Literature DB >> 34196677

Polatuzumab vedotin as a salvage and bridging treatment in relapsed or refractory large B-cell lymphomas.

Nora Liebers1,2, Johannes Duell3, Donnacha Fitzgerald1,4, Andrea Kerkhoff5, Daniel Noerenberg6, Eva Kaebisch6, Fabian Acker7, Stephan Fuhrmann8, Corinna Leng9, Manfred Welslau10, Jens Chemnitz11, Jan-Moritz Middeke12, Thomas Weber13, Udo Holtick14, Ralf Trappe15, Roald Pfannes16, Ruediger Liersch17, Christian Spoer18, Stefan Fuxius19, Niklas Gebauer20, Léandra Caillé1, Thomas Geer21, Christian Koenecke22, Ulrich Keller9, Rainer Claus23, Dimitrios Mougiakakos24, Stephanie Mayer25, Andreas Huettmann26, Christiane Pott27, Arne Trummer28, Gerald Wulf29, Uta Brunnberg7, Lars Bullinger6, Georg Hess30, Carsten Mueller-Tidow1,2, Bertram Glass8, Georg Lenz5, Peter Dreger1, Sascha Dietrich1,2,4.   

Abstract

The antibody-drug conjugate polatuzumab vedotin (pola) has recently been approved in combination with bendamustine and rituximab (pola-BR) for patients with refractory or relapsed (r/r) large B-cell lymphoma (LBCL). To investigate the efficacy of pola-BR in a real-world setting, we retrospectively analyzed 105 patients with LBCL who were treated in 26 German centers under the national compassionate use program. Fifty-four patients received pola as a salvage treatment and 51 patients were treated with pola with the intention to bridge to chimeric antigen receptor (CAR) T-cell therapy (n = 41) or allogeneic hematopoietic cell transplantation (n = 10). Notably, patients in the salvage and bridging cohort had received a median of 3 prior treatment lines. In the salvage cohort, the best overall response rate was 48.1%. The 6-month progression-free survival and overall survival (OS) was 27.7% and 49.6%, respectively. In the bridging cohort, 51.2% of patients could be successfully bridged with pola to the intended CAR T-cell therapy. The combination of pola bridging and successful CAR T-cell therapy resulted in a 6-month OS of 77.9% calculated from pola initiation. Pola vedotin-rituximab without a chemotherapy backbone demonstrated encouraging overall response rates up to 40%, highlighting both an appropriate alternative for patients unsuitable for chemotherapy and a new treatment option for bridging before leukapheresis in patients intended for CAR T-cell therapy. Furthermore, 7 of 12 patients with previous failure of CAR T-cell therapy responded to a pola-containing regimen. These findings suggest that pola may serve as effective salvage and bridging treatment of r/r LBCL patients.
© 2021 by The American Society of Hematology.

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Year:  2021        PMID: 34196677     DOI: 10.1182/bloodadvances.2020004155

Source DB:  PubMed          Journal:  Blood Adv        ISSN: 2473-9529


  7 in total

Review 1.  Preparing for CAR T cell therapy: patient selection, bridging therapies and lymphodepletion.

Authors:  Leila Amini; Sara K Silbert; Nirali N Shah; Mohamed Abou-El-Enein; Shannon L Maude; Loretta J Nastoupil; Carlos A Ramos; Renier J Brentjens; Craig S Sauter
Journal:  Nat Rev Clin Oncol       Date:  2022-03-22       Impact factor: 66.675

Review 2.  CAR T-Cell Therapy Predictive Response Markers in Diffuse Large B-Cell Lymphoma and Therapeutic Options After CART19 Failure.

Authors:  Ana Carolina Caballero; Laura Escribà-Garcia; Carmen Alvarez-Fernández; Javier Briones
Journal:  Front Immunol       Date:  2022-07-06       Impact factor: 8.786

Review 3.  Monoclonal Antibodies in the Treatment of Diffuse Large B-Cell Lymphoma: Moving beyond Rituximab.

Authors:  Sotirios G Papageorgiou; Thomas P Thomopoulos; Athanasios Liaskas; Theodoros P Vassilakopoulos
Journal:  Cancers (Basel)       Date:  2022-04-10       Impact factor: 6.575

Review 4.  Novel Immune-Based treatments for Diffuse Large B-Cell Lymphoma: The Post-CAR T Cell Era.

Authors:  Suheil Albert Atallah-Yunes; Michael J Robertson; Utpal P Davé; Paola Ghione; Fabiana Perna
Journal:  Front Immunol       Date:  2022-06-01       Impact factor: 8.786

5.  Results of a United Kingdom real-world study of polatuzumab vedotin, bendamustine, and rituximab for relapsed/refractory DLBCL.

Authors:  Michael Northend; William Wilson; Wendy Osborne; Christopher P Fox; Andrew J Davies; Dima El-Sharkawi; Elizabeth H Phillips; Hau Wui Sim; Shalal Sadullah; Nimish Shah; Ying Ying Peng; Iman Qureshi; Juanah Addada; Rocio Figueroa Mora; Neil Phillips; Andrea Kuhnl; Elizabeth Davies; David Wrench; Pamela McKay; Indrani Karpha; Anna Cowley; Richard Karim; Sarah Challenor; Vikram Singh; Cathy Burton; Rebecca Auer; Chris Williams; Joel Cunningham; Angus Broom; Anita Arasaretnam; Claire Roddie; Tobias Menne; William Townsend
Journal:  Blood Adv       Date:  2022-05-10

6.  Case Report: Subtotal Lymphoid and Total Marrow Irradiation as Bridge Therapy to CD19-Directed CAR T Cells in a Chemorefractory DLBCL With Leukemic Involvement.

Authors:  Simonetta Saldi; Vincenzo Maria Perriello; Lorenza Falini; Loredana Ruggeri; Christian Fulcheri; Sara Ciardelli; Alessandra Innocente; Stelvio Ballanti; Nicodemo Baffa; Leonardo Flenghi; Antonio Pierini; Cynthia Aristei; Brunangelo Falini
Journal:  Front Immunol       Date:  2022-07-14       Impact factor: 8.786

Review 7.  Combination strategies to optimize the efficacy of chimeric antigen receptor T cell therapy in haematological malignancies.

Authors:  Xinyi Xiao; Yazhuo Wang; Zhengbang Zou; Yufei Yang; Xinyu Wang; Xin Xin; Sanfang Tu; Yuhua Li
Journal:  Front Immunol       Date:  2022-08-23       Impact factor: 8.786

  7 in total

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