Brentuximab vedotin consolidation after autologous stem cell transplantation for Hodgkin lymphoma: A Fondazione Italiana Linfomi real-life experience.


Journal

Hematological oncology
ISSN: 1099-1069
Titre abrégé: Hematol Oncol
Pays: England
ID NLM: 8307268

Informations de publication

Date de publication:
Feb 2022
Historique:
revised: 17 10 2021
received: 31 08 2021
accepted: 18 10 2021
pubmed: 26 10 2021
medline: 15 2 2022
entrez: 25 10 2021
Statut: ppublish

Résumé

The standard management for relapsed or refractory classical Hodgkin lymphoma (cHL) is salvage therapy followed by autologous stem cell transplantation (ASCT). This strategy allows almost 50% of patients to be cured. Post-ASCT maintenance treatment with brentuximab vedotin (BV) confers improved progression-free survival (PFS) to cHL patients at high risk of relapse. We investigated the outcome of 105 cHL patients receiving post-ASCT BV maintenance in the real-life setting of 23 Italian hematology centers. This population included naïve patients and those previously exposed to BV. Median follow-up was 20 months. Patients presented a median of two lines of treatment pre-ASCT, with 51% receiving BV. Twenty-nine percent of patients had at least two high-risk factors (refractory disease, complete response [CR] less than 12 months, extranodal disease at relapse), while 16% presented none. At PET-CT, a Deauville score (DS) of 1-3 was reported in 75% and 78% of pre- and post-ASCT evaluations, respectively. Grade 3-4 adverse events (AEs), mainly peripheral neuropathy, were observed in 16% of patients. Three-year PFS and overall survival (OS) were 62% and 86%, respectively. According to BV exposure, 3-year PFS and OS were 54% and 71%, respectively, for naïve and 77% and 96%, respectively, for previously exposed patients. Refractory disease (hazard ratio [HR] 4.46; p = 0.003) and post-ASCT DS 4-5 (HR 3.14; p = 0.005) were the only two factors significantly associated with PFS reduction in multivariable analysis. Post-ASCT BV maintenance is an effective, safe treatment option for cHL naïve patients and those previously exposed to BV.

Identifiants

pubmed: 34694649
doi: 10.1002/hon.2939
pmc: PMC9298220
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
Brentuximab Vedotin 7XL5ISS668

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

31-39

Subventions

Organisme : Takeda

Informations de copyright

© 2021 The Authors. Hematological Oncology published by John Wiley & Sons Ltd.

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Auteurs

Fulvio Massaro (F)

PhD Program in Clinical and Experimental Medicine, University of Modena and Reggio Emilia, Modena, Italy.
Hematology Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Vincenzo Pavone (V)

Department of Hematology and Bone Marrow Transplant, Hospital Card. G. Panico, Tricase, Italy.

Piero Maria Stefani (PM)

Hematology Unit, General Hospital Ca' Foncello, Treviso, Italy.

Barbara Botto (B)

Division of Hematology, Città della Salute e della Scienza Hospital and University, Torino, Italy.

Alessandro Pulsoni (A)

Department of Translational and Precision Medicine, Sapienza University, Rome, Italy.

Caterina Patti (C)

Division of Onco-Hematology, Azienda Villa Sofia-Cervello, Palermo, Italy.

Maria Cantonetti (M)

Unit of Lymphoproliferative Disorders, Policlinico Tor Vergata, Rome, Italy.

Andrea Visentin (A)

Hematology and Clinical Immunology Unit, Department of Medicine (DIMED), University of Padua, Padua, Italy.

Potito Rosario Scalzulli (PR)

Department of Hematology, Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.

Andrea Rossi (A)

Hematology, Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.

Sara Galimberti (S)

Division of Hematology, Department of Clinical and Experimental Medicine, University of Pisa, Italy.

Michele Cimminiello (M)

Hematology, San Carlo Hospital, Potenza, Italy.

Guido Gini (G)

Division of Hematology, Azienda Ospedaliera Universitaria Ospedali Riuniti, Ancona, Italy.

Maurizio Musso (M)

Department of Oncology, Hematology and BMT Unit, Casa di Cura La Maddalena, Palermo, Italy.

Marco Sorio (M)

Department of Clinical and Experimental Medicine, Hematology and Bone Marrow Transplant Unit, University of Verona, Verona, Italy.

Annalisa Arcari (A)

Hematology Unit, Ospedale Guglielmo da Saliceto, Piacenza, Italy.

Vittorio Ruggero Zilioli (VR)

Division of Hematology, ASST Grande Ospedale Metropolitano Niguarda, Milano, Italy.

Mario Luppi (M)

Department of Medical and Surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Donato Mannina (D)

Unit of Haematology, Azienda Ospedaliera Papardo, Messina, Italy.

Alberto Fabbri (A)

Hematology, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.

Giuseppe Pietrantuono (G)

Hematology and Stem Cell Transplantation Unit, IRCCS Centro di Riferimento Oncologico della Basilicata, Rionero in Vulture, Italy.

Ombretta Annibali (O)

Unit of Haematology and Stem Cell Transplantation, Campus Bio-Medico University, Rome, Italy.

Agostino Tafuri (A)

Department of Clinical and Molecular Medicine and Hematology, Sant'Andrea - University Hospital - Sapienza, University of Rome, Rome, Italy.

Eleonora Prete (E)

Department of Hematology and Bone Marrow Transplant, Hospital Card. G. Panico, Tricase, Italy.

Antonino Mulè (A)

Division of Onco-Hematology, Azienda Villa Sofia-Cervello, Palermo, Italy.

Elisa Barbolini (E)

Gruppo Amici dell'Ematologia GRADE-Onlus Foundation, Reggio Emilia, Italy.

Luigi Marcheselli (L)

Fondazione Italiana Linfomi Onlus, Modena, Italy.

Stefano Luminari (S)

Hematology Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Francesco Merli (F)

Hematology Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

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