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OUTCOME AND PROGNOSTIC FACTORS IN PATIENTS WITH ADVANCED HODGKIN LYMPHOMA WHO REMAIN PET/CT-POSITIVE AFTER 2 CYCLES OF ABVD: REAL-LIFE EXPERIENCE IN A MULTICENTER SETTING IN GREECE.
Author(s): ,
Theodoros Vassilakopoulos
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Phivi Rondogianni
Affiliations:
Department of Nuclear Medicine,'Evangelismos' General Hospital,Athens,Greece
,
Athanasios Liaskas
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Ioannis Assimakopoulos
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Maria Arapaki
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Chrysovalantou Chatzidimitriou
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Ilianna Konstantinou
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Marina Bellia
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Georgios Boutsikas
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Sofia Chatziioannou
Affiliations:
Department of Nuclear Medicine,Biomedical Research Foundation, Academy of Athens,Αθήνα,Greece
,
Maria Moschogianni
Affiliations:
Department of Haematology,Athens Medical Center, Psychikon Branch,Athens,Greece
,
Maria Dimou
Affiliations:
1st Propaedeutic Department of Internal Medicine,'Laikon' General Hospital,Athens,Greece
,
Vassilis Prassopoulos
Affiliations:
Department of Nuclear Medicine,'Hygeia' General Hospital,Athens,Greece
,
Marina Siakantari
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Sotiris Papageorgiou
Affiliations:
2nd Propaedeutic Department of Internal Medicine,'Attikon' General Hospital,Athens,Greece
,
Flora Kondopidou
Affiliations:
2nd Department of Internal Medicine,'Ippokration' General Hospital,Athens,Greece
,
Pantelis Tsirkinidis
Affiliations:
Department of Haematology,401 General Military Hospital,Athens,Greece
,
Dimitris Boutsis
Affiliations:
Department of Haematology, Athens Navy Hospital,Athens,Greece
,
Christos Poziopoulos
Affiliations:
Department of Haematology,Metropolitan Hospital,Athens,Greece
,
Eleftheria Hatzimichael
Affiliations:
Department of Haematology,University of Ioannina,Ioannina,Greece
,
Argyro Koumarianou
Affiliations:
Department of Haematology,Metropolitan Hospital,Athens,Greece
,
Stamatis Karakatsanis
Affiliations:
3rd Department of Internal Medicine,'Sotiria' General Hospital,Athens,Greece
,
Nikolaos Kanellias
Affiliations:
Department of Clinical Therapeutics, National and Kapodistrian University of Athens,'Alexandra' General Hospital,Athens,Greece
,
Theodoros Marinakis
Affiliations:
Department of Haematology,'G.Gennimatas' General Hospital,Athens,Greece
,
Maria Palassopoulou
Affiliations:
Department of Haematology, University of Thessaly,University Hospital of Larissa,Larissa,Greece
,
Emmanouil Spanoudakis
Affiliations:
Department of Haematology, Democritus University of Thrace,University Hospital of Alexandroupolis,Alexandroupolis,Greece
,
Maria Kotsopoulou
Affiliations:
Department of Haematology,'Metaxa' Anticancer Hospital, Piraeus,Greece
,
Dimitra Liapi
Affiliations:
Department of Haematology,'Venizelion' General Hospital,Heraklion,Greece
,
Sotiris Sachanas
Affiliations:
Department of Haematology,Athens Medical Center, Psychikon Branch,Athens,Greece
,
Maria Christina Kyrtsoni
Affiliations:
1st Propaedeutic Department of Internal Medicine,'Laikon' General Hospital,Athens,Greece
,
Eleni Variami
Affiliations:
1st Department of Internal Medicine,'Laikon' General Hospital,Athens,Greece
,
Nora-Athina Vyniou
Affiliations:
1st Department of Internal Medicine,'Laikon' General Hospital,Athens,Greece
,
Xanthi Giakoumi
Affiliations:
Department of Haematology,Athens Medical Center, Psychikon Branch,Athens,Greece
,
Maria Efstathopoulou
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Dimitris Galopoulos
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Ilias Pessach
Affiliations:
1st Propaedeutic Department of Internal Medicine,'Laikon' General Hospital,Athens,Greece
,
Theodoros Iliakis
Affiliations:
1st Propaedeutic Department of Internal Medicine,'Laikon' General Hospital,Athens,Greece
,
Vassilios Pardalis
Affiliations:
1st Propaedeutic Department of Internal Medicine,'Laikon' General Hospital,Athens,Greece
,
Aikaterini Mainda
Affiliations:
Department of Nuclear Medicine,Athens Medical Center,Athens,Greece
,
Meletios-Athanasios Dimopoulos
Affiliations:
Department of Clinical Therapeutics, National and Kapodistrian University of Athens,'Alexandra' General Hospital,Athens,Greece
,
Ioannis Datseris
Affiliations:
Department of Nuclear Medicine,'Evangelismos' General Hospital,Athens,Greece
,
Eleni Plata
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Panagiotis Panagiotidis
Affiliations:
1st Propaedeutic Department of Internal Medicine,'Laikon' General Hospital,Athens,Greece
,
Kostas Konstantopoulos
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
,
Gerasimos Pangalis
Affiliations:
Department of Haematology,Athens Medical Center, Psychikon Branch,Athens,Greece
Maria Angelopoulou
Affiliations:
Department of Haematology and Bone Marrow Transplant Unit, National and Kapodistrian University of Athens,'Laikon' General Hospital,Athens,Greece
EHA Library. Vassilakopoulos T. 06/09/21; 325532; EP774
Assoc. Prof. Theodoros Vassilakopoulos
Assoc. Prof. Theodoros Vassilakopoulos
Contributions
Abstract
Presentation during EHA2021: All e-poster presentations will be made available as of Friday, June 11, 2021 (09:00 CEST) and will be accessible for on-demand viewing until August 15, 2021 on the Virtual Congress platform.

Abstract: EP774

Type: E-Poster Presentation

Session title: Hodgkin lymphoma - Clinical

Background
Positive PET/CT after 2 cycles of ABVD (interim PET, iPET) has a strong adverse prognostic significance in patients with advanced Hodgkin lymphoma (HL), who continue treatment with ABVD. These patients could be successfully salvaged by treatment escalation to BEACOPP, but more “real-life” data are needed in order to predict their outcome. 

Aims
The aim of this study is the evaluation of treatment strategies, patient outcome and potential prognostic factors in iPET positive (iPET+) patients in 15 hematological departments of Greece.

Methods
This is a retrospective study of 282 patients with advanced HL according to GHSG (stages III/IV or IIB with bulky mediastinal and/or extranodal disease), who received 2 cycles of ABVD and underwent PET/CT. iPET was evaluated according to the Deauville 5-point scale score (D5PSS) and scores 4 and 5 were considered positive (residual uptake >liver). In case of PET positivity, further treatment strategy (intensification to BEACOPP or not) was at the treating physician’s discretion, as this study reflects every-day clinical practice. However, consistent strategies have been followed within the same Department. Radiotherapy was also at physician’s discretion. 

Results
iPET was negative in 77% and positive in 23% of patients respectively. 62 out of 65 iPET(+) patients were ≤60 years old and consisted the study population, as they were eligible for treatment intensification. Of these patients, 37 received intensified treatment: 36 with BEACOPP (of whom 31 received BEACOPP-escalated, 2 BEACOPP-14 and 3 BEACOPP-baseline) and 1 with ESHAP. 25 patients continued with ABVD due to individual Department’s treatment strategy (n=18), or, in 7 patients, because of treating physician’s decision or due to misclassification as D5PSS 3. The 5-year progression free survival (PFS) was 53% in the whole population of iPET(+) patients. It was 59% vs 41% for patients who received intensified treatment or continued with ABVD respectively (p=0.09). In Departments which did not follow the treatment intensification strategy the 5-year PFS was 32% for patients who continued with ABVD. Patients who remained iPET(+) with D5PSS 4 had 5-year PFS 60% vs 37%  for patients with D5PSS 5 (p=0.13). Apart from patient’s age, no other potential prognostic factor associated with disease extent or aggressiveness affected the outcome of iPET(+) patients. Surprisingly, patients <45 years old had inferior outcome in univariate analysis. In multivariate analysis, D5PSS 5 (vs 4) was an independent adverse prognostic factor for PFS (HR: 2.789, 95% CI: 1.049-7.416, p=0.04), whereas continuation with ABVD vs treatment intensification was of borderline significance (HR: 2.434, 95% CI: 0.934-6.340, p=0.069).

Conclusion
Our study provides “real-life” data confirming the adverse outcome of iPET(+) patients as well as the remarkable efficacy of treatment intensification with BEACOPP-escalated. Of note, the 5-year PFS almost reached 60% despite the fact that the study included patients with “strictly” advanced-stage disease, without admixing early stages with adverse characteristics. Conventional prognostic factors may be replaced by different scores of iPET positivity. However, larger studies are needed in order to confirm and extend these results in order to draw safe conclusions. 

Keyword(s):

Presentation during EHA2021: All e-poster presentations will be made available as of Friday, June 11, 2021 (09:00 CEST) and will be accessible for on-demand viewing until August 15, 2021 on the Virtual Congress platform.

Abstract: EP774

Type: E-Poster Presentation

Session title: Hodgkin lymphoma - Clinical

Background
Positive PET/CT after 2 cycles of ABVD (interim PET, iPET) has a strong adverse prognostic significance in patients with advanced Hodgkin lymphoma (HL), who continue treatment with ABVD. These patients could be successfully salvaged by treatment escalation to BEACOPP, but more “real-life” data are needed in order to predict their outcome. 

Aims
The aim of this study is the evaluation of treatment strategies, patient outcome and potential prognostic factors in iPET positive (iPET+) patients in 15 hematological departments of Greece.

Methods
This is a retrospective study of 282 patients with advanced HL according to GHSG (stages III/IV or IIB with bulky mediastinal and/or extranodal disease), who received 2 cycles of ABVD and underwent PET/CT. iPET was evaluated according to the Deauville 5-point scale score (D5PSS) and scores 4 and 5 were considered positive (residual uptake >liver). In case of PET positivity, further treatment strategy (intensification to BEACOPP or not) was at the treating physician’s discretion, as this study reflects every-day clinical practice. However, consistent strategies have been followed within the same Department. Radiotherapy was also at physician’s discretion. 

Results
iPET was negative in 77% and positive in 23% of patients respectively. 62 out of 65 iPET(+) patients were ≤60 years old and consisted the study population, as they were eligible for treatment intensification. Of these patients, 37 received intensified treatment: 36 with BEACOPP (of whom 31 received BEACOPP-escalated, 2 BEACOPP-14 and 3 BEACOPP-baseline) and 1 with ESHAP. 25 patients continued with ABVD due to individual Department’s treatment strategy (n=18), or, in 7 patients, because of treating physician’s decision or due to misclassification as D5PSS 3. The 5-year progression free survival (PFS) was 53% in the whole population of iPET(+) patients. It was 59% vs 41% for patients who received intensified treatment or continued with ABVD respectively (p=0.09). In Departments which did not follow the treatment intensification strategy the 5-year PFS was 32% for patients who continued with ABVD. Patients who remained iPET(+) with D5PSS 4 had 5-year PFS 60% vs 37%  for patients with D5PSS 5 (p=0.13). Apart from patient’s age, no other potential prognostic factor associated with disease extent or aggressiveness affected the outcome of iPET(+) patients. Surprisingly, patients <45 years old had inferior outcome in univariate analysis. In multivariate analysis, D5PSS 5 (vs 4) was an independent adverse prognostic factor for PFS (HR: 2.789, 95% CI: 1.049-7.416, p=0.04), whereas continuation with ABVD vs treatment intensification was of borderline significance (HR: 2.434, 95% CI: 0.934-6.340, p=0.069).

Conclusion
Our study provides “real-life” data confirming the adverse outcome of iPET(+) patients as well as the remarkable efficacy of treatment intensification with BEACOPP-escalated. Of note, the 5-year PFS almost reached 60% despite the fact that the study included patients with “strictly” advanced-stage disease, without admixing early stages with adverse characteristics. Conventional prognostic factors may be replaced by different scores of iPET positivity. However, larger studies are needed in order to confirm and extend these results in order to draw safe conclusions. 

Keyword(s):

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