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Real-life experience with the combination of polatuzumab vedotin, rituximab, and bendamustine in aggressive B-cell lymphomas.
Dimou, Maria; Papageorgiou, Sotirios G; Stavroyianni, Niki; Katodritou, Eirini; Tsirogianni, Maria; Kalpadakis, Christina; Banti, Anastasia; Arapaki, Maria; Iliakis, Theodoros; Bouzani, Maria; Verrou, Eugenia; Spanoudakis, Emmanouil; Giannouli, Stavroula; Marinakis, Theodoros; Mandala, Evdokia; Mparmparousi, Despoina; Sachanas, Sotirios; Dalekou-Tsolakou, Maria; Hatzimichael, Eleftheria; Vadikolia, Chryssa; Violaki, Vasiliki; Poziopoulos, Christos; Tsirkinidis, Pantelis; Chatzileontiadou, Sofia; Vervessou, Elissavet; Ximeri, Maria; Sioni, Anastasia; Konstantinidou, Pavlina; Kyrtsonis, Marie-Christine; Siakantaris, Marina P; Angelopoulou, Maria K; Pappa, Vassiliki; Konstantopoulos, Kostas; Panayiotidis, Panayiotis; Vassilakopoulos, Theodoros P.
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  • Dimou M; First Department of Internal Medicine, Propaedeutic, Haematology Clinical Trial Unit, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Papageorgiou SG; Second Department of Internal Medicine, Propaedeutic, Hematology Unit, University General Hospital "Attikon", National and Kapodistrian University of Athens, Athens, Greece.
  • Stavroyianni N; Department of Hematology, Papanikolaou Hospital, Thessaloniki, Greece.
  • Katodritou E; Department of Hematology, Theagenion Cancer Hospital, Thessaloniki, Greece.
  • Tsirogianni M; Department of Hematology, Aghios Savvas Anticancer Hospital, Athens, Greece.
  • Kalpadakis C; Department of Hematology, University of Crete, Iraklion, Crete, Greece.
  • Banti A; Hematology Department, Papageorgiou Hospital, Thessaloniki, Greece.
  • Arapaki M; Department of Haematology and Bone Marrow Transplantation, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Iliakis T; First Department of Internal Medicine, Propaedeutic, Haematology Clinical Trial Unit, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Bouzani M; Department of Hematology and Lymphoma, Evangelismos General Hospital, Athens, Greece.
  • Verrou E; Department of Hematology, Theagenion Cancer Hospital, Thessaloniki, Greece.
  • Spanoudakis E; Department of Hematology, Democritus University of Trace, Alexandroupolis, Greece.
  • Giannouli S; Second Department of Internal Medicine, Ippokrateion General Hospital, Athens, Greece.
  • Marinakis T; Department of Clinical Hematology, "G. Gennimatas" General Hospital, Athens, Greece.
  • Mandala E; Forth Department of Medicine, Faculty of Medicine, Aristotle University of Thessaloniki, Hippokration Hospital, Thessaloniki, Greece.
  • Mparmparousi D; Department of Therapeutics, National and Kapodistrian University of Athens, Alexandra Hospital, Athens, Greece.
  • Sachanas S; Department of Hematology, Athens Medical Center, Athens, Greece.
  • Dalekou-Tsolakou M; General Hospital of Kalamata, Kalamata, Greece.
  • Hatzimichael E; Department of Hematology, Faculty of Medicine, School of Health Sciences, University of Ioannina, Ioannina, Greece.
  • Vadikolia C; Department of Hematology, 424 Army Hospital, Thessaloniki, Greece.
  • Violaki V; Department of Hematology, Chania General Hospital, Chania, Greece.
  • Poziopoulos C; Department of Hematology, Metropolitan Hospital, N. Faliron, Athens, Greece.
  • Tsirkinidis P; Department of Hematology, 401 Army Hospital, Athens, Greece.
  • Chatzileontiadou S; Hematology Unit, 1st Department of Internal Medicine, Aristotle University of Thessaloniki, AHEPA Hospital, Thessaloniki, Greece.
  • Vervessou E; Department of Hematology, Henry Dynant Hospital, Athens, Greece.
  • Ximeri M; Department of Hematology, University of Crete, Iraklion, Crete, Greece.
  • Sioni A; Department of Hematology, Aghios Savvas Anticancer Hospital, Athens, Greece.
  • Konstantinidou P; Department of Hematology, Theagenion Cancer Hospital, Thessaloniki, Greece.
  • Kyrtsonis MC; First Department of Internal Medicine, Propaedeutic, Haematology Clinical Trial Unit, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Siakantaris MP; Department of Haematology and Bone Marrow Transplantation, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Angelopoulou MK; Department of Haematology and Bone Marrow Transplantation, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Pappa V; Second Department of Internal Medicine, Propaedeutic, Hematology Unit, University General Hospital "Attikon", National and Kapodistrian University of Athens, Athens, Greece.
  • Konstantopoulos K; Department of Haematology and Bone Marrow Transplantation, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Panayiotidis P; First Department of Internal Medicine, Propaedeutic, Haematology Clinical Trial Unit, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
  • Vassilakopoulos TP; Department of Haematology and Bone Marrow Transplantation, Laikon General Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Hematol Oncol ; 39(3): 336-348, 2021 Aug.
Article en En | MEDLINE | ID: mdl-33583077
ABSTRACT
Transplant-ineligible relapsed/refractory (rr) diffuse large B-cell lymphoma (DLBCL) patients represent an unmet medical need. Polatuzumab vedotin (Pola), an anti-CD79b antibody-drug-conjugate (ADG), with bendamustine- rituximab(BR) has recently gained approval for these patients, both in the USA and Europe, based on the GO29365 phase IIb trial. Real-life data with Pola are extremely limited. We report the outcomes of 61 Greek patients, who received Pola-(B)R mainly within a compassionate use program. Treatment was given for up to six 21-day cycles. Bendamustine was omitted in three cases due to previous short-lived responses. Fourty-nine rrDLBCL(efficacy cohort-EC) and 58 rr aggressive B-NHL (safety cohort-SC) patients received at least 1 Pola-BR cycle. Twenty-one (43%) patients of the EC responded with 12/49 (25%) CR and 9/49 (18%) PR as best response. Median progression-free survival, overall survival and duration of response were 4.0, 8.5, and 8.5 months respectively, while 55% of patients experienced a grade ≥3 adverse event, mainly hematologic. Treatment discontinuations and death during treatment were mainly due to disease progression. Twenty-two (41%) patients received further treatment; 11/22 are still alive, including one after CAR-T cells, and two after stem cell transplantation. Our data confirm that Pola-BR is a promising treatment for rrDLBCL patients, inducing an adequate response rate with acceptable toxicity. Pola-BR could be used as bridging therapy before further consolidative treatments.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma de Células B Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma de Células B Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Año: 2021 Tipo del documento: Article