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Positron Emission Tomography-Computed Tomography (PET-CT) After Induction Therapy Is Highly Predictive of Patient Outcome in Follicular Lymphoma: Analysis of PET-CT in a Subset of PRIMA Trial Participants

Identifieur interne : 004520 ( PascalFrancis/Curation ); précédent : 004519; suivant : 004521

Positron Emission Tomography-Computed Tomography (PET-CT) After Induction Therapy Is Highly Predictive of Patient Outcome in Follicular Lymphoma: Analysis of PET-CT in a Subset of PRIMA Trial Participants

Auteurs : Judith Trotman ; Marion Fournier [France] ; Thierry Lamy [France] ; John Francis Seymour [Australie] ; Anne Sonet [France] ; Andrea Janikova [République tchèque] ; Ofer Shpilberg [Israël] ; Emmanuel Gyan [France] ; Hervé Tilly [France] ; Jane Estell ; Cecily Forsyth [Australie] ; Didier Decaudin [France] ; Bettina Fabiani [France] ; Jean Gabarre [France] ; Bruno Salles [France] ; Eric Van Den Neste [Belgique] ; Danielle Canioni [France] ; Etienne Garin [France] ; Michael Fulham [Australie] ; Thierry Vander Borght [France] ; Gilles Salles [France]

Source :

RBID : Pascal:11-0380678

Descripteurs français

English descriptors

Abstract

Purpose The utility of [18F]fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET-CT) in assessing response at the end of induction therapy is well documented in Hodgkin's and diffuse large B-cell lymphomas, but its role in follicular lymphoma (FL) remains undetermined. We investigated the prognostic significance of PET-CT performed after first-line therapy in patients with FL treated in the prospective Primary Rituximab and Maintenance (PRIMA) study. Patients and Methods Results of PET-CT scans performed after induction immunochemotherapy were recorded retrospectively. Patients went on to either observation or rituximab maintenance per protocol independent of the PET-CT result. Patient characteristics and outcomes were then evaluated. Results Of 122 PET-CT scans performed at the end of the induction immunochemotherapy, 32 (26%) were reported as positive by the local investigator. Initial demographic or disease characteristics did not differ between PET-CT-positive (PET-positive) and PET-CT-negative (PET-negative) patients. PET status correlated with conventional response criteria (P<.001). Patients remaining PET positive had a significantly (P< .001) inferior progression-free survival at 42 months of 32.9% (95% CI, 17.2% to 49.5%) compared with 70.7% (95% CI, 59.3% to 79.4%) in those who became PET negative. PET status, but not conventional response (complete response or complete response unconfirmed v partial response) according to IWC 1999, was an independent predictive factor for lymphoma progression. The risk of death was also increased in PET-positive patients (hazard ratio 7.0; P = .0011). Conclusion [18F]FDG PET-CT status at the end of immunochemotherapy induction in patients with FL is strongly predictive of outcome and should be considered a meaningful clinical end point in future studies.
pA  
A01 01  1    @0 0732-183X
A03   1    @0 J. clin. oncol.
A05       @2 29
A06       @2 23
A08 01  1  ENG  @1 Positron Emission Tomography-Computed Tomography (PET-CT) After Induction Therapy Is Highly Predictive of Patient Outcome in Follicular Lymphoma: Analysis of PET-CT in a Subset of PRIMA Trial Participants
A11 01  1    @1 TROTMAN (Judith)
A11 02  1    @1 FOURNIER (Marion)
A11 03  1    @1 LAMY (Thierry)
A11 04  1    @1 SEYMOUR (John Francis)
A11 05  1    @1 SONET (Anne)
A11 06  1    @1 JANIKOVA (Andrea)
A11 07  1    @1 SHPILBERG (Ofer)
A11 08  1    @1 GYAN (Emmanuel)
A11 09  1    @1 TILLY (Hervé)
A11 10  1    @1 ESTELL (Jane)
A11 11  1    @1 FORSYTH (Cecily)
A11 12  1    @1 DECAUDIN (Didier)
A11 13  1    @1 FABIANI (Bettina)
A11 14  1    @1 GABARRE (Jean)
A11 15  1    @1 SALLES (Bruno)
A11 16  1    @1 DEN NESTE (Eric Van)
A11 17  1    @1 CANIONI (Danielle)
A11 18  1    @1 GARIN (Etienne)
A11 19  1    @1 FULHAM (Michael)
A11 20  1    @1 BORGHT (Thierry Vander)
A11 21  1    @1 SALLES (Gilles)
A14 01      @1 Concord Hospital @3 INC @Z 1 aut. @Z 10 aut.
A14 02      @1 Royal Prince Alfred Hospital and Sydney Medical School, University of Sydney @2 Sydney @3 AUS @Z 19 aut.
A14 03      @1 Peter MacCallum Cancer Center and University of Melbourne @2 Melbourne @3 AUS @Z 4 aut.
A14 04      @1 Wyong Hospital @2 Kanwal @3 AUS @Z 11 aut.
A14 05      @1 Hospices Civils de Lyon, Groupe d'Etude des Lymphomes de l'Adulte, Recherche Clinique, Hôpital Lyon sud, Pierre-Benite @3 FRA @Z 2 aut.
A14 06      @1 Centre Hospitalier Universitaire (CHU) de Rennes, L'Institut National de la Sante et de la Recherche Médicale (INSERM) U917, Universite de Rennes @3 FRA @Z 3 aut.
A14 07      @1 CHU de Rennes @2 Rennes @3 FRA @Z 18 aut.
A14 08      @1 CHU de Tours @2 Tours @3 FRA @Z 8 aut.
A14 09      @1 Centre Henri Becquerel, INSERM U918, Universite de Rouen @2 Rouen @3 FRA @Z 9 aut.
A14 10      @1 Institut Curie @3 FRA @Z 12 aut.
A14 11      @1 Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Antoine @3 FRA @Z 13 aut.
A14 12      @1 Hôpital de la Pitie Salpetriere @3 FRA @Z 14 aut.
A14 13      @1 Hôpital Necker @2 Paris @3 FRA @Z 17 aut.
A14 14      @1 Centre Hospitalier @2 Chalons-Saône @3 FRA @Z 15 aut.
A14 15      @1 Hospices Civils de Lyon, Universite Lyon1 @3 FRA @Z 21 aut.
A14 16      @1 Universite Catholique de Louvain (UCL), Mont-Godinne Medical Center @2 Yvoir @3 FRA @Z 5 aut. @Z 20 aut.
A14 17      @1 UCL Saint-Luc @2 Brussels @3 BEL @Z 16 aut.
A14 18      @1 University Hospital Brno @2 Brno @3 CZE @Z 6 aut.
A14 19      @1 Rabin Medical Center @2 Petah-Tikva @3 ISR @Z 7 aut.
A14 20      @1 Tel Aviv University @2 Tel Aviv @3 ISR @Z 7 aut.
A20       @1 3194-3200
A21       @1 2011
A23 01      @0 ENG
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A60       @1 P @3 C
A61       @0 A
A64 01  1    @0 Journal of clinical oncology
A66 01      @0 USA
C01 01    ENG  @0 Purpose The utility of [18F]fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET-CT) in assessing response at the end of induction therapy is well documented in Hodgkin's and diffuse large B-cell lymphomas, but its role in follicular lymphoma (FL) remains undetermined. We investigated the prognostic significance of PET-CT performed after first-line therapy in patients with FL treated in the prospective Primary Rituximab and Maintenance (PRIMA) study. Patients and Methods Results of PET-CT scans performed after induction immunochemotherapy were recorded retrospectively. Patients went on to either observation or rituximab maintenance per protocol independent of the PET-CT result. Patient characteristics and outcomes were then evaluated. Results Of 122 PET-CT scans performed at the end of the induction immunochemotherapy, 32 (26%) were reported as positive by the local investigator. Initial demographic or disease characteristics did not differ between PET-CT-positive (PET-positive) and PET-CT-negative (PET-negative) patients. PET status correlated with conventional response criteria (P<.001). Patients remaining PET positive had a significantly (P< .001) inferior progression-free survival at 42 months of 32.9% (95% CI, 17.2% to 49.5%) compared with 70.7% (95% CI, 59.3% to 79.4%) in those who became PET negative. PET status, but not conventional response (complete response or complete response unconfirmed v partial response) according to IWC 1999, was an independent predictive factor for lymphoma progression. The risk of death was also increased in PET-positive patients (hazard ratio 7.0; P = .0011). Conclusion [18F]FDG PET-CT status at the end of immunochemotherapy induction in patients with FL is strongly predictive of outcome and should be considered a meaningful clinical end point in future studies.
C02 01  X    @0 002B04
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C07 01  X  FRE  @0 Exploration radioisotopique @5 37
C07 01  X  ENG  @0 Radionuclide study @5 37
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N21       @1 262
N44 01      @1 OTO
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Judith Trotman
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Jane Estell
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<title xml:lang="en" level="a">Positron Emission Tomography-Computed Tomography (PET-CT) After Induction Therapy Is Highly Predictive of Patient Outcome in Follicular Lymphoma: Analysis of PET-CT in a Subset of PRIMA Trial Participants</title>
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<name sortKey="Janikova, Andrea" sort="Janikova, Andrea" uniqKey="Janikova A" first="Andrea" last="Janikova">Andrea Janikova</name>
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<author>
<name sortKey="Shpilberg, Ofer" sort="Shpilberg, Ofer" uniqKey="Shpilberg O" first="Ofer" last="Shpilberg">Ofer Shpilberg</name>
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<name sortKey="Estell, Jane" sort="Estell, Jane" uniqKey="Estell J" first="Jane" last="Estell">Jane Estell</name>
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<name sortKey="Forsyth, Cecily" sort="Forsyth, Cecily" uniqKey="Forsyth C" first="Cecily" last="Forsyth">Cecily Forsyth</name>
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<s1>Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Antoine</s1>
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<name sortKey="Den Neste, Eric Van" sort="Den Neste, Eric Van" uniqKey="Den Neste E" first="Eric Van" last="Den Neste">Eric Van Den Neste</name>
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<s1>UCL Saint-Luc</s1>
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<name sortKey="Borght, Thierry Vander" sort="Borght, Thierry Vander" uniqKey="Borght T" first="Thierry Vander" last="Borght">Thierry Vander Borght</name>
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<series>
<title level="j" type="main">Journal of clinical oncology</title>
<title level="j" type="abbreviated">J. clin. oncol.</title>
<idno type="ISSN">0732-183X</idno>
<imprint>
<date when="2011">2011</date>
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<title level="j" type="main">Journal of clinical oncology</title>
<title level="j" type="abbreviated">J. clin. oncol.</title>
<idno type="ISSN">0732-183X</idno>
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<keywords scheme="KwdEn" xml:lang="en">
<term>B cell neoplasm</term>
<term>Cancerology</term>
<term>Clinical trial</term>
<term>Computerized axial tomography</term>
<term>Emission tomography</term>
<term>Follicular lymphoma</term>
<term>Human</term>
<term>Induction treatment</term>
<term>Lymphoid neoplasm</term>
<term>Positron emission tomography</term>
<term>Prognosis</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Tomoscintigraphie</term>
<term>Tomographie par émission de positons</term>
<term>Traitement induction</term>
<term>Tomodensitométrie</term>
<term>Homme</term>
<term>Pronostic</term>
<term>Lymphome folliculaire</term>
<term>Essai clinique</term>
<term>Cancérologie</term>
<term>Hémopathie maligne lymphoïde</term>
<term>Hémopathie lymphoïde B</term>
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<front>
<div type="abstract" xml:lang="en">Purpose The utility of [
<sup>18</sup>
F]fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET-CT) in assessing response at the end of induction therapy is well documented in Hodgkin's and diffuse large B-cell lymphomas, but its role in follicular lymphoma (FL) remains undetermined. We investigated the prognostic significance of PET-CT performed after first-line therapy in patients with FL treated in the prospective Primary Rituximab and Maintenance (PRIMA) study. Patients and Methods Results of PET-CT scans performed after induction immunochemotherapy were recorded retrospectively. Patients went on to either observation or rituximab maintenance per protocol independent of the PET-CT result. Patient characteristics and outcomes were then evaluated. Results Of 122 PET-CT scans performed at the end of the induction immunochemotherapy, 32 (26%) were reported as positive by the local investigator. Initial demographic or disease characteristics did not differ between PET-CT-positive (PET-positive) and PET-CT-negative (PET-negative) patients. PET status correlated with conventional response criteria (P<.001). Patients remaining PET positive had a significantly (P< .001) inferior progression-free survival at 42 months of 32.9% (95% CI, 17.2% to 49.5%) compared with 70.7% (95% CI, 59.3% to 79.4%) in those who became PET negative. PET status, but not conventional response (complete response or complete response unconfirmed v partial response) according to IWC 1999, was an independent predictive factor for lymphoma progression. The risk of death was also increased in PET-positive patients (hazard ratio 7.0; P = .0011). Conclusion [
<sup>18</sup>
F]FDG PET-CT status at the end of immunochemotherapy induction in patients with FL is strongly predictive of outcome and should be considered a meaningful clinical end point in future studies.</div>
</front>
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<s1>Hôpital Necker</s1>
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<sZ>5 aut.</sZ>
<sZ>20 aut.</sZ>
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<s0>Purpose The utility of [
<sup>18</sup>
F]fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET-CT) in assessing response at the end of induction therapy is well documented in Hodgkin's and diffuse large B-cell lymphomas, but its role in follicular lymphoma (FL) remains undetermined. We investigated the prognostic significance of PET-CT performed after first-line therapy in patients with FL treated in the prospective Primary Rituximab and Maintenance (PRIMA) study. Patients and Methods Results of PET-CT scans performed after induction immunochemotherapy were recorded retrospectively. Patients went on to either observation or rituximab maintenance per protocol independent of the PET-CT result. Patient characteristics and outcomes were then evaluated. Results Of 122 PET-CT scans performed at the end of the induction immunochemotherapy, 32 (26%) were reported as positive by the local investigator. Initial demographic or disease characteristics did not differ between PET-CT-positive (PET-positive) and PET-CT-negative (PET-negative) patients. PET status correlated with conventional response criteria (P<.001). Patients remaining PET positive had a significantly (P< .001) inferior progression-free survival at 42 months of 32.9% (95% CI, 17.2% to 49.5%) compared with 70.7% (95% CI, 59.3% to 79.4%) in those who became PET negative. PET status, but not conventional response (complete response or complete response unconfirmed v partial response) according to IWC 1999, was an independent predictive factor for lymphoma progression. The risk of death was also increased in PET-positive patients (hazard ratio 7.0; P = .0011). Conclusion [
<sup>18</sup>
F]FDG PET-CT status at the end of immunochemotherapy induction in patients with FL is strongly predictive of outcome and should be considered a meaningful clinical end point in future studies.</s0>
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<s0>002B19B</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Tomoscintigraphie</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Emission tomography</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Tomocentelleografía</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Tomographie par émission de positons</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Positron emission tomography</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Tomografía emisión positrones</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Traitement induction</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Induction treatment</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Tratamiento inductivo</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Tomodensitométrie</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Computerized axial tomography</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Tomodensitometría</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Homme</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Human</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Pronostic</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Prognosis</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Pronóstico</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Lymphome folliculaire</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Follicular lymphoma</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Linfoma folicular</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Essai clinique</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Clinical trial</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Ensayo clínico</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Cancérologie</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Cancerology</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Cancerología</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Hémopathie maligne lymphoïde</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Lymphoid neoplasm</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Hémopathie lymphoïde B</s0>
<s4>CD</s4>
<s5>97</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>B cell neoplasm</s0>
<s4>CD</s4>
<s5>97</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Exploration radioisotopique</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Radionuclide study</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Exploración radioisotópica</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Imagerie médicale</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Medical imagery</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Imaginería médica</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Radiodiagnostic</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Radiodiagnosis</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Radiodiagnóstico</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Hémopathie maligne</s0>
<s2>NM</s2>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Malignant hemopathy</s0>
<s2>NM</s2>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Hemopatía maligna</s0>
<s2>NM</s2>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Cancer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Cancer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Cáncer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Lymphome non hodgkinien</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Non Hodgkin lymphoma</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Linfoma no Hodgkin</s0>
<s5>41</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Syndrome lymphoprolifératif</s0>
<s2>NM</s2>
<s5>42</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Lymphoproliferative syndrome</s0>
<s2>NM</s2>
<s5>42</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Linfoproliferativo síndrome</s0>
<s2>NM</s2>
<s5>42</s5>
</fC07>
<fN21>
<s1>262</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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