneous group of aggressive non-Hodgkin lymphomas with poor outcomes on current therapy. We investigated whether response assessed with PET/CT combined with baseline total metabolic tumor volume (TMTV) could detect early relapse or refractory disease. From 7 European centers, 140 patients with nodal PTCL who underwent baseline PET/CT were selected. Forty-three had interim PET (iPET) performed after 2 cycles (iPET2), 95 had iPET performed after 3 or 4 cycles (iPET3/4… Show more
“…Additionally, the use of SUV metrics as prognostic factors when pooling data from several PET systems would be affected by reconstruction inconsistencies. Finally, the delineation of metabolically active tumor volume, which is increasingly being used as a prognosticator in lymphoma patients (19,20), is strongly affected by the use of advanced reconstruction algorithms (21). For these reasons, it seems preferable to pursue ongoing harmonization efforts with programs such as EARL or QIBA.…”
When evaluating F-FDG PET images with the Deauville score (DS), the quantification of tumor and reference organs limits the problem of optical misinterpretation. Compared with conventional reconstruction algorithms, point-spread function (PSF) modeling increases SUVs significantly in tumors but only moderately in the liver, which could affect the DS. We investigated whether the choice of the reconstruction algorithm affects the DS and whether discordance affects the capability ofF-FDG PET to stratify lymphoma patients. Overall, 126 patients with diffuse large B-cell lymphoma were included (56 female and 70 male; median age, 65 y; range, 20-88 y). PET data were reconstructed with the unfiltered PSF method. Additionally, a 6-mm filter was applied to PSF images to meet the requirements of the EANM Research Ltd. (EARL) harmonization program from the European Association of Nuclear Medicine (EANM) (PSF). One hundred interim PET (i-PET) and 95 end-of-treatment PET (EoT-PET) studies were analyzed. SUV in the liver and aorta was determined using automatic volumes of interest and compared with SUV in the residual mass with the highest F-FDG uptake. For i-PET, using PSF and PSF, we classified patients as responders and nonresponders in 60 and 40 cases versus 63 and 37 cases, respectively. Five cases of major discordance (5.0%) occurred (i.e., changes from responder to nonresponder). For Eot-PET, patients were classified using PSF and PSF as responders and nonresponders in 69 and 26 cases versus 72 and 23 cases, respectively. Three cases of major discordance (3.2%) occurred. Concordance (Cohen unweighted κ) between the PSF and the PSF DS was 0.82 (95% confidence interval, 0.73-0.91) for i-PET and 0.89 (95% confidence interval, 0.81-0.96) for EoT-PET. The median follow-up periods were 28.4 and 27.4 mo for i-PET and EoT-PET, respectively. Kaplan-Meier analysis showed statistically significant differences in progression-free survival and overall survival among responders and nonresponders no matter which reconstruction was used for i-PET and EoT-PET. Neither DS nor risk stratification of diffuse large B-cell lymphoma patients is affected by the choice of PET reconstruction. Specifically, the use of PSF is not an issue in routine clinical processes or in multicenter trials. These findings have to be confirmed in escalation and deescalation procedures based on early i-PET.
“…Additionally, the use of SUV metrics as prognostic factors when pooling data from several PET systems would be affected by reconstruction inconsistencies. Finally, the delineation of metabolically active tumor volume, which is increasingly being used as a prognosticator in lymphoma patients (19,20), is strongly affected by the use of advanced reconstruction algorithms (21). For these reasons, it seems preferable to pursue ongoing harmonization efforts with programs such as EARL or QIBA.…”
When evaluating F-FDG PET images with the Deauville score (DS), the quantification of tumor and reference organs limits the problem of optical misinterpretation. Compared with conventional reconstruction algorithms, point-spread function (PSF) modeling increases SUVs significantly in tumors but only moderately in the liver, which could affect the DS. We investigated whether the choice of the reconstruction algorithm affects the DS and whether discordance affects the capability ofF-FDG PET to stratify lymphoma patients. Overall, 126 patients with diffuse large B-cell lymphoma were included (56 female and 70 male; median age, 65 y; range, 20-88 y). PET data were reconstructed with the unfiltered PSF method. Additionally, a 6-mm filter was applied to PSF images to meet the requirements of the EANM Research Ltd. (EARL) harmonization program from the European Association of Nuclear Medicine (EANM) (PSF). One hundred interim PET (i-PET) and 95 end-of-treatment PET (EoT-PET) studies were analyzed. SUV in the liver and aorta was determined using automatic volumes of interest and compared with SUV in the residual mass with the highest F-FDG uptake. For i-PET, using PSF and PSF, we classified patients as responders and nonresponders in 60 and 40 cases versus 63 and 37 cases, respectively. Five cases of major discordance (5.0%) occurred (i.e., changes from responder to nonresponder). For Eot-PET, patients were classified using PSF and PSF as responders and nonresponders in 69 and 26 cases versus 72 and 23 cases, respectively. Three cases of major discordance (3.2%) occurred. Concordance (Cohen unweighted κ) between the PSF and the PSF DS was 0.82 (95% confidence interval, 0.73-0.91) for i-PET and 0.89 (95% confidence interval, 0.81-0.96) for EoT-PET. The median follow-up periods were 28.4 and 27.4 mo for i-PET and EoT-PET, respectively. Kaplan-Meier analysis showed statistically significant differences in progression-free survival and overall survival among responders and nonresponders no matter which reconstruction was used for i-PET and EoT-PET. Neither DS nor risk stratification of diffuse large B-cell lymphoma patients is affected by the choice of PET reconstruction. Specifically, the use of PSF is not an issue in routine clinical processes or in multicenter trials. These findings have to be confirmed in escalation and deescalation procedures based on early i-PET.
“…Eine zunehmende Anzahl von Studien berichtet von der prognostischen Aussagekraft prätherapeutischer oder (seltener) Interim-Response (semi)quantitativer [18F]FDG-PET-Parameter, welche neben SUV-Werten auch metabolisches Tumorvolumen (MTV) und totale Glykolyse im Lymphomgewebe (TLG, Produkt aus MTV und mittlerem SUV) umfassen. Die bisherigen Ergebnisse lassen auf eine Anwendbarkeit über ein breites Spektrum verschiedener Lymphomsubtypen schließen, welches u. a. Hodgkin-Lymphome, DLBCL, follikuläre Lymphome, MALT-Lymphome und T-Zell-Lymphome umfasst [32][33][34][35][36][37]. Diese prognostische Aussagekraft, welche in den meisten Fällen auf die Vorhersage des progressionsfreien Überlebens (PFS, "progression-free survival") oder Gesamtüberlebens (OS, "overall survival") abzielt, ließ sich für Patienten unter verschiedenen Therapien nachweisen.…”
Section: Quantitative Parameter Und Prognostikunclassified
Lymphome: KlassifikationLymphome bilden eine heterogene Gruppe maligner Tumoren, welche der noch umfangreicheren Gruppe der hämatoonkologischen Erkrankungen zugeordnet werden kann. Mit 48 % der jährlichen Neuerkrankungen liegen Lymphome innerhalb dieser Gruppe klar vor Leukämien (35 %) und Myelomen (18 %) [1]. Unverändert gebräuchlich ist die Unterscheidung in Hodgkin-Lymphome (HL) und Non-Hodgkin-Lymphome (NHL), zumal sich HL nicht nur histologisch von der NHL-Gruppe unterscheiden, sondern auch hinsichtlich des klinischen Verlaufs und der sehr guten Prognose unter Standard-Chemotherapie. Innerhalb der NHL-Gruppe wird einerseits histologisch zwischen den häufigeren B-Zell-Lymphomen (ca. 85 %) und den selteneren T-und NK("natural killer")-Zell-Lymphomen (ca. 15 %) unterschieden, anderseits -und für die Hybridbildgebung von größerer Relevanz -auf Basis der REAL-Klassifikation grob zwischen schnell wachsenden aggressiven Lymphomen und langsam wachsenden, allerdings unheilbaren, indolenten Lymphomen [2]. Das häufigste aggressive Lymphom stellt dabei das diffuse großzellige B-Zell-Lymphom (DLBCL) mit 33 % aller NHL dar, das häufigste indolente Lymphom das follikuläre Lymphom mit 25 % aller NHL. Neben diesen beiden Hauptvertretern, welche den B-Zell-Lymphomen zugeordnet werden, werden hinsichtlich der Inzidenz (mit 5-10 % der NHL) auch folgende Subtypen häufiger angetroffen: die Marginalzonenlymphome (10 % aller NHL, mit dem MALT-Lymphom als häufigster Variante); das Mantelzelllym-Korrespondenzadresse Assoc. Prof. PD Dr.
“…Notably, many previous studies have also shown that pretherapeutic SUVs, metabolic tumor volumes (MTV), and total lesion glycolysis (TLG) extracted from [ 18 F]FDG‐PET enable outcome prognostication in a variety of histological subtypes, including HL, DLBCL, FL, and also T‐cell lymphomas . In addition, [ 18 F]FDG‐PET has also been evaluated as a tool for risk stratification in clinical trials, and several studies to investigate this topic are still ongoing.…”
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